WO2017123657A1 - Cyclic dinucleotides for treating conditions associated with sting activity such as cancer - Google Patents

Cyclic dinucleotides for treating conditions associated with sting activity such as cancer Download PDF

Info

Publication number
WO2017123657A1
WO2017123657A1 PCT/US2017/013049 US2017013049W WO2017123657A1 WO 2017123657 A1 WO2017123657 A1 WO 2017123657A1 US 2017013049 W US2017013049 W US 2017013049W WO 2017123657 A1 WO2017123657 A1 WO 2017123657A1
Authority
WO
WIPO (PCT)
Prior art keywords
compound
cancer
alkyl
independently selected
group
Prior art date
Application number
PCT/US2017/013049
Other languages
French (fr)
Inventor
Gary Glick
Shomir Ghosh
Edward James Olhava
William R. Roush
Roger Jones
Original Assignee
Gary Glick
Shomir Ghosh
Edward James Olhava
Roush William R
Roger Jones
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gary Glick, Shomir Ghosh, Edward James Olhava, Roush William R, Roger Jones filed Critical Gary Glick
Priority to US16/069,201 priority Critical patent/US10723756B2/en
Publication of WO2017123657A1 publication Critical patent/WO2017123657A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7084—Compounds having two nucleosides or nucleotides, e.g. nicotinamide-adenine dinucleotide, flavine-adenine dinucleotide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Definitions

  • This disclosure features chemical entities (e.g., a compound that modulates (e.g., agonizes) Stimulator of Interferon Genes (STING), or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that are useful, e.g., for treating a condition, disease or disorder in which a decrease or increase in STING activity (e.g., a decrease, e.g., a condition, disease or disorder associated with repressed or impaired STING signaling) contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human).
  • This disclosure also features compositions as well as other methods of using and making the same.
  • STING also known as transmembrane protein 173 (TMEM173) and MPYS/MITA/ERIS, is a protein that in humans is encoded by the TMEM173 gene. STING has been shown to play a role in innate immunity. STING induces type I interferon production when cells are infected with intracellular pathogens, such as viruses, mycobacteria and intracellular parasites. Type I interferon, mediated by STING, protects infected cells and nearby cells from local infection in an autocrine and paracrine manner. The STING pathway is a pathway that is involved in the detection of cytosolic DNA.
  • the STING signaling pathway is activated by cyclic dinucleotides (CDNs), which may be produced by bacteria or produced by antigen presenting cells in response to sensing cytosolic DNA.
  • CDNs cyclic dinucleotides
  • Unmodified CDNs have been shown to induce type I interferon and other co-regulated genes, which in turn facilitate the development of a specific immune response (see, e.g., Wu and Sun, et al., Science 2013, 339, 826-830).
  • WO 2015/077354 discloses the use of STING agonists for the treatment of cancer.
  • This disclosure features chemical entities (e.g., a compound that modulates (e.g., agonizes) Stimulator of Interferon Genes (STING), or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that are useful, e.g., for treating a condition, disease or disorder in which a decrease or increase in STING activity (e.g., a decrease, e.g., a condition, disease or disorder associated with repressed or impaired STING signaling) contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human).
  • a compound that modulates e.g., agonizes
  • STING Stimulator of Interferon Genes
  • a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound e.g., for treating a
  • the chemical entities described herein induce an immune response in a subject (e.g., a human). In certain embodiments, the chemical entities described herein induce STING-dependent type I interferon production in a subject (e.g., a human).
  • An "agonist" of STING includes compounds that, at the protein level, directly bind or modify STING such that an activity of STING is increased, e.g., by activation, stabilization, altered distribution, or otherwise.
  • Certain compounds described herein that agonize STING to a lesser extent than a STING full agonist can function in assays as antagonists as well as agonists. These compounds antagonize activation of STING by a STING full agonist because they prevent the full effect of STING interaction. However, the compounds also, on their own, activate some STING activity, typically less than a corresponding amount of the STING full agonist. Such compounds may be referred to as "partial agonists of STING".
  • the compounds described herein are agonists (e.g. full agonists) of STING.
  • the compounds described herein are partial agonists of STING.
  • a receptor exists in an active (Ra) and an inactive (Ri) conformation.
  • Certain compounds that affect the receptor can alter the ratio of Ra to Ri (Ra/Ri).
  • a full agonist increases the ratio of Ra/Ri and can cause a "maximal", saturating effect.
  • a partial agonist when bound to the receptor, gives a response that is lower than that elicited by a full agonist (e.g., an endogenous agonist).
  • the Ra/Ri for a partial agonist is less than for a full agonist.
  • the potency of a partial agonist may be greater or less than that of the full agonist.
  • the partial agonists of STING described herein provide advantages with regard to treating the disorders described herein.
  • the partial agonists of STING described herein exhibit intrinsic activities that are expected to be both (i) high enough to induce an anti-tumor response (i.e., kill one or more tumor cells) and (ii) low enough to reduce the likelihood of producing toxicity-related side effects.
  • partial agonists can antagonize activation of STING by a STING full agonist because they prevent the full effect of STING interaction, thereby reducing the activity of the STING full agonist.
  • this antagonism can also modulate (e.g., reduce) the toxicity profile of the STING full agonist. Accordingly, this disclosure contemplates methods in which the partial agonists of STING described herein are combined with one (or more) full agonists of STING (e.g., as described anywhere herein) to provide therapeutic drug combinations that are both efficacious and exhibit relatively low toxicity.
  • compounds of Formula A, or a pharmaceutically acceptable salt thereof are featured:
  • X 1 and X 5 can each be independently“up” or“down.”
  • compounds of Formula B, or a pharmaceutically acceptable salt thereof are featured:
  • A, B, X, X’, G 1 , G 2 , X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , L 1 , L 2 , R 1A , R 1B , R 2A , and R2B can be as defined anywhere herein.
  • X 1 and X 5 can each be independently“up” or “down.”
  • A, B, X, X’, G 1 , G 2 , X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , L 1 , L 2 , R1A, R1B, R2A, and R2B can be as defined anywhere herein.
  • compounds of Formula A’, or a pharmaceutically acceptable salt thereof are featured:
  • A, B, X, X’, X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , L 1 , L 2 , R 1A , R 1B , R 2A , and R 2B can be as defined anywhere herein.
  • X 1 and X 5 can each be independently“up” or“down.”
  • X 1 and X 5 can each be independently“up” or“down.”
  • compounds of Formula I-A, or a pharmaceutically acceptable salt thereof are featured:
  • compositions are featured that include a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same) and one or more pharmaceutically acceptable excipients.
  • methods for modulating (e.g., agonizing) STING activity include contacting STING with a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
  • a chemical entity described herein e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same.
  • Methods include in vitro methods, e.g., contacting a sample that includes one or more cells comprising STING (e.g., innate immune cells, e.g., mast cells, macrophages, dendritic cells (DCs), and natural killer cells) with the chemical entity.
  • STING e.g., innate immune cells, e.g., mast cells, macrophages, dendritic cells (DCs), and natural killer cells
  • the contacting can, in some cases, induce an immune response sufficient to kill at least one of the one or more cancer cells.
  • Methods can also include in vivo methods; e.g., administering the chemical entity to a subject (e.g., a human) having a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease (e.g., cancer; e.g., a refractory cancer).
  • a subject e.g., a human
  • methods of treating cancer include administering to a subject in need of such treatment an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
  • methods of inducing an immune response e.g., an innate immune response
  • an immune response e.g., an innate immune response
  • methods of inducing an immune response include administering to the subject an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
  • a chemical entity described herein e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same.
  • methods of inducing induce STING-dependent type I interferon production in a subject in need thereof include administering to the subject an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
  • a chemical entity described herein e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same.
  • methods of treatment of a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease include administering to a subject in need of such treatment an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
  • a chemical entity described herein e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same.
  • methods of treatment include administering to a subject having a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
  • a chemical entity described herein e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same.
  • methods of treatment that include administering to a subject a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same), wherein the chemical entity is administered in an amount effective to treat a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease, thereby treating the disease.
  • a chemical entity described herein e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same
  • Embodiments can include one or more of the following features.
  • the chemical entity can be administered in combination with one or more additional cancer therapies (e.g., surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy or gene therapy, or a combination thereof; e.g., chemotherapy that includes administering one or more (e.g., two, three, four, five, six, or more) additional chemotherapeutic agents.
  • additional cancer therapies e.g., surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy or gene therapy, or a combination thereof; e.g., chemotherapy that includes administering one or more (e.g., two, three, four, five, six, or more) additional chemotherapeutic agents.
  • Non-limiting examples of additional chemotherapeutic agents is selected from an alkylating agent (e.g., cisplatin, carboplatin, mechlorethamine, cyclophosphamide, chlorambucil, ifosfamide and/or oxaliplatin); an anti-metabolite (e.g.,azathioprine and/or mercaptopurine); a terpenoid (e.g., a vinca alkaloid and/or a taxane; e.g., Vincristine, Vinblastine, Vinorelbine and/or Vindesine Taxol, Pacllitaxel and/or Docetaxel); a topoisomerase (e.g., a type I topoisomerase and/or a type 2 topoisomerase; e.g., camptothecins, such as irinotecan and/or topotecan;.
  • an alkylating agent e.g.,
  • Non-limiting examples of cancer include melanoma, cervical cancer, breast cancer, ovarian cancer, prostate cancer, testicular cancer, urothelial carcinoma, bladder cancer, non-small cell lung cancer, small cell lung cancer, sarcoma, colorectal adenocarcinoma, gastrointestinal stromal tumors, gastroesophageal carcinoma, colorectal cancer, pancreatic cancer, kidney cancer, hepatocellular cancer, malignant mesothelioma, leukemia, lymphoma, myelodysplasia syndrome, multiple myeloma, transitional cell carcinoma, neuroblastoma, plasma cell neoplasms, Wilm's tumor, or hepatocellular carcinoma.
  • the cancer can be a refractory cancer.
  • the chemical entity can be administered intratumorally.
  • the methods can further include identifying the subject.
  • the term“STING” is meant to include, without limitation, nucleic acids, polynucleotides, oligonucleotides, sense and antisense polynucleotide strands, complementary sequences, peptides, polypeptides, proteins, homologous and/or orthologous STING molecules, isoforms, precursors, mutants, variants, derivatives, splice variants, alleles, different species, and active fragments thereof.
  • the term“acceptable” with respect to a formulation, composition or ingredient, as used herein, means having no persistent detrimental effect on the general health of the subject being treated.
  • API refers to an active pharmaceutical ingredient.
  • an effective amount or“therapeutically effective amount,” as used herein, refer to a sufficient amount of a chemical entity (e.g., a compound exhibiting activity as a mitochondrial uncoupling agent or a pharmaceutically acceptable salt and/or hydrate and/or cocrystal thereof; e.g., a compound, such as niclosamide or a pharmaceutically acceptable salt and/or hydrate and/or cocrystal thereof; e.g., a compound, such as a niclosamide analog, or a pharmaceutically acceptable salt and/or hydrate and/or cocrystal thereof) being administered which will relieve to some extent one or more of the symptoms of the disease or condition being treated.
  • a chemical entity e.g., a compound exhibiting activity as a mitochondrial uncoupling agent or a pharmaceutically acceptable salt and/or hydrate and/or cocrystal thereof; e.g., a compound, such as niclosamide or a pharmaceutically acceptable salt and/or hydrate and/or cocrystal thereof
  • an“effective amount” for therapeutic uses is the amount of the composition comprising a compound as disclosed herein required to provide a clinically significant decrease in disease symptoms.
  • An appropriate“effective” amount in any individual case is determined using any suitable technique, such as a dose escalation study.
  • excipient or “pharmaceutically acceptable excipient” means a pharmaceutically-acceptable material, composition, or vehicle, such as a liquid or solid filler, diluent, carrier, solvent, or encapsulating material.
  • each component is“pharmaceutically acceptable” in the sense of being compatible with the other ingredients of a pharmaceutical formulation, and suitable for use in contact with the tissue or organ of humans and animals without excessive toxicity, irritation, allergic response, immunogenicity, or other problems or complications, commensurate with a reasonable benefit/risk ratio.
  • pharmaceutically acceptable salt refers to a formulation of a compound that does not cause significant irritation to an organism to which it is administered and does not abrogate the biological activity and properties of the compound.
  • pharmaceutically acceptable salts are obtained by reacting a compound described herein, with acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid and the like.
  • pharmaceutically acceptable salts are obtained by reacting a compound having acidic group described herein with a base to form a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, and salts with amino acids such as arginine, lysine, and the like, or by other methods previously determined.
  • a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, and salts with amino acids such as arginine, lysine, and the like, or by other methods previously determined.
  • Examples of a salt that the compounds described hereinform with a base include the following: salts thereof with inorganic bases such as sodium, potassium, magnesium, calcium, and aluminum; salts thereof with organic bases such as methylamine, ethylamine and ethanolamine; salts thereof with basic amino acids such as lysine and ornithine; and ammonium salt.
  • the salts may be acid addition salts, which are specifically exemplified by acid addition salts with the following: mineral acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, and phosphoric acid:organic acids such as formic acid, acetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, tartaric acid, citric acid, methanesulfonic acid, and ethanesulfonic acid; acidic amino acids such as aspartic acid and glutamic acid.
  • mineral acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, and phosphoric acid
  • organic acids such as formic acid, acetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, tart
  • pharmaceutical composition refers to a mixture of a compound described herein with other chemical components (referred to collectively herein as “excipients”), such as carriers, stabilizers, diluents, dispersing agents, suspending agents, and/or thickening agents.
  • excipients such as carriers, stabilizers, diluents, dispersing agents, suspending agents, and/or thickening agents.
  • the pharmaceutical composition facilitates administration of the compound to an organism. Multiple techniques of administering a compound exist in the art including, but not limited to: rectal, oral, intravenous, aerosol, parenteral, ophthalmic, pulmonary, and topical administration.
  • subject refers to an animal, including, but not limited to, a primate (e.g., human), monkey, cow, pig, sheep, goat, horse, dog, cat, rabbit, rat, or mouse.
  • primate e.g., human
  • monkey cow, pig, sheep, goat
  • horse dog, cat, rabbit, rat
  • patient is used interchangeably herein in reference, for example, to a mammalian subject, such as a human.
  • treat in the context of treating a disease or disorder, are meant to include alleviating or abrogating a disorder, disease, or condition, or one or more of the symptoms associated with the disorder, disease, or condition; or to slowing the progression, spread or worsening of a disease, disorder or condition or of one or more symptoms thereof.
  • The“treatment of cancer” refers to one or more of the following effects: (1) inhibition, to some extent, of tumor growth, including, (i) slowing down and (ii) complete growth arrest; (2) reduction in the number of tumor cells; (3) maintaining tumor size; (4) reduction in tumor size; (5) inhibition, including (i) reduction, (ii) slowing down or (iii) complete prevention, of tumor cell infiltration into peripheral organs; (6) inhibition, including (i) reduction, (ii) slowing down or (iii) complete prevention, of metastasis; (7) enhancement of anti-tumor immune response, which may result in (i) maintaining tumor size, (ii) reducing tumor size, (iii) slowing the growth of a tumor, (iv) reducing, slowing or preventing invasion and/or (8) relief, to some extent, of the severity or number of one or more symptoms associated with the disorder.
  • halo refers to fluoro (F), chloro (Cl), bromo (Br), or iodo (I
  • alkyl refers to a hydrocarbon chain that may be a straight chain or branched chain, containing the indicated number of carbon atoms.
  • C 1-10 indicates that the group may have from 1 to 10 (inclusive) carbon atoms in it.
  • Non-limiting examples include methyl, ethyl, iso-propyl, tert-butyl, n-hexyl.
  • haloalkyl refers to an alkyl, in which one or more hydrogen atoms is/are replaced with an independently selected halo.
  • alkoxy refers to an -O-alkyl radical (e.g., -OCH 3 ).
  • alkylene refers to a divalent alkyl (e.g., -CH 2 -).
  • alkenyl refers to a hydrocarbon chain that may be a straight chain or branched chain having one or more carbon-carbon double bonds.
  • the alkenyl moiety contains the indicated number of carbon atoms. For example, C2-6 indicates that the group may have from 2 to 6 (inclusive) carbon atoms in it.
  • alkynyl refers to a hydrocarbon chain that may be a straight chain or branched chain having one or more carbon-carbon triple bonds.
  • the alkynyl moiety contains the indicated number of carbon atoms. For example, C2-6 indicates that the group may have from 2 to 6 (inclusive) carbon atoms in it.
  • aryl refers to a 6-carbon monocyclic, 10-carbon bicyclic, or 14-carbon tricyclic aromatic ring system wherein 0, 1, 2, 3, or 4 atoms of each ring may be substituted by a substituent.
  • aryl groups include phenyl, naphthyl and the like.
  • cycloalkyl as used herein includes saturated cyclic hydrocarbon groups having 3 to 10 carbons, preferably 3 to 8 carbons, and more preferably 3 to 6 carbons, wherein the cycloalkyl group may be optionally substituted.
  • Preferred cycloalkyl groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl.
  • heteroaryl refers to an aromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2, 3, or 4 atoms of each ring may be substituted by a substituent.
  • heteroaryl groups include pyridyl, furyl or furanyl, imidazolyl, benzimidazolyl, pyrimidinyl, thiophenyl or thienyl, quinolinyl, indolyl, thiazolyl, and the like.
  • heterocyclyl refers to a nonaromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2 or 3 atoms of each ring may be substituted by a substituent.
  • heterocyclyl groups include piperazinyl, pyrrolidinyl, dioxanyl, morpholinyl, tetrahydrofuranyl, and the like.
  • atoms making up the compounds of the present embodiments are intended to include all isotopic forms of such atoms.
  • Isotopes include those atoms having the same atomic number but different mass numbers.
  • isotopes of hydrogen include tritium and deuterium
  • isotopes of carbon include 13 C and 14 C.
  • This disclosure features chemical entities (e.g., a compound that modulates (e.g., agonizes) Stimulator of Interferon Genes (STING), or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that are useful, e.g., for treating a condition, disease or disorder in which a decrease or increase in STING activity (e.g., a decrease, e.g., a condition, disease or disorder associated with repressed or impaired STING signaling) contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human).
  • a compound that modulates e.g., agonizes
  • STING Stimulator of Interferon Genes
  • a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound e.g., for treating a
  • the chemical entities described herein induce an immune response in a subject (e.g., a human). In certain embodiments, the chemical entities described herein induce STING-dependent type I interferon production in a subject (e.g., a human).
  • This disclosure also features compositions as well as other methods of using and making the same.
  • Formula I Compounds In one aspect, compounds of Formula A, or a pharmaceutically acceptable salt thereof,
  • a and B are each independently selected from the group consisting of Formulae (i), (ii), (iii), and (iv):
  • G 1 is a bond connecting (i) the carbon directly attached to X 2 and (ii) the carbon directly attached to C(R 2A )(R 2B )(X 6 ); or is C(R G1A )(R G1B );
  • G 2 is a bond connecting (i) the carbon directly attached to X 4 and (ii) the carbon directly attached to C(R 1A )(R 1B )(X 3 ); or is C(R G2A )(R G2B );
  • Y 1 and Y 2 are each independently selected from the group consisting of–OH, - OR a1 , O-, -SH, -SR a1 , S-; and–NR b1 R c1 ;
  • R 1A and R 1B are each independently selected from the group consisting of H; halo; C 1-4 alkyl; C 1-4 haloalkyl; C 2-4 alkenyl; C 2-4 alkynyl; and C3-5 cycloalkyl, which is optionally substituted with from 1-4 independently selected C 1-4 alkyl; or R 1A and R 1B , together with the carbon atom to which each is attached, form a C3-5 cycloalkyl or heterocyclyl, including from 4-5 ring atoms, wherein from 1-2 (e.g., 1) ring atoms are independently selected from the group consisting of nitrogen and oxygen (e.g oxetane), wherein the C3-5 cycloalkyl or heterocyclyl ring
  • R 2A and R 2B are each independently selected from the group consisting of H; halo; C 1-4 alkyl; C 1-4 haloalkyl; C 2-4 alkenyl; C 2-4 alkynyl; and C3-5 cycloalkyl, which is optionally substituted with from 1-4 independently selected C 1-4 alkyl; or R 2A and R 2B , together with the carbon atom to which each is attached, form a C3-5 cycloalkyl or heterocyclyl, including from 4-5 ring atoms, wherein from 1-2 (e.g., 1) ring atoms are independently selected from the group consisting of nitrogen and oxygen (e.g., oxetane), wherein the C3-5 cycloalkyl or heterocyclyl ring can each be optionally substituted with from 1-4 independently selected C 1-4 alkyl, Z 1 is N or C-R 4 ;
  • Z1’ is N or C-H
  • Z2 is N or C-R 4’ ;
  • Z 2’ is N or C-H
  • Z3 is N-R 3 or C-R 4 ; each occurrence of R a1 is independently selected from the group consisting of: ⁇ C 1-10 alkyl optionally substituted with from 1-3 R A ;
  • heterocyclyl including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 R C ;
  • heterocyclyl as defined above-C 1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the heterocyclyl is optionally substituted with from 1-5 R C ;
  • R b1 and R c1 taken together with the nitrogen atom to which each is attached form a heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 R C ; (e.g., azetidinyl, morpholino, piperidinyl); each occurrence of R G1A , R G1B , R G1A , R G1B , R 4 , R 4’ , R 5 , R 6 , and R 6’ is independently selected from the group consisting of: H; R a1 ; halo, -CN, -NO2, -N3, -OH, - OR a1 , -SH, -SR a1 , -C(O)H, -C(O)R a1 , -C(O)NR c1 R d1 , -C(O)
  • R’ and R’’ are each independently selected from H and C 1-4 alkyl;
  • R’ and R’’ are each independently selected from H and
  • R’’ and R’’ are each independently selected from the group consisting of H, C 1-4 alkyl, -SO2(C 1-6 alkyl), -C(O)(C 1-6 alkyl), and - C(O)O(C 1-6 alkyl);
  • G 1 is a bond connecting (i) the carbon directly attached to X 2 and (ii) the carbon directly attached to C(R 2A )(R 2B )(X 6 ); or is C(R G1A )(R G1B );
  • G 2 is a bond connecting (i) the carbon directly attached to X 4 and (ii) the carbon directly attached to C(R 1A )(R 1B )(X 3 ); or is C(R G2A )(R G2B );
  • Y 1 and Y 2 are each independently selected from the group consisting of–OH, - OR a1 , O-, -SH, -SR a1 , S-; and–NR b1 R c1 ;
  • R 1A and R 1B are each independently selected from the group consisting of H; halo; C 1-4 alkyl; C 1-4 haloalkyl; C 2-4 alkenyl; C 2-4 alkynyl; and C3-5 cycloalkyl, which is optionally substituted with from 1-4 independently selected C 1-4 alkyl; or R 1A and R 1B , together with the carbon atom to which each is attached, form a C3-5 cycloalkyl or heterocyclyl, including from 4-5 ring atoms, wherein from 1-2 (e.g., 1) ring atoms are independently selected from the group consisting of nitrogen and oxygen (e.g oxetane), wherein the C3-5 cycloalkyl or heterocyclyl ring
  • R 2A and R 2B are each independently selected from the group consisting of H; halo; C 1-4 alkyl; C 1-4 haloalkyl; C 2-4 alkenyl; C 2-4 alkynyl; and C3-5 cycloalkyl, which is optionally substituted with from 1-4 independently selected C 1-4 alkyl; or R 2A and R 2B , together with the carbon atom to which each is attached, form a C3-5 cycloalkyl or heterocyclyl, including from 4-5 ring atoms, wherein from 1-2 (e.g., 1) ring atoms are independently selected from the group consisting of nitrogen and oxygen (e.g., oxetane), wherein the C3-5 cycloalkyl or heterocyclyl ring can each be optionally substituted with from 1-4 independently selected C 1-4 alkyl, Z 1 is N or C-R 4 ;
  • Z1’ is N or C-H
  • Z2 is N or C-R 4’ ;
  • Z 2’ is N or C-H
  • Z 3 is N-R 3 or C-R 4 ; each occurrence of R a1 is independently selected from the group consisting of: ⁇ C 1-10 alkyl optionally substituted with from 1-3 R A ;
  • heterocyclyl including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 R C ;
  • heterocyclyl as defined above-C 1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the heterocyclyl is optionally substituted with from 1-5 R C ;
  • R’ and R’’ are each independently selected from H and C 1-4 alkyl;
  • R’ and R’’ are each independently selected from H and C 1-4 alkyl;
  • R’’ and R’’ are each independently selected from the group consisting of H, C 1-4 alkyl, -SO2(C 1-6 alkyl), -C(O)(C 1-6 alkyl), and - C(O)O(C 1-6 alkyl);
  • ⁇ (heteroaryl as defined above)-(CH 2 ) 0-2 , wherein the CH 2 (when present) serves as the point of attachment, and wherein the phenyl is optionally substituted with from 1-5 substituents independently selected from halo, C 1-4 alkyl, -CF3, -OCH 3 , -SCH 3 , -OCF3, -NO2, -N3, -NH 2 , -NH(C 1-4 alkyl), -N(C 1-4 alkyl)2, -C(O)(C 1-4 alkyl), -C(O)OH, -C(O)O(C 1-4 alkyl), - SO2(CH 3 ), and cyclopropyl; and In some embodiments, one, two, three, four, five, six, seven, or eight of the following apply:
  • X 1 and X 5 cannot both be -OR a1 when each occurrence of R a1 is C 1-10 alkyl optionally substituted with from 1-3 R A (e.g., when each occurrence of R a1 is C 1-4 alkyl optionally substituted with from 1-2 R A ; when each occurrence of R a1 is C 1-4 alkyl; e.g., when each occurrence of R a1 is methyl or ethyl);
  • X 1 and X 5 cannot both be -OR a1 when each occurrence of R a1 is heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 R C ; (in certain of these embodiments, the heterocyclyl, includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., optionally substituted pyranyl or piperidinyl);
  • X 1 and X 5 cannot both be -OR a1 when each occurrence of R a1 is when each occurrence of R a1 is (heterocyclyl as defined above)-C 1-6 alkylene; in certain of these embodiments, the heterocyclyl, includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., optionally substituted pyranyl or piperidinyl);
  • X 1 and X 5 cannot both be -OC(O)R a1 when each occurrence of R a1 is C 1-10 alkyl optionally substituted with from 1-3 R A (e.g., when each occurrence of R a1 is C 1-4 alkyl optionally substituted with from 1-2 R A ; e.g., when each occurrence of R a1 is C 1-4 alkyl; e.g., when each occurrence of R a1 is methyl);
  • X 1 and X 5 cannot both be -OC(O)R a1 when each occurrence of R a1 is C6-10 aryl (e.g., phenyl) optionally substituted with from 1-5 R D ; and
  • ⁇ halo e.g., -F
  • R a1 ⁇ -OC(O)R a1 (e.g., when each occurrence of R a1 is C6-10 aryl (e.g., phenyl) optionally substituted with from 1-5 R D ); or
  • ⁇ -OR a1 e.g., when each occurrence of R a1 is C 1-10 alkyl optionally substituted with from 1-3 R A (e.g., when each occurrence of R a1 is C 1-4 alkyl optionally substituted with from 1-2 R A ; when each occurrence of R a1 is C 1-4 alkyl; e.g., when each occurrence of R a1 is methyl or ethyl).
  • the compounds have formula (B). In some embodiments, the compounds have formula (I).
  • X and X’ are each O.
  • G 1 is a bond connecting (i) the carbon directly attached to X 2 and (ii) the carbon directly attached to C(R 2A )(R 2B )(X 6 ).
  • G 2 is a bond connecting (i) the carbon directly attached to X 4 and (ii) the carbon directly attached to C(R 1A )(R 1B )(X 3 ).
  • X and X’ are each O
  • G 1 is a bond connecting (i) the carbon directly attached to X 2 and (ii) the carbon directly attached to C(R 2A )(R 2B )(X 6 )
  • G 2 is a bond connecting (i) the carbon directly attached to X 4 and (ii) the carbon directly attached to C(R 1A )(R 1B )(X 3 )
  • the compound has formula (A’), (B’), or (I-A) described previously.
  • a and B are each independently selected from the group consisting of formula (i) and formula (ii). In certain embodiments, A has formula (i), and B has formula (ii); or A has formula (ii), and B has formula (i). In other embodiments, A has formula (ii), and B has formula (ii). In still other embodiments, A has formula (i), and B has formula (i).
  • each occurrence of Z 1 is N, and Z 1’ is N.
  • R 5 is -NR b1 R c1 (e.g., -NH 2 or -NHR c1 ).
  • each occurrence of Z 1 is N, Z 1’ is N, and R 5 is -NR b1 R c1 (e.g., -NH 2 or -NHR c1 ).
  • R 4 and/or R 6 is H; or R 4 is other than H, and R 6 is H.
  • each occurrence of Z 1 is N, and Z 1’ is N.
  • R 5 is -OH.
  • each occurrence of Z 1 is N, Z 1’ is N, and R 5 is -OH.
  • R 6 is H.
  • R 4 is H; in other embodiments, R 4 is other than H.
  • each occurrence of Z 1 is N; Z 1’ is N; R 5 is -OH; R 6 is H; and R 4 is H.
  • each occurrence of Z 2 is N, Z 2’ is. N, and Z 3 is N-R 3 (e.g., N-H).
  • R 6’ is -NR b1 R c1 (e.g., -NH 2 or -NHR c1 ).
  • each occurrence of Z 2 is N, Z 2’ is. N, Z 3 is N-R 3 (e.g., N-H), and R 6’ is - NR b1 R c1 (e.g., -NH 2 or -NHR c1 ).
  • R 4’ is H; in other embodiments, R 4’ is other than H.
  • each of X 2 , X 3 , X 4 and X 6 is O.
  • X 1 is–F, -OH, -OR a1 , -OC(O)H, -OC(O)R a1 , or - OC(O)NR b1 R c1 (in certain embodiment, X 1 is other than–F).
  • X 1 is–F, -OH or -OR a1 (in certain embodiment, X 1 is other than–F).
  • X 5 is–F, -OH, -OR a1 , -OC(O)H, -OC(O)R a1 , or - OC(O)NR b1 R c1 (in certain embodiment, X 5 is other than–F).
  • X 5 is–F, -OH or -OR a1 (in certain embodiment, X 5 is other than–F).
  • X 1 and X 5 can be the same or different.
  • X 1 and X 5 are each independently selected from–F, -OH, -OR a1 , -OC(O)H, -OC(O)R a1 , or -OC(O)NR b1 R c1 (in certain embodiment, X 5 is other than –F).
  • X 1 and X 5 are each independently selected from–F, -OH or -OR a1 (in certain embodiment, X 5 is other than–F).
  • one of X 1 and X 5 is other than halo.
  • one of X 1 and X 5 is other than -F.
  • one of X 1 and X 5 is other than -OR a1 .
  • R a1 is:
  • ⁇ C 1-10 alkyl optionally substituted with from 1-3 R A (e.g., when each occurrence of R a1 is C 1-4 alkyl optionally substituted with from 1-2 R A ; when each occurrence of R a1 is C 1-4 alkyl; e.g., when each occurrence of R a1 is methyl or ethyl); and/or
  • heterocyclyl including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 R C ;
  • the heterocyclyl includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., R a1 is optionally substituted pyanyl or piperidinyl); and/or ⁇ (heterocyclyl as defined above)-C 1-6 alkylene; in certain of these embodiments, the heterocyclyl portion includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., optionally substituted pyanyl or piperidinyl).
  • one of X 1 and X 5 is other than -OC(O)R a1 .
  • R a1 is:
  • ⁇ C 1-10 alkyl optionally substituted with from 1-3 R A (e.g., when each occurrence of R a1 is C 1-4 alkyl optionally substituted with from 1-2 R A ; when each occurrence of R a1 is C 1-4 alkyl; e.g., when each occurrence of R a1 is methyl; and/or ⁇ C6-10 aryl (e.g., phenyl) optionally substituted with from 1-5 R D .
  • one of X 1 and X 5 is other than -OC(O)NR b1 R c1 .
  • one of X 1 and X 5 is other than -OH and halo. In certain embodiments, one of X 1 and X 5 is other than -OH and -F.
  • one of X 1 and X 5 is other than -OH, halo (e.g., -F), -OR a1 , and -OC(O)R a1 .
  • one of X 1 and X 5 is other than -OH, halo (e.g., -F), -OR a1 , - OC(O)R a1 , and -OC(O)NR b1 R c1 .
  • one of X 1 and X 5 is selected from the group consisting of -NR b1 R c1 , - + NR b2 R c2 R d2 , -NR d1 C(O)H, -NR d1 C(O)R a1 , -NR d1 C(O)OR a1 , - NR d1 C(O)NR b1 R c1 , -NR d1 S(O)R a1 , -NR d1 S(O)2R a1 , and -NR d1 S(O)2NR b1 R c1 ; and the other is as defined anywhere herein.
  • one of X 1 and X 5 is selected from the group consisting of -NR b1 R c1 , - + NR b2 R c2 R d2 , -NR d1 C(O)H, -NR d1 C(O)R a1 , -NR d1 C(O)OR a1 , and - NR d1 C(O)NR b1 R c1 ; and the other is as defined anywhere herein.
  • one of X 1 and X 5 is selected from the group consisting of -NR b1 R c1 and - + NR b2 R c2 R d2 ; and the other is as defined anywhere herein.
  • one of X 1 and X 5 is selected from the group consisting– NH 2 , - + NH 3 , and NHR c1 ; and the other is as defined anywhere herein.
  • each of X 1 and X 5 is independently selected from the group consisting of -NR b1 R c1 , - + NR b2 R c2 R d2 , -NR d1 C(O)H, -NR d1 C(O)R a1 , -NR d1 C(O)OR a1 , - NR d1 C(O)NR b1 R c1 , -NR d1 S(O)R a1 , -NR d1 S(O)2R a1 , and -NR d1 S(O)2NR b1 R c1 .
  • each of X 1 and X 5 is independently selected from the group consisting of -NR b1 R c1 , - + NR b2 R c2 R d2 , -NR d1 C(O)H, -NR d1 C(O)R a1 , -NR d1 C(O)OR a1 , and -NR d1 C(O)NR b1 R c1 .
  • each of X 1 and X 5 is independently selected from the group consisting of -NR b1 R c1 and - + NR b2 R c2 R d2 .
  • each of X 1 and X 5 is independently selected from the group consisting–NH 2 , - + NH 3 , and NHR c1 .
  • the carbon directly attached to X 1 and the carbon directly attached to X 5 both have the (R)-configuration.
  • the carbon directly attached to X 1 and the carbon directly attached to X 5 both have the (S)-configuration. In some embodiments, the carbon directly attached to X 1 and the carbon directly attached to X 5 have opposite configurations (i.e., one has the (R)-configuration, and the other has the (S)-configuration).
  • L 1 and L 2 In some embodiments, L 1 is .
  • Y 1 is -OH, -OR a1 , O-, -SH, -SR a1 , or S. In certain embodiments, . Y 1 is -OH, -OR a1 , or O- (e.g., -OR a1 or O-).
  • Y 1 is -SH or S-.
  • L 1 has the RP configuration, or L 1 has the SP configuration.
  • L 2 is .
  • Y 2 is -OH, -OR a1 , O-, -SH, -SR a1 , or S.
  • . Y 2 is -OH, -OR a1 , or O- (e.g., -OR a1 or O-).
  • Y 2 is -SH or S-.
  • L 2 has the RP configuration, or L 2 has the SP configuration.
  • L 1 is , and L 2 is .
  • Y 1 and Y 2 can be the same or different.
  • Y 1 and Y 2 are each independently selected from is - OH, -OR a1 , O-, -SH, -SR a1 , or S; e.g., -OR a1 or O-; e.g., -SH or S-; e.g., S-.
  • Y 1 and Y 2 are each O-.
  • Y 1 and Y 2 are each -SH or S-.
  • L 1 and L 2 both have the RP configuration or both have the SP configuration.
  • one of L 1 and L 2 has the RP configuration, and the other has the SP configuration.
  • R 1A and R 1B are each H. In some embodiments, R 2A and R 2B are each H. In some embodiments, R 1A and R 1B are each H, and R 2A and R 2B are each H.
  • Y 1 and Y 2 are each independently selected from -OH, -OR a1 , O-, -SH, -SR a1 , or S; . and
  • a and B are each independently selected from the group consisting of: formula (i) and formula (ii).
  • Embodiments can include any one or more of the features delineated in claims 19- 70.
  • each occurrence of Z 1 is N, Z 1’ is N, and R 5 is -NR b1 R c1 (e.g., -NH 2 or -NHR c1 ); and in certain of these embodiments, R 4 and/or R 6 is H; or R 4 is other than H, and R 6 is H; and/or
  • each occurrence of Z 1 is N, Z 1’ is N, and R 5 is -OH; in certain of these embodiments, R 6 is H; in certain of these embodiments, R 4 is H; in other embodiments, R 4 is other than H; and/or
  • each occurrence of Z 2 is N, Z 2’ is. N, Z 3 is N-R 3 (e.g., N-H), and R 6’ is -NR b1 R c1 (e.g., -NH 2 or -NHR c1 ); and in certain of these embodiments, R 4’ is H; in other embodiments, R 4’ is other than H.
  • Embodiments can include any one or more of the features delineated in claims 19- 70.
  • the compound has formula (II):
  • Embodiments can include any one or more of the features delineated in claims 19- 71.
  • the compound has formula (V):
  • each of X 2 , X 3 , X 4 and X 6 is O;
  • Y 1 and Y 2 are each independently selected from -OH, -OR a1 , O-, -SH, -SR a1 , or S; . and
  • a and B are each independently selected from the group consisting of: formula (i) and formula (ii).
  • Embodiments can include any one or more of the features delineated in claims 72- 85.
  • Representative and non-limiting examples of formula I compounds are provided in Table 1.
  • a chemical entity e.g., a compound that modulates (e.g., agonizes or partially agonizes) STING, or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination thereof) is administered as a pharmaceutical composition that includes the chemical entity and one or more pharmaceutically acceptable excipients, and optionally one or more additional therapeutic agents as described herein.
  • a pharmaceutical composition that includes the chemical entity and one or more pharmaceutically acceptable excipients, and optionally one or more additional therapeutic agents as described herein.
  • the chemical entities can be administered in combination with one or more conventional pharmaceutical excipients.
  • Pharmaceutically acceptable excipients include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, self-emulsifying drug delivery systems (SEDDS) such as d- ⁇ -tocopherol polyethylene glycol 1000 succinate, surfactants used in pharmaceutical dosage forms such as Tweens, poloxamers or other similar polymeric delivery matrices, serum proteins, such as human serum albumin, buffer substances such as phosphates, tris, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium-chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium, sodium
  • Cyclodextrins such as ⁇ -, ⁇ , and ⁇ -cyclodextrin, or chemically modified derivatives such as hydroxyalkylcyclodextrins, including 2- and 3- hydroxypropyl- ⁇ -cyclodextrins, or other solubilized derivatives can also be used to enhance delivery of compounds described herein.
  • Dosage forms or compositions containing a chemical entity as described herein in the range of 0.005% to 100% with the balance made up from non-toxic excipient may be prepared.
  • the contemplated compositions may contain 0.001%-100% of a chemical entity provided herein, in one embodiment 0.1-95%, in another embodiment 75-85%, in a further embodiment 20-80%.
  • the chemical entities described herein or a pharmaceutical composition thereof can be administered to subject in need thereof by any accepted route of administration.
  • Acceptable routes of administration include, but are not limited to, buccal, cutaneous, endocervical, endosinusial, endotracheal, enteral, epidural, interstitial, intra-abdominal, intra-arterial, intrabronchial, intrabursal, intracerebral, intracisternal, intracoronary, intradermal, intraductal, intraduodenal, intradural, intraepidermal, intraesophageal, intragastric, intragingival, intraileal, intralymphatic, intramedullary, intrameningeal, intramuscular, intraovarian, intraperitoneal, intraprostatic, intrapulmonary, intrasinal, intraspinal, intrasynovial, intratesticular, intrathecal, intratubular, intratumoral, intrauterine, intravascular, intravenous, nasal, nasogastric
  • compositions can be formulated for parenteral administration, e.g., formulated for injection via the intravenous, intramuscular, sub-cutaneous, or even intraperitoneal routes.
  • parenteral administration e.g., intratumoral
  • Such compositions can be prepared as injectables, either as liquid solutions or suspensions; solid forms suitable for use to prepare solutions or suspensions upon the addition of a liquid prior to injection can also be prepared; and the preparations can also be emulsified.
  • injectables either as liquid solutions or suspensions
  • solid forms suitable for use to prepare solutions or suspensions upon the addition of a liquid prior to injection can also be prepared; and the preparations can also be emulsified.
  • the preparation of such formulations will be known to those of skill in the art in light of the present disclosure.
  • the pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions; formulations including sesame oil, peanut oil, or aqueous propylene glycol; and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions.
  • the form must be sterile and must be fluid to the extent that it may be easily injected. It also should be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms, such as bacteria and fungi.
  • the carrier also can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and vegetable oils.
  • the proper fluidity can be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion, and by the use of surfactants.
  • the prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like.
  • isotonic agents for example, sugars or sodium chloride.
  • Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.
  • Sterile injectable solutions are prepared by incorporating the active compounds in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filtered sterilization.
  • dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above.
  • the preferred methods of preparation are vacuum-drying and freeze-drying techniques, which yield a powder of the active ingredient, plus any additional desired ingredient from a previously sterile-filtered solution thereof.
  • Intratumoral injections are discussed, e.g., in Lammers, et al.,“Effect of Intratumoral Injection on the Biodistribution and the Therapeutic Potential of HPMA Copolymer-Based Drug Delivery Systems” Neoplasia.2006, 10, 788–795.
  • Pharmacologically acceptable excipients usable in the rectal composition as a gel, cream, enema, or rectal suppository include, without limitation, any one or more of cocoa butter glycerides, synthetic polymers such as polyvinylpyrrolidone, PEG (like PEG ointments), glycerine, glycerinated gelatin, hydrogenated vegetable oils, poloxamers, mixtures of polyethylene glycols of various molecular weights and fatty acid esters of polyethylene glycol Vaseline, anhydrous lanolin, shark liver oil, sodium saccharinate, menthol, sweet almond oil, sorbitol, sodium benzoate, anoxid SBN, vanilla essential oil, aerosol, parabens in phenoxyethanol, sodium methyl p-oxybenzoate, sodium propyl p- oxybenzoate, diethylamine, carbomers, carbopol, methyloxybenzoate, macrogol cetostearyl ether, cocoyl caprylo
  • suppositories can be prepared by mixing the chemical entities described herein with suitable non-irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at ambient temperature but liquid at body temperature and therefore melt in the rectum and release the active compound.
  • suitable non-irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at ambient temperature but liquid at body temperature and therefore melt in the rectum and release the active compound.
  • compositions for rectal administration are in the form of an enema.
  • the compounds described herein or a pharmaceutical composition thereof are suitable for local delivery to the digestive or GI tract by way of oral administration (e.g., solid or liquid dosage forms.).
  • Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules.
  • the chemical entity is mixed with one or more pharmaceutically acceptable excipients, such as sodium citrate or dicalcium phosphate and/or: a) fillers or extenders such as starches, lactose, sucrose, glucose, mannitol, and silicic acid, b) binders such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidinone, sucrose, and acacia, c) humectants such as glycerol, d) disintegrating agents such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption accelerators such as quaternary ammonium compounds, g) wetting agents such as, for example, cetyl alcohol and glycerol mono
  • the dosage form may also comprise buffering agents.
  • Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.
  • the compositions will take the form of a unit dosage form such as a pill or tablet and thus the composition may contain, along with a chemical entity provided herein, a diluent such as lactose, sucrose, dicalcium phosphate, or the like; a lubricant such as magnesium stearate or the like; and a binder such as starch, gum acacia, polyvinylpyrrolidine, gelatin, cellulose, cellulose derivatives or the like.
  • a diluent such as lactose, sucrose, dicalcium phosphate, or the like
  • a lubricant such as magnesium stearate or the like
  • a binder such as starch, gum acacia, polyvinylpyrrolidine, gelatin, cellulose, cellulose derivatives or the like.
  • a powder, marume, solution or suspension (e.g., in propylene carbonate, vegetable oils, PEG’s, poloxamer 124 or triglycerides) is encapsulated in a capsule (gelatin or cellulose base capsule).
  • Unit dosage forms in which one or more chemical entities provided herein or additional active agents are physically separated are also contemplated; e.g., capsules with granules (or tablets in a capsule) of each drug; two-layer tablets; two- compartment gel caps, etc. Enteric coated or delayed release oral dosage forms are also contemplated.
  • physiologically acceptable compounds include wetting agents, emulsifying agents, dispersing agents or preservatives that are particularly useful for preventing the growth or action of microorganisms.
  • Various preservatives are well known and include, for example, phenol and ascorbic acid.
  • the excipients are sterile and generally free of undesirable matter. These compositions can be sterilized by conventional, well-known sterilization techniques. For various oral dosage form excipients such as tablets and capsules sterility is not required. The USP/NF standard is usually sufficient.
  • solid oral dosage forms can further include one or more components that chemically and/or structurally predispose the composition for delivery of the chemical entity to the stomach or the lower GI; e.g., the ascending colon and/or transverse colon and/or distal colon and/or small bowel.
  • Exemplary formulation techniques are described in, e.g., Filipski, K.J., et al., Current Topics in Medicinal Chemistry, 2013, 13, 776-802, which is incorporated herein by reference in its entirety.
  • Examples include upper-GI targeting techniques, e.g., Accordion Pill (Intec Pharma), floating capsules, and materials capable of adhering to mucosal walls.
  • Upper-GI targeting techniques e.g., Accordion Pill (Intec Pharma)
  • floating capsules e.g., floating capsules, and materials capable of adhering to mucosal walls.
  • enteric/pH-responsive coatings and excipients are available. These materials are typically polymers that are designed to dissolve or erode at specific pH ranges, selected based upon the GI region of desired drug release. These materials also function to protect acid labile drugs from gastric fluid or limit exposure in cases where the active ingredient may be irritating to the upper GI (e.g., hydroxypropyl methylcellulose phthalate series, Coateric (polyvinyl acetate phthalate), cellulose acetate phthalate, hydroxypropyl methylcellulose acetate succinate, Eudragit series (methacrylic acid–methyl methacrylate copolymers), and Marcoat).
  • hydroxypropyl methylcellulose phthalate series Coateric (polyvinyl acetate phthalate), cellulose acetate phthalate, hydroxypropyl methylcellulose acetate succinate, Eudragit series (methacrylic acid–methyl methacrylate copolymers), and Marcoat).
  • Ocular compositions can include, without limitation, one or more of any of the following: viscogens (e.g., Carboxymethylcellulose, Glycerin, Polyvinylpyrrolidone, Polyethylene glycol); Stabilizers (e.g., Pluronic (triblock copolymers), Cyclodextrins); Preservatives (e.g., Benzalkonium chloride, ETDA, SofZia (boric acid, propylene glycol, sorbitol, and zinc chloride; Alcon Laboratories, Inc.), Purite (stabilized oxychloro complex; Allergan, Inc.)).
  • viscogens e.g., Carboxymethylcellulose, Glycerin, Polyvinylpyrrolidone, Polyethylene glycol
  • Stabilizers e.g., Pluronic (triblock copolymers), Cyclodextrins
  • Preservatives e.g., Benzalkonium chloride, ETDA, SofZ
  • Topical compositions can include ointments and creams.
  • Ointments are semisolid preparations that are typically based on petrolatum or other petroleum derivatives.
  • Creams containing the selected active agent are typically viscous liquid or semisolid emulsions, often either oil-in-water or water-in-oil.
  • Cream bases are typically water-washable, and contain an oil phase, an emulsifier and an aqueous phase.
  • the oil phase also sometimes called the“internal” phase, is generally comprised of petrolatum and a fatty alcohol such as cetyl or stearyl alcohol; the aqueous phase usually, although not necessarily, exceeds the oil phase in volume, and generally contains a humectant.
  • compositions described herein can include one or more one or more of the following: lipids, interbilayer crosslinked multilamellar vesicles, biodegradeable poly(D,L-lactic-co-glycolic acid) [PLGA]-based or poly anhydride-based nanoparticles or microparticles, and nanoporous particle-supported lipid bilayers.
  • the dosages may be varied depending on the requirement of the patient, the severity of the condition being treating and the particular compound being employed. Determination of the proper dosage for a particular situation can be determined by one skilled in the medical arts.
  • the total daily dosage may be divided and administered in portions throughout the day or by means providing continuous delivery.
  • the compounds described herein are administered at a dosage of from about 0.001 mg/Kg to about 500 mg/Kg (e.g., from about 0.001 mg/Kg to about 200 mg/Kg; from about 0.01 mg/Kg to about 200 mg/Kg; from about 0.01 mg/Kg to about 150 mg/Kg; from about 0.01 mg/Kg to about 100 mg/Kg; from about 0.01 mg/Kg to about 50 mg/Kg; from about 0.01 mg/Kg to about 10 mg/Kg; from about 0.01 mg/Kg to about 5 mg/Kg; from about 0.01 mg/Kg to about 1 mg/Kg; from about 0.01 mg/Kg to about 0.5 mg/Kg; from about 0.01 mg/Kg to about 0.1 mg/Kg; from about 0.1 mg/Kg to about 200 mg/Kg; from about 0.1 mg/Kg to about 150 mg/Kg; from about 0.1 mg/Kg to about 100 mg/Kg; from about 0.1 mg
  • the foregoing dosages can be administered on a daily basis (e.g., as a single dose or as two or more divided doses) or non-daily basis (e.g., every other day, every two days, every three days, once weekly, twice weeks, once every two weeks, once a month).
  • a daily basis e.g., as a single dose or as two or more divided doses
  • non-daily basis e.g., every other day, every two days, every three days, once weekly, twice weeks, once every two weeks, once a month.
  • the period of administration of a compound described herein is for 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 1 1 days, 12 days, 13 days, 14 days, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, 11 weeks, 12 weeks, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, or more.
  • a period of during which administration is stopped is for 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 11 days, 12 days, 13 days, 14 days, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, 11 weeks, 12 weeks, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, or more.
  • a therapeutic compound is administered to an individual for a period of time followed by a separate period of time.
  • a therapeutic compound is administered for a first period and a second period following the first period, with administration stopped during the second period, followed by a third period where administration of the therapeutic compound is started and then a fourth period following the third period where administration is stopped.
  • the period of administration of a therapeutic compound followed by a period where administration is stopped is repeated for a determined or undetermined period of time.
  • a period of administration is for 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 11 days, 12 days, 13 days, 14 days, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, 11 weeks, 12 weeks, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, or more.
  • a period of during which administration is stopped is for 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 11 days, 12 days, 13 days, 14 days, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, 11 weeks, 12 weeks, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, or more.
  • methods for treating a subject having condition, disease or disorder in which a decrease or increase in STING activity contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., immune disorders, cancer) are provided.
  • the chemical entities described herein induce an immune response in a subject (e.g., a human).
  • the chemical entities described herein induce STING-dependent type I interferon production in a subject (e.g., a human). Indications
  • the condition, disease or disorder is cancer.
  • cancer include melanoma, carcinoma, lymphoma, blastoma, sarcoma, and leukemia or lymphoid malignancies. More particular examples of such cancers include breast cancer, colon cancer, rectal cancer, colorectal cancer, kidney or renal cancer, clear cell cancer lung cancer including small-cell lung cancer, non- small cell lung cancer, adenocarcinoma of the lung and squamous carcinoma of the lung, squamous cell cancer (e.g.
  • epithelial squamous cell cancer cervical cancer, ovarian cancer, prostate cancer, prostatic neoplasms, liver cancer, bladder cancer, cancer of the peritoneum, hepatocellular cancer, gastric or stomach cancer including gastrointestinal cancer, gastrointestinal stromal tumor, pancreatic cancer, head and neck cancer, glioblastoma, retinoblastoma, astrocytoma, thecomas, arrhenoblastomas, hepatoma, hematologic malignancies including non-Hodgkins lymphoma (NHL), multiple myeloma, myelodysplasia disorders, myeloproliferative disorders, chronic myelogenous leukemia, and acute hematologic malignancies, endometrial or uterine carcinoma, endometriosis, endometrial stromal sarcoma, fibrosarcomas, choriocarcinoma, salivary gland carcinoma, vulval cancer, thyroid cancer, es
  • the cancer is melanoma.
  • the condition, disease or disorder is a neurological disorder, which includes disorders that involve the central nervous system (brain, brainstem and cerebellum), the peripheral nervous system (including cranial nerves), and the autonomic nervous system (parts of which are located in both central and peripheral nervous system).
  • Non-limiting examples of cancer include acquired epileptiform aphasia; acute disseminated encephalomyelitis; adrenoleukodystrophy; age-related macular degeneration; agenesis of the corpus callosum; agnosia; Aicardi syndrome; Alexander disease; Alpers' disease; alternating hemiplegia; Alzheimer's disease; Vascular dementia; amyotrophic lateral sclerosis; anencephaly; Angelman syndrome; angiomatosis; anoxia; aphasia; apraxia; arachnoid cysts; arachnoiditis; Anronl-Chiari malformation; arteriovenous malformation; Asperger syndrome; ataxia telegiectasia; attention deficit hyperactivity disorder; autism; autonomic dysfunction; back pain; Batten disease; Behcet's disease; Bell's palsy; benign essential blepharospasm; benign focal; amyotrophy; benign intracranial hypertension; Bin
  • the condition, disease or disorder is an autoimmune diseases.
  • autoimmune diseases Non-limiting examples include rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, inflammatory bowel diseases (IBDs) comprising Crohn disease (CD) and ulcerative colitis (UC), which are chronic inflammatory conditions with polygenic susceptibility.
  • IBDs inflammatory bowel diseases
  • CD Crohn disease
  • UC ulcerative colitis
  • the condition is an inflammatory bowel disease.
  • the condition is Crohn’s disease, autoimmune colitis, iatrogenic autoimmune colitis, ulcerative colitis, colitis induced by one or more chemotherapeutic agents, colitis induced by treatment with adoptive cell therapy, colitis associated by one or more alloimmune diseases (such as graft-vs-host disease, e.g., acute graft vs. host disease and chronic graft vs. host disease), radiation enteritis, collagenous colitis, lymphocytic colitis, microscopic colitis, and radiation enteritis.
  • the condition is alloimmune disease (such as graft-vs-host disease, e.g., acute graft vs.
  • graft vs. host disease e.g., celiac disease, irritable bowel syndrome, rheumatoid arthritis, lupus, scleroderma, psoriasis, cutaneous T-cell lymphoma, uveitis, and mucositis (e.g., oral mucositis, esophageal mucositis or intestinal mucositis).
  • celiac disease irritable bowel syndrome
  • rheumatoid arthritis lupus
  • scleroderma psoriasis
  • cutaneous T-cell lymphoma e.g., uveitis
  • mucositis e.g., oral mucositis, esophageal mucositis or intestinal mucositis.
  • modulation of the immune system by STING provides for the treatment of diseases, including diseases caused by foreign agents.
  • exemplary infections by foreign agents which may be treated and/or prevented by the method of the present invention include an infection by a bacterium (e.g., a Gram-positive or Gram- negative bacterium), an infection by a fungus, an infection by a parasite, and an infection by a virus.
  • the infection is a bacterial infection (e.g., infection by E.
  • the infection is a fungal infection (e.g. infection by a mould, a yeast, or a higher fungus).
  • the infection is a parasitic infection (e.g., infection by a single-celled or multicellular parasite, including Giardia duodenalis, Cryptosporidium parvum, Cyclospora cayetanensis, and Toxoplasma gondiz).
  • the infection is a viral infection (e.g., infection by a virus associated with AIDS, avian flu, chickenpox, cold sores, common cold, gastroenteritis, glandular fever, influenza, measles, mumps, pharyngitis, pneumonia, rubella, SARS, and lower or upper respiratory tract infection (e.g., respiratory syncytial virus)).
  • a viral infection e.g., infection by a virus associated with AIDS, avian flu, chickenpox, cold sores, common cold, gastroenteritis, glandular fever, influenza, measles, mumps, pharyngitis, pneumonia, rubella, SARS, and lower or upper respiratory tract infection (e.g., respiratory syncytial virus)).
  • condition, disease or disorder is hepatits B (see, e.g., WO 2015/061294).
  • condition, disease or disorder is mucositis, also known as stomatitits, which can occur as a result of chemotherapy or radiation therapy, either alone or in combination as well as damage caused by exposure to radiation outside of the context of radiation therapy.
  • the condition, disease or disorder is uveitis, which is inflammation of the uvea (e.g., anterior uveitis, e.g., iridocyclitis or LTDis; intermediate uveitis (also known as pars planitis); posterior uveitis; or chorioretinitis, e.g., pan-uveitis).
  • uveitis inflammation of the uvea
  • anterior uveitis e.g., iridocyclitis or ulceris
  • intermediate uveitis also known as pars planitis
  • posterior uveitis e.g., pan-uveitis
  • chorioretinitis e.g., pan-uveitis
  • This disclosure contemplates both monotherapy regimens as well as combination therapy regimens.
  • the methods described herein can further include administering one or more additional therapies (e.g., one or more additional therapeutic agents and/or one or more therapeutic regimens) in combination with administration of the compounds described herein.
  • the methods described herein can further include administering one or more additional cancer therapies.
  • the one or more additional cancer therapies can include, without limitation, surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy, cancer vaccines (e.g., HPV vaccine, hepatitis B vaccine, Oncophage, Provenge) and gene therapy, as well as combinations thereof.
  • Immunotherapy including, without limitation, adoptive cell therapy, the derivation of stem cells and/or dendritic cells, blood transfusions, lavages, and/or other treatments, including, without limitation, freezing a tumor.
  • the one or more additional cancer therapies is chemotherapy, which can include administering one or more additional chemotherapeutic agents.
  • the additional chemotherapeutic agent is an immunomodulatory moiety, e.g., an immune checkpoint inhibitor.
  • the immune checkpoint inhibitor targets an immune checkpoint receptor selected from the group consisting of CTLA-4, PD-1, PD-L1, PD-1– PD-L1, PD-1– PD- L2, interleukin ⁇ 2 (IL ⁇ 2), indoleamine 2,3-dioxygenase (IDO), IL ⁇ 10, transforming growth factor- ⁇ (TGF ⁇ ), T cell immunoglobulin and mucin 3 (TIM3 or HAVCR2), Galectin 9– TIM3, Phosphatidylserine– TIM3, lymphocyte activation gene 3 protein (LAG3), MHC class II– LAG3, 4 ⁇ 1BB–4 ⁇ 1BB ligand, OX40–OX40 ligand, GITR, GITR ligand– GITR, CD27, CD70-CD27, TNFRSF25, TNFRSF25–TL1A, CD40L, CD40–CD40 ligand, HVEM–LIGHT–LTA, HVEM
  • the immune checkpoint inhibitor is selected from the group consisting of: Urelumab, PF ⁇ 05082566, MEDI6469, TRX518, Varlilumab, CP ⁇ 870893, Pembrolizumab (PD1), Nivolumab (PD1), Atezolizumab (formerly MPDL3280A) (PDL1), MEDI4736 (PD-L1), Avelumab (PD-L1), PDR001 (PD1), BMS ⁇ 986016, MGA271, Lirilumab, IPH 2 201, Emactuzumab, INCB024360, Galunisertib, Ulocuplumab, BKT140, Bavituximab, CC ⁇ 90002, Bevacizumab, and MNRP1685A, and MGA271.
  • the additional chemotherapeutic agent is a STING agonist.
  • the STING agonist can comprise a flavonoid.
  • suitable flavonoids include, but are not limited to, 10- (carboxymethyl)-9(10H)acridone (CMA), 5,6- Dimethylxanthenone-4-acetic acid (DMXAA), methoxyvone, 6, 4'-dimethoxyflavone, 4'- methoxyflavone, 3', 6 '-dihydroxyflavone, 7, 2'- dihydroxyflavone, daidzein, formononetin, retusin 7-methyl ether, xanthone, or any combination thereof.
  • CMA carboxymethyl-9(10H)acridone
  • DMXAA 5,6- Dimethylxanthenone-4-acetic acid
  • methoxyvone 6, 4'-dimethoxyflavone, 4'- methoxyflavone, 3', 6 '-dihydroxyfla
  • the STING agonist can be 10-(carboxymethyl)-9(10H)acridone (CMA). In some aspects, the STING agonist can be 5,6-Dimethylxanthenone-4-acetic acid (DMXAA). In some aspects, the STING agonist can be methoxyvone. In some aspects, the STING agonist can be 6, 4'-dimethoxyflavone. In some aspects, the STING agonist can be 4'- methoxyflavone. In some aspects, the STING agonist can be 3', 6 '-dihydroxyflavone. In some aspects, the STING agonist can be 7, 2 '-dihydroxyflavone. In some aspects, the STING agonist can be daidzein.
  • the STING agonist can be formononetin. In some aspects, the STING agonist can be retusin 7-methyl ether. In some aspects, the STING agonist can be xanthone. In some aspects, the STING agonist can be any combination of the above flavonoids.
  • the flavonoid comprises DMXAA.
  • the additional chemotherapeutic agent is an alkylating agent. Alkylating agents are so named because of their ability to alkylate many nucleophilic functional groups under conditions present in cells, including, but not limited to cancer cells.
  • an alkylating agent includes, but is not limited to, Cisplatin, carboplatin, mechlorethamine, cyclophosphamide, chlorambucil, ifosfamide and/or oxaliplatin.
  • alkylating agents can function by impairing cell function by forming covalent bonds with the amino, carboxyl, sulfhydryl, and phosphate groups in biologically important molecules or they can work by modifying a cell's DNA.
  • an alkylating agent is a synthetic, semisynthetic or derivative.
  • the additional chemotherapeutic agent is an anti- metabolite.
  • Anti-metabolites masquerade as purines or pyrimidines, the building-blocks of DNA and in general, prevent these substances from becoming incorporated in to DNA during the "S" phase (of the cell cycle), stopping normal development and division. Anti- metabolites can also affect RNA synthesis.
  • an antimetabolite includes, but is not limited to azathioprine and/or mercaptopurine.
  • an anti- metabolite is a synthetic, semisynthetic or derivative.
  • the additional chemotherapeutic agent is a plant alkaloid and/or terpenoid. These alkaloids are derived from plants and block cell division by, in general, preventing microtubule function.
  • a plant alkaloid and/or terpenoid is a vinca alkaloid, a podophyllotoxin and/or a taxane.
  • Vinca alkaloids in general, bind to specific sites on tubulin, inhibiting the assembly of tubulin into microtubules, generally during the M phase of the cell cycle.
  • a vinca alkaloid is derived, without limitation, from the Madagascar periwinkle, Catharanthus roseus (formerly known as Vinca rosea).
  • a vinca alkaloid includes, without limitation, Vincristine, Vinblastine, Vinorelbine and/or Vindesine.
  • a taxane includes, but is not limited, to Taxol, Paclitaxel and/or Docetaxel.
  • a plant alkaloid or terpernoid is a synthetic, semisynthetic or derivative.
  • a podophyllotoxin is, without limitation, an etoposide and/or teniposide.
  • a taxane is, without limitation, docetaxel and/or ortataxel.
  • a cancer therapeutic is a topoisomerase. Topoisomerases are essential enzymes that maintain the topology of DNA.
  • a topoisomerase is, without limitation, a type I topoisomerase inhibitor or a type II topoisomerase inhibitor.
  • a type I topoisomerase inhibitor is, without limitation, a camptothecin.
  • a camptothecin is, without limitation, exatecan, irinotecan, lurtotecan, topotecan, BNP 1350, CKD 602, DB 67 (AR67) and/or ST 1481.
  • a type II topoisomerase inhibitor is, without limitation, epipodophyllotoxin.
  • an epipodophyllotoxin is, without limitation, an amsacrine, etoposid, etoposide phosphate and/or teniposide.
  • a topoisomerase is a synthetic, semisynthetic or derivative, including those found in nature such as, without limitation, epipodophyllotoxins, substances naturally occurring in the root of American Mayapple (Podophyllum peltatum).
  • the additional chemotherapeutic agent is a stilbenoid.
  • a stilbenoid includes, but is not limited to, Resveratrol, Piceatannol, Pinosylvin, Pterostilbene, Alpha-Viniferin, Ampelopsin A, Ampelopsin E, Diptoindonesin C, Diptoindonesin F, Epsilon- Vinferin, Flexuosol A, Gnetin H, Hemsleyanol D, Hopeaphenol, Trans-Diptoindonesin B, Astringin, Piceid and Diptoindonesin A.
  • a stilbenoid is a synthetic, semisynthetic or derivative.
  • the additional chemotherapeutic agent is a cytotoxic antibiotic.
  • a cytotoxic antibiotic is, without limitation, an actinomycin, an anthracenedione, an anthracycline, thalidomide, dichloroacetic acid, nicotinic acid, 2- deoxyglucose and/or chlofazimine.
  • an actinomycin is, without limitation, actinomycin D, bacitracin, colistin (polymyxin E) and/or polymyxin B.
  • an antracenedione is, without limitation, mitoxantrone and/or pixantrone.
  • an anthracycline is, without limitation, bleomycin, doxorubicin (Adriamycin), daunorubicin (daunomycin), epirubicin, idarubicin, mitomycin, plicamycin and/or valrubicin.
  • a cytotoxic antibiotic is a synthetic, semisynthetic or derivative.
  • the additional chemotherapeutic agent is selected from endostatin, angiogenin, angiostatin, chemokines, angioarrestin, angiostatin (plasminogen fragment), basement-membrane collagen-derived anti-angiogenic factors (tumstatin, canstatin, or arrestin), anti-angiogenic antithrombin III, signal transduction inhibitors, cartilage-derived inhibitor (CDI), CD59 complement fragment, fibronectin fragment, gro- beta, heparinases, heparin hexasaccharide fragment, human chorionic gonadotropin (hCG), interferon alpha/beta/gamma, interferon inducible protein (IP-10), interleukin-12, kringle 5 (plasminogen fragment), metalloproteinase inhibitors (TIMPs), 2-methoxyestradiol, placental ribonuclease inhibitor, plasminogen activator inhibitor, platelet factor-4 (PF4), prolactin
  • the additional chemotherapeutic agent is selected from abiraterone acetate, altretamine, anhydrovinblastine, auristatin, bexarotene, bicalutamide, BMS 184476, 2,3,4,5,6-pentafluoro-N-(3-fluoro-4-methoxyphenyl)benzene sulfonamide, bleomycin, N,N-dimethyl-L-valyl-L-valyl-N-methyl-L-valyl-L-proly-1-Lproline-t- butylamide, cachectin, cemadotin, chlorambucil, cyclophosphamide, 3′,4′-didehydro-4′- deoxy-8′-norvin-caleukoblastine, docetaxol, doxetaxel, cyclophosphamide, carboplatin, carmustine, cisplatin, cryptophycin, cycl
  • the additional chemotherapeutic agent is platinum, cisplatin, carboplatin, oxaliplatin, mechlorethamine, cyclophosphamide, chlorambucil, azathioprine, mercaptopurine, vincristine, vinblastine, vinorelbine, vindesine, etoposide and teniposide, paclitaxel, docetaxel, irinotecan, topotecan, amsacrine, etoposide, etoposide phosphate, teniposide, 5-fluorouracil, leucovorin, methotrexate, gemcitabine, taxane, leucovorin, mitomycin C, tegafur-uracil, idarubicin, fludarabine, mitoxantrone, ifosfamide and doxorubicin.
  • Additional agents include inhibitors of mTOR (mammalian target of rapamycin), including but not limited to rapamycin, everolimus, temsirolimus and deforolimus.
  • the additional chemotherapeutic agent can be selected from those delineated in U.S. Patent 7,927,613, which is incorporated herein by reference in its entirety.
  • the second therapeutic agent or regimen is administered to the subject prior to contacting with or administering the chemical entity (e.g., about one hour prior, or about 6 hours prior, or about 12 hours prior, or about 24 hours prior, or about 48 hours prior, or about 1 week prior, or about 1 month prior).
  • the second therapeutic agent or regimen is administered to the subject at about the same time as contacting with or administering the chemical entity.
  • the second therapeutic agent or regimen and the chemical entity are provided to the subject simultaneously in the same dosage form.
  • the second therapeutic agent or regimen and the chemical entity are provided to the subject concurrently in separate dosage forms.
  • the second therapeutic agent or regimen is administered to the subject after contacting with or administering the chemical entity (e.g., about one hour after, or about 6 hours after, or about 12 hours after, or about 24 hours after, or about 48 hours after, or about 1 week after, or about 1 month after).
  • the chemical entity e.g., about one hour after, or about 6 hours after, or about 12 hours after, or about 24 hours after, or about 48 hours after, or about 1 week after, or about 1 month after.
  • the methods described herein further include the step of identifying a subject (e.g., a patient) in need of such treatment (e.g., by way of biopsy, endoscopy, or other conventional method known in the art).
  • the STING protein can serve as a biomarker for certain types of cancer, e.g., colon cancer and prostate cancer.
  • identifying a subject can include assaying the patient’s tumor microenvironment for the absence of T-cells and/or presence of exhausted T-cells, e.g., patients having one or more cold tumors. Such patients can include those that are resistant to treatment with checkpoint inhibitors.
  • such patients can be treated with a chemical entity herein, e.g., to recruit T-cells into the tumor, and in some cases, further treated with one or more checkpoint inhibitors, e.g., once the T-cells become exhausted.
  • the chemical entities, methods, and compositions described herein can be administered to certain treatment-resistant patient populations (e.g., patients resistant to checkpoint inhibitors; e.g., patients having one or more cold tumors, e.g., tumors lacking T-cells or exhausted T-cells).

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Organic Chemistry (AREA)
  • Epidemiology (AREA)
  • Biochemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Biotechnology (AREA)
  • Endocrinology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

This disclosure features dinucleotide compounds that modulate Stimulator of Interferon Genes (STING) activity, for use for example in the treatment of cancer. This disclosure also features compositions as well as other methods of using and making the same. A and B are each independently selected from the group consisting of Formulae (i), (ii), (iii), and (iv):

Description

CYCLIC DINUCLEOTIDES FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY SUCH AS CANCER
CROSS REFERENCE TO RELATED APPLICATIONS
This application claims the benefit of United States Provisional Application No. 62/277,273, filed on January 11, 2016 and United States Provisional Application No. 62/436,795, filed on December 20, 2016, each of which is incorporated herein by reference in its entirety.
TECHNICAL FIELD
This disclosure features chemical entities (e.g., a compound that modulates (e.g., agonizes) Stimulator of Interferon Genes (STING), or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that are useful, e.g., for treating a condition, disease or disorder in which a decrease or increase in STING activity (e.g., a decrease, e.g., a condition, disease or disorder associated with repressed or impaired STING signaling) contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human). This disclosure also features compositions as well as other methods of using and making the same.
BACKGROUND
STING, also known as transmembrane protein 173 (TMEM173) and MPYS/MITA/ERIS, is a protein that in humans is encoded by the TMEM173 gene. STING has been shown to play a role in innate immunity. STING induces type I interferon production when cells are infected with intracellular pathogens, such as viruses, mycobacteria and intracellular parasites. Type I interferon, mediated by STING, protects infected cells and nearby cells from local infection in an autocrine and paracrine manner. The STING pathway is a pathway that is involved in the detection of cytosolic DNA.
The STING signaling pathway is activated by cyclic dinucleotides (CDNs), which may be produced by bacteria or produced by antigen presenting cells in response to sensing cytosolic DNA. Unmodified CDNs have been shown to induce type I interferon and other co-regulated genes, which in turn facilitate the development of a specific immune response (see, e.g., Wu and Sun, et al., Science 2013, 339, 826-830). WO 2015/077354 discloses the use of STING agonists for the treatment of cancer. SUMMARY
This disclosure features chemical entities (e.g., a compound that modulates (e.g., agonizes) Stimulator of Interferon Genes (STING), or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that are useful, e.g., for treating a condition, disease or disorder in which a decrease or increase in STING activity (e.g., a decrease, e.g., a condition, disease or disorder associated with repressed or impaired STING signaling) contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human). In certain embodiments, the chemical entities described herein induce an immune response in a subject (e.g., a human). In certain embodiments, the chemical entities described herein induce STING-dependent type I interferon production in a subject (e.g., a human). This disclosure also features compositions as well as other methods of using and making the same. An "agonist" of STING includes compounds that, at the protein level, directly bind or modify STING such that an activity of STING is increased, e.g., by activation, stabilization, altered distribution, or otherwise.
Certain compounds described herein that agonize STING to a lesser extent than a STING full agonist can function in assays as antagonists as well as agonists. These compounds antagonize activation of STING by a STING full agonist because they prevent the full effect of STING interaction. However, the compounds also, on their own, activate some STING activity, typically less than a corresponding amount of the STING full agonist. Such compounds may be referred to as "partial agonists of STING".
In some embodiments, the compounds described herein are agonists (e.g. full agonists) of STING. In other embodiments, the compounds described herein are partial agonists of STING. Generally, a receptor exists in an active (Ra) and an inactive (Ri) conformation. Certain compounds that affect the receptor can alter the ratio of Ra to Ri (Ra/Ri). For example, a full agonist increases the ratio of Ra/Ri and can cause a "maximal", saturating effect. A partial agonist, when bound to the receptor, gives a response that is lower than that elicited by a full agonist (e.g., an endogenous agonist). Thus, the Ra/Ri for a partial agonist is less than for a full agonist. However, the potency of a partial agonist may be greater or less than that of the full agonist.
While not wishing to be bound by theory, it is believed that the partial agonists of STING described herein provide advantages with regard to treating the disorders described herein. By way of example, the partial agonists of STING described herein exhibit intrinsic activities that are expected to be both (i) high enough to induce an anti-tumor response (i.e., kill one or more tumor cells) and (ii) low enough to reduce the likelihood of producing toxicity-related side effects. As discussed above, partial agonists can antagonize activation of STING by a STING full agonist because they prevent the full effect of STING interaction, thereby reducing the activity of the STING full agonist. It is believed that this antagonism can also modulate (e.g., reduce) the toxicity profile of the STING full agonist. Accordingly, this disclosure contemplates methods in which the partial agonists of STING described herein are combined with one (or more) full agonists of STING (e.g., as described anywhere herein) to provide therapeutic drug combinations that are both efficacious and exhibit relatively low toxicity. In one aspect, compounds of Formula A, or a pharmaceutically acceptable salt thereof, are featured:
Figure imgf000005_0001
in which A, B, X, X’, G1, G2, X1, X2, X3, X4, X5, X6, L1, L2, R1A, R1B, R2A, and R2B can be as defined anywhere herein. X1 and X5 can each be independently“up” or“down.” In another aspect, compounds of Formula B, or a pharmaceutically acceptable salt thereof, are featured:
Figure imgf000006_0001
in which A, B, X, X’, G1, G2, X1, X2, X3, X4, X5, X6, L1, L2, R1A, R1B, R2A, and R2B can be as defined anywhere herein. X1 and X5 can each be independently“up” or “down.”
In one aspect, compounds of Formula I, or a pharmaceutically acceptable salt thereof, are featured:
Figure imgf000006_0002
in which A, B, X, X’, G1, G2, X1, X2, X3, X4, X5, X6, L1, L2, R1A, R1B, R2A, and R2B can be as defined anywhere herein. In one aspect, compounds of Formula A’, or a pharmaceutically acceptable salt thereof, are featured:
Figure imgf000007_0001
in which A, B, X, X’, X1, X2, X3, X4, X5, X6, L1, L2, R1A, R1B, R2A, and R2B can be as defined anywhere herein. X1 and X5 can each be independently“up” or“down.”
In another aspect, compounds of Formula B’, or a pharmaceutically acceptable salt thereof, are featured:
Figure imgf000007_0002
(B’),
in which A, B, X, X’, X1, X2, X3, X4, X5, X6, L1, L2, R1A, R1B, R2A, and R2B can be as defined anywhere herein. X1 and X5 can each be independently“up” or“down.” In another aspect, compounds of Formula I-A, or a pharmaceutically acceptable salt thereof, are featured:
Figure imgf000007_0003
in which A, B, X, X’, X1, X2, X3, X4, X5, X6, L1, L2, R1A, R1B, R2A, and R2B can be as defined anywhere herein. In one aspect, pharmaceutical compositions are featured that include a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same) and one or more pharmaceutically acceptable excipients. In one aspect, methods for modulating (e.g., agonizing) STING activity are featured that include contacting STING with a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same). Methods include in vitro methods, e.g., contacting a sample that includes one or more cells comprising STING (e.g., innate immune cells, e.g., mast cells, macrophages, dendritic cells (DCs), and natural killer cells) with the chemical entity. The contacting can, in some cases, induce an immune response sufficient to kill at least one of the one or more cancer cells. Methods can also include in vivo methods; e.g., administering the chemical entity to a subject (e.g., a human) having a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease (e.g., cancer; e.g., a refractory cancer). In another aspect, methods of treating cancer are featured that include administering to a subject in need of such treatment an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
In a further aspect, methods of inducing an immune response (e.g., an innate immune response) in a subject in need thereof are featured that include administering to the subject an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
In another aspect, methods of inducing induce STING-dependent type I interferon production in a subject in need thereof are featured that include administering to the subject an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
In a further aspect, methods of treatment of a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease are featured that include administering to a subject in need of such treatment an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
In another aspect, methods of treatment are featured that include administering to a subject having a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
In a further aspect, methods of treatment that include administering to a subject a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same), wherein the chemical entity is administered in an amount effective to treat a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease, thereby treating the disease.
Embodiments can include one or more of the following features.
The chemical entity can be administered in combination with one or more additional cancer therapies (e.g., surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy or gene therapy, or a combination thereof; e.g., chemotherapy that includes administering one or more (e.g., two, three, four, five, six, or more) additional chemotherapeutic agents. Non-limiting examples of additional chemotherapeutic agents is selected from an alkylating agent (e.g., cisplatin, carboplatin, mechlorethamine, cyclophosphamide, chlorambucil, ifosfamide and/or oxaliplatin); an anti-metabolite (e.g.,azathioprine and/or mercaptopurine); a terpenoid (e.g., a vinca alkaloid and/or a taxane; e.g., Vincristine, Vinblastine, Vinorelbine and/or Vindesine Taxol, Pacllitaxel and/or Docetaxel); a topoisomerase (e.g., a type I topoisomerase and/or a type 2 topoisomerase; e.g., camptothecins, such as irinotecan and/or topotecan;. amsacrine, etoposide, etoposide phosphate and/or teniposide); a cytotoxic antibiotic (e.g., actinomycin, anthracyclines, doxorubicin, daunorubicin, valrubicin, idarubicin, epirubicin, bleomycin, plicamycin and/or mitomycin); a hormone (e.g., a lutenizing hormone releasing hormone agonist; e.g., leuprolidine, goserelin, triptorelin, histrelin, bicalutamide, flutamide and/or nilutamide); an antibody (e.g., Abciximab, Adalimumab, Alemtuzumab, Atlizumab, Basiliximab, Belimumab, Bevacizumab, Bretuximab vedotin, Canakinumab, Cetuximab, Ceertolizumab pegol, Daclizumab, Denosumab, Eculizumab, Efalizumab, Gemtuzumab, Golimumab, Golimumab, Ibritumomab tiuxetan, Infliximab, Ipilimumab, Muromonab-CD3, Natalizumab, Ofatumumab, Omalizumab, Palivizumab, Panitumuab, Ranibizumab, Rituximab, Tocilizumab, Tositumomab and/or Trastuzumab); an anti- angiogenic agent; a cytokine; a thrombotic agent; a growth inhibitory agent; an anti- helminthic agent; and an immune checkpoint inhibitor that targets an immune checkpoint receptor selected from the group consisting of CTLA-4, PD-1, PD-L1, PD-1– PD-L1, PD- 1– PD-L2, interleukin‑2 (IL‑2), indoleamine 2,3-dioxygenase (IDO), IL‑10, transforming growth factor-β (TGFβ), T cell immunoglobulin and mucin 3 (TIM3 or HAVCR2), Galectin 9– TIM3, Phosphatidylserine– TIM3, lymphocyte activation gene 3 protein (LAG3), MHC class II– LAG3, 4‑1BB–4‑1BB ligand, OX40–OX40 ligand, GITR, GITR ligand– GITR, CD27, CD70-CD27, TNFRSF25, TNFRSF25–TL1A, CD40L, CD40– CD40 ligand, HVEM–LIGHT–LTA, HVEM, HVEM– BTLA, HVEM– CD160, HVEM – LIGHT, HVEM–BTLA–CD160, CD80, CD80– PDL-1, PDL2– CD80, CD244, CD48 – CD244, CD244, ICOS, ICOS–ICOS ligand, B7‑H3, B7‑H4, VISTA, TMIGD2, HHLA2–TMIGD2, Butyrophilins, including BTNL2, Siglec family, TIGIT and PVR family members, KIRs, ILTs and LIRs, NKG2D and NKG2A, MICA and MICB, CD244, CD28, CD86– CD28, CD86– CTLA, CD80– CD28, CD39, CD73 Adenosine–CD39– CD73, CXCR4–CXCL12, Phosphatidylserine, TIM3, Phosphatidylserine – TIM3, SIRPA–CD47, VEGF, Neuropilin, CD160, CD30, and CD155 (e.g., CTLA-4 or PD1 or PD-L1). The subject can have cancer; e.g., the subject has undergone and/or is undergoing and/or will undergo one or more cancer therapies.
Non-limiting examples of cancer include melanoma, cervical cancer, breast cancer, ovarian cancer, prostate cancer, testicular cancer, urothelial carcinoma, bladder cancer, non-small cell lung cancer, small cell lung cancer, sarcoma, colorectal adenocarcinoma, gastrointestinal stromal tumors, gastroesophageal carcinoma, colorectal cancer, pancreatic cancer, kidney cancer, hepatocellular cancer, malignant mesothelioma, leukemia, lymphoma, myelodysplasia syndrome, multiple myeloma, transitional cell carcinoma, neuroblastoma, plasma cell neoplasms, Wilm's tumor, or hepatocellular carcinoma. In certain embodiments, the cancer can be a refractory cancer.
The chemical entity can be administered intratumorally.
The methods can further include identifying the subject.
Other embodiments include those described in the Detailed Description and/or in the claims. Additional Definitions
To facilitate understanding of the disclosure set forth herein, a number of additional terms are defined below. Generally, the nomenclature used herein and the laboratory procedures in organic chemistry, medicinal chemistry, and pharmacology described herein are those well-known and commonly employed in the art. Unless defined otherwise, all technical and scientific terms used herein generally have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. Each of the patents, applications, published applications, and other publications that are mentioned throughout the specification are incorporated herein by reference in their entireties.
As used herein, the term“STING” is meant to include, without limitation, nucleic acids, polynucleotides, oligonucleotides, sense and antisense polynucleotide strands, complementary sequences, peptides, polypeptides, proteins, homologous and/or orthologous STING molecules, isoforms, precursors, mutants, variants, derivatives, splice variants, alleles, different species, and active fragments thereof. The term“acceptable” with respect to a formulation, composition or ingredient, as used herein, means having no persistent detrimental effect on the general health of the subject being treated.
“API” refers to an active pharmaceutical ingredient.
The terms“effective amount” or“therapeutically effective amount,” as used herein, refer to a sufficient amount of a chemical entity (e.g., a compound exhibiting activity as a mitochondrial uncoupling agent or a pharmaceutically acceptable salt and/or hydrate and/or cocrystal thereof; e.g., a compound, such as niclosamide or a pharmaceutically acceptable salt and/or hydrate and/or cocrystal thereof; e.g., a compound, such as a niclosamide analog, or a pharmaceutically acceptable salt and/or hydrate and/or cocrystal thereof) being administered which will relieve to some extent one or more of the symptoms of the disease or condition being treated. The result includes reduction and/or alleviation of the signs, symptoms, or causes of a disease, or any other desired alteration of a biological system. For example, an“effective amount” for therapeutic uses is the amount of the composition comprising a compound as disclosed herein required to provide a clinically significant decrease in disease symptoms. An appropriate“effective” amount in any individual case is determined using any suitable technique, such as a dose escalation study.
The term “excipient” or “pharmaceutically acceptable excipient” means a pharmaceutically-acceptable material, composition, or vehicle, such as a liquid or solid filler, diluent, carrier, solvent, or encapsulating material. In one embodiment, each component is“pharmaceutically acceptable” in the sense of being compatible with the other ingredients of a pharmaceutical formulation, and suitable for use in contact with the tissue or organ of humans and animals without excessive toxicity, irritation, allergic response, immunogenicity, or other problems or complications, commensurate with a reasonable benefit/risk ratio. See, e.g., Remington: The Science and Practice of Pharmacy, 21st ed.; Lippincott Williams & Wilkins: Philadelphia, PA, 2005; Handbook of Pharmaceutical Excipients, 6th ed.; Rowe et al., Eds.; The Pharmaceutical Press and the American Pharmaceutical Association: 2009; Handbook of Pharmaceutical Additives, 3rd ed.; Ash and Ash Eds.; Gower Publishing Company: 2007; Pharmaceutical Preformulation and Formulation, 2nd ed.; Gibson Ed.; CRC Press LLC: Boca Raton, FL, 2009.
The term“pharmaceutically acceptable salt” refers to a formulation of a compound that does not cause significant irritation to an organism to which it is administered and does not abrogate the biological activity and properties of the compound. In certain instances, pharmaceutically acceptable salts are obtained by reacting a compound described herein, with acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid and the like. In some instances, pharmaceutically acceptable salts are obtained by reacting a compound having acidic group described herein with a base to form a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, and salts with amino acids such as arginine, lysine, and the like, or by other methods previously determined. The pharmacologically acceptable salt s not specifically limited as far as it can be used in medicaments. Examples of a salt that the compounds described hereinform with a base include the following: salts thereof with inorganic bases such as sodium, potassium, magnesium, calcium, and aluminum; salts thereof with organic bases such as methylamine, ethylamine and ethanolamine; salts thereof with basic amino acids such as lysine and ornithine; and ammonium salt. The salts may be acid addition salts, which are specifically exemplified by acid addition salts with the following: mineral acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, and phosphoric acid:organic acids such as formic acid, acetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, tartaric acid, citric acid, methanesulfonic acid, and ethanesulfonic acid; acidic amino acids such as aspartic acid and glutamic acid.
The term“pharmaceutical composition” refers to a mixture of a compound described herein with other chemical components (referred to collectively herein as “excipients”), such as carriers, stabilizers, diluents, dispersing agents, suspending agents, and/or thickening agents. The pharmaceutical composition facilitates administration of the compound to an organism. Multiple techniques of administering a compound exist in the art including, but not limited to: rectal, oral, intravenous, aerosol, parenteral, ophthalmic, pulmonary, and topical administration.
The term“subject” refers to an animal, including, but not limited to, a primate (e.g., human), monkey, cow, pig, sheep, goat, horse, dog, cat, rabbit, rat, or mouse. The terms “subject” and“patient” are used interchangeably herein in reference, for example, to a mammalian subject, such as a human.
The terms“treat,”“treating,” and“treatment,” in the context of treating a disease or disorder, are meant to include alleviating or abrogating a disorder, disease, or condition, or one or more of the symptoms associated with the disorder, disease, or condition; or to slowing the progression, spread or worsening of a disease, disorder or condition or of one or more symptoms thereof. The“treatment of cancer”, refers to one or more of the following effects: (1) inhibition, to some extent, of tumor growth, including, (i) slowing down and (ii) complete growth arrest; (2) reduction in the number of tumor cells; (3) maintaining tumor size; (4) reduction in tumor size; (5) inhibition, including (i) reduction, (ii) slowing down or (iii) complete prevention, of tumor cell infiltration into peripheral organs; (6) inhibition, including (i) reduction, (ii) slowing down or (iii) complete prevention, of metastasis; (7) enhancement of anti-tumor immune response, which may result in (i) maintaining tumor size, (ii) reducing tumor size, (iii) slowing the growth of a tumor, (iv) reducing, slowing or preventing invasion and/or (8) relief, to some extent, of the severity or number of one or more symptoms associated with the disorder. The term "halo" refers to fluoro (F), chloro (Cl), bromo (Br), or iodo (I).
The term "alkyl" refers to a hydrocarbon chain that may be a straight chain or branched chain, containing the indicated number of carbon atoms. For example, C1-10 indicates that the group may have from 1 to 10 (inclusive) carbon atoms in it. Non-limiting examples include methyl, ethyl, iso-propyl, tert-butyl, n-hexyl.
The term "haloalkyl" refers to an alkyl, in which one or more hydrogen atoms is/are replaced with an independently selected halo.
The term "alkoxy" refers to an -O-alkyl radical (e.g., -OCH3). The term "alkylene" refers to a divalent alkyl (e.g., -CH2-).
The term "alkenyl" refers to a hydrocarbon chain that may be a straight chain or branched chain having one or more carbon-carbon double bonds. The alkenyl moiety contains the indicated number of carbon atoms. For example, C2-6 indicates that the group may have from 2 to 6 (inclusive) carbon atoms in it.
The term "alkynyl" refers to a hydrocarbon chain that may be a straight chain or branched chain having one or more carbon-carbon triple bonds. The alkynyl moiety contains the indicated number of carbon atoms. For example, C2-6 indicates that the group may have from 2 to 6 (inclusive) carbon atoms in it.
The term "aryl" refers to a 6-carbon monocyclic, 10-carbon bicyclic, or 14-carbon tricyclic aromatic ring system wherein 0, 1, 2, 3, or 4 atoms of each ring may be substituted by a substituent. Examples of aryl groups include phenyl, naphthyl and the like.
The term "cycloalkyl" as used herein includes saturated cyclic hydrocarbon groups having 3 to 10 carbons, preferably 3 to 8 carbons, and more preferably 3 to 6 carbons, wherein the cycloalkyl group may be optionally substituted. Preferred cycloalkyl groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl.
The term "heteroaryl" refers to an aromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2, 3, or 4 atoms of each ring may be substituted by a substituent. Examples of heteroaryl groups include pyridyl, furyl or furanyl, imidazolyl, benzimidazolyl, pyrimidinyl, thiophenyl or thienyl, quinolinyl, indolyl, thiazolyl, and the like.
The term "heterocyclyl" refers to a nonaromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2 or 3 atoms of each ring may be substituted by a substituent. Examples of heterocyclyl groups include piperazinyl, pyrrolidinyl, dioxanyl, morpholinyl, tetrahydrofuranyl, and the like.
In addition, atoms making up the compounds of the present embodiments are intended to include all isotopic forms of such atoms. Isotopes, as used herein, include those atoms having the same atomic number but different mass numbers. By way of general example and without limitation, isotopes of hydrogen include tritium and deuterium, and isotopes of carbon include 13C and 14C. The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features and advantages of the invention will be apparent from the description and drawings, and from the claims. DETAILED DESCRIPTION
This disclosure features chemical entities (e.g., a compound that modulates (e.g., agonizes) Stimulator of Interferon Genes (STING), or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that are useful, e.g., for treating a condition, disease or disorder in which a decrease or increase in STING activity (e.g., a decrease, e.g., a condition, disease or disorder associated with repressed or impaired STING signaling) contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human). In certain embodiments, the chemical entities described herein induce an immune response in a subject (e.g., a human). In certain embodiments, the chemical entities described herein induce STING-dependent type I interferon production in a subject (e.g., a human). This disclosure also features compositions as well as other methods of using and making the same. Formula I Compounds In one aspect, compounds of Formula A, or a pharmaceutically acceptable salt thereof,
Figure imgf000017_0001
wherein:
A and B are each independently selected from the group consisting of Formulae (i), (ii), (iii), and (iv):
Figure imgf000017_0002
Figure imgf000017_0003
X and X’ are each independently selected from the group consisting of O, S, S(O), SO2, CH2, CHF, CF2, CH2O, OCH2, CH2CH2, CH=CH, NR3, and N(O-)R3; G1 is a bond connecting (i) the carbon directly attached to X2 and (ii) the carbon directly attached to C(R2A)(R2B)(X6); or is C(RG1A)(RG1B);
G2 is a bond connecting (i) the carbon directly attached to X4 and (ii) the carbon directly attached to C(R1A)(R1B)(X3); or is C(RG2A)(RG2B); X1 and X5 are each independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, halo (e.g., F), -CN, -NO2, -N3, -OH, -ORa1, -SH, -SRa1, -C(O)H, - C(O)Ra1, -C(O)NRc1Rd1, -C(O)OH, -C(O)ORa1, -OC(O)H, -OC(O)Ra1, -OC(O)NRb1Rc1, - -C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, - NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1; X2, X3, X4 and X6 are each independently selected from the group consisting of O and S;
Figure imgf000018_0001
Y1 and Y2 are each independently selected from the group consisting of–OH, - ORa1, O-, -SH, -SRa1, S-; and–NRb1Rc1; R1A and R1B are each independently selected from the group consisting of H; halo; C1-4 alkyl; C1-4 haloalkyl; C2-4 alkenyl; C2-4 alkynyl; and C3-5 cycloalkyl, which is optionally substituted with from 1-4 independently selected C1-4 alkyl; or R1A and R1B, together with the carbon atom to which each is attached, form a C3-5 cycloalkyl or heterocyclyl, including from 4-5 ring atoms, wherein from 1-2 (e.g., 1) ring atoms are independently selected from the group consisting of nitrogen and oxygen (e.g oxetane), wherein the C3-5 cycloalkyl or heterocyclyl ring can each be optionally substituted with from 1-4 independently selected C1-4 alkyl;
R2A and R2B are each independently selected from the group consisting of H; halo; C1-4 alkyl; C1-4 haloalkyl; C2-4 alkenyl; C2-4 alkynyl; and C3-5 cycloalkyl, which is optionally substituted with from 1-4 independently selected C1-4 alkyl; or R2A and R2B, together with the carbon atom to which each is attached, form a C3-5 cycloalkyl or heterocyclyl, including from 4-5 ring atoms, wherein from 1-2 (e.g., 1) ring atoms are independently selected from the group consisting of nitrogen and oxygen (e.g., oxetane), wherein the C3-5 cycloalkyl or heterocyclyl ring can each be optionally substituted with from 1-4 independently selected C1-4 alkyl, Z1 is N or C-R4;
Z1’ is N or C-H;
Z2 is N or C-R4’;
Z2’ is N or C-H;
Z3 is N-R3 or C-R4; each occurrence of Ra1 is independently selected from the group consisting of: ● C1-10 alkyl optionally substituted with from 1-3 RA;
● C1-10 haloalkyl optionally substituted with from 1-3 RA;
● C2-10 alkenyl optionally substituted with from 1-3 RB,
● C2-10 alkynyl optionally substituted with from 1-3 RB,
● C3-10 cycloalkyl optionally substituted with from 1-5 RC;
● (C3-10 cycloalkyl)-C1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the C3-10 cycloalkyl optionally substituted with from 1-5 RC;
● heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RC;
● (heterocyclyl as defined above)-C1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the heterocyclyl is optionally substituted with from 1-5 RC;
● C6-10 aryl optionally substituted with from 1-5 RD;
● heteroaryl including from 5-10 ring atoms, wherein from 1-4 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RD; and ● (heteroaryl as defined above)-C1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the heteroaryl optionally substituted with from 1-5 RD; each occurrence of R3, Rb1, Rc1, Rd1, and Re1 is independently selected from the group consisting of: H; Ra1; -C(O)H, -C(O)Ra1, -C(O)NRc1Rd1, -C(O)ORa1, -OC(O)H, -- C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, - S(O)2Ra1, and -S(O)2NRb1Rc1; or
Rb1 and Rc1 taken together with the nitrogen atom to which each is attached form a heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RC; (e.g., azetidinyl, morpholino, piperidinyl); each occurrence of RG1A, RG1B, RG1A, RG1B, R4, R4’, R5, R6, and R6’ is independently selected from the group consisting of: H; Ra1; halo, -CN, -NO2, -N3, -OH, - ORa1, -SH, -SRa1, -C(O)H, -C(O)Ra1, -C(O)NRc1Rd1, -C(O)OH, -C(O)ORa1, -OC(O)H, - OC(O)Ra1, -OC(O)NRb1Rc1, --C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, - N+Rb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, -NRc1C(O)ORa1, -NRd1C(O)NRb1Rc1, - NRd1S(O)Ra1, -NRd1S(O)2Ra1, -NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1; each occurrence of RA is independently selected from the group consisting of: - CN; -OH; C1-6 alkoxy; C1-6 haloalkoxy; -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl; -C(O)OH; -C(O)O(C1-6 alkyl); and - NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), -C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl); each occurrence of RB is independently selected from the group consisting of: halo; -CN; -OH; C1-6 alkoxy; C1-6 haloalkoxy; -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl; -C(O)OH; -C(O)O(C1-6 alkyl); and - NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), -C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl);; each occurrence of RC is independently selected from the group consisting of: C1- 6 alkyl; C1-4 haloalkyl; halo; -CN; -OH; oxo; C1-6 alkoxy; C1-6 haloalkoxy; -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl; -C(O)(C1-6 alkyl); -C(O)OH; -C(O)O(C1-6 alkyl); and -NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), - C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl); each occurrence of RD is independently selected from the group consisting of: ● C1-6 alkyl optionally substituted with from 1-2 substituents independently selected from the group consisting of:–OH, C1-4 alkoxy; C1-4 haloalkoxy; -NH2, -NH(C1-4 alkyl), and -N(C1-4 alkyl)2;
● C1-4 haloalkyl;
● C2-4 alkenyl;
● C2-4 alkynyl;
● halo;
● -CN;
● -NO2;
● -N3;
● -OH;
● C1-6 alkoxy;
● C1-6 haloalkoxy;
● -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl;
● -SO2NRR’, wherein R’ and R’’ are each independently selected from H and
C1-4 alkyl;
● -C(O)(C1-6 alkyl); ● -C(O)OH;
● -C(O)O(C1-6 alkyl);
● -SO2(C1-6 alkyl),
● -NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), -C(O)(C1-6 alkyl), and - C(O)O(C1-6 alkyl);
● (C3-10 cycloalkyl)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the C3-10 cycloalkyl is optionally substituted with from 1-5 independently selected C1-4 alkyl; ● (heterocyclyl as defined above)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the heterocyclyl is optionally substituted with from 1-5 independently selected C1-4 alkyl; ● (phenyl)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the phenyl is optionally substituted with from 1-5 substituents independently selected from halo, C1-4 alkyl, -CF3, -OCH3, - SCH3, -OCF3, -NO2, -N3, -NH2, -NH(C1-4 alkyl), -N(C1-4 alkyl)2, - C(O)(C1-4 alkyl), -C(O)OH, -C(O)O(C1-4 alkyl), -SO2(CH3), and cyclopropyl; and
● (heteroaryl as defined above)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the phenyl is optionally substituted with from 1-5 substituents independently selected from halo, C1-4 alkyl, -CF3, -OCH3, -SCH3, -OCF3, -NO2, -N3, -NH2, -NH(C1-4 alkyl), -N(C1-4 alkyl)2, -C(O)(C1-4 alkyl), -C(O)OH, -C(O)O(C1-4 alkyl), - SO2(CH3), and cyclopropyl. In another aspect, of compounds having formula (A) can be as defined as follows: A and B are each independently selected from the group consisting of Formulae (i), (ii), (iii), and (iv):
Figure imgf000023_0001
X and X’ are each independently selected from the group consisting of O, S, S(O), SO2, CH2, CHF, CF2, CH2O, OCH2, CH2CH2, CH=CH, NR3, and N(O-)R3; G1 is a bond connecting (i) the carbon directly attached to X2 and (ii) the carbon directly attached to C(R2A)(R2B)(X6); or is C(RG1A)(RG1B);
G2 is a bond connecting (i) the carbon directly attached to X4 and (ii) the carbon directly attached to C(R1A)(R1B)(X3); or is C(RG2A)(RG2B); X1 and X5 are each independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, halo (e.g., F), -CN, -NO2, -N3, -OH, -ORa1, -SH, -SRa1, -C(O)H, - C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -OC(O)H, -OC(O)Ra1, -OC(O)NRb1Rc1, - -C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, - NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1; X2, X3, X4 and X6 are each independently selected from the group consisting of O and S;
Figure imgf000023_0002
Figure imgf000024_0001
Y1 and Y2 are each independently selected from the group consisting of–OH, - ORa1, O-, -SH, -SRa1, S-; and–NRb1Rc1; R1A and R1B are each independently selected from the group consisting of H; halo; C1-4 alkyl; C1-4 haloalkyl; C2-4 alkenyl; C2-4 alkynyl; and C3-5 cycloalkyl, which is optionally substituted with from 1-4 independently selected C1-4 alkyl; or R1A and R1B, together with the carbon atom to which each is attached, form a C3-5 cycloalkyl or heterocyclyl, including from 4-5 ring atoms, wherein from 1-2 (e.g., 1) ring atoms are independently selected from the group consisting of nitrogen and oxygen (e.g oxetane), wherein the C3-5 cycloalkyl or heterocyclyl ring can each be optionally substituted with from 1-4 independently selected C1-4 alkyl;
R2A and R2B are each independently selected from the group consisting of H; halo; C1-4 alkyl; C1-4 haloalkyl; C2-4 alkenyl; C2-4 alkynyl; and C3-5 cycloalkyl, which is optionally substituted with from 1-4 independently selected C1-4 alkyl; or R2A and R2B, together with the carbon atom to which each is attached, form a C3-5 cycloalkyl or heterocyclyl, including from 4-5 ring atoms, wherein from 1-2 (e.g., 1) ring atoms are independently selected from the group consisting of nitrogen and oxygen (e.g., oxetane), wherein the C3-5 cycloalkyl or heterocyclyl ring can each be optionally substituted with from 1-4 independently selected C1-4 alkyl, Z1 is N or C-R4;
Z1’ is N or C-H;
Z2 is N or C-R4’;
Z2’ is N or C-H;
Z3 is N-R3 or C-R4; each occurrence of Ra1 is independently selected from the group consisting of: ● C1-10 alkyl optionally substituted with from 1-3 RA;
● C1-10 haloalkyl optionally substituted with from 1-3 RA;
● C2-10 alkenyl optionally substituted with from 1-3 RB,
● C2-10 alkynyl optionally substituted with from 1-3 RB,
● C3-10 cycloalkyl optionally substituted with from 1-5 RC;
● (C3-10 cycloalkyl)-C1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the C3-10 cycloalkyl optionally substituted with from 1-5 RC;
● heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RC;
● (heterocyclyl as defined above)-C1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the heterocyclyl is optionally substituted with from 1-5 RC;
● C6-10 aryl optionally substituted with from 1-5 RD;
● heteroaryl including from 5-10 ring atoms, wherein from 1-4 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RD; and ● (heteroaryl as defined above)-C1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the heteroaryl optionally substituted with from 1-5 RD; each occurrence of Rb1 and Rc1 is independently selected from the group consisting of: H; Ra1; -C(O)H, -C(O)Ra1, -C(O)NRb3Rc3, -C(O)ORa1, -OC(O)H, --C(=NRe2)NRb3Rc3, -NRd3C(=NRe2) NRb3Rc3, - NRb3Rc3, -S(O)Ra1, -S(O) NRb3Rc3, -S(O)2Ra1, and -S(O)2 NRb3Rc3; or
Rb1 and Rc1 taken together with the nitrogen atom to which each is attached form a heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RC; (e.g., azetidinyl, morpholino, piperidinyl); each occurrence of R3, Rd1, and Re1 is independently selected from the group consisting of: H; Ra1; -C(O)H, -C(O)Ra1, -C(O)NRb3Rc3, -C(O)ORa1, -OC(O)H, -- C(=NRe2)NRb3Rc3, -NRd3C(=NRe2)NRb3Rc3, -NRb3Rc3, -S(O)Ra1, -S(O)NRb3Rc3, - S(O)2Ra1, and -S(O)2NRb3Rc3; each occurrence of Rb2, Rc2, and Rd2 is independently selected from the group consisting of: H and C1-6 alkyl optionally substituted with from 1-2 RA; each occurrence of Rb3, Rc3, Rd3, and Re2 is independently selected from the group consisting of: H; C1-6 alkyl optionally substituted with from 1-2 RA; -SO2(C1-6 alkyl), - C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl); each occurrence of RG1A, RG1B, RG1A, RG1B, R4, R4’, R5, R6, and R6’ is independently selected from the group consisting of: H; Ra1; halo, -CN, -NO2, -N3, -OH, - ORa1, -SH, -SRa1, -C(O)H, -C(O)Ra1, -C(O) NRb1Rc1, -C(O)OH, -C(O)ORa1, -OC(O)H, - OC(O)Ra1, -OC(O)NRb1Rc1, --C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, - +NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRc1C(O)ORa1, -NRd1C(O)NRb1Rc1, - NRd1S(O)Ra1, -NRd1S(O)2Ra1, -NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1; each occurrence of RA is independently selected from the group consisting of: - CN; -OH; C1-6 alkoxy; C1-6 haloalkoxy; -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl; -C(O)OH; -C(O)O(C1-6 alkyl); and - NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), -C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl); each occurrence of RB is independently selected from the group consisting of: halo; -CN; -OH; C1-6 alkoxy; C1-6 haloalkoxy; -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl; -C(O)OH; -C(O)O(C1-6 alkyl); and - NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), -C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl);; each occurrence of RC is independently selected from the group consisting of: C1- 6 alkyl; C1-4 haloalkyl; halo; -CN; -OH; oxo; C1-6 alkoxy; C1-6 haloalkoxy; -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl; -C(O)(C1-6 alkyl); -C(O)OH; -C(O)O(C1-6 alkyl); and -NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), - C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl); each occurrence of RD is independently selected from the group consisting of: ● C1-6 alkyl optionally substituted with from 1-2 substituents independently selected from the group consisting of:–OH, C1-4 alkoxy; C1-4 haloalkoxy; -NH2, -NH(C1-4 alkyl), and -N(C1-4 alkyl)2;
● C1-4 haloalkyl;
● C2-4 alkenyl;
● C2-4 alkynyl;
● halo;
● -CN;
● -NO2;
● -N3;
● -OH;
● C1-6 alkoxy;
● C1-6 haloalkoxy;
● -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl;
● -SO2NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl;
● -C(O)(C1-6 alkyl); ● -C(O)OH;
● -C(O)O(C1-6 alkyl);
● -SO2(C1-6 alkyl),
● -NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), -C(O)(C1-6 alkyl), and - C(O)O(C1-6 alkyl);
● (C3-10 cycloalkyl)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the C3-10 cycloalkyl is optionally substituted with from 1-5 independently selected C1-4 alkyl; ● (heterocyclyl as defined above)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the heterocyclyl is optionally substituted with from 1-5 independently selected C1-4 alkyl; ● (phenyl)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the phenyl is optionally substituted with from 1-5 substituents independently selected from halo, C1-4 alkyl, -CF3, -OCH3, - SCH3, -OCF3, -NO2, -N3, -NH2, -NH(C1-4 alkyl), -N(C1-4 alkyl)2, - C(O)(C1-4 alkyl), -C(O)OH, -C(O)O(C1-4 alkyl), -SO2(CH3), and cyclopropyl;
● (heteroaryl as defined above)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the phenyl is optionally substituted with from 1-5 substituents independently selected from halo, C1-4 alkyl, -CF3, -OCH3, -SCH3, -OCF3, -NO2, -N3, -NH2, -NH(C1-4 alkyl), -N(C1-4 alkyl)2, -C(O)(C1-4 alkyl), -C(O)OH, -C(O)O(C1-4 alkyl), - SO2(CH3), and cyclopropyl; and In some embodiments, one, two, three, four, five, six, seven, or eight of the following apply:
(a) X1 and X5 cannot both be-OH: (b) X1 and X5 cannot both be halo (e.g., X1 and X5 cannot both be -F); in certain embodiments, when A and B are each independently selected from formula (i) and formula (ii), then X1 and X5 cannot both be halo (e.g., X1 and X5 cannot both be -F);
(c) X1 and X5 cannot both be -ORa1 when each occurrence of Ra1 is C1-10 alkyl optionally substituted with from 1-3 RA (e.g., when each occurrence of Ra1 is C1-4 alkyl optionally substituted with from 1-2 RA; when each occurrence of Ra1 is C1-4 alkyl; e.g., when each occurrence of Ra1 is methyl or ethyl);
(d) X1 and X5 cannot both be -ORa1 when each occurrence of Ra1 is heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RC; (in certain of these embodiments, the heterocyclyl, includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., optionally substituted pyranyl or piperidinyl);
(e) X1 and X5 cannot both be -ORa1 when each occurrence of Ra1 is when each occurrence of Ra1 is (heterocyclyl as defined above)-C1-6 alkylene; in certain of these embodiments, the heterocyclyl, includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., optionally substituted pyranyl or piperidinyl);
(f) X1 and X5 cannot both be -OC(O)Ra1 when each occurrence of Ra1 is C1-10 alkyl optionally substituted with from 1-3 RA (e.g., when each occurrence of Ra1 is C1-4 alkyl optionally substituted with from 1-2 RA; e.g., when each occurrence of Ra1 is C1-4 alkyl; e.g., when each occurrence of Ra1 is methyl);
(g) X1 and X5 cannot both be -OC(O)Ra1 when each occurrence of Ra1 is C6-10 aryl (e.g., phenyl) optionally substituted with from 1-5 RD; and
(h) when one of X1 and X5 is -OH, then the other of X1 and X5 cannot be:
● halo (e.g., -F);
● -OC(O)NRb1Rc1;
● -OC(O)Ra1 (e.g., when each occurrence of Ra1 is C6-10 aryl (e.g., phenyl) optionally substituted with from 1-5 RD); or
● -ORa1 (e.g., when each occurrence of Ra1 is C1-10 alkyl optionally substituted with from 1-3 RA (e.g., when each occurrence of Ra1 is C1-4 alkyl optionally substituted with from 1-2 RA; when each occurrence of Ra1 is C1-4 alkyl; e.g., when each occurrence of Ra1 is methyl or ethyl). Variables X, X’, G1, and G1
In some embodiments, the compounds have formula (B). In some embodiments, the compounds have formula (I).
In some embodiments, X and X’ are each O. In some embodiments, G1 is a bond connecting (i) the carbon directly attached to X2 and (ii) the carbon directly attached to C(R2A)(R2B)(X6). In some embodiments, G2 is a bond connecting (i) the carbon directly attached to X4 and (ii) the carbon directly attached to C(R1A)(R1B)(X3).
In some embodiments, X and X’ are each O, G1 is a bond connecting (i) the carbon directly attached to X2 and (ii) the carbon directly attached to C(R2A)(R2B)(X6), G2 is a bond connecting (i) the carbon directly attached to X4 and (ii) the carbon directly attached to C(R1A)(R1B)(X3), and the compound has formula (A’), (B’), or (I-A) described previously. Variables A and B
In some embodiments, A and B are each independently selected from the group consisting of formula (i) and formula (ii). In certain embodiments, A has formula (i), and B has formula (ii); or A has formula (ii), and B has formula (i). In other embodiments, A has formula (ii), and B has formula (ii). In still other embodiments, A has formula (i), and B has formula (i).
In some embodiments, each occurrence of Z1 is N, and Z1’ is N. In some embodiments, R5 is -NRb1Rc1 (e.g., -NH2 or -NHRc1). In some embodiments, each occurrence of Z1 is N, Z1’ is N, and R5 is -NRb1Rc1 (e.g., -NH2 or -NHRc1). In certain of these embodiments, R4 and/or R6 is H; or R4 is other than H, and R6 is H.
In some embodiments, each occurrence of Z1 is N, and Z1’ is N. In some embodiments, R5 is -OH. In some embodiments, each occurrence of Z1 is N, Z1’ is N, and R5 is -OH. In certain of these embodiments, R6 is H. In certain of these embodiments, R4 is H; in other embodiments, R4 is other than H. For example, each occurrence of Z1 is N; Z1’ is N; R5 is -OH; R6 is H; and R4 is H.
In some embodiments, each occurrence of Z2 is N, Z2’ is. N, and Z3 is N-R3 (e.g., N-H). In some embodiments, R6’ is -NRb1Rc1 (e.g., -NH2 or -NHRc1). In some embodiments, each occurrence of Z2 is N, Z2’ is. N, Z3 is N-R3 (e.g., N-H), and R6’ is - NRb1Rc1 (e.g., -NH2 or -NHRc1). In certain of these embodiments, R4’ is H; in other embodiments, R4’ is other than H. Variables X2, X3, X4 and X6
In some embodiments, each of X2, X3, X4 and X6 is O. Variables X1 and X5
In some embodiments, X1 is -OH, -ORa1, -F, -SH, -SRa1, -OC(O)H, -OC(O)Ra1, - OC(O)NRb1Rc1, -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, - NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, - NRd1S(O)2Ra1, or -NRd1S(O)2NRb1Rc1 (in certain embodiment, X1 is other than–F).
In certain embodiments, X1 is -OH, -ORa1, -OC(O)H, -OC(O)Ra1, -OC(O)NRb1Rc1, -F, -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, or - NRd1S(O)2NRb1Rc1 (in certain embodiment, X1 is other than–F).
In certain embodiments, X1 is–F, -OH, -ORa1, -OC(O)H, -OC(O)Ra1, or - OC(O)NRb1Rc1 (in certain embodiment, X1 is other than–F).
In certain embodiments, X1 is–F, -OH or -ORa1 (in certain embodiment, X1 is other than–F).
In certain embodiments, X1 is–OH. In other embodiments, X1 is -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, - +NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, - NRd1S(O)Ra1, -NRd1S(O)2Ra1, or -NRd1S(O)2NRb1Rc1.; e.g., -NRb1Rc1 or -+NRb1Rc1Rd1; e.g.,–NH2, -+NH3, or NHRc1. In other embodiments, X1 is -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, - +NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, - NRd1S(O)Ra1, -NRd1S(O)2Ra1, or -NRd1S(O)2NRb1Rc1.; e.g., -NRb1Rc1 or -+NRb1Rc1Rd1; e.g.,–NH2, -+NH3, or NHRc1, each of X2, X3, X4 and X6 is O. In some embodiments, the carbon directly attached to X1 has the (R)-configuration. In some embodiments, the carbon directly attached to X1 has the (S)-configuration. In some embodiments, X5 is -OH, -ORa1, -F, -SH, -SRa1, -OC(O)H, -OC(O)Ra1, - OC(O)NRb1Rc1, -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, - NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, - NRd1S(O)2Ra1, or -NRd1S(O)2NRb1Rc1 (in certain embodiment, X5 is other than–F). In certain embodiments, X5 is -OH, -ORa1, -OC(O)H, -OC(O)Ra1, -OC(O)NRb1Rc1, -F, -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, or - NRd1S(O)2NRb1Rc1 (in certain embodiment, X5 is other than–F).
In certain embodiments, X5 is–F, -OH, -ORa1, -OC(O)H, -OC(O)Ra1, or - OC(O)NRb1Rc1 (in certain embodiment, X5 is other than–F).
In certain embodiments, X5 is–F, -OH or -ORa1 (in certain embodiment, X5 is other than–F).
In certain embodiments, X5 is–OH. In other embodiments, X5 is -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, - +NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, - NRd1S(O)Ra1, -NRd1S(O)2Ra1, or -NRd1S(O)2NRb1Rc1.; e.g., -NRb1Rc1 or -+NRb1Rc1Rd1; e.g.,–NH2, -+NH3, or NHRc1.
In other embodiments, X5 is -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, - +NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, - NRd1S(O)Ra1, -NRd1S(O)2Ra1, or -NRd1S(O)2NRb1Rc1.; e.g., -NRb1Rc1 or -+NRb1Rc1Rd1; e.g.,–NH2, -+NH3, or NHRc1, and each of X2, X3, X4 and X6 is O. In some embodiments, the carbon directly attached to X5 has the (R)-configuration. In some embodiments, the carbon directly attached to X5 has the (S)-configuration. In some embodiments, X1 and X5 are each independently selected from -OH, -ORa1, -F, -SH, -SRa1, -OC(O)H, -OC(O)Ra1, -OC(O)NRb1Rc1, -NO2, -N3, - NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, or - NRd1S(O)2NRb1Rc1 (in certain embodiment, X1 and/or X5 is other than–F). X1 and X5 can be the same or different. In certain embodiments, X1 and X5 are each independently selected from -OH, - ORa1, -OC(O)H, -OC(O)Ra1, -OC(O)NRb1Rc1, -F, -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, - NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, - NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, or -NRd1S(O)2NRb1Rc1 (in certain embodiment, X5 is other than–F).
In certain embodiments, X1 and X5 are each independently selected from–F, -OH, -ORa1, -OC(O)H, -OC(O)Ra1, or -OC(O)NRb1Rc1 (in certain embodiment, X5 is other than –F).
In certain embodiments, X1 and X5 are each independently selected from–F, -OH or -ORa1 (in certain embodiment, X5 is other than–F).
In certain embodiments, X1 and X5 are each–OH. In other embodiments, X1 and X5 are each independently selected from -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, or - NRd1S(O)2NRb1Rc1.; e.g., -NRb1Rc1 or -+NRb1Rc1Rd1; e.g.,–NH2, -+NH3, or NHRc1. In other embodiments, X1 and X5 are each independently selected from -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, or - NRd1S(O)2NRb1Rc1.; e.g., -NRb1Rc1 or -+NRb1Rc1Rd1; e.g.,–NH2, -+NH3, or NHRc1, and each of X2, X3, X4 and X6 is O. In some embodiments, one of X1 and X5 is other than -OH.
In some embodiments, one of X1 and X5 is other than halo.
In some embodiments, one of X1 and X5 is other than -F.
In some embodiments, one of X1 and X5 is other than -ORa1. In certain of these embodiments, Ra1 is:
● C1-10 alkyl optionally substituted with from 1-3 RA (e.g., when each occurrence of Ra1 is C1-4 alkyl optionally substituted with from 1-2 RA; when each occurrence of Ra1 is C1-4 alkyl; e.g., when each occurrence of Ra1 is methyl or ethyl); and/or
● heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RC; (in certain of these embodiments, the heterocyclyl, includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., Ra1 is optionally substituted pyanyl or piperidinyl); and/or ● (heterocyclyl as defined above)-C1-6 alkylene; in certain of these embodiments, the heterocyclyl portion includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., optionally substituted pyanyl or piperidinyl). In some embodiments, one of X1 and X5 is other than -OC(O)Ra1. In certain of these embodiments, Ra1 is:
● C1-10 alkyl optionally substituted with from 1-3 RA (e.g., when each occurrence of Ra1 is C1-4 alkyl optionally substituted with from 1-2 RA; when each occurrence of Ra1 is C1-4 alkyl; e.g., when each occurrence of Ra1 is methyl; and/or ● C6-10 aryl (e.g., phenyl) optionally substituted with from 1-5 RD. In some embodiments, one of X1 and X5 is other than -OC(O)NRb1Rc1.
In some embodiments, one of X1 and X5 is other than -OH and halo. In certain embodiments, one of X1 and X5 is other than -OH and -F.
In some embodiments, one of X1 and X5 is other than -OH, halo (e.g., -F), -ORa1, and -OC(O)Ra1.
In some embodiments, one of X1 and X5 is other than -OH, halo (e.g., -F), -ORa1, - OC(O)Ra1, and -OC(O)NRb1Rc1.
In some embodiments, one of X1 and X5 is selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -SH, -SRa1, -C(O)H, -C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, - +NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, - NRd1S(O)Ra1, -NRd1S(O)2Ra1, -NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1; and the other is as defined anywhere herein.
In certain embodiments, one of X1 and X5 is selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -C(O)H, -C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, - NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, - NRd1S(O)2Ra1, -NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and - S(O)2NRb1Rc1; and the other is as defined anywhere herein.
In certain embodiments, one of X1 and X5 is selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -C(O)H, -C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, - NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, - NRd1S(O)2Ra1, and -NRd1S(O)2NRb1Rc1; and the other is as defined anywhere herein.
In certain embodiments, one of X1 and X5 is selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, - +NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, - NRd1S(O)Ra1, -NRd1S(O)2Ra1, and -NRd1S(O)2NRb1Rc1; and the other is as defined anywhere herein.
In certain embodiments, one of X1 and X5 is selected from the group consisting of -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and - NRd1S(O)2NRb1Rc1; and the other is as defined anywhere herein.
In certain embodiments, one of X1 and X5 is selected from the group consisting of -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, - NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and -NRd1S(O)2NRb1Rc1; and the other is as defined anywhere herein.
In certain embodiments, one of X1 and X5 is selected from the group consisting of -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, and - NRd1C(O)NRb1Rc1; and the other is as defined anywhere herein.
In certain embodiments, one of X1 and X5 is selected from the group consisting of -NRb1Rc1 and -+NRb2Rc2Rd2; and the other is as defined anywhere herein.
In certain embodiments, one of X1 and X5 is selected from the group consisting– NH2, -+NH3, and NHRc1; and the other is as defined anywhere herein. In some embodiments, each of X1 and X5 is independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -SH, -SRa1, -C(O)H, -C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, - NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, - NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, -NRd1S(O)2NRb1Rc1, -S(O)Ra1, - S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1.
In certain embodiments, each of X1 and X5 is independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -C(O)H, -C(O)Ra1, - C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, - NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, - NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, -NRd1S(O)2NRb1Rc1, -S(O)Ra1, - S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1. In certain embodiments, each of X1 and X5 is independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -C(O)H, -C(O)Ra1, - C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, - NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, - NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and -NRd1S(O)2NRb1Rc1.
In certain embodiments, each of X1 and X5 is independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, - NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, - NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and -NRd1S(O)2NRb1Rc1. In certain embodiments, each of X1 and X5 is independently selected from the group consisting of -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and - NRd1S(O)2NRb1Rc1.
In certain embodiments, each of X1 and X5 is independently selected from the group consisting of -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, - NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and -NRd1S(O)2NRb1Rc1.
In certain embodiments, each of X1 and X5 is independently selected from the group consisting of -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, and -NRd1C(O)NRb1Rc1.
In certain embodiments, each of X1 and X5 is independently selected from the group consisting of -NRb1Rc1 and -+NRb2Rc2Rd2.
In certain embodiments, each of X1 and X5 is independently selected from the group consisting–NH2, -+NH3, and NHRc1. In some embodiments, the carbon directly attached to X1 and the carbon directly attached to X5 both have the (R)-configuration.
In some embodiments, the carbon directly attached to X1 and the carbon directly attached to X5 both have the (S)-configuration. In some embodiments, the carbon directly attached to X1 and the carbon directly attached to X5 have opposite configurations (i.e., one has the (R)-configuration, and the other has the (S)-configuration). Variables L1 and L2 In some embodiments, L1 is . In some embodiments, Y1 is -OH, -ORa1, O-, -SH, -SRa1, or S. In certain embodiments, .Y1 is -OH, -ORa1, or O- (e.g., -ORa1 or O-). In other embodiments, Y1 is -SH or S-. In certain of these embodiments, L1 has the RP configuration, or L1 has the SP configuration. In some embodiments, L2 is . In some embodiments, Y2 is -OH, -ORa1, O-, -SH, -SRa1, or S. In certain embodiments, .Y2 is -OH, -ORa1, or O- (e.g., -ORa1 or O-). In other embodiments, Y2 is -SH or S-. In certain of these embodiments, L2 has the RP configuration, or L2 has the SP configuration. In some embodiments, L1 is , and L2 is . Y1 and Y2 can be the same or different. In some embodiments, Y1 and Y2 are each independently selected from is - OH, -ORa1, O-, -SH, -SRa1, or S; e.g., -ORa1 or O-; e.g., -SH or S-; e.g., S-.
In certain embodiments, Y1 and Y2 are each O-.
In certain embodiments, Y1 and Y2 are each -SH or S-. In certain of these embodiments, L1 and L2 both have the RP configuration or both have the SP configuration. In other of these embodiments, one of L1 and L2 has the RP configuration, and the other has the SP configuration. Variables R1A and R1B and R2A and R2B
In some embodiments, R1A and R1B are each H. In some embodiments, R2A and R2B are each H. In some embodiments, R1A and R1B are each H, and R2A and R2B are each H. Non-Limiting Combinations
In some embodiments of formula (A), (B), (I), (A’), (B’), or (I-A):
X1 and X5 are each independently selected from the group consisting of -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and - each of X2, X3, X4 and X6 is O;
Figure imgf000039_0001
Y1 and Y2 are each independently selected from -OH, -ORa1, O-, -SH, -SRa1, or S; .and
A and B are each independently selected from the group consisting of: formula (i) and formula (ii).
Embodiments can include any one or more of the features delineated in claims 19- 70. In some embodiments of formula (A), (B), (I), (A’), (B’), or (I-A):
X1 and X5 are each independently selected from the group consisting of -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and - each of X2, X3, X4 and X6 is O;
Figure imgf000039_0002
Y1 and Y2 are each independently selected from -OH, -ORa1, O-, -SH, -SRa1, or S; .and A and B are each independently selected from the group consisting of: formula (i) and formula (ii);
and optionally:
each occurrence of Z1 is N, Z1’ is N, and R5 is -NRb1Rc1 (e.g., -NH2 or -NHRc1); and in certain of these embodiments, R4 and/or R6 is H; or R4 is other than H, and R6 is H; and/or
each occurrence of Z1 is N, Z1’ is N, and R5 is -OH; in certain of these embodiments, R6 is H; in certain of these embodiments, R4 is H; in other embodiments, R4 is other than H; and/or
each occurrence of Z2 is N, Z2’ is. N, Z3 is N-R3 (e.g., N-H), and R6’ is -NRb1Rc1 (e.g., -NH2 or -NHRc1); and in certain of these embodiments, R4’ is H; in other embodiments, R4’ is other than H.
Embodiments can include any one or more of the features delineated in claims 19- 70. In some embodiments, the compound has formula (II):
Figure imgf000040_0001
Figure imgf000041_0001
Embodiments can include any one or more of the features delineated in claims 19- 71. In some embodiments, the compound has formula (V):
Figure imgf000042_0001
in which,
X11 and X51 are each independently selected from the group consisting of -NO2, - N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and - NRd1S(O)2NRb1Rc1;
each of X2, X3, X4 and X6 is O;
Figure imgf000042_0002
Y1 and Y2 are each independently selected from -OH, -ORa1, O-, -SH, -SRa1, or S; .and
A and B are each independently selected from the group consisting of: formula (i) and formula (ii).
Embodiments can include any one or more of the features delineated in claims 72- 85. Representative and non-limiting examples of formula I compounds are provided in Table 1.
Table 1
Figure imgf000043_0001
Figure imgf000044_0001
Pharmaceutical Compositions and Administration
General
In some embodiments, a chemical entity (e.g., a compound that modulates (e.g., agonizes or partially agonizes) STING, or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination thereof) is administered as a pharmaceutical composition that includes the chemical entity and one or more pharmaceutically acceptable excipients, and optionally one or more additional therapeutic agents as described herein.
In some embodiments, the chemical entities can be administered in combination with one or more conventional pharmaceutical excipients. Pharmaceutically acceptable excipients include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, self-emulsifying drug delivery systems (SEDDS) such as d-α-tocopherol polyethylene glycol 1000 succinate, surfactants used in pharmaceutical dosage forms such as Tweens, poloxamers or other similar polymeric delivery matrices, serum proteins, such as human serum albumin, buffer substances such as phosphates, tris, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium-chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethyl cellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, and wool fat. Cyclodextrins such as α-,●, and γ-cyclodextrin, or chemically modified derivatives such as hydroxyalkylcyclodextrins, including 2- and 3- hydroxypropyl-β-cyclodextrins, or other solubilized derivatives can also be used to enhance delivery of compounds described herein. Dosage forms or compositions containing a chemical entity as described herein in the range of 0.005% to 100% with the balance made up from non-toxic excipient may be prepared. The contemplated compositions may contain 0.001%-100% of a chemical entity provided herein, in one embodiment 0.1-95%, in another embodiment 75-85%, in a further embodiment 20-80%. Actual methods of preparing such dosage forms are known, or will be apparent, to those skilled in this art; for example, see Remington: The Science and Practice of Pharmacy, 22nd Edition (Pharmaceutical Press, London, UK.2012). Routes of Administration and Composition Components
In some embodiments, the chemical entities described herein or a pharmaceutical composition thereof can be administered to subject in need thereof by any accepted route of administration. Acceptable routes of administration include, but are not limited to, buccal, cutaneous, endocervical, endosinusial, endotracheal, enteral, epidural, interstitial, intra-abdominal, intra-arterial, intrabronchial, intrabursal, intracerebral, intracisternal, intracoronary, intradermal, intraductal, intraduodenal, intradural, intraepidermal, intraesophageal, intragastric, intragingival, intraileal, intralymphatic, intramedullary, intrameningeal, intramuscular, intraovarian, intraperitoneal, intraprostatic, intrapulmonary, intrasinal, intraspinal, intrasynovial, intratesticular, intrathecal, intratubular, intratumoral, intrauterine, intravascular, intravenous, nasal, nasogastric, oral, parenteral, percutaneous, peridural, rectal, respiratory (inhalation), subcutaneous, sublingual, submucosal, topical, transdermal, transmucosal, transtracheal, ureteral, urethral and vaginal. In certain embodiments, a preferred route of administration is parenteral (e.g., intratumoral). Compositions can be formulated for parenteral administration, e.g., formulated for injection via the intravenous, intramuscular, sub-cutaneous, or even intraperitoneal routes. Typically, such compositions can be prepared as injectables, either as liquid solutions or suspensions; solid forms suitable for use to prepare solutions or suspensions upon the addition of a liquid prior to injection can also be prepared; and the preparations can also be emulsified. The preparation of such formulations will be known to those of skill in the art in light of the present disclosure.
The pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions; formulations including sesame oil, peanut oil, or aqueous propylene glycol; and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. In all cases the form must be sterile and must be fluid to the extent that it may be easily injected. It also should be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms, such as bacteria and fungi.
The carrier also can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and vegetable oils. The proper fluidity can be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion, and by the use of surfactants. The prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.
Sterile injectable solutions are prepared by incorporating the active compounds in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum-drying and freeze-drying techniques, which yield a powder of the active ingredient, plus any additional desired ingredient from a previously sterile-filtered solution thereof.
Intratumoral injections are discussed, e.g., in Lammers, et al.,“Effect of Intratumoral Injection on the Biodistribution and the Therapeutic Potential of HPMA Copolymer-Based Drug Delivery Systems” Neoplasia.2006, 10, 788–795. Pharmacologically acceptable excipients usable in the rectal composition as a gel, cream, enema, or rectal suppository, include, without limitation, any one or more of cocoa butter glycerides, synthetic polymers such as polyvinylpyrrolidone, PEG (like PEG ointments), glycerine, glycerinated gelatin, hydrogenated vegetable oils, poloxamers, mixtures of polyethylene glycols of various molecular weights and fatty acid esters of polyethylene glycol Vaseline, anhydrous lanolin, shark liver oil, sodium saccharinate, menthol, sweet almond oil, sorbitol, sodium benzoate, anoxid SBN, vanilla essential oil, aerosol, parabens in phenoxyethanol, sodium methyl p-oxybenzoate, sodium propyl p- oxybenzoate, diethylamine, carbomers, carbopol, methyloxybenzoate, macrogol cetostearyl ether, cocoyl caprylocaprate, isopropyl alcohol, propylene glycol, liquid paraffin, xanthan gum, carboxy-metabisulfite, sodium edetate, sodium benzoate, potassium metabisulfite, grapefruit seed extract, methyl sulfonyl methane (MSM) , lactic acid, glycine, vitamins, such as vitamin A and E and potassium acetate.
In certain embodiments, suppositories can be prepared by mixing the chemical entities described herein with suitable non-irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at ambient temperature but liquid at body temperature and therefore melt in the rectum and release the active compound. In other embodiments, compositions for rectal administration are in the form of an enema. In other embodiments, the compounds described herein or a pharmaceutical composition thereof are suitable for local delivery to the digestive or GI tract by way of oral administration (e.g., solid or liquid dosage forms.).
Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the chemical entity is mixed with one or more pharmaceutically acceptable excipients, such as sodium citrate or dicalcium phosphate and/or: a) fillers or extenders such as starches, lactose, sucrose, glucose, mannitol, and silicic acid, b) binders such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidinone, sucrose, and acacia, c) humectants such as glycerol, d) disintegrating agents such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption accelerators such as quaternary ammonium compounds, g) wetting agents such as, for example, cetyl alcohol and glycerol monostearate, h) absorbents such as kaolin and bentonite clay, and i) lubricants such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof. In the case of capsules, tablets and pills, the dosage form may also comprise buffering agents. Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.
In one embodiment, the compositions will take the form of a unit dosage form such as a pill or tablet and thus the composition may contain, along with a chemical entity provided herein, a diluent such as lactose, sucrose, dicalcium phosphate, or the like; a lubricant such as magnesium stearate or the like; and a binder such as starch, gum acacia, polyvinylpyrrolidine, gelatin, cellulose, cellulose derivatives or the like. In another solid dosage form, a powder, marume, solution or suspension (e.g., in propylene carbonate, vegetable oils, PEG’s, poloxamer 124 or triglycerides) is encapsulated in a capsule (gelatin or cellulose base capsule). Unit dosage forms in which one or more chemical entities provided herein or additional active agents are physically separated are also contemplated; e.g., capsules with granules (or tablets in a capsule) of each drug; two-layer tablets; two- compartment gel caps, etc. Enteric coated or delayed release oral dosage forms are also contemplated.
Other physiologically acceptable compounds include wetting agents, emulsifying agents, dispersing agents or preservatives that are particularly useful for preventing the growth or action of microorganisms. Various preservatives are well known and include, for example, phenol and ascorbic acid.
In certain embodiments the excipients are sterile and generally free of undesirable matter. These compositions can be sterilized by conventional, well-known sterilization techniques. For various oral dosage form excipients such as tablets and capsules sterility is not required. The USP/NF standard is usually sufficient.
In certain embodiments, solid oral dosage forms can further include one or more components that chemically and/or structurally predispose the composition for delivery of the chemical entity to the stomach or the lower GI; e.g., the ascending colon and/or transverse colon and/or distal colon and/or small bowel. Exemplary formulation techniques are described in, e.g., Filipski, K.J., et al., Current Topics in Medicinal Chemistry, 2013, 13, 776-802, which is incorporated herein by reference in its entirety.
Examples include upper-GI targeting techniques, e.g., Accordion Pill (Intec Pharma), floating capsules, and materials capable of adhering to mucosal walls.
Other examples include lower-GI targeting techniques. For targeting various regions in the intestinal tract, several enteric/pH-responsive coatings and excipients are available. These materials are typically polymers that are designed to dissolve or erode at specific pH ranges, selected based upon the GI region of desired drug release. These materials also function to protect acid labile drugs from gastric fluid or limit exposure in cases where the active ingredient may be irritating to the upper GI (e.g., hydroxypropyl methylcellulose phthalate series, Coateric (polyvinyl acetate phthalate), cellulose acetate phthalate, hydroxypropyl methylcellulose acetate succinate, Eudragit series (methacrylic acid–methyl methacrylate copolymers), and Marcoat). Other techniques include dosage forms that respond to local flora in the GI tract, Pressure-controlled colon delivery capsule, and Pulsincap. Ocular compositions can include, without limitation, one or more of any of the following: viscogens (e.g., Carboxymethylcellulose, Glycerin, Polyvinylpyrrolidone, Polyethylene glycol); Stabilizers (e.g., Pluronic (triblock copolymers), Cyclodextrins); Preservatives (e.g., Benzalkonium chloride, ETDA, SofZia (boric acid, propylene glycol, sorbitol, and zinc chloride; Alcon Laboratories, Inc.), Purite (stabilized oxychloro complex; Allergan, Inc.)).
Topical compositions can include ointments and creams. Ointments are semisolid preparations that are typically based on petrolatum or other petroleum derivatives. Creams containing the selected active agent are typically viscous liquid or semisolid emulsions, often either oil-in-water or water-in-oil. Cream bases are typically water-washable, and contain an oil phase, an emulsifier and an aqueous phase. The oil phase, also sometimes called the“internal” phase, is generally comprised of petrolatum and a fatty alcohol such as cetyl or stearyl alcohol; the aqueous phase usually, although not necessarily, exceeds the oil phase in volume, and generally contains a humectant. The emulsifier in a cream formulation is generally a nonionic, anionic, cationic or amphoteric surfactant. As with other carriers or vehicles, an ointment base should be inert, stable, nonirritating and non- sensitizing. In any of the foregoing embodiments, pharmaceutical compositions described herein can include one or more one or more of the following: lipids, interbilayer crosslinked multilamellar vesicles, biodegradeable poly(D,L-lactic-co-glycolic acid) [PLGA]-based or poly anhydride-based nanoparticles or microparticles, and nanoporous particle-supported lipid bilayers. Dosages
The dosages may be varied depending on the requirement of the patient, the severity of the condition being treating and the particular compound being employed. Determination of the proper dosage for a particular situation can be determined by one skilled in the medical arts. The total daily dosage may be divided and administered in portions throughout the day or by means providing continuous delivery. In some embodiments, the compounds described herein are administered at a dosage of from about 0.001 mg/Kg to about 500 mg/Kg (e.g., from about 0.001 mg/Kg to about 200 mg/Kg; from about 0.01 mg/Kg to about 200 mg/Kg; from about 0.01 mg/Kg to about 150 mg/Kg; from about 0.01 mg/Kg to about 100 mg/Kg; from about 0.01 mg/Kg to about 50 mg/Kg; from about 0.01 mg/Kg to about 10 mg/Kg; from about 0.01 mg/Kg to about 5 mg/Kg; from about 0.01 mg/Kg to about 1 mg/Kg; from about 0.01 mg/Kg to about 0.5 mg/Kg; from about 0.01 mg/Kg to about 0.1 mg/Kg; from about 0.1 mg/Kg to about 200 mg/Kg; from about 0.1 mg/Kg to about 150 mg/Kg; from about 0.1 mg/Kg to about 100 mg/Kg; from about 0.1 mg/Kg to about 50 mg/Kg; from about 0.1 mg/Kg to about 10 mg/Kg; from about 0.1 mg/Kg to about 5 mg/Kg; from about 0.1 mg/Kg to about 1 mg/Kg; from about 0.1 mg/Kg to about 0.5 mg/Kg). Regimens
The foregoing dosages can be administered on a daily basis (e.g., as a single dose or as two or more divided doses) or non-daily basis (e.g., every other day, every two days, every three days, once weekly, twice weeks, once every two weeks, once a month).
In some embodiments, the period of administration of a compound described herein is for 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 1 1 days, 12 days, 13 days, 14 days, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, 11 weeks, 12 weeks, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, or more. In a further embodiment, a period of during which administration is stopped is for 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 11 days, 12 days, 13 days, 14 days, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, 11 weeks, 12 weeks, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, or more. In an embodiment, a therapeutic compound is administered to an individual for a period of time followed by a separate period of time. In another embodiment, a therapeutic compound is administered for a first period and a second period following the first period, with administration stopped during the second period, followed by a third period where administration of the therapeutic compound is started and then a fourth period following the third period where administration is stopped. In an aspect of this embodiment, the period of administration of a therapeutic compound followed by a period where administration is stopped is repeated for a determined or undetermined period of time. In a further embodiment, a period of administration is for 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 11 days, 12 days, 13 days, 14 days, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, 11 weeks, 12 weeks, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, or more. In a further embodiment, a period of during which administration is stopped is for 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 11 days, 12 days, 13 days, 14 days, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks, 10 weeks, 11 weeks, 12 weeks, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, or more. Methods of Treatment
In some embodiments, methods for treating a subject having condition, disease or disorder in which a decrease or increase in STING activity (e.g., a decrease, e.g., repressed or impaired STING signaling) contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., immune disorders, cancer) are provided. In certain embodiments, the chemical entities described herein induce an immune response in a subject (e.g., a human). In certain embodiments, the chemical entities described herein induce STING-dependent type I interferon production in a subject (e.g., a human). Indications
In some embodiments, the condition, disease or disorder is cancer. Non-limiting examples of cancer include melanoma, carcinoma, lymphoma, blastoma, sarcoma, and leukemia or lymphoid malignancies. More particular examples of such cancers include breast cancer, colon cancer, rectal cancer, colorectal cancer, kidney or renal cancer, clear cell cancer lung cancer including small-cell lung cancer, non- small cell lung cancer, adenocarcinoma of the lung and squamous carcinoma of the lung, squamous cell cancer (e.g. epithelial squamous cell cancer), cervical cancer, ovarian cancer, prostate cancer, prostatic neoplasms, liver cancer, bladder cancer, cancer of the peritoneum, hepatocellular cancer, gastric or stomach cancer including gastrointestinal cancer, gastrointestinal stromal tumor, pancreatic cancer, head and neck cancer, glioblastoma, retinoblastoma, astrocytoma, thecomas, arrhenoblastomas, hepatoma, hematologic malignancies including non-Hodgkins lymphoma (NHL), multiple myeloma, myelodysplasia disorders, myeloproliferative disorders, chronic myelogenous leukemia, and acute hematologic malignancies, endometrial or uterine carcinoma, endometriosis, endometrial stromal sarcoma, fibrosarcomas, choriocarcinoma, salivary gland carcinoma, vulval cancer, thyroid cancer, esophageal carcinomas, hepatic carcinoma, anal carcinoma, penile carcinoma, nasopharyngeal carcinoma, laryngeal carcinomas, Kaposi's sarcoma, mast cell sarcoma, ovarian sarcoma, uterine sarcoma, melanoma, malignant mesothelioma, skin carcinomas, Schwannoma, oligodendroglioma, neuroblastomas, neuroectodermal tumor, rhabdomyosarcoma, osteogenic sarcoma, leiomyosarcomas, Ewing Sarcoma, peripheral primitive neuroectodermal tumor, urinary tract carcinomas, thyroid carcinomas, Wilm's tumor, as well as abnormal vascular proliferation associated with phakomatoses, edema (such as that associated with brain tumors), and Meigs' syndrome. In some cases, the cancer is melanoma. In some embodiments, the condition, disease or disorder is a neurological disorder, which includes disorders that involve the central nervous system (brain, brainstem and cerebellum), the peripheral nervous system (including cranial nerves), and the autonomic nervous system (parts of which are located in both central and peripheral nervous system). Non-limiting examples of cancer include acquired epileptiform aphasia; acute disseminated encephalomyelitis; adrenoleukodystrophy; age-related macular degeneration; agenesis of the corpus callosum; agnosia; Aicardi syndrome; Alexander disease; Alpers' disease; alternating hemiplegia; Alzheimer's disease; Vascular dementia; amyotrophic lateral sclerosis; anencephaly; Angelman syndrome; angiomatosis; anoxia; aphasia; apraxia; arachnoid cysts; arachnoiditis; Anronl-Chiari malformation; arteriovenous malformation; Asperger syndrome; ataxia telegiectasia; attention deficit hyperactivity disorder; autism; autonomic dysfunction; back pain; Batten disease; Behcet's disease; Bell's palsy; benign essential blepharospasm; benign focal; amyotrophy; benign intracranial hypertension; Binswanger's disease; blepharospasm; Bloch Sulzberger syndrome; brachial plexus injury; brain abscess; brain injury; brain tumors (including glioblastoma multiforme); spinal tumor; Brown-Sequard syndrome; Canavan disease; carpal tunnel syndrome; causalgia; central pain syndrome; central pontine myelinolysis; cephalic disorder; cerebral aneurysm; cerebral arteriosclerosis; cerebral atrophy; cerebral gigantism; cerebral palsy; Charcot-Marie-Tooth disease; chemotherapy-induced neuropathy and neuropathic pain; Chiari malformation; chorea; chronic inflammatory demyelinating polyneuropathy; chronic pain; chronic regional pain syndrome; Coffin Lowry syndrome; coma, including persistent vegetative state; congenital facial diplegia; corticobasal degeneration; cranial arteritis; craniosynostosis; Creutzfeldt-Jakob disease; cumulative trauma disorders; Cushing's syndrome; cytomegalic inclusion body disease; cytomegalovirus infection; dancing eyes-dancing feet syndrome; Dandy-Walker syndrome; Dawson disease; De Morsier's syndrome; Dejerine-Klumke palsy; dementia; dermatomyositis; diabetic neuropathy; diffuse sclerosis; dysautonomia; dysgraphia; dyslexia; dystonias; early infantile epileptic encephalopathy; empty sella syndrome; encephalitis; encephaloceles; encephalotrigeminal angiomatosis; epilepsy; Erb's palsy; essential tremor; Fabry's disease; Fahr's syndrome; fainting; familial spastic paralysis; febrile seizures; Fisher syndrome; Friedreich's ataxia; fronto-temporal dementia and other “tauopathies”; Gaucher's disease; Gerstmann's syndrome; giant cell arteritis; giant cell inclusion disease; globoid cell leukodystrophy; Guillain-Barre syndrome; HTLV-1- associated myelopathy; Hallervorden-Spatz disease; head injury; headache; hemifacial spasm; hereditary spastic paraplegia; heredopathia atactica polyneuritiformis; herpes zoster oticus; herpes zoster; Hirayama syndrome; HIV-associated dementia and neuropathy (also neurological manifestations of AIDS); holoprosencephaly; Huntington's disease and other polyglutamine repeat diseases; hydranencephaly; hydrocephalus; hypercortisolism; hypoxia; immune-mediated encephalomyelitis; inclusion body myositis; incontinentia pigmenti; infantile phytanic acid storage disease; infantile refsum disease; infantile spasms; inflammatory myopathy; intracranial cyst; intracranial hypertension; Joubert syndrome; Kearns-Sayre syndrome; Kennedy disease Kinsbourne syndrome; Klippel Feil syndrome; Krabbe disease; Kugelberg-Welander disease; kuru; Lafora disease; Lambert-Eaton myasthenic syndrome; Landau-Kleffner syndrome; lateral medullary (Wallenberg) syndrome; learning disabilities; Leigh's disease; Lennox-Gustaut syndrome; Lesch-Nyhan syndrome; leukodystrophy; Lewy body dementia; Lissencephaly; locked-in syndrome; Lou Gehrig's disease (i.e., motor neuron disease or amyotrophic lateral sclerosis); lumbar disc disease; Lyme disease—neurological sequelae; Machado-Joseph disease; macrencephaly; megalencephaly; Melkersson-Rosenthal syndrome; Menieres disease; meningitis; Menkes disease; metachromatic leukodystrophy; microcephaly; migraine; Miller Fisher syndrome; mini-strokes; mitochondrial myopathies; Mobius syndrome; monomelic amyotrophy; motor neuron disease; Moyamoya disease; mucopolysaccharidoses; milti-infarct dementia; multifocal motor neuropathy; multiple sclerosis and other demyelinating disorders; multiple system atrophy with postural hypotension; p muscular dystrophy; myasthenia gravis; myelinoclastic diffuse sclerosis; myoclonic encephalopathy of infants; myoclonus; myopathy; myotonia congenital; narcolepsy; neurofibromatosis; neuroleptic malignant syndrome; neurological manifestations of AIDS; neurological sequelae of lupus; neuromyotonia; neuronal ceroid lipofuscinosis; neuronal migration disorders; Niemann-Pick disease; O'Sullivan-McLeod syndrome; occipital neuralgia; occult spinal dysraphism sequence; Ohtahara syndrome; olivopontocerebellar atrophy; opsoclonus myoclonus; optic neuritis; orthostatic hypotension; overuse syndrome; paresthesia; Parkinson's disease; paramyotonia congenital; paraneoplastic diseases; paroxysmal attacks; Parry Romberg syndrome; Pelizaeus-Merzbacher disease; periodic paralyses; peripheral neuropathy; painful neuropathy and neuropathic pain; persistent vegetative state; pervasive developmental disorders; photic sneeze reflex; phytanic acid storage disease; Pick's disease; pinched nerve; pituitary tumors; polymyositis; porencephaly; post-polio syndrome; postherpetic neuralgia; postinfectious encephalomyelitis; postural hypotension; Prader-Willi syndrome; primary lateral sclerosis; prion diseases; progressive hemifacial atrophy; progressive multifocal leukoencephalopathy; progressive sclerosing poliodystrophy; progressive supranuclear palsy; pseudotumor cerebri; Ramsay-Hunt syndrome (types I and II); Rasmussen's encephalitis; reflex sympathetic dystrophy syndrome; Refsum disease; repetitive motion disorders; repetitive stress injuries; restless legs syndrome; retrovirus- associated myelopathy; Rett syndrome; Reye's syndrome; Saint Vitus dance; Sandhoff disease; Schilder's disease; schizencephaly; septo-optic dysplasia; shaken baby syndrome; shingles; Shy-Drager syndrome; Sjögren's syndrome; sleep apnea; Soto's syndrome; spasticity; spina bifida; spinal cord injury; spinal cord tumors; spinal muscular atrophy; Stiff-Person syndrome; stroke; Sturge-Weber syndrome; subacute sclerosing panencephalitis; subcortical arteriosclerotic encephalopathy; Sydenham chorea; syncope; syringomyelia; tardive dyskinesia; Tay-Sachs disease; temporal arteritis; tethered spinal cord syndrome; Thomsen disease; thoracic outlet syndrome; Tic Douloureux; Todd's paralysis; Tourette syndrome; transient ischemic attack; transmissible spongiform encephalopathies; transverse myelitis; traumatic brain injury; tremor; trigeminal neuralgia; tropical spastic paraparesis; tuberous sclerosis; vascular dementia (multi-infarct dementia); vasculitis including temporal arteritis; Von Hippel-Lindau disease; Wallenberg's syndrome; Werdnig-Hoffman disease; West syndrome; whiplash; Williams syndrome; Wildon's disease; and Zellweger syndrome. In some embodiments, the condition, disease or disorder is an autoimmune diseases. Non-limiting examples include rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, inflammatory bowel diseases (IBDs) comprising Crohn disease (CD) and ulcerative colitis (UC), which are chronic inflammatory conditions with polygenic susceptibility. In certain embodiments, the condition is an inflammatory bowel disease. In certain embodiments, the condition is Crohn’s disease, autoimmune colitis, iatrogenic autoimmune colitis, ulcerative colitis, colitis induced by one or more chemotherapeutic agents, colitis induced by treatment with adoptive cell therapy, colitis associated by one or more alloimmune diseases (such as graft-vs-host disease, e.g., acute graft vs. host disease and chronic graft vs. host disease), radiation enteritis, collagenous colitis, lymphocytic colitis, microscopic colitis, and radiation enteritis. In certain of these embodiments, the condition is alloimmune disease (such as graft-vs-host disease, e.g., acute graft vs. host disease and chronic graft vs. host disease), celiac disease, irritable bowel syndrome, rheumatoid arthritis, lupus, scleroderma, psoriasis, cutaneous T-cell lymphoma, uveitis, and mucositis (e.g., oral mucositis, esophageal mucositis or intestinal mucositis).
In some embodiments, modulation of the immune system by STING provides for the treatment of diseases, including diseases caused by foreign agents. Exemplary infections by foreign agents which may be treated and/or prevented by the method of the present invention include an infection by a bacterium (e.g., a Gram-positive or Gram- negative bacterium), an infection by a fungus, an infection by a parasite, and an infection by a virus. In one embodiment of the present invention, the infection is a bacterial infection (e.g., infection by E. coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Salmonella spp., Staphylococcus aureus, Streptococcus spp., or vancomycin-resistant enterococcus). In another embodiment, the infection is a fungal infection (e.g. infection by a mould, a yeast, or a higher fungus). In still another embodiment, the infection is a parasitic infection (e.g., infection by a single-celled or multicellular parasite, including Giardia duodenalis, Cryptosporidium parvum, Cyclospora cayetanensis, and Toxoplasma gondiz). In yet another embodiment, the infection is a viral infection (e.g., infection by a virus associated with AIDS, avian flu, chickenpox, cold sores, common cold, gastroenteritis, glandular fever, influenza, measles, mumps, pharyngitis, pneumonia, rubella, SARS, and lower or upper respiratory tract infection (e.g., respiratory syncytial virus)).
In some embodiments, the condition, disease or disorder is hepatits B (see, e.g., WO 2015/061294).
In some embodiments, the condition, disease or disorder is mucositis, also known as stomatitits, which can occur as a result of chemotherapy or radiation therapy, either alone or in combination as well as damage caused by exposure to radiation outside of the context of radiation therapy.
In some embodiments, the condition, disease or disorder is uveitis, which is inflammation of the uvea (e.g., anterior uveitis, e.g., iridocyclitis or iritis; intermediate uveitis (also known as pars planitis); posterior uveitis; or chorioretinitis, e.g., pan-uveitis). Combination therapy
This disclosure contemplates both monotherapy regimens as well as combination therapy regimens.
In some embodiments, the methods described herein can further include administering one or more additional therapies (e.g., one or more additional therapeutic agents and/or one or more therapeutic regimens) in combination with administration of the compounds described herein. In certain embodiments, the methods described herein can further include administering one or more additional cancer therapies.
The one or more additional cancer therapies can include, without limitation, surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy, cancer vaccines (e.g., HPV vaccine, hepatitis B vaccine, Oncophage, Provenge) and gene therapy, as well as combinations thereof. Immunotherapy, including, without limitation, adoptive cell therapy, the derivation of stem cells and/or dendritic cells, blood transfusions, lavages, and/or other treatments, including, without limitation, freezing a tumor. In some embodiments, the one or more additional cancer therapies is chemotherapy, which can include administering one or more additional chemotherapeutic agents. In certain embodiments, the additional chemotherapeutic agent is an immunomodulatory moiety, e.g., an immune checkpoint inhibitor. In certain of these embodiments, the immune checkpoint inhibitor targets an immune checkpoint receptor selected from the group consisting of CTLA-4, PD-1, PD-L1, PD-1– PD-L1, PD-1– PD- L2, interleukin‑2 (IL‑2), indoleamine 2,3-dioxygenase (IDO), IL‑10, transforming growth factor-β (TGFβ), T cell immunoglobulin and mucin 3 (TIM3 or HAVCR2), Galectin 9– TIM3, Phosphatidylserine– TIM3, lymphocyte activation gene 3 protein (LAG3), MHC class II– LAG3, 4‑1BB–4‑1BB ligand, OX40–OX40 ligand, GITR, GITR ligand– GITR, CD27, CD70-CD27, TNFRSF25, TNFRSF25–TL1A, CD40L, CD40–CD40 ligand, HVEM–LIGHT–LTA, HVEM, HVEM– BTLA, HVEM– CD160, HVEM– LIGHT, HVEM–BTLA–CD160, CD80, CD80– PDL-1, PDL2– CD80, CD244, CD48– CD244, CD244, ICOS, ICOS–ICOS ligand, B7‑H3, B7‑H4, VISTA, TMIGD2, HHLA2– TMIGD2, Butyrophilins, including BTNL2, Siglec family, TIGIT and PVR family members, KIRs, ILTs and LIRs, NKG2D and NKG2A, MICA and MICB, CD244, CD28, CD86– CD28, CD86– CTLA, CD80– CD28, CD39, CD73 Adenosine–CD39–CD73, CXCR4–CXCL12, Phosphatidylserine, TIM3, Phosphatidylserine– TIM3, SIRPA–CD47, VEGF, Neuropilin, CD160, CD30, and CD155; e.g., CTLA-4 or PD1 or PD-L1). See, e.g., Postow, M. J. Clin. Oncol.2015, 33, 1.
In certain of these embodiments, the immune checkpoint inhibitor is selected from the group consisting of: Urelumab, PF‑05082566, MEDI6469, TRX518, Varlilumab, CP‑870893, Pembrolizumab (PD1), Nivolumab (PD1), Atezolizumab (formerly MPDL3280A) (PDL1), MEDI4736 (PD-L1), Avelumab (PD-L1), PDR001 (PD1), BMS‑986016, MGA271, Lirilumab, IPH2201, Emactuzumab, INCB024360, Galunisertib, Ulocuplumab, BKT140, Bavituximab, CC‑90002, Bevacizumab, and MNRP1685A, and MGA271. In certain embodiments, the additional chemotherapeutic agent is a STING agonist. For example, the STING agonist can comprise a flavonoid. Suitable flavonoids include, but are not limited to, 10- (carboxymethyl)-9(10H)acridone (CMA), 5,6- Dimethylxanthenone-4-acetic acid (DMXAA), methoxyvone, 6, 4'-dimethoxyflavone, 4'- methoxyflavone, 3', 6 '-dihydroxyflavone, 7, 2'- dihydroxyflavone, daidzein, formononetin, retusin 7-methyl ether, xanthone, or any combination thereof. In some aspects, the STING agonist can be 10-(carboxymethyl)-9(10H)acridone (CMA). In some aspects, the STING agonist can be 5,6-Dimethylxanthenone-4-acetic acid (DMXAA). In some aspects, the STING agonist can be methoxyvone. In some aspects, the STING agonist can be 6, 4'-dimethoxyflavone. In some aspects, the STING agonist can be 4'- methoxyflavone. In some aspects, the STING agonist can be 3', 6 '-dihydroxyflavone. In some aspects, the STING agonist can be 7, 2 '-dihydroxyflavone. In some aspects, the STING agonist can be daidzein. In some aspects, the STING agonist can be formononetin. In some aspects, the STING agonist can be retusin 7-methyl ether. In some aspects, the STING agonist can be xanthone. In some aspects, the STING agonist can be any combination of the above flavonoids. Thus, for example, in some embodiments the flavonoid comprises DMXAA. In certain embodiments, the additional chemotherapeutic agent is an alkylating agent. Alkylating agents are so named because of their ability to alkylate many nucleophilic functional groups under conditions present in cells, including, but not limited to cancer cells. In a further embodiment, an alkylating agent includes, but is not limited to, Cisplatin, carboplatin, mechlorethamine, cyclophosphamide, chlorambucil, ifosfamide and/or oxaliplatin. In an embodiment, alkylating agents can function by impairing cell function by forming covalent bonds with the amino, carboxyl, sulfhydryl, and phosphate groups in biologically important molecules or they can work by modifying a cell's DNA. In a further embodiment an alkylating agent is a synthetic, semisynthetic or derivative. In certain embodiments, the additional chemotherapeutic agent is an anti- metabolite. Anti-metabolites masquerade as purines or pyrimidines, the building-blocks of DNA and in general, prevent these substances from becoming incorporated in to DNA during the "S" phase (of the cell cycle), stopping normal development and division. Anti- metabolites can also affect RNA synthesis. In an embodiment, an antimetabolite includes, but is not limited to azathioprine and/or mercaptopurine. In a further embodiment an anti- metabolite is a synthetic, semisynthetic or derivative. In certain embodiments, the additional chemotherapeutic agent is a plant alkaloid and/or terpenoid. These alkaloids are derived from plants and block cell division by, in general, preventing microtubule function. In an embodiment, a plant alkaloid and/or terpenoid is a vinca alkaloid, a podophyllotoxin and/or a taxane. Vinca alkaloids, in general, bind to specific sites on tubulin, inhibiting the assembly of tubulin into microtubules, generally during the M phase of the cell cycle. In an embodiment, a vinca alkaloid is derived, without limitation, from the Madagascar periwinkle, Catharanthus roseus (formerly known as Vinca rosea). In an embodiment, a vinca alkaloid includes, without limitation, Vincristine, Vinblastine, Vinorelbine and/or Vindesine. In an embodiment, a taxane includes, but is not limited, to Taxol, Paclitaxel and/or Docetaxel. In a further embodiment a plant alkaloid or terpernoid is a synthetic, semisynthetic or derivative. In a further embodiment, a podophyllotoxin is, without limitation, an etoposide and/or teniposide. In an embodiment, a taxane is, without limitation, docetaxel and/or ortataxel. [021] In an embodiment, a cancer therapeutic is a topoisomerase. Topoisomerases are essential enzymes that maintain the topology of DNA. Inhibition of type I or type II topoisomerases interferes with both transcription and replication of DNA by upsetting proper DNA supercoiling. In a further embodiment, a topoisomerase is, without limitation, a type I topoisomerase inhibitor or a type II topoisomerase inhibitor. In an embodiment a type I topoisomerase inhibitor is, without limitation, a camptothecin. In another embodiment, a camptothecin is, without limitation, exatecan, irinotecan, lurtotecan, topotecan, BNP 1350, CKD 602, DB 67 (AR67) and/or ST 1481. In an embodiment, a type II topoisomerase inhibitor is, without limitation, epipodophyllotoxin. In a further embodiment an epipodophyllotoxin is, without limitation, an amsacrine, etoposid, etoposide phosphate and/or teniposide. In a further embodiment a topoisomerase is a synthetic, semisynthetic or derivative, including those found in nature such as, without limitation, epipodophyllotoxins, substances naturally occurring in the root of American Mayapple (Podophyllum peltatum). In certain embodiments, the additional chemotherapeutic agent is a stilbenoid. In a further embodiment, a stilbenoid includes, but is not limited to, Resveratrol, Piceatannol, Pinosylvin, Pterostilbene, Alpha-Viniferin, Ampelopsin A, Ampelopsin E, Diptoindonesin C, Diptoindonesin F, Epsilon- Vinferin, Flexuosol A, Gnetin H, Hemsleyanol D, Hopeaphenol, Trans-Diptoindonesin B, Astringin, Piceid and Diptoindonesin A. In a further embodiment a stilbenoid is a synthetic, semisynthetic or derivative. In certain embodiments, the additional chemotherapeutic agent is a cytotoxic antibiotic. In an embodiment, a cytotoxic antibiotic is, without limitation, an actinomycin, an anthracenedione, an anthracycline, thalidomide, dichloroacetic acid, nicotinic acid, 2- deoxyglucose and/or chlofazimine. In an embodiment, an actinomycin is, without limitation, actinomycin D, bacitracin, colistin (polymyxin E) and/or polymyxin B. In another embodiment, an antracenedione is, without limitation, mitoxantrone and/or pixantrone. In a further embodiment, an anthracycline is, without limitation, bleomycin, doxorubicin (Adriamycin), daunorubicin (daunomycin), epirubicin, idarubicin, mitomycin, plicamycin and/or valrubicin. In a further embodiment a cytotoxic antibiotic is a synthetic, semisynthetic or derivative. In certain embodiments, the additional chemotherapeutic agent is selected from endostatin, angiogenin, angiostatin, chemokines, angioarrestin, angiostatin (plasminogen fragment), basement-membrane collagen-derived anti-angiogenic factors (tumstatin, canstatin, or arrestin), anti-angiogenic antithrombin III, signal transduction inhibitors, cartilage-derived inhibitor (CDI), CD59 complement fragment, fibronectin fragment, gro- beta, heparinases, heparin hexasaccharide fragment, human chorionic gonadotropin (hCG), interferon alpha/beta/gamma, interferon inducible protein (IP-10), interleukin-12, kringle 5 (plasminogen fragment), metalloproteinase inhibitors (TIMPs), 2-methoxyestradiol, placental ribonuclease inhibitor, plasminogen activator inhibitor, platelet factor-4 (PF4), prolactin 16 kD fragment, proliferin-related protein (PRP), various retinoids, tetrahydrocortisol-S, thrombospondin-1 (TSP-1), transforming growth factor-beta (TGF- β), vasculostatin, vasostatin (calreticulin fragment) and the like. In certain embodiments, the additional chemotherapeutic agent is selected from abiraterone acetate, altretamine, anhydrovinblastine, auristatin, bexarotene, bicalutamide, BMS 184476, 2,3,4,5,6-pentafluoro-N-(3-fluoro-4-methoxyphenyl)benzene sulfonamide, bleomycin, N,N-dimethyl-L-valyl-L-valyl-N-methyl-L-valyl-L-proly-1-Lproline-t- butylamide, cachectin, cemadotin, chlorambucil, cyclophosphamide, 3′,4′-didehydro-4′- deoxy-8′-norvin-caleukoblastine, docetaxol, doxetaxel, cyclophosphamide, carboplatin, carmustine, cisplatin, cryptophycin, cyclophosphamide, cytarabine, dacarbazine (DTIC), dactinomycin, daunorubicin, decitabine dolastatin, doxorubicin (adriamycin), etoposide, 5- fluorouracil, finasteride, flutamide, hydroxyurea and hydroxyureataxanes, ifosfamide, liarozole, lonidamine, lomustine (CCNU), MDV3100, mechlorethamine (nitrogen mustard), melphalan, mivobulin isethionate, rhizoxin, sertenef, streptozocin, mitomycin, methotrexate, taxanes, nilutamide, onapristone, paclitaxel, prednimustine, procarbazine, RPR109881, stramustine phosphate, tamoxifen, tasonermin, taxol, tretinoin, vinblastine, vincristine, vindesine sulfate, and vinflunine. In certain embodiments, the additional chemotherapeutic agent is platinum, cisplatin, carboplatin, oxaliplatin, mechlorethamine, cyclophosphamide, chlorambucil, azathioprine, mercaptopurine, vincristine, vinblastine, vinorelbine, vindesine, etoposide and teniposide, paclitaxel, docetaxel, irinotecan, topotecan, amsacrine, etoposide, etoposide phosphate, teniposide, 5-fluorouracil, leucovorin, methotrexate, gemcitabine, taxane, leucovorin, mitomycin C, tegafur-uracil, idarubicin, fludarabine, mitoxantrone, ifosfamide and doxorubicin. Additional agents include inhibitors of mTOR (mammalian target of rapamycin), including but not limited to rapamycin, everolimus, temsirolimus and deforolimus. In still other embodiments, the additional chemotherapeutic agent can be selected from those delineated in U.S. Patent 7,927,613, which is incorporated herein by reference in its entirety. In certain embodiments, the second therapeutic agent or regimen is administered to the subject prior to contacting with or administering the chemical entity (e.g., about one hour prior, or about 6 hours prior, or about 12 hours prior, or about 24 hours prior, or about 48 hours prior, or about 1 week prior, or about 1 month prior).
In other embodiments, the second therapeutic agent or regimen is administered to the subject at about the same time as contacting with or administering the chemical entity. By way of example, the second therapeutic agent or regimen and the chemical entity are provided to the subject simultaneously in the same dosage form. As another example, the second therapeutic agent or regimen and the chemical entity are provided to the subject concurrently in separate dosage forms.
In still other embodiments, the second therapeutic agent or regimen is administered to the subject after contacting with or administering the chemical entity (e.g., about one hour after, or about 6 hours after, or about 12 hours after, or about 24 hours after, or about 48 hours after, or about 1 week after, or about 1 month after). Patient Selection
In some embodiments, the methods described herein further include the step of identifying a subject (e.g., a patient) in need of such treatment (e.g., by way of biopsy, endoscopy, or other conventional method known in the art). In certain embodiments, the STING protein can serve as a biomarker for certain types of cancer, e.g., colon cancer and prostate cancer. In other embodiments, identifying a subject can include assaying the patient’s tumor microenvironment for the absence of T-cells and/or presence of exhausted T-cells, e.g., patients having one or more cold tumors. Such patients can include those that are resistant to treatment with checkpoint inhibitors. In certain embodiments, such patients can be treated with a chemical entity herein, e.g., to recruit T-cells into the tumor, and in some cases, further treated with one or more checkpoint inhibitors, e.g., once the T-cells become exhausted. In some embodiments, the chemical entities, methods, and compositions described herein can be administered to certain treatment-resistant patient populations (e.g., patients resistant to checkpoint inhibitors; e.g., patients having one or more cold tumors, e.g., tumors lacking T-cells or exhausted T-cells). Compound Preparation and Biological Assays
As can be appreciated by the skilled artisan, methods of synthesizing the compounds of the formulae herein will be evident to those of ordinary skill in the art. For example, the compounds described herein can be synthesized using methods described in, e.g., US 2015/0056224, the contents of each of which are hereby incorporated by reference in their entirety. Synthetic chemistry transformations and protecting group methodologies (protection and deprotection) useful in synthesizing the compounds described herein are known in the art and include, for example, those such as described in R. Larock, Comprehensive Organic Transformations, VCH Publishers (1989); T. W. Greene and RGM. Wuts, Protective Groups in Organic Synthesis, 2d. Ed., John Wiley and Sons (1991); L. Fieser and M. Fieser, Fieser and Fieser's Reagents for Organic Synthesis, John Wiley and Sons (1994); and L. Paquette, ed., Encyclopedia of Reagents for Organic Synthesis, John Wiley and Sons (1995), and subsequent editions thereof. Compounds can be assayed using the procedures described in, e.g., WO 2015/077354. A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. Accordingly, other embodiments are within the scope of the following claims.

Claims

WHAT IS CLAIMED IS: 1. A compound of Formula I:
Figure imgf000066_0001
or a pharmaceutically acceptable salt thereof, wherein: A and B are each independently selected from the group consisting of Formulae (i), (ii), (iii), and (iv):
Figure imgf000066_0002
X and X’ are each independently selected from the group consisting of O, S, S(O), SO2, CH2, CHF, CF2, CH2O, OCH2, CH2CH2, CH=CH, NR3, and N(O-)R3; G1 is a bond connecting (i) the carbon directly attached to X2 and (ii) the carbon directly attached to C(R2A)(R2B)(X6); or is C(RG1A)(RG1B); G2 is a bond connecting (i) the carbon directly attached to X4 and (ii) the carbon directly attached to C(R1A)(R1B)(X3); or is C(RG2A)(RG2B); X1 and X5 are each independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, halo (e.g., F), -CN, -NO2, -N3, -OH, -ORa1, -SH, -SRa1, -C(O)H, - C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -OC(O)H, -OC(O)Ra1, -OC(O)NRb1Rc1, - -C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, - NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1; X2, X3, X4 and X6 are each independently selected from the group consisting of O and S;
Figure imgf000067_0001
Y1 and Y2 are each independently selected from the group consisting of–OH, - ORa1, O-, -SH, -SRa1, S-; and–NRb1Rc1; R1A and R1B are each independently selected from the group consisting of H; halo; C1-4 alkyl; C1-4 haloalkyl; C2-4 alkenyl; C2-4 alkynyl; and C3-5 cycloalkyl, which is optionally substituted with from 1-4 independently selected C1-4 alkyl; or R1A and R1B, together with the carbon atom to which each is attached, form a C3-5 cycloalkyl or heterocyclyl, including from 4-5 ring atoms, wherein from 1-2 (e.g., 1) ring atoms are independently selected from the group consisting of nitrogen and oxygen (e.g oxetane), wherein the C3-5 cycloalkyl or heterocyclyl ring can each be optionally substituted with from 1-4 independently selected C1-4 alkyl; R2A and R2B are each independently selected from the group consisting of H; halo; C1-4 alkyl; C1-4 haloalkyl; C2-4 alkenyl; C2-4 alkynyl; and C3-5 cycloalkyl, which is optionally substituted with from 1-4 independently selected C1-4 alkyl; or R2A and R2B, together with the carbon atom to which each is attached, form a C3-5 cycloalkyl or heterocyclyl, including from 4-5 ring atoms, wherein from 1-2 (e.g., 1) ring atoms are independently selected from the group consisting of nitrogen and oxygen (e.g., oxetane), wherein the C3-5 cycloalkyl or heterocyclyl ring can each be optionally substituted with from 1-4 independently selected C1-4 alkyl, Z1 is N or C-R4;
Z1’ is N or C-H;
Z2 is N or C-R4’;
Z2’ is N or C-H;
Z3 is N-R3 or C-R4; each occurrence of Ra1 is independently selected from the group consisting of: ● C1-10 alkyl optionally substituted with from 1-3 RA;
● C1-10 haloalkyl optionally substituted with from 1-3 RA;
● C2-10 alkenyl optionally substituted with from 1-3 RB,
● C2-10 alkynyl optionally substituted with from 1-3 RB,
● C3-10 cycloalkyl optionally substituted with from 1-5 RC;
● (C3-10 cycloalkyl)-C1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the C3-10 cycloalkyl optionally substituted with from 1-5 RC;
● heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RC;
● (heterocyclyl as defined above)-C1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the heterocyclyl is optionally substituted with from 1-5 RC; ● C6-10 aryl optionally substituted with from 1-5 RD;
● heteroaryl including from 5-10 ring atoms, wherein from 1-4 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RD; and ● (heteroaryl as defined above)-C1-6 alkylene, wherein the alkylene serves as the point of attachment, and wherein the heteroaryl optionally substituted with from 1-5 RD; each occurrence of Rb1 and Rc1 is independently selected from the group consisting of: H; Ra1; -C(O)H, -C(O)Ra1, -C(O)NRb3Rc3, -C(O)ORa1, -OC(O)H, --C(=NRe2)NRb3Rc3, -NRd3C(=NRe2) NRb3Rc3, - NRb3Rc3, -S(O)Ra1, -S(O) NRb3Rc3, -S(O)2Ra1, and -S(O)2 NRb3Rc3; or
Rb1 and Rc1 taken together with the nitrogen atom to which each is attached form a heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RC; (e.g., azetidinyl, morpholino, piperidinyl); each occurrence of R3, Rd1, and Re1 is independently selected from the group consisting of: H; Ra1; -C(O)H, -C(O)Ra1, -C(O)NRb3Rc3, -C(O)ORa1, -OC(O)H, -- C(=NRe2)NRb3Rc3, -NRd3C(=NRe2)NRb3Rc3, -NRb3Rc3, -S(O)Ra1, -S(O)NRb3Rc3, - S(O)2Ra1, and -S(O)2NRb3Rc3; each occurrence of Rb2, Rc2, and Rd2 is independently selected from the group consisting of: H and C1-6 alkyl optionally substituted with from 1-2 RA; each occurrence of Rb3, Rc3, Rd3, and Re2 is independently selected from the group consisting of: H; C1-6 alkyl optionally substituted with from 1-2 RA; -SO2(C1-6 alkyl), - C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl); each occurrence of RG1A, RG1B, RG1A, RG1B, R4, R4’, R5, R6, and R6’ is independently selected from the group consisting of: H; Ra1; halo, -CN, -NO2, -N3, -OH, - ORa1, -SH, -SRa1, -C(O)H, -C(O)Ra1, -C(O) NRb1Rc1, -C(O)OH, -C(O)ORa1, -OC(O)H, - OC(O)Ra1, -OC(O)NRb1Rc1, --C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, - +NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRc1C(O)ORa1, -NRd1C(O)NRb1Rc1, - NRd1S(O)Ra1, -NRd1S(O)2Ra1, -NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1; each occurrence of RA is independently selected from the group consisting of: - CN; -OH; C1-6 alkoxy; C1-6 haloalkoxy; -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl; -C(O)OH; -C(O)O(C1-6 alkyl); and - NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), -C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl); each occurrence of RB is independently selected from the group consisting of: halo; -CN; -OH; C1-6 alkoxy; C1-6 haloalkoxy; -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl; -C(O)OH; -C(O)O(C1-6 alkyl); and - NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), -C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl);; each occurrence of RC is independently selected from the group consisting of: C1- 6 alkyl; C1-4 haloalkyl; halo; -CN; -OH; oxo; C1-6 alkoxy; C1-6 haloalkoxy; -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl; -C(O)(C1-6 alkyl); -C(O)OH; -C(O)O(C1-6 alkyl); and -NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), - C(O)(C1-6 alkyl), and -C(O)O(C1-6 alkyl); each occurrence of RD is independently selected from the group consisting of: ● C1-6 alkyl optionally substituted with from 1-2 substituents independently selected from the group consisting of:–OH, C1-4 alkoxy; C1-4 haloalkoxy; -NH2, -NH(C1-4 alkyl), and -N(C1-4 alkyl)2;
● C1-4 haloalkyl;
● C2-4 alkenyl;
● C2-4 alkynyl;
● halo;
● -CN; ● -N3;
● -OH;
● C1-6 alkoxy;
● C1-6 haloalkoxy;
● -C(O)NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl;
● -SO2NRR’, wherein R’ and R’’ are each independently selected from H and C1-4 alkyl;
● -C(O)(C1-6 alkyl);
● -C(O)OH;
● -C(O)O(C1-6 alkyl);
● -SO2(C1-6 alkyl),
● -NR’’R’’’, wherein R’’ and R’’’ are each independently selected from the group consisting of H, C1-4 alkyl, -SO2(C1-6 alkyl), -C(O)(C1-6 alkyl), and - C(O)O(C1-6 alkyl);
● (C3-10 cycloalkyl)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the C3-10 cycloalkyl is optionally substituted with from 1-5 independently selected C1-4 alkyl; ● (heterocyclyl as defined above)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the heterocyclyl is optionally substituted with from 1-5 independently selected C1-4 alkyl; ● (phenyl)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the phenyl is optionally substituted with from 1-5 substituents independently selected from halo, C1-4 alkyl, -CF3, -OCH3, - SCH3, -OCF3, -NO2, -N3, -NH2, -NH(C1-4 alkyl), -N(C1-4 alkyl)2, - C(O)(C1-4 alkyl), -C(O)OH, -C(O)O(C1-4 alkyl), -SO2(CH3), and cyclopropyl;
● (heteroaryl as defined above)-(CH2)0-2, wherein the CH2 (when present) serves as the point of attachment, and wherein the phenyl is optionally substituted with from 1-5 substituents independently selected from halo, C1-4 alkyl, -CF3, -OCH3, -SCH3, -OCF3, -NO2, -N3, -NH2, -NH(C1-4 alkyl), -N(C1-4 alkyl)2, -C(O)(C1-4 alkyl), -C(O)OH, -C(O)O(C1-4 alkyl), - SO2(CH3), and cyclopropyl; and wherein it is provided:
(a) X1 and X5 cannot both be-OH:
(b) X1 and X5 cannot both be halo (e.g., X1 and X5 cannot both be -F); in certain embodiments, when A and B are each independently selected from formula (i) and formula (ii), then X1 and X5 cannot both be halo (e.g., X1 and X5 cannot both be -F);
(c) X1 and X5 cannot both be -ORa1 when each occurrence of Ra1 is C1-10 alkyl optionally substituted with from 1-3 RA (e.g., when each occurrence of Ra1 is C1-4 alkyl optionally substituted with from 1-2 RA; when each occurrence of Ra1 is C1-4 alkyl; e.g., when each occurrence of Ra1 is methyl or ethyl);
(d) X1 and X5 cannot both be -ORa1 when each occurrence of Ra1 is heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RC; (in certain of these embodiments, the heterocyclyl, includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., Ra1 is optionally substituted pyanyl or piperidinyl);
(e) X1 and X5 cannot both be -ORa1 when each occurrence of Ra1 is (heterocyclyl as defined above)-C1-6 alkylene; in certain of these embodiments, the heterocyclyl, portion includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., optionally substituted pyanyl or piperidinyl);
(f) X1 and X5 cannot both be -OC(O)Ra1 when each occurrence of Ra1 is C1-10 alkyl optionally substituted with from 1-3 RA (e.g., when each occurrence of Ra1 is C1-4 alkyl optionally substituted with from 1-2 RA; when each occurrence of Ra1 is C1-4 alkyl; e.g., when each occurrence of Ra1 is methyl;
(g) X1 and X5 cannot both be -OC(O)Ra1 when when each occurrence of Ra1 is C6- 10 aryl (e.g., phenyl) optionally substituted with from 1-5 RD); and
(h) when one of X1 and X5 is -OH, then the other of X1 and X5 cannot be:
● halo (e.g., -F);
● -OC(O)NRb1Rc1;
● -OC(O)Ra1 (e.g., when each occurrence of Ra1 is C6-10 aryl (e.g., phenyl) optionally substituted with from 1-5 RD); or
● -ORa1 (e.g., when each occurrence of Ra1 is C1-10 alkyl optionally
substituted with from 1-3 RA (e.g., when each occurrence of Ra1 is C1-4 alkyl optionally substituted with from 1-2 RA; when each occurrence of Ra1 is C1-4 alkyl; e.g., when each occurrence of Ra1 is methyl or ethyl).
2. The compound of claim 1, wherein the compound has formula (B):
Figure imgf000073_0001
3. The compound of claim 1 or 2, wherein the compound has formula (I):
Figure imgf000074_0001
4. The compound of any one of claims 1-3, wherein the carbon directly attached to X1 has the (R)-configuration.
5. The compound of any one of claims 1-3, wherein the carbon directly attached to X1 has the (S)-configuration.
6. The compound of any one of claims 1-5, wherein the carbon directly attached to X5 has the (R)-configuration.
7. The compound of any one of claims 1-5, wherein the carbon directly attached to X5 has the (S)-configuration.
8. The compound of any one of claims 1-7, wherein X and X’ are each O.
9. The compound of any one of claims 1-8, wherein G1 is a bond connecting (i) the carbon directly attached to X2 and (ii) the carbon directly attached to C(R2A)(R2B)(X6).
10. The compound of any one of claims 1-9, wherein G2 is a bond connecting (i) the carbon directly attached to X4 and (ii) the carbon directly attached to
C(R1A)(R1B)(X3).
11. The compound of claim 1, wherein X and X’ are each O, G1 is a bond connecting (i) the carbon directly attached to X2 and (ii) the carbon directly attached to C(R2A)(R2B)(X6); or is C(RG1A)(RG1B); G2 is a bond connecting (i) the carbon directly attached to X4 and (ii) the carbon directly attached to C(R1A)(R1B)(X3), and the compound has formula (A’):
Figure imgf000075_0001
12. The compound of claim 11, wherein X and X’ are each O, G1 is a bond connecting (i) the carbon directly attached to X2 and (ii) the carbon directly attached to C(R2A)(R2B)(X6); or is C(RG1A)(RG1B); G2 is a bond connecting (i) the carbon directly attached to X4 and (ii) the carbon directly attached to C(R1A)(R1B)(X3), and the compound has formula (B’):
Figure imgf000075_0002
13. The compound of claim 1, wherein X and X’ are each O, G1 is a bond connecting (i) the carbon directly attached to X2 and (ii) the carbon directly attached to C(R2A)(R2B)(X6); or is C(RG1A)(RG1B); G2 is a bond connecting (i) the carbon directly attached to X4 and (ii) the carbon directly attached to C(R1A)(R1B)(X3), and the compound has formula (I-A):
Figure imgf000076_0001
14. The compound of any one of claims 1-13, wherein A and B are each independently selected from the group consisting of:
Figure imgf000076_0002
15. The compound of any one of claims 1-14, wherein the compound has the following formula:
Figure imgf000076_0003
16. The compound of any one of claims 1-14, wherein the compound has the following formula:
Figure imgf000077_0001
17. The compound of any one of claims 1-14, wherein the compound has the following formul
Figure imgf000077_0002
18. The compound of any one of claims 1-14, wherein the compound has the following formula:
Figure imgf000077_0003
19. The compound of any one of claims 1-16 and 18, wherein each occurrence of Z1 is N, and Z1’ is N.
20. The compound of any one of claims 1-16, 18 and 19, wherein R5 is - NRb1Rc1 (e.g., -NH2 or -NHRc1; e.g., in certain embodiments, R4 and/or R6 is H; or R4 is other than H, and R6 is H).
21. The compound of any one of claims 1-16 and 18 and 19, wherein R5 is - OH.
22. The compound of claim 21, wherein R6 is H (e.g., in certain embodiments, R4 is H; in other embodiments, R4 is other than H).
23. The compound of any one of claims 1-17, wherein each occurrence of Z2 is N, Z2’ is. N, and Z3 is N-R3 (e.g., N-H).
24. The compound of any one of claims 1-17 and 23, wherein R6’ is -NRb1Rc1 (e.g., -NH2 or -NHRc1; e.g., in certain embodiments, R4’ is H; in other embodiments, R4’ is other than H).
25. The compound of any one of claims 1-24, wherein one of X1 and X5 is other than -OH.
26. The compound of any one of claims 1-25, wherein one of X1 and X5 is other than halo.
27. The compound of any one of claims 1-26, wherein one of X1 and X5 is other than -F.
28. The compound of any one of claims 1-27, wherein one of X1 and X5 is other than -ORa1.
29. The compound of claim 28, wherein Ra1 is:
● C1-10 alkyl optionally substituted with from 1-3 RA (e.g., when each
occurrence of Ra1 is C1-4 alkyl optionally substituted with from 1-2 RA; when each occurrence of Ra1 is C1-4 alkyl; e.g., when each occurrence of Ra1 is methyl or ethyl); and/or
● heterocyclyl, including from 3-10 ring atoms, wherein from 1-3 ring atoms are independently selected from the group consisting of nitrogen, oxygen and sulfur, and which is optionally substituted with from 1-5 RC; (in certain of these embodiments, the heterocyclyl, includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., optionally substituted pyanyl or
piperidinyl); and/or
● (heterocyclyl as defined above)-C1-6 alkylene; in certain of these embodiments, the heterocyclyl portion includes from 5-7 ring atoms; e.g., 6 ring atoms, e.g., optionally substituted pyanyl or piperidinyl).
30. The compound of any one of claims 1-29, wherein one of X1 and X5 is other than -OC(O)Ra1.
31. The compound of claim 30, wherein Ra1 is:
● C1-10 alkyl optionally substituted with from 1-3 RA (e.g., when each
occurrence of Ra1 is C1-4 alkyl optionally substituted with from 1-2 RA; when each occurrence of Ra1 is C1-4 alkyl; e.g., when each occurrence of Ra1 is methyl); and/or
● when each occurrence of Ra1 is C6-10 aryl (e.g., phenyl) optionally substituted with from 1-5 RD.
32. The compound of any one of claims 1-31, wherein one of X1 and X5 is other than -OC(O)NRb1Rc1.
33. The compound of any one of claims 1-27, wherein one of X1 and X5 is other than -OH and halo.
34. The compound of any one of claims 1-27 and 33, wherein one of X1 and X5 is other than -OH and -F.
35. The compound of any one of claims 1-31, 33 and 34, wherein one of X1 and X5 is other than -OH, halo, -ORa1 (e.g., when Ra1 is as defined in claim 29), and - OC(O)Ra1 (e.g., when Ra1 is as defined in claim 31).
36. The compound of any one of claims 1-31 and 33-35, wherein one of X1 and X5 is other than -OH, halo, -ORa1 (e.g., when Ra1 is as defined in claim 29), - OC(O)Ra1 (e.g., when Ra1 is as defined in claim 31), and -OC(O)NRb1Rc1.
37. The compound of claim 35 or 36, wherein halo is -F.
38. The compound of any one of claims 1-37, wherein one of X1 and X5 is selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -SH, - SRa1, -C(O)H, -C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -C(=NRe1)NRb1Rc1, - NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, -NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1; and the other is as defined in claim 1.
39. The compound of any one of claims 1-38, wherein one of X1 and X5 is selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, - C(O)H, -C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -C(=NRe1)NRb1Rc1, - NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, -NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1; and the other is as defined in claim 1.
40. The compound of any one of claims 1-39, wherein one of X1 and X5 is selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, - C(O)H, -C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, -C(=NRe1)NRb1Rc1, - NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and - NRd1S(O)2NRb1Rc1; and the other is as defined in claim 1.
41. The compound of any one of claims 1-40, wherein one of X1 and X5 is selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, - NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and - NRd1S(O)2NRb1Rc1; and the other is as defined in claim 1.
42. The compound of any one of claims 1-41, wherein one of X1 and X5 is selected from the group consisting of -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, - +NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, - NRd1S(O)Ra1, -NRd1S(O)2Ra1, and -NRd1S(O)2NRb1Rc1; and the other is as defined in claim 1.
43. The compound of any one of claims 1-42, wherein one of X1 and X5 is selected from the group consisting of -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and - NRd1S(O)2NRb1Rc1; and the other is as defined in claim 1.
44. The compound of any one of claims 1-43, wherein one of X1 and X5 is selected from the group consisting of -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, and -NRd1C(O)NRb1Rc1; and the other is as defined in claim 1.
45. The compound of any one of claims 1-44, wherein one of X1 and X5 is selected from the group consisting of -NRb1Rc1 and -+NRb2Rc2Rd2; and the other is as defined in claim 1.
46. The compound of any one of claims 1-45, wherein one of X1 and X5 is selected from the group consisting–NH2, -+NH3, and NHRc1; and the other is as defined in claim 1.
47. The compound of any one of claims 1-37, wherein each of X1 and X5 is independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, - NO2, -N3, -SH, -SRa1, -C(O)H, -C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, - C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, - NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1.
48. The compound of any one of claims 1-37 and 47, wherein each of X1 and X5 is independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, - CN, -NO2, -N3, -C(O)H, -C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, - C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, - NRd1S(O)2NRb1Rc1, -S(O)Ra1, -S(O)NRb1Rc1, -S(O)2Ra1, and -S(O)2NRb1Rc1.
49. The compound of any one of claims 1-37, 47, and 48, wherein each of X1 and X5 is independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -C(O)H, -C(O)Ra1, -C(O)NRb1Rc1, -C(O)OH, -C(O)ORa1, - C(=NRe1)NRb1Rc1, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, - NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1.
50. The compound of any one of claims 1-37 and 47-49, wherein each of X1 and X5 is independently selected from the group consisting of H, C1-4 alkyl, C1-4 haloalkyl, -CN, -NO2, -N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, - NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, - NRd1S(O)2Ra1, and -NRd1S(O)2NRb1Rc1.
51. The compound of any one of claims 1-37 and 47-50, wherein each of X1 and X5 is independently selected from the group consisting of -NO2, -N3, - NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb2Rc2Rd2, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and - NRd1S(O)2NRb1Rc1.
52. The compound of any one of claims 1-37 and 47-51, wherein each of X1 and X5 is independently selected from the group consisting of -NRb1Rc1, -+NRb2Rc2Rd2, - NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, - NRd1S(O)2Ra1, and -NRd1S(O)2NRb1Rc1.
53. The compound of any one of claims 1-37 and 47-52, wherein each of X1 and X5 is independently selected from the group consisting of -NRb1Rc1, -+NRb2Rc2Rd2, - NRd1C(O)H, -NRd1C(O)Ra1, -NRd1C(O)ORa1, and -NRd1C(O)NRb1Rc1.
54. The compound of any one of claims 1-37 and 47-53, wherein each of X1 and X5 is independently selected from the group consisting of -NRb1Rc1 and - +NRb2Rc2Rd2.
55. The compound of any one of claims 1-37 and 47-54, wherein each of X1 and X5 is independently selected from the group consisting–NH2, -+NH3, and NHRc1.
56. The compound of any one of claims 1-55, wherein each of X2, X3, X4 and X6 is O.
57. The compound of any one of claims 1-56, wherein L1 is .
58. The compound of any one of claims 1-57, wherein Y1 is -OH, -ORa1, O-, - SH, -SRa1, or S..
59. The compound of any one of claims 1-58, wherein Y1 is -OH, -ORa1, or O- .
60. The compound of any one of claims 1-58, wherein Y1 is -SH or S-.
61. The compound of claim 60, wherein L1 has the RP configuration.
62. The compound of claim 60, wherein L1 has the SP configuration.
63. The compound of any one of claims 1-62, wherein L2 is .
64. The compound of any one of claims 1-63, wherein Y2 is -OH, -ORa1, O-, - SH, -SRa1, or S..
65. The compound of any one of claims 1-64, wherein Y2 is -OH, -ORa1, or O- .
66. The compound of any one of claims 1-64, wherein Y2 is S-.
67. The compound of claim 66, wherein L2 has the RP configuration.
68. The compound of claim 66, wherein L2 has the SP configuration.
69. The compound of any one of claims 1-68, wherein R1A and R1B are each H.
70. The compound of any one of claims 1-69, wherein R2A and R2B are each H.
71. The compound of claim 1, wherein the compound has formula (V):
wherein,
Figure imgf000085_0001
X11 and X51 are each independently selected from the group consisting of -NO2, - N3, -NRd1C(=NRe1)NRb1Rc1, -NRb1Rc1, -+NRb1Rc1Rd1, -NRd1C(O)H, -NRd1C(O)Ra1, - NRd1C(O)ORa1, -NRd1C(O)NRb1Rc1, -NRd1S(O)Ra1, -NRd1S(O)2Ra1, and - NRd1S(O)2NRb1Rc1;
each of X2, X3, X4 and X6 is O;
Figure imgf000085_0002
Y1 and Y2 are each independently selected from -OH, -ORa1, O-, -SH, -SRa1, or S; .and
A and B are each independently selected from the group consisting of:
Figure imgf000086_0001
72. The compound of claim 71, wherein A has formula (i), and B has formula (ii); or A has formula (ii), and B has formula (ii); or A has formula (i), and B has formula (i); or A has formula (ii), and B has formula (i).
73. The compound of claim 71 or 72, wherein each occurrence of Z1 is N, and Z1’ is N.
74. The compound of any one of claims 71-73, wherein R5 is -NRb1Rc1 (e.g., - NH2 or -NHRc1; e.g., in certain embodiments, R4 and/or R6 is H; or R4 is other than H, and R6 is H).
75. The compound of any one of claims 71-73, wherein R5 is -OH, and R6 is H (e.g., in certain embodiments, R4 is H; in other embodiments, R4 is other than H).
76. The compound of any one of claims 71-75, wherein each occurrence of Z2 is N, Z2’ is. N, and Z3 is N-R3 (e.g., N-H).
77. The compound of any one of claims 71-76, wherein R6’ is -NRb1Rc1 (e.g., - NH2 or -NHRc1; e.g., in certain embodiments, R4’ is H; in other embodiments, R4’ is other than H).
78. The compound of any one of claims 71-77, wherein X11 and X51 are each independently selected from the group consisting of -NRb1Rc1 and -+NRb1Rc1Rd1.
79. The compound of any one of claims 71-78, wherein X11 and X51 are each independently selected from the group consisting of–NH2, -+NH3, and NHRc1.
80. The compound of any one of claims 71-79, wherein X11 and X51 are each - +NH3.
81. The compound of any one of claims 71-80, wherein Y1 and Y2 are each O- .
82. The compound of any one of claims 71-80, wherein Y1 and Y2 are each S-.
83. The compound of claim 82, wherein L1 and L2 both have the RP configuration or both have the SP configuration.
84. The compound of claim 82, wherein one of L1 and L2 has the RP configuration, and the other has the SP configuration.
85. The compound of any one of claims 71-84, wherein R1A and R1B are each H, and R2A and R2B are each H.
86. The compound of claim 1, wherein the compound is a compound delineated in Table 1.
87. A pharmaceutical composition comprising a compound or salt as claimed in any one of claims 1-86 and one or more pharmaceutically acceptable excipients.
88. A method for modulating STING activity, the method comprising contacting STING with a compound as claimed in any one of claims 1-86; or a pharmaceutical composition as claimed in claim 87.
89. The method of claim 88, wherein the modulating comprises agonizing STING.
90. The method of claim 88, wherein the modulating comprises partially agonizing STING.
91. The method of claim 88, wherein the modulating comprises antagonizing STING
92. The method of any one of claims 88-91, which is carried out in vitro.
93. The method of claim 92, wherein the method comprises contacting a sample comprising one or more cells comprising STING with the compound.
94. The method of claim 93, wherein at least one of the one or more cells is an innate immune cell (e.g., mast cells, macrophages, dendritic cells (DCs), and natural killer cells).
95. The method of claim 94, wherein said contacting induces an immune response sufficient to kill at least one of the one or more cancer cells.
96. The method of claim 93, wherein the sample further comprises one or more cancer cells (e.g., wherein the cancer is selected from the group consisting of melanoma, cervical cancer, breast cancer, ovarian cancer, prostate cancer, testicular cancer, urothelial carcinoma, bladder cancer, non-small cell lung cancer, small cell lung cancer, sarcoma, colorectal adenocarcinoma, gastrointestinal stromal tumors, gastroesophageal carcinoma, colorectal cancer, pancreatic cancer, kidney cancer, hepatocellular cancer, malignant mesothelioma, leukemia, lymphoma, myelodysplasia syndrome, multiple myeloma, transitional cell carcinoma, neuroblastoma, plasma cell neoplasms, Wilm's tumor, or hepatocellular carcinoma).
97. The method of claim 88-91, which is carried out in vivo.
98. The method of claim 97, wherein the method comprises administering the compound to a subject having a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease.
99. The method of claim 98, wherein the subject is a human.
100. The method of claim 98, wherein the disease is cancer.
101. The method of claim 100, wherein the cancer is selected from the group consisting of melanoma, cervical cancer, breast cancer, ovarian cancer, prostate cancer, testicular cancer, urothelial carcinoma, bladder cancer, non-small cell lung cancer, small cell lung cancer, sarcoma, colorectal adenocarcinoma, gastrointestinal stromal tumors, gastroesophageal carcinoma, colorectal cancer, pancreatic cancer, kidney cancer, hepatocellular cancer, malignant mesothelioma, leukemia, lymphoma, myelodysplasia syndrome, multiple myeloma, transitional cell carcinoma, neuroblastoma, plasma cell neoplasms, Wilm's tumor, or hepatocellular carcinoma.
102. The method of claim 100 or 101, wherein the cancer is a refractory cancer.
103. The method of claim 98, wherein the compound is administered in combination with one or more additional cancer therapies.
104. The method of claim 103, wherein the one or more additional cancer therapies comprises surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy or gene therapy, or a combination thereof.
105. The method of claim 104, wherein chemotherapy comprises administering one or more additional chemotherapeutic agents.
106. The method of claim 105, wherein the one or more additional chemotherapeutic agents is selected from an alkylating agent (e.g., cisplatin, carboplatin, mechlorethamine, cyclophosphamide, chlorambucil, ifosfamide and/or oxaliplatin); an anti-metabolite (e.g.,azathioprine and/or mercaptopurine); a terpenoid (e.g., a vinca alkaloid and/or a taxane; e.g., Vincristine, Vinblastine, Vinorelbine and/or Vindesine Taxol, Pacllitaxel and/or Docetaxel); a topoisomerase (e.g., a type I topoisomerase and/or a type 2 topoisomerase; e.g., camptothecins, such as irinotecan and/or topotecan;. amsacrine, etoposide, etoposide phosphate and/or teniposide); a cytotoxic antibiotic (e.g., actinomycin, anthracyclines, doxorubicin, daunorubicin, valrubicin, idarubicin, epirubicin, bleomycin, plicamycin and/or mitomycin); a hormone (e.g., a lutenizing hormone releasing hormone agonist; e.g., leuprolidine, goserelin, triptorelin, histrelin, bicalutamide, flutamide and/or nilutamide); an antibody (e.g., Abciximab, Adalimumab, Alemtuzumab, Atlizumab, Basiliximab, Belimumab, Bevacizumab, Bretuximab vedotin, Canakinumab, Cetuximab, Ceertolizumab pegol, Daclizumab, Denosumab, Eculizumab, Efalizumab, Gemtuzumab, Golimumab, Golimumab, Ibritumomab tiuxetan, Infliximab, Ipilimumab, Muromonab-CD3, Natalizumab, Ofatumumab, Omalizumab, Palivizumab, Panitumuab, Ranibizumab, Rituximab, Tocilizumab, Tositumomab and/or Trastuzumab); an anti- angiogenic agent; a cytokine; a thrombotic agent; a growth inhibitory agent; an anti- helminthic agent; and an immune checkpoint inhibitor that targets an immune checkpoint receptor selected from the group consisting of CTLA-4, PD-1, PD-L1, PD-1– PD-L1, PD- 1– PD-L2, interleukin‑2 (IL‑2), indoleamine 2,3-dioxygenase (IDO), IL‑10, transforming growth factor-β (TGFβ), T cell immunoglobulin and mucin 3 (TIM3 or HAVCR2), Galectin 9– TIM3, Phosphatidylserine– TIM3, lymphocyte activation gene 3 protein (LAG3), MHC class II– LAG3, 4‑1BB–4‑1BB ligand, OX40–OX40 ligand, GITR, GITR ligand– GITR, CD27, CD70-CD27, TNFRSF25, TNFRSF25–TL1A, CD40L, CD40– CD40 ligand, HVEM–LIGHT–LTA, HVEM, HVEM– BTLA, HVEM– CD160, HVEM – LIGHT, HVEM–BTLA–CD160, CD80, CD80– PDL-1, PDL2– CD80, CD244, CD48 – CD244, CD244, ICOS, ICOS–ICOS ligand, B7‑H3, B7‑H4, VISTA, TMIGD2, HHLA2–TMIGD2, Butyrophilins, including BTNL2, Siglec family, TIGIT and PVR family members, KIRs, ILTs and LIRs, NKG2D and NKG2A, MICA and MICB, CD244, CD28, CD86– CD28, CD86– CTLA, CD80– CD28, CD39, CD73 Adenosine–CD39– CD73, CXCR4–CXCL12, Phosphatidylserine, TIM3, Phosphatidylserine – TIM3, SIRPA–CD47, VEGF, Neuropilin, CD160, CD30, and CD155 (e.g., CTLA-4 or PD1 or PD-L1).
107. The method of any one of claims 98-106, wherein the compound is administered intratumorally.
108. A method of treating cancer, comprising administering to a subject in need of such treatment an effective amount of a compound as claimed in any one of claims 1- 86, or a pharmaceutical composition as claimed in claim 87.
109. The method of claim 108, wherein the cancer is selected from the group consisting of melanoma, cervical cancer, breast cancer, ovarian cancer, prostate cancer, testicular cancer, urothelial carcinoma, bladder cancer, non-small cell lung cancer, small cell lung cancer, sarcoma, colorectal adenocarcinoma, gastrointestinal stromal tumors, gastroesophageal carcinoma, colorectal cancer, pancreatic cancer, kidney cancer, hepatocellular cancer, malignant mesothelioma, leukemia, lymphoma, myelodysplasia syndrome, multiple myeloma, transitional cell carcinoma, neuroblastoma, plasma cell neoplasms, Wilm's tumor, or hepatocellular carcinoma.
110. The method of claim 108 or 109, wherein the cancer is a refractory cancer.
111. The method of claim 108, wherein the compound is administered in combination with one or more additional cancer therapies.
112. The method of claim 111, wherein the one or more additional cancer therapies comprises surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy or gene therapy, or a combination thereof.
113. The method of claim 112, wherein chemotherapy comprises administering one or more additional chemotherapeutic agents.
114. The method of claim 113, wherein the one or more additional chemotherapeutic agents is selected from an alkylating agent (e.g., cisplatin, carboplatin, mechlorethamine, cyclophosphamide, chlorambucil, ifosfamide and/or oxaliplatin); an anti-metabolite (e.g.,azathioprine and/or mercaptopurine); a terpenoid (e.g., a vinca alkaloid and/or a taxane; e.g., Vincristine, Vinblastine, Vinorelbine and/or Vindesine Taxol, Pacllitaxel and/or Docetaxel); a topoisomerase (e.g., a type I topoisomerase and/or a type 2 topoisomerase; e.g., camptothecins, such as irinotecan and/or topotecan;. amsacrine, etoposide, etoposide phosphate and/or teniposide); a cytotoxic antibiotic (e.g., actinomycin, anthracyclines, doxorubicin, daunorubicin, valrubicin, idarubicin, epirubicin, bleomycin, plicamycin and/or mitomycin); a hormone (e.g., a lutenizing hormone releasing hormone agonist; e.g., leuprolidine, goserelin, triptorelin, histrelin, bicalutamide, flutamide and/or nilutamide); an antibody (e.g., Abciximab, Adalimumab, Alemtuzumab, Atlizumab, Basiliximab, Belimumab, Bevacizumab, Bretuximab vedotin, Canakinumab, Cetuximab, Ceertolizumab pegol, Daclizumab, Denosumab, Eculizumab, Efalizumab, Gemtuzumab, Golimumab, Golimumab, Ibritumomab tiuxetan, Infliximab, Ipilimumab, Muromonab-CD3, Natalizumab, Ofatumumab, Omalizumab, Palivizumab, Panitumuab, Ranibizumab, Rituximab, Tocilizumab, Tositumomab and/or Trastuzumab); an anti- angiogenic agent; a cytokine; a thrombotic agent; a growth inhibitory agent; an anti- helminthic agent; and an immune checkpoint inhibitor that targets an immune checkpoint receptor selected from the group consisting of CTLA-4, PD-1, PD-L1, PD-1– PD-L1, PD- 1– PD-L2, interleukin‑2 (IL‑2), indoleamine 2,3-dioxygenase (IDO), IL‑10, transforming growth factor-β (TGFβ), T cell immunoglobulin and mucin 3 (TIM3 or HAVCR2), Galectin 9– TIM3, Phosphatidylserine– TIM3, lymphocyte activation gene 3 protein (LAG3), MHC class II– LAG3, 4‑1BB–4‑1BB ligand, OX40–OX40 ligand, GITR, GITR ligand– GITR, CD27, CD70-CD27, TNFRSF25, TNFRSF25–TL1A, CD40L, CD40– CD40 ligand, HVEM–LIGHT–LTA, HVEM, HVEM– BTLA, HVEM– CD160, HVEM – LIGHT, HVEM–BTLA–CD160, CD80, CD80– PDL-1, PDL2– CD80, CD244, CD48 – CD244, CD244, ICOS, ICOS–ICOS ligand, B7‑H3, B7‑H4, VISTA, TMIGD2, HHLA2–TMIGD2, Butyrophilins, including BTNL2, Siglec family, TIGIT and PVR family members, KIRs, ILTs and LIRs, NKG2D and NKG2A, MICA and MICB, CD244, CD28, CD86– CD28, CD86– CTLA, CD80– CD28, CD39, CD73 Adenosine–CD39– CD73, CXCR4–CXCL12, Phosphatidylserine, TIM3, Phosphatidylserine – TIM3, SIRPA–CD47, VEGF, Neuropilin, CD160, CD30, and CD155 (e.g., CTLA-4 or PD1 or PD-L1).
115. The method of any one of claims 108-114, wherein the compound is administered intratumorally.
116. A method of inducing an immune response in a subject in need thereof, the method comprising administering to the subject an effective amount of a compound as claimed in any one of claims 1-86, or a pharmaceutical composition as claimed in claim 87.
117. The method of claim 116, wherein the subject has cancer.
118. The method of claim 117, wherein the subject has undergone and/or is undergoing and/or will undergo one or more cancer therapies.
119. The method of claim 117, wherein the cancer selected from the group consisting of melanoma, cervical cancer, breast cancer, ovarian cancer, prostate cancer, testicular cancer, urothelial carcinoma, bladder cancer, non-small cell lung cancer, small cell lung cancer, sarcoma, colorectal adenocarcinoma, gastrointestinal stromal tumors, gastroesophageal carcinoma, colorectal cancer, pancreatic cancer, kidney cancer, hepatocellular cancer, malignant mesothelioma, leukemia, lymphoma, myelodysplasia syndrome, multiple myeloma, transitional cell carcinoma, neuroblastoma, plasma cell neoplasms, Wilm's tumor, or hepatocellular carcinoma .
120. The method of claim 119, wherein the cancer is a refractory cancer.
121. The method of claim 116, wherein the immune response is an innate immune response.
122. The method of claim 121, wherein the at least one or more cancer therapies comprises surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy or gene therapy, or a combination thereof.
123. The method of claim 122, wherein chemotherapy comprises administering one or more additional chemotherapeutic agents.
124. The method of claim 123, wherein the one or more additional chemotherapeutic agents is selected from alkylating agent (e.g., cisplatin, carboplatin, mechlorethamine, cyclophosphamide, chlorambucil, ifosfamide and/or oxaliplatin); an anti-metabolite (e.g.,azathioprine and/or mercaptopurine); a terpenoid (e.g., a vinca alkaloid and/or a taxane; e.g., Vincristine, Vinblastine, Vinorelbine and/or Vindesine Taxol, Pacllitaxel and/or Docetaxel); a topoisomerase (e.g., a type I topoisomerase and/or a type 2 topoisomerase; e.g., camptothecins, such as irinotecan and/or topotecan;. amsacrine, etoposide, etoposide phosphate and/or teniposide); a cytotoxic antibiotic (e.g., actinomycin, anthracyclines, doxorubicin, daunorubicin, valrubicin, idarubicin, epirubicin, bleomycin, plicamycin and/or mitomycin); a hormone (e.g., a lutenizing hormone releasing hormone agonist; e.g., leuprolidine, goserelin, triptorelin, histrelin, bicalutamide, flutamide and/or nilutamide); an antibody (e.g., Abciximab, Adalimumab, Alemtuzumab, Atlizumab, Basiliximab, Belimumab, Bevacizumab, Bretuximab vedotin, Canakinumab, Cetuximab, Ceertolizumab pegol, Daclizumab, Denosumab, Eculizumab, Efalizumab, Gemtuzumab, Golimumab, Golimumab, Ibritumomab tiuxetan, Infliximab, Ipilimumab, Muromonab-CD3, Natalizumab, Ofatumumab, Omalizumab, Palivizumab, Panitumuab, Ranibizumab, Rituximab, Tocilizumab, Tositumomab and/or Trastuzumab); an anti- angiogenic agent; a cytokine; a thrombotic agent; a growth inhibitory agent; an anti- helminthic agent; and an immune checkpoint inhibitor that targets an immune checkpoint receptor selected from the group consisting of CTLA-4, PD-1, PD-L1, PD-1– PD-L1, PD- 1– PD-L2, interleukin‑2 (IL‑2), indoleamine 2,3-dioxygenase (IDO), IL‑10, transforming growth factor-β (TGFβ), T cell immunoglobulin and mucin 3 (TIM3 or HAVCR2), Galectin 9– TIM3, Phosphatidylserine– TIM3, lymphocyte activation gene 3 protein (LAG3), MHC class II– LAG3, 4‑1BB–4‑1BB ligand, OX40–OX40 ligand, GITR, GITR ligand– GITR, CD27, CD70-CD27, TNFRSF25, TNFRSF25–TL1A, CD40L, CD40– CD40 ligand, HVEM–LIGHT–LTA, HVEM, HVEM– BTLA, HVEM– CD160, HVEM – LIGHT, HVEM–BTLA–CD160, CD80, CD80– PDL-1, PDL2– CD80, CD244, CD48 – CD244, CD244, ICOS, ICOS–ICOS ligand, B7‑H3, B7‑H4, VISTA, TMIGD2, HHLA2–TMIGD2, Butyrophilins, including BTNL2, Siglec family, TIGIT and PVR family members, KIRs, ILTs and LIRs, NKG2D and NKG2A, MICA and MICB, CD244, CD28, CD86– CD28, CD86– CTLA, CD80– CD28, CD39, CD73 Adenosine–CD39– CD73, CXCR4–CXCL12, Phosphatidylserine, TIM3, Phosphatidylserine – TIM3, SIRPA–CD47, VEGF, Neuropilin, CD160, CD30, and CD155 (e.g., CTLA-4 or PD1 or PD-L1).
125. A method of inducing STING-dependent type I interferon production in a subject in need thereof, the method comprising administering to the subject an effective amount of a compound as claimed in any one of claims 1-86, or a pharmaceutical composition as claimed in claim 87.
126. The method of claim 125, wherein the subject has cancer.
127. The method of claim 126, wherein the wherein the subject has undergone and/or is undergoing and/or will undergo one or more cancer therapies cancer is a refractory cancer.
128. The method of claim 126, wherein the cancer selected from the group consisting of melanoma, cervical cancer, breast cancer, ovarian cancer, prostate cancer, testicular cancer, urothelial carcinoma, bladder cancer, non-small cell lung cancer, small cell lung cancer, sarcoma, colorectal adenocarcinoma, gastrointestinal stromal tumors, gastroesophageal carcinoma, colorectal cancer, pancreatic cancer, kidney cancer, hepatocellular cancer, malignant mesothelioma, leukemia, lymphoma, myelodysplasia syndrome, multiple myeloma, transitional cell carcinoma, neuroblastoma, plasma cell neoplasms, Wilm's tumor, or hepatocellular carcinoma.
129. The method of claim 128, wherein the cancer is a refractory cancer.
130. The method of claim 125, wherein the one or more additional cancer therapies comprises surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy or gene therapy, or a combination thereof.
131. The method of claim 130, wherein at least one of the one or more additional cancer therapies is chemotherapy.
132. The method of claim 131, wherein chemotherapy comprises administering one or more additional chemotherapeutic agents.
133. The method of claim 132, wherein the one or more additional
chemotherapeutic agents is selected from alkylating agent (e.g., cisplatin, carboplatin, mechlorethamine, cyclophosphamide, chlorambucil, ifosfamide and/or oxaliplatin); an anti-metabolite (e.g.,azathioprine and/or mercaptopurine); a terpenoid (e.g., a vinca alkaloid and/or a taxane; e.g., Vincristine, Vinblastine, Vinorelbine and/or Vindesine Taxol, Pacllitaxel and/or Docetaxel); a topoisomerase (e.g., a type I topoisomerase and/or a type 2 topoisomerase; e.g., camptothecins, such as irinotecan and/or topotecan;.
amsacrine, etoposide, etoposide phosphate and/or teniposide); a cytotoxic antibiotic (e.g., actinomycin, anthracyclines, doxorubicin, daunorubicin, valrubicin, idarubicin, epirubicin, bleomycin, plicamycin and/or mitomycin); a hormone (e.g., a lutenizing hormone releasing hormone agonist; e.g., leuprolidine, goserelin, triptorelin, histrelin, bicalutamide, flutamide and/or nilutamide); an antibody (e.g., Abciximab, Adalimumab, Alemtuzumab, Atlizumab, Basiliximab, Belimumab, Bevacizumab, Bretuximab vedotin, Canakinumab, Cetuximab, Ceertolizumab pegol, Daclizumab, Denosumab, Eculizumab, Efalizumab, Gemtuzumab, Golimumab, Golimumab, Ibritumomab tiuxetan, Infliximab, Ipilimumab, Muromonab-CD3, Natalizumab, Ofatumumab, Omalizumab, Palivizumab, Panitumuab, Ranibizumab, Rituximab, Tocilizumab, Tositumomab and/or Trastuzumab); an anti-angiogenic agent; a cytokine; a thrombotic agent; a growth inhibitory agent; an anti-helminthic agent; and an immune checkpoint inhibitor that targets an immune checkpoint receptor selected from the group consisting of CTLA-4, PD-1, PD-L1, PD-1– PD-L1, PD-1– PD-L2, interleukin‑2 (IL‑2), indoleamine 2,3-dioxygenase (IDO), IL‑10, transforming growth factor-β (TGFβ), T cell immunoglobulin and mucin 3 (TIM3 or HAVCR2), Galectin 9– TIM3, Phosphatidylserine– TIM3, lymphocyte activation gene 3 protein (LAG3), MHC class II– LAG3, 4‑1BB–4‑1BB ligand, OX40–OX40 ligand, GITR, GITR ligand– GITR, CD27, CD70-CD27, TNFRSF25, TNFRSF25–TL1A, CD40L, CD40–CD40 ligand, HVEM–LIGHT–LTA, HVEM, HVEM– BTLA, HVEM– CD160, HVEM– LIGHT, HVEM–BTLA–CD160, CD80, CD80– PDL-1, PDL2– CD80, CD244, CD48– CD244, CD244, ICOS, ICOS–ICOS ligand, B7‑H3, B7‑H4, VISTA, TMIGD2, HHLA2–TMIGD2, Butyrophilins, including BTNL2, Siglec family, TIGIT and PVR family members, KIRs, ILTs and LIRs, NKG2D and NKG2A, MICA and MICB, CD244, CD28, CD86– CD28, CD86– CTLA, CD80– CD28, CD39, CD73 Adenosine–CD39–CD73, CXCR4–CXCL12, Phosphatidylserine, TIM3, Phosphatidylserine– TIM3, SIRPA–CD47, VEGF, Neuropilin, CD160, CD30, and CD155 (e.g., CTLA-4 or PD1 or PD-L1) .
134. A method of treatment of a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease, comprising administering to a subject in need of such treatment an effective amount of a compound as claimed in any one of claims 1-86, or a pharmaceutical composition as claimed in claim 87.
135. A method of treatment comprising administering to a subject having a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease an effective amount of a compound as claimed in any one of claims 1-86, or a pharmaceutical composition as claimed in claim 87.
136. A method of treatment comprising administering to a subject a compound as claimed in any one of claims 1-86, or a pharmaceutical composition as claimed in claim 87, wherein the compound or composition is administered in an amount effective to treat a disease in which repressed or impaired STING signaling contributes to the pathology and/or symptoms and/or progression of the disease, thereby treating the disease.
137. The method of any one of claims 134-136, wherein the disease is cancer.
138. The method of claim 137, wherein the cancer is selected from the group consisting of melanoma, cervical cancer, breast cancer, ovarian cancer, prostate cancer, testicular cancer, urothelial carcinoma, bladder cancer, non-small cell lung cancer, small cell lung cancer, sarcoma, colorectal adenocarcinoma, gastrointestinal stromal tumors, gastroesophageal carcinoma, colorectal cancer, pancreatic cancer, kidney cancer, hepatocellular cancer, malignant mesothelioma, leukemia, lymphoma, myelodysplasia syndrome, multiple myeloma, transitional cell carcinoma, neuroblastoma, plasma cell neoplasms, Wilm's tumor, or hepatocellular carcinoma.
139. The method of claim 137 or 138, wherein the cancer is a refractory cancer.
140. The method of any one of claims 134-139, wherein the compound is administered in combination with one or more additional cancer therapies.
141. The method of claim 140, wherein the one or more additional cancer therapies comprises surgery, radiotherapy, chemotherapy, toxin therapy, immunotherapy, cryotherapy or gene therapy, or a combination thereof.
142. The method of claim 141, wherein chemotherapy comprises administering one or more additional chemotherapeutic agents.
143. The method of claim 142, wherein the one or more additional chemotherapeutic agents is selected from an alkylating agent (e.g., cisplatin, carboplatin, mechlorethamine, cyclophosphamide, chlorambucil, ifosfamide and/or oxaliplatin); an anti-metabolite (e.g.,azathioprine and/or mercaptopurine); a terpenoid (e.g., a vinca alkaloid and/or a taxane; e.g., Vincristine, Vinblastine, Vinorelbine and/or Vindesine Taxol, Pacllitaxel and/or Docetaxel); a topoisomerase (e.g., a type I topoisomerase and/or a type 2 topoisomerase; e.g., camptothecins, such as irinotecan and/or topotecan;. amsacrine, etoposide, etoposide phosphate and/or teniposide); a cytotoxic antibiotic (e.g., actinomycin, anthracyclines, doxorubicin, daunorubicin, valrubicin, idarubicin, epirubicin, bleomycin, plicamycin and/or mitomycin); a hormone (e.g., a lutenizing hormone releasing hormone agonist; e.g., leuprolidine, goserelin, triptorelin, histrelin, bicalutamide, flutamide and/or nilutamide); an antibody (e.g., Abciximab, Adalimumab, Alemtuzumab, Atlizumab, Basiliximab, Belimumab, Bevacizumab, Bretuximab vedotin, Canakinumab, Cetuximab, Ceertolizumab pegol, Daclizumab, Denosumab, Eculizumab, Efalizumab, Gemtuzumab, Golimumab, Golimumab, Ibritumomab tiuxetan, Infliximab, Ipilimumab, Muromonab-CD3, Natalizumab, Ofatumumab, Omalizumab, Palivizumab, Panitumuab, Ranibizumab, Rituximab, Tocilizumab, Tositumomab and/or Trastuzumab); an anti- angiogenic agent; a cytokine; a thrombotic agent; a growth inhibitory agent; an anti- helminthic agent; and an immune checkpoint inhibitor that targets an immune checkpoint receptor selected from the group consisting of CTLA-4, PD-1, PD-L1, PD-1– PD-L1, PD- 1– PD-L2, interleukin‑2 (IL‑2), indoleamine 2,3-dioxygenase (IDO), IL‑10, transforming growth factor-β (TGFβ), T cell immunoglobulin and mucin 3 (TIM3 or HAVCR2), Galectin 9– TIM3, Phosphatidylserine– TIM3, lymphocyte activation gene 3 protein (LAG3), MHC class II– LAG3, 4‑1BB–4‑1BB ligand, OX40–OX40 ligand, GITR, GITR ligand– GITR, CD27, CD70-CD27, TNFRSF25, TNFRSF25–TL1A, CD40L, CD40– CD40 ligand, HVEM–LIGHT–LTA, HVEM, HVEM– BTLA, HVEM– CD160, HVEM – LIGHT, HVEM–BTLA–CD160, CD80, CD80– PDL-1, PDL2– CD80, CD244, CD48 – CD244, CD244, ICOS, ICOS–ICOS ligand, B7‑H3, B7‑H4, VISTA, TMIGD2, HHLA2–TMIGD2, Butyrophilins, including BTNL2, Siglec family, TIGIT and PVR family members, KIRs, ILTs and LIRs, NKG2D and NKG2A, MICA and MICB, CD244, CD28, CD86– CD28, CD86– CTLA, CD80– CD28, CD39, CD73 Adenosine–CD39– CD73, CXCR4–CXCL12, Phosphatidylserine, TIM3, Phosphatidylserine – TIM3, SIRPA–CD47, VEGF, Neuropilin, CD160, CD30, and CD155 (e.g., CTLA-4 or PD1 or PD-L1).
144. The method of any one of claims 134-143, wherein the compound is administered intratumorally.
145. The method of any one of claims 98-144, wherein the method further comprises identifying the subject..
PCT/US2017/013049 2016-01-11 2017-01-11 Cyclic dinucleotides for treating conditions associated with sting activity such as cancer WO2017123657A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US16/069,201 US10723756B2 (en) 2016-01-11 2017-01-11 Cyclic dinucleotides for treating conditions associated with STING activity such as cancer

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201662277273P 2016-01-11 2016-01-11
US62/277,273 2016-01-11
US201662436795P 2016-12-20 2016-12-20
US62/436,795 2016-12-20

Publications (1)

Publication Number Publication Date
WO2017123657A1 true WO2017123657A1 (en) 2017-07-20

Family

ID=58010368

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2017/013049 WO2017123657A1 (en) 2016-01-11 2017-01-11 Cyclic dinucleotides for treating conditions associated with sting activity such as cancer

Country Status (2)

Country Link
US (1) US10723756B2 (en)
WO (1) WO2017123657A1 (en)

Cited By (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018152450A1 (en) 2017-02-17 2018-08-23 Eisai R&D Management Co., Ltd. Cyclic di-nucleotides compounds for the treatment of cancer
WO2018190719A2 (en) 2017-04-13 2018-10-18 Aduro Biotech Holdings, Europe B.V. Anti-sirp alpha antibodies
US10106574B2 (en) 2015-08-13 2018-10-23 Merck Sharp & Dohme Corp. Cyclic di-nucleotide compounds as sting agonists
WO2019046496A1 (en) * 2017-08-31 2019-03-07 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
WO2019046500A1 (en) * 2017-08-31 2019-03-07 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
WO2019043634A2 (en) 2017-08-30 2019-03-07 Beijing Xuanyi Pharmasciences Co., Ltd. Cyclic di-nucleotides as stimulator of interferon genes modulators
WO2019046498A1 (en) * 2017-08-31 2019-03-07 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
WO2019074887A1 (en) * 2017-10-10 2019-04-18 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
CN109694397A (en) * 2017-10-23 2019-04-30 上海弘翊生物科技有限公司 Cyclic annular dinucleotides compound, preparation method and application
WO2019084060A1 (en) 2017-10-24 2019-05-02 Silverback Therapeutics, Inc. Conjugates and methods of use thereof for selective delivery of immune-modulatory agents
WO2019092660A1 (en) 2017-11-10 2019-05-16 Takeda Pharmaceutical Company Limited Sting modulator compounds, and methods of making and using
WO2019173587A1 (en) * 2018-03-08 2019-09-12 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
US10413612B2 (en) 2016-08-30 2019-09-17 Dana-Farber Cancer Institute, Inc. Method of treating cancer with a biomaterial and a toll-like receptor agonist
US10414747B2 (en) 2016-10-04 2019-09-17 Merck Sharp & Dohme Corp. Benzo[b]thiophene compounds as sting agonists
WO2019180683A1 (en) 2018-03-23 2019-09-26 Takeda Pharmaceutical Company Limited Sting modulator compounds with sulfamate linkages, and methods of making and using
WO2019193543A1 (en) 2018-04-06 2019-10-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3'3'-cyclic dinucleotides
WO2019193542A1 (en) 2018-04-06 2019-10-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'3'-cyclic dinucleotides
WO2019193533A1 (en) 2018-04-06 2019-10-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'2'-cyclic dinucleotides
US10449211B2 (en) 2015-03-10 2019-10-22 Aduro Biotech, Inc. Compositions and methods for activating “stimulator of interferon gene”—dependent signalling
WO2019211799A1 (en) 2018-05-03 2019-11-07 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'3'-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide
WO2019232392A1 (en) 2018-06-01 2019-12-05 Eisai R&D Management Co., Ltd. Methods for the treatment of bladder cancer
US10519188B2 (en) 2016-03-18 2019-12-31 Immunesensor Therapeutics, Inc. Cyclic di-nucleotide compounds and methods of use
WO2020056008A1 (en) 2018-09-12 2020-03-19 Silverback Therapeutics, Inc. Compositions for the treatment of disease with immune stimulatory conjugates
WO2020057546A1 (en) 2018-09-21 2020-03-26 上海迪诺医药科技有限公司 Cyclic dinucleotide analogue, pharmaceutical composition thereof, and application
WO2020074004A1 (en) * 2018-10-12 2020-04-16 上海济煜医药科技有限公司 Cyclic dinucleotide compound and uses thereof
WO2020089815A1 (en) 2018-10-31 2020-05-07 Novartis Ag Antibody conjugates comprising sting agonist
WO2020106741A1 (en) * 2018-11-19 2020-05-28 Ifm Due, Inc. Compounds and compositions for treating conditions associated with sting activity
WO2020178770A1 (en) 2019-03-07 2020-09-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3'3'-cyclic dinucleotides and prodrugs thereof
WO2020178769A1 (en) 2019-03-07 2020-09-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'3'-cyclic dinucleotides and prodrugs thereof
WO2020178768A1 (en) 2019-03-07 2020-09-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3'3'-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide as sting modulator
US10793557B2 (en) 2018-04-03 2020-10-06 Merck Sharp & Dohme Corp. Sting agonist compounds
WO2020227159A2 (en) 2019-05-03 2020-11-12 Flagship Pioneering Innovations V, Inc. Methods of modulating immune activity
US10875872B2 (en) 2018-07-31 2020-12-29 Incyte Corporation Heteroaryl amide compounds as sting activators
CN112424212A (en) * 2018-07-17 2021-02-26 詹森生物科技公司 Cyclic dinucleotides as STING agonists
US10947227B2 (en) 2018-05-25 2021-03-16 Incyte Corporation Tricyclic heterocyclic compounds as sting activators
US10966999B2 (en) 2017-12-20 2021-04-06 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3′3′ cyclic dinucleotides with phosphonate bond activating the sting adaptor protein
WO2021067644A1 (en) 2019-10-01 2021-04-08 Silverback Therapeutics, Inc. Combination therapy with immune stimulatory conjugates
US10980825B2 (en) 2016-12-01 2021-04-20 Takeda Pharmaceutical Company Limited Cyclic dinucleotide
US11008344B2 (en) 2018-07-31 2021-05-18 Incyte Corporation Tricyclic heteroaryl compounds as STING activators
US11033569B2 (en) 2016-07-06 2021-06-15 Sperovie Biosciences, Inc. Compounds,Compositions, and methods for the treatment of disease
US11098077B2 (en) 2016-07-05 2021-08-24 Chinook Therapeutics, Inc. Locked nucleic acid cyclic dinucleotide compounds and uses thereof
WO2021168274A1 (en) 2020-02-21 2021-08-26 Silverback Therapeutics, Inc. Nectin-4 antibody conjugates and uses thereof
US11110106B2 (en) 2018-10-29 2021-09-07 Venenum Biodesign, LLC Sting agonists for treating bladder cancer and solid tumors
WO2021206158A1 (en) 2020-04-10 2021-10-14 小野薬品工業株式会社 Method of cancer therapy
US11161864B2 (en) 2018-10-29 2021-11-02 Venenum Biodesign, LLC Sting agonists
US11203610B2 (en) 2017-12-20 2021-12-21 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2′3′ cyclic dinucleotides with phosphonate bond activating the sting adaptor protein
WO2022006327A1 (en) 2020-07-01 2022-01-06 Silverback Therapeutics, Inc. Anti-asgr1 antibody conjugates and uses thereof
US11285131B2 (en) 2017-08-04 2022-03-29 Merck Sharp & Dohme Corp. Benzo[b]thiophene STING agonists for cancer treatment
US11312772B2 (en) 2017-08-04 2022-04-26 Merck Sharp & Dohme Corp. Combinations of PD-1 antagonists and benzo [b] thiophene STING agonists for cancer treatment
WO2022083584A1 (en) * 2020-10-20 2022-04-28 泰励生物科技（上海）有限公司 Multifunctional cyclic dinucleotide and use thereof
US11453697B1 (en) 2015-08-13 2022-09-27 Merck Sharp & Dohme Llc Cyclic di-nucleotide compounds as sting agonists
US11466047B2 (en) 2017-05-12 2022-10-11 Merck Sharp & Dohme Llc Cyclic di-nucleotide compounds as sting agonists
US11584774B2 (en) 2017-09-11 2023-02-21 F-star Therapeutics, Inc. Compounds, compositions, and methods for the treatment of disease
US11596692B1 (en) 2018-11-21 2023-03-07 Incyte Corporation PD-L1/STING conjugates and methods of use
RU2795220C2 (en) * 2018-06-01 2023-05-02 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Methods for treatment of bladder cancer
US11638716B2 (en) 2017-08-31 2023-05-02 F-star Therapeutics, Inc. Compounds, compositions, and methods for the treatment of disease
US11685761B2 (en) 2017-12-20 2023-06-27 Merck Sharp & Dohme Llc Cyclic di-nucleotide compounds as sting agonists
US11691990B2 (en) 2018-08-16 2023-07-04 Eisai R&D Management Co., Ltd Salts of compounds and crystals thereof
US11702430B2 (en) 2018-04-03 2023-07-18 Merck Sharp & Dohme Llc Aza-benzothiophene compounds as STING agonists
US11707531B2 (en) 2017-09-11 2023-07-25 F-star Therapeutics, Inc. Compounds, compositions, and methods for the treatment of disease
US11725024B2 (en) 2020-11-09 2023-08-15 Takeda Pharmaceutical Company Limited Antibody drug conjugates
US11787833B2 (en) 2019-05-09 2023-10-17 Aligos Therapeutics, Inc. Modified cyclic dinucleoside compounds as sting modulators

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019195658A1 (en) 2018-04-05 2019-10-10 Dana-Farber Cancer Institute, Inc. Sting levels as a biomarker for cancer immunotherapy
US20220305048A1 (en) 2019-08-26 2022-09-29 Dana-Farber Cancer Institute, Inc. Use of heparin to promote type 1 interferon signaling
WO2021228832A1 (en) 2020-05-11 2021-11-18 Erytech Pharma Red cell extracellular vesicles (rcevs) containing cargoes and methods of use and production thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050203051A1 (en) * 2004-03-15 2005-09-15 David Karaolis Method for inhibiting cancer cell proliferation or increasing cancer cell apoptosis
US7927613B2 (en) 2002-02-15 2011-04-19 University Of South Florida Pharmaceutical co-crystal compositions
WO2014179335A1 (en) * 2013-04-29 2014-11-06 Memorial Sloan Kettering Cancer Center Compositions and methods for altering second messenger signaling
US20150056224A1 (en) 2013-05-18 2015-02-26 Aduro Biotech, Inc. Compositions and methods for activating stimulator of interferon gene-dependent signalling
WO2015061294A2 (en) 2013-10-21 2015-04-30 Philadelphia Health & Education Corporation D/B/A/ Use of sting agonists to treat chronic hepatitis b virus infection
WO2015077354A1 (en) 2013-11-19 2015-05-28 The University Of Chicago Use of sting agonist as cancer treatment

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7927613B2 (en) 2002-02-15 2011-04-19 University Of South Florida Pharmaceutical co-crystal compositions
US20050203051A1 (en) * 2004-03-15 2005-09-15 David Karaolis Method for inhibiting cancer cell proliferation or increasing cancer cell apoptosis
WO2014179335A1 (en) * 2013-04-29 2014-11-06 Memorial Sloan Kettering Cancer Center Compositions and methods for altering second messenger signaling
US20150056224A1 (en) 2013-05-18 2015-02-26 Aduro Biotech, Inc. Compositions and methods for activating stimulator of interferon gene-dependent signalling
WO2015061294A2 (en) 2013-10-21 2015-04-30 Philadelphia Health & Education Corporation D/B/A/ Use of sting agonists to treat chronic hepatitis b virus infection
WO2015077354A1 (en) 2013-11-19 2015-05-28 The University Of Chicago Use of sting agonist as cancer treatment

Non-Patent Citations (16)

* Cited by examiner, † Cited by third party
Title
"Encyclopedia of Reagents for Organic Synthesis", 1995, JOHN WILEY AND SONS
"Handbook of Pharmaceutical Additives", 2007, GOWER PUBLISHING COMPANY
"Handbook of Pharmaceutical Excipients", 2009, THE PHARMACEUTICAL PRESS
"Pharmaceutical Preformulation and Formulation", 2009, CRC PRESS LLC
"Remington: The Science and Practice of Pharmacy", 2005, LIPPINCOTT WILLIAMS & WILKINS
"Remington: The Science and Practice of Pharmacy. 22nd Ed.", 2012, PHARMACEUTICAL PRESS
ANDRZEJ GRAJKOWSKI ET AL: "Convenient Synthesis of a Propargylated Cyclic (3'-5') Diguanylic Acid and Its "Click" Conjugation to a Biotinylated Azide", BIOCONJUGATE CHEMISTRY, vol. 21, no. 11, 17 November 2010 (2010-11-17), pages 2147 - 2152, XP055205485, ISSN: 1043-1802, DOI: 10.1021/bc1003857 *
FILIPSKI, K.J. ET AL., CURRENT TOPICS IN MEDICINAL CHEMISTRY, vol. 13, 2013, pages 776 - 802
L. FIESER; M. FIESER: "Fieser and Fieser's Reagents for Organic Synthesis", 1994, JOHN WILEY AND SONS
LAMMERS ET AL.: "Effect of Intratumoral Injection on the Biodistribution and the Therapeutic Potential of HPMA Copolymer-Based Drug Delivery Systems", NEOPLASIA, vol. 10, 2006, pages 788 - 795
MICHAEL SMIETANA ET AL: "Solid-Phase Synthesis and Screening of Macrocyclic Nucleotide-Hybrid Compounds Targeted to Hepatitis?C?NS5B", CHEMISTRY - A EUROPEAN JOURNAL, vol. 10, no. 1, 5 January 2004 (2004-01-05), pages 173 - 181, XP055193155, ISSN: 0947-6539, DOI: 10.1002/chem.200305402 *
POSTOW, M. J., CLIN. ONCOL., vol. 33, 2015, pages 1
R. LAROCK: "Comprehensive Organic Transformations", 1989, VCH PUBLISHERS
T. W. GREENE; RGM. WUTS: "Protective Groups in Organic Synthesis", 1991, JOHN WILEY AND SONS
WU; SUN ET AL., SCIENCE, vol. 339, 2013, pages 826 - 830
YILING LUO ET AL: "Differential binding of 2'-biotinylated analogs of c-di-GMP with c-di-GMP riboswitches and binding proteins", MOLECULAR BIOSYSTEMS, vol. 8, no. 3, 19 December 2011 (2011-12-19), GB, pages 772 - 778, XP055355933, ISSN: 1742-206X, DOI: 10.1039/C2MB05338A *

Cited By (124)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10449211B2 (en) 2015-03-10 2019-10-22 Aduro Biotech, Inc. Compositions and methods for activating “stimulator of interferon gene”—dependent signalling
US11040053B2 (en) 2015-03-10 2021-06-22 Chinook Therapeutics, Inc. Compositions and methods for activating “stimulator of interferon gene”13 dependent signalling
US11453697B1 (en) 2015-08-13 2022-09-27 Merck Sharp & Dohme Llc Cyclic di-nucleotide compounds as sting agonists
US10106574B2 (en) 2015-08-13 2018-10-23 Merck Sharp & Dohme Corp. Cyclic di-nucleotide compounds as sting agonists
US10766919B2 (en) 2015-08-13 2020-09-08 Merck Sharp & Dohme Corp. Cyclic di-nucleotide compounds as sting agonists
US10759825B2 (en) 2015-08-13 2020-09-01 Merck Sharp & Dohme Corp. Cyclic di-nucleotide compounds as STING agonists
US10738074B2 (en) 2015-08-13 2020-08-11 Merck Sharp & Dohme Corp. Cyclic di-nucleotide compounds as STING agonists
US11299512B2 (en) 2016-03-18 2022-04-12 Immunesensor Therapeutics, Inc. Cyclic di-nucleotide compounds and methods of use
US10519188B2 (en) 2016-03-18 2019-12-31 Immunesensor Therapeutics, Inc. Cyclic di-nucleotide compounds and methods of use
US11098077B2 (en) 2016-07-05 2021-08-24 Chinook Therapeutics, Inc. Locked nucleic acid cyclic dinucleotide compounds and uses thereof
US11033569B2 (en) 2016-07-06 2021-06-15 Sperovie Biosciences, Inc. Compounds,Compositions, and methods for the treatment of disease
US11744845B2 (en) 2016-07-06 2023-09-05 F-star Therapeutics, Inc. Compounds,compositions, and methods for the treatment of disease
US11021539B2 (en) 2016-08-30 2021-06-01 Dana-Farber Cancer Institute, Inc. Drug delivery compositions and uses thereof
US10413612B2 (en) 2016-08-30 2019-09-17 Dana-Farber Cancer Institute, Inc. Method of treating cancer with a biomaterial and a toll-like receptor agonist
US10435469B2 (en) 2016-08-30 2019-10-08 Dana-Farber Cancer Institute, Inc. Drug delivery compositions and uses thereof
US10836826B2 (en) 2016-08-30 2020-11-17 Dana-Farber Cancer Institute, Inc. Drug delivery compositions and uses thereof
US10414747B2 (en) 2016-10-04 2019-09-17 Merck Sharp & Dohme Corp. Benzo[b]thiophene compounds as sting agonists
US10730849B2 (en) 2016-10-04 2020-08-04 Merck Sharp & Dohme Corp. Benzo[b]thiophene compounds as STING agonists
US10703738B2 (en) 2016-10-04 2020-07-07 Merck Sharp & Dohme Corp. Benzo[b]thiophene compounds as STING agonists
US11666594B2 (en) 2016-12-01 2023-06-06 Takeda Pharmaceutical Company Limited Antibody-drug conjugates comprising a cyclic dinucleotide
US10980825B2 (en) 2016-12-01 2021-04-20 Takeda Pharmaceutical Company Limited Cyclic dinucleotide
EP4008403A1 (en) 2017-02-17 2022-06-08 Eisai R&D Management Co., Ltd. Cyclic di-nucleotides compounds for the treatment of cancer
WO2018152450A1 (en) 2017-02-17 2018-08-23 Eisai R&D Management Co., Ltd. Cyclic di-nucleotides compounds for the treatment of cancer
US10618930B2 (en) 2017-02-17 2020-04-14 Eisai R&D Management Co., Ltd. Compounds for the treatment of cancer
US11339188B2 (en) 2017-02-17 2022-05-24 Eisai R&D Management Co., Ltd. Compounds for the treatment of cancer
US10246480B2 (en) 2017-02-17 2019-04-02 Eisai R&D Management Co., Ltd. Compounds for the treatment of cancer
WO2018152453A1 (en) 2017-02-17 2018-08-23 Eisai R&D Management Co., Ltd. Cyclic di-nucleotides derivative for the treatment of cancer
WO2018190719A2 (en) 2017-04-13 2018-10-18 Aduro Biotech Holdings, Europe B.V. Anti-sirp alpha antibodies
US11466047B2 (en) 2017-05-12 2022-10-11 Merck Sharp & Dohme Llc Cyclic di-nucleotide compounds as sting agonists
US11285131B2 (en) 2017-08-04 2022-03-29 Merck Sharp & Dohme Corp. Benzo[b]thiophene STING agonists for cancer treatment
US11312772B2 (en) 2017-08-04 2022-04-26 Merck Sharp & Dohme Corp. Combinations of PD-1 antagonists and benzo [b] thiophene STING agonists for cancer treatment
WO2019043634A2 (en) 2017-08-30 2019-03-07 Beijing Xuanyi Pharmasciences Co., Ltd. Cyclic di-nucleotides as stimulator of interferon genes modulators
US11773132B2 (en) 2017-08-30 2023-10-03 Beijing Xuanyi Pharmasciences Co., Ltd. Cyclic di-nucleotides as stimulator of interferon genes modulators
JP2020532529A (en) * 2017-08-31 2020-11-12 ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ Cyclic dinucleotide as an anticancer drug
CN111032672A (en) * 2017-08-31 2020-04-17 百时美施贵宝公司 Cyclic dinucleotides as anticancer agents
CN111051328B (en) * 2017-08-31 2023-11-03 百时美施贵宝公司 Cyclic dinucleotides as anticancer agents
US11667663B2 (en) 2017-08-31 2023-06-06 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
KR20200042939A (en) * 2017-08-31 2020-04-24 브리스톨-마이어스 스큅 컴퍼니 Cyclic dinucleotide as an anticancer agent
US20200223883A1 (en) * 2017-08-31 2020-07-16 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
KR20200042938A (en) * 2017-08-31 2020-04-24 브리스톨-마이어스 스큅 컴퍼니 Cyclic dinucleotide as an anticancer agent
US11638716B2 (en) 2017-08-31 2023-05-02 F-star Therapeutics, Inc. Compounds, compositions, and methods for the treatment of disease
WO2019046496A1 (en) * 2017-08-31 2019-03-07 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
CN111051328A (en) * 2017-08-31 2020-04-21 百时美施贵宝公司 Cyclic dinucleotides as anticancer agents
CN111051327B (en) * 2017-08-31 2023-11-03 百时美施贵宝公司 Cyclic dinucleotides as anticancer agents
WO2019046500A1 (en) * 2017-08-31 2019-03-07 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
KR102674630B1 (en) 2017-08-31 2024-06-11 브리스톨-마이어스 스큅 컴퍼니 Cyclic dinucleotides as anticancer agents
JP7208225B2 (en) 2017-08-31 2023-01-18 ブリストル－マイヤーズ スクイブ カンパニー Cyclic dinucleotides as anticancer agents
KR102651946B1 (en) 2017-08-31 2024-03-26 브리스톨-마이어스 스큅 컴퍼니 Cyclic dinucleotides as anticancer agents
JP2020532539A (en) * 2017-08-31 2020-11-12 ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ Cyclic dinucleotide as an anticancer drug
JP7209697B2 (en) 2017-08-31 2023-01-20 ブリストル－マイヤーズ スクイブ カンパニー Cyclic dinucleotides as anticancer agents
JP2020532542A (en) * 2017-08-31 2020-11-12 ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ Cyclic dinucleotide as an anticancer drug
CN111051327A (en) * 2017-08-31 2020-04-21 百时美施贵宝公司 Cyclic dinucleotides as anticancer agents
JP7316263B2 (en) 2017-08-31 2023-07-27 ブリストル－マイヤーズ スクイブ カンパニー Cyclic dinucleotides as anticancer agents
CN111032672B (en) * 2017-08-31 2024-09-13 百时美施贵宝公司 Cyclic dinucleotides as anticancer agents
WO2019046498A1 (en) * 2017-08-31 2019-03-07 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
US10947263B2 (en) 2017-08-31 2021-03-16 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
US10953032B2 (en) 2017-08-31 2021-03-23 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
US11584774B2 (en) 2017-09-11 2023-02-21 F-star Therapeutics, Inc. Compounds, compositions, and methods for the treatment of disease
US11707531B2 (en) 2017-09-11 2023-07-25 F-star Therapeutics, Inc. Compounds, compositions, and methods for the treatment of disease
WO2019074887A1 (en) * 2017-10-10 2019-04-18 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
CN111344297B (en) * 2017-10-10 2023-10-20 百时美施贵宝公司 Cyclic dinucleotides as anticancer agents
CN111344297A (en) * 2017-10-10 2020-06-26 百时美施贵宝公司 Cyclic dinucleotides as anticancer agents
US11660311B2 (en) 2017-10-10 2023-05-30 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
CN109694397A (en) * 2017-10-23 2019-04-30 上海弘翊生物科技有限公司 Cyclic annular dinucleotides compound, preparation method and application
WO2019084060A1 (en) 2017-10-24 2019-05-02 Silverback Therapeutics, Inc. Conjugates and methods of use thereof for selective delivery of immune-modulatory agents
US12054512B2 (en) 2017-11-10 2024-08-06 Takeda Pharmaceutical Company Limited Sting modulator compounds, and methods of making and using
US11542293B2 (en) 2017-11-10 2023-01-03 Takeda Pharmaceutical Company Limited Sting modulator compounds, and methods of making and using
WO2019092660A1 (en) 2017-11-10 2019-05-16 Takeda Pharmaceutical Company Limited Sting modulator compounds, and methods of making and using
US11203610B2 (en) 2017-12-20 2021-12-21 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2′3′ cyclic dinucleotides with phosphonate bond activating the sting adaptor protein
US10966999B2 (en) 2017-12-20 2021-04-06 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3′3′ cyclic dinucleotides with phosphonate bond activating the sting adaptor protein
US11685761B2 (en) 2017-12-20 2023-06-27 Merck Sharp & Dohme Llc Cyclic di-nucleotide compounds as sting agonists
CN111801341A (en) * 2018-03-08 2020-10-20 百时美施贵宝公司 Cyclic dinucleotides as anticancer agents
US11945834B2 (en) 2018-03-08 2024-04-02 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
CN111801341B (en) * 2018-03-08 2023-10-24 百时美施贵宝公司 Cyclic dinucleotides as anticancer agents
WO2019173587A1 (en) * 2018-03-08 2019-09-12 Bristol-Myers Squibb Company Cyclic dinucleotides as anticancer agents
EP4242212A2 (en) 2018-03-23 2023-09-13 Takeda Pharmaceutical Company Limited Sting modulator compounds with sulfamate linkages, and methods of making and using
WO2019180683A1 (en) 2018-03-23 2019-09-26 Takeda Pharmaceutical Company Limited Sting modulator compounds with sulfamate linkages, and methods of making and using
US11702430B2 (en) 2018-04-03 2023-07-18 Merck Sharp & Dohme Llc Aza-benzothiophene compounds as STING agonists
US10793557B2 (en) 2018-04-03 2020-10-06 Merck Sharp & Dohme Corp. Sting agonist compounds
US11149052B2 (en) 2018-04-06 2021-10-19 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2′3′-cyclic dinucleotides
WO2019193533A1 (en) 2018-04-06 2019-10-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'2'-cyclic dinucleotides
WO2019193542A1 (en) 2018-04-06 2019-10-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'3'-cyclic dinucleotides
WO2019193543A1 (en) 2018-04-06 2019-10-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3'3'-cyclic dinucleotides
US11292812B2 (en) 2018-04-06 2022-04-05 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3′3′-cyclic dinucleotides
WO2019211799A1 (en) 2018-05-03 2019-11-07 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'3'-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide
US11713317B2 (en) 2018-05-25 2023-08-01 Incyte Corporation Tricyclic heterocyclic compounds as sting activators
US10947227B2 (en) 2018-05-25 2021-03-16 Incyte Corporation Tricyclic heterocyclic compounds as sting activators
RU2795220C2 (en) * 2018-06-01 2023-05-02 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Methods for treatment of bladder cancer
WO2019232392A1 (en) 2018-06-01 2019-12-05 Eisai R&D Management Co., Ltd. Methods for the treatment of bladder cancer
CN112424212A (en) * 2018-07-17 2021-02-26 詹森生物科技公司 Cyclic dinucleotides as STING agonists
JP2021531277A (en) * 2018-07-17 2021-11-18 ヤンセン・バイオテック・インコーポレイテッドJanssen Biotech, Inc. Cyclic dinucleotide as a STING agonist
US11912722B2 (en) 2018-07-31 2024-02-27 Incyte Corporation Tricyclic heteroaryl compounds as sting activators
US11008344B2 (en) 2018-07-31 2021-05-18 Incyte Corporation Tricyclic heteroaryl compounds as STING activators
US10875872B2 (en) 2018-07-31 2020-12-29 Incyte Corporation Heteroaryl amide compounds as sting activators
US11427597B2 (en) 2018-07-31 2022-08-30 Incyte Corporation Heteroaryl amide compounds as sting activators
US11691990B2 (en) 2018-08-16 2023-07-04 Eisai R&D Management Co., Ltd Salts of compounds and crystals thereof
WO2020056008A1 (en) 2018-09-12 2020-03-19 Silverback Therapeutics, Inc. Compositions for the treatment of disease with immune stimulatory conjugates
WO2020057546A1 (en) 2018-09-21 2020-03-26 上海迪诺医药科技有限公司 Cyclic dinucleotide analogue, pharmaceutical composition thereof, and application
EP3868773A4 (en) * 2018-10-12 2022-07-13 Shanghai Jemincare Pharmaceuticals Co., Ltd. Cyclic dinucleotide compound and uses thereof
WO2020074004A1 (en) * 2018-10-12 2020-04-16 上海济煜医药科技有限公司 Cyclic dinucleotide compound and uses thereof
CN112867727B (en) * 2018-10-12 2024-05-17 上海济煜医药科技有限公司 Cyclic dinucleotide compounds and uses thereof
US11401295B2 (en) 2018-10-12 2022-08-02 Shanghai Jemincare Pharmaceuticals Co., Ltd. Cyclic dinucleotide compound and uses thereof
CN112867727A (en) * 2018-10-12 2021-05-28 上海济煜医药科技有限公司 Cyclic dinucleoside compound and application thereof
US11161864B2 (en) 2018-10-29 2021-11-02 Venenum Biodesign, LLC Sting agonists
US11110106B2 (en) 2018-10-29 2021-09-07 Venenum Biodesign, LLC Sting agonists for treating bladder cancer and solid tumors
US11883420B2 (en) 2018-10-29 2024-01-30 Venenum Biodesign, LLC Sting agonists for treating bladder cancer and solid tumors
WO2020089815A1 (en) 2018-10-31 2020-05-07 Novartis Ag Antibody conjugates comprising sting agonist
WO2020106741A1 (en) * 2018-11-19 2020-05-28 Ifm Due, Inc. Compounds and compositions for treating conditions associated with sting activity
US11596692B1 (en) 2018-11-21 2023-03-07 Incyte Corporation PD-L1/STING conjugates and methods of use
TWI844631B (en) * 2019-03-07 2024-06-11 捷克科學院有機化學與生物化學研究所 3'3'-cyclic dinucleotides with carbocyclic nucleotide
US11766447B2 (en) 2019-03-07 2023-09-26 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3′3′-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide as sting modulator
WO2020178768A1 (en) 2019-03-07 2020-09-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3'3'-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide as sting modulator
WO2020178769A1 (en) 2019-03-07 2020-09-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'3'-cyclic dinucleotides and prodrugs thereof
WO2020178770A1 (en) 2019-03-07 2020-09-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3'3'-cyclic dinucleotides and prodrugs thereof
WO2020227159A2 (en) 2019-05-03 2020-11-12 Flagship Pioneering Innovations V, Inc. Methods of modulating immune activity
US11787833B2 (en) 2019-05-09 2023-10-17 Aligos Therapeutics, Inc. Modified cyclic dinucleoside compounds as sting modulators
WO2021067644A1 (en) 2019-10-01 2021-04-08 Silverback Therapeutics, Inc. Combination therapy with immune stimulatory conjugates
US11179473B2 (en) 2020-02-21 2021-11-23 Silverback Therapeutics, Inc. Nectin-4 antibody conjugates and uses thereof
WO2021168274A1 (en) 2020-02-21 2021-08-26 Silverback Therapeutics, Inc. Nectin-4 antibody conjugates and uses thereof
WO2021206158A1 (en) 2020-04-10 2021-10-14 小野薬品工業株式会社 Method of cancer therapy
WO2022006327A1 (en) 2020-07-01 2022-01-06 Silverback Therapeutics, Inc. Anti-asgr1 antibody conjugates and uses thereof
US11541126B1 (en) 2020-07-01 2023-01-03 Silverback Therapeutics, Inc. Anti-ASGR1 antibody TLR8 agonist comprising conjugates and uses thereof
WO2022083584A1 (en) * 2020-10-20 2022-04-28 泰励生物科技（上海）有限公司 Multifunctional cyclic dinucleotide and use thereof
US11725024B2 (en) 2020-11-09 2023-08-15 Takeda Pharmaceutical Company Limited Antibody drug conjugates

Also Published As

Publication number Publication date
US20190031708A1 (en) 2019-01-31
US10723756B2 (en) 2020-07-28

Similar Documents

Publication Publication Date Title
US10723756B2 (en) Cyclic dinucleotides for treating conditions associated with STING activity such as cancer
US10961270B2 (en) Compounds and compositions for treating conditions associated with sting activity
US20190345191A1 (en) Cyclic dinucleotide analogs for treating conditions associated with sting (stimulator of interferon genes) activity
WO2020150417A2 (en) Compounds and compositions for treating conditions associated with sting activity
US20200172534A1 (en) Compounds and compositions for treating conditions associated with sting activity
WO2020010155A1 (en) Compounds and compositions for treating conditions associated with sting activity
WO2020236586A1 (en) N-hetaryl-squaramide compounds for treating conditions associated with sting activity
EP3911314A1 (en) Compounds and compositions for treating conditions associated with sting activity
WO2020106741A1 (en) Compounds and compositions for treating conditions associated with sting activity
US20220227760A1 (en) Compounds and compositions for treating conditions associated with sting activity
WO2021067791A1 (en) Oxalamide compounds and compositions for treating conditions associated with sting activity
US20220024906A1 (en) Compounds and compositions for treating conditions associated with sting activity
US20240101556A1 (en) Compounds and compositions for treating conditions associated with sting activity
EP4274660A1 (en) Compounds and compositions for treating conditions associated with sting activity
US20220024919A1 (en) Compounds and compositions for treating conditions associated with sting activity
EP4274824A1 (en) Heterobicyclic compounds having an urea or analogue and their compositions for treating conditions associated with sting activity
US20240076285A1 (en) Compounds and compositions for treating conditions associated with sting activity
WO2022015938A1 (en) Compounds and compositions for treating conditions associated with sting activity
WO2022150549A1 (en) Oxalamide compounds and compositions for treating conditions associated with sting activity
WO2022133098A2 (en) Compounds and compositions for treating conditions associated with sting activity
WO2023137041A1 (en) Compounds and compositions for treating conditions associated with sting activity
WO2024064358A1 (en) Compounds and compositions for treating conditions associated with sting activity

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17704335

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 17704335

Country of ref document: EP

Kind code of ref document: A1