WO2014023813A1 - Alkylpyrimidine derivatives for the treatment of viral infections and further diseases - Google Patents

Alkylpyrimidine derivatives for the treatment of viral infections and further diseases Download PDF

Info

Publication number
WO2014023813A1
WO2014023813A1 PCT/EP2013/066673 EP2013066673W WO2014023813A1 WO 2014023813 A1 WO2014023813 A1 WO 2014023813A1 EP 2013066673 W EP2013066673 W EP 2013066673W WO 2014023813 A1 WO2014023813 A1 WO 2014023813A1
Authority
WO
WIPO (PCT)
Prior art keywords
alkyl
compound
carboxylic
pharmaceutically acceptable
formula
Prior art date
Application number
PCT/EP2013/066673
Other languages
French (fr)
Inventor
David Craig Mc Gowan
Tim Hugo Maria Jonckers
Pierre Jean-Marie Bernard Raboisson
Original Assignee
Janssen R&D Ireland
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
Priority to BR112015002524-2A priority Critical patent/BR112015002524B1/en
Priority to CA2879617A priority patent/CA2879617C/en
Priority to KR1020217004007A priority patent/KR102280589B1/en
Priority to JP2015525892A priority patent/JP6302906B2/en
Priority to ES13748289T priority patent/ES2707885T3/en
Priority to IN478MUN2015 priority patent/IN2015MN00478A/en
Priority to CN201380042284.4A priority patent/CN104781239B/en
Priority to EP13748289.9A priority patent/EP2882721B1/en
Priority to US14/420,066 priority patent/US9284304B2/en
Priority to NZ703731A priority patent/NZ703731A/en
Priority to MX2015001829A priority patent/MX369417B/en
Priority to MYPI2015000167A priority patent/MY183534A/en
Priority to SG11201500814UA priority patent/SG11201500814UA/en
Priority to AU2013301450A priority patent/AU2013301450B2/en
Application filed by Janssen R&D Ireland filed Critical Janssen R&D Ireland
Priority to DK13748289.9T priority patent/DK2882721T3/en
Priority to UAA201500301A priority patent/UA115558C2/en
Priority to KR1020157003081A priority patent/KR102216479B1/en
Priority to EA201590343A priority patent/EA029266B1/en
Publication of WO2014023813A1 publication Critical patent/WO2014023813A1/en
Priority to IL236700A priority patent/IL236700A/en
Priority to PH12015500274A priority patent/PH12015500274A1/en
Priority to ZA2015/00921A priority patent/ZA201500921B/en
Priority to HK15108264.5A priority patent/HK1207636A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48—Two nitrogen atoms
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48—Two nitrogen atoms
    • C07D239/49—Two nitrogen atoms with an aralkyl radical, or substituted aralkyl radical, attached in position 5, e.g. trimethoprim
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Definitions

  • This invention relates to alkylpyrimidine derivatives, processes for their preparation, pharmaceutical compositions, and their use in treatment and /or therapy of diseases.
  • the present invention relates to the use of alkylpyrimidine derivatives in the treatment of viral infections, immune or inflammatory disorders, whereby the modulation, or agonism, of toll-like-receptors (TLRs) is involved.
  • TLRs toll-like-receptors
  • Toll-Like Receptors are primary transmembrane proteins characterized by an extracellular leucine rich domain and a cytoplasmic extension that contains a conserved region.
  • the innate immune system can recognize pathogen-associated molecular patterns via these TLRs expressed on the cell surface of certain types of immune cells. Recognition of foreign pathogens activates the production of cytokines and upregulation of co-stimulatory molecules on phagocytes. This leads to the modulation of T cell behaviour.
  • TLRs TLRs
  • TLR14 TLR14
  • TLR14 TLR14
  • IFNalfa interferon
  • HCV hepatitis C virus
  • IFN inducers offer the potential advantages of reduced immunogenicity and convenience of administration.
  • novel IFN inducers are potentially effective new class of drugs for treating virus infections.
  • Ri is hydrogen, fluorine, hydroxyl, amine, C h alky], C 1-e alkylamino, alkoxy, Ca-y cycloalkyl, C 4 . 7 heterocycle, aryl, bicyclic heterocycle, arylalkyl, heteroaryl, heteroarylalkyl, aryloxy, heteroaryloxy, carboxylic acid, carboxylic ester, carboxylic amide each of which is optionally substituted by one or more substituents
  • halogen independently selected from halogen, hydroxyl, amino, C1-3 alkyl, di-(Ci.6)alkylamino, (Ci-4)alkoxy-(C 1-4 )alkyl, C 1j3 alkylamino, C ā‡ alkyl, C ā‡ alkoxy, C ā‡ cycloalkyl, carboxylic acid, carboxylic ester, carboxylic amide, heterocycle, aryl, alkenyl, alkynyl, arylalkyl, heteroaryl, heteroarylalkyl, or nitrile,
  • R 2 is C1-3 alkyl, each of which is optionally substituted by one or more substituents independently selected from halogen, hydroxyl, amino, nitrile, carboxylic acid, carboxylic ester, carboxylic amide, C 1-3 alkyl, C 1-3 alkoxy or C 3-6 cycloalkyl, sulfone, sulfoxide, or nitrile, with the proviso that N-(2-amino-5-phenethylpyrimidine-4-yl)-N-pentylamine is excluded.
  • the current invention relates to compounds of formula (I) wherein R-i is a heterocycle and R 2 is C 1-6 alkyl substituted with, for example, a hydroxyl group.
  • the present invention provides compounds of formula (I) wherein R-i is hydrogen and wherein R 2 is C 1-6 alkyl, each of which is optionally substituted by one or more substituents independently selected from halogen, hydroxyl, amino, nitrile, carboxylic acid, carboxylic ester, carboxylic amide, C 1-3 alkyl, C 1-3 alkoxy or C 3-6 cycloalkyl, sulfone, sulfoxide, or nitrile.
  • the compounds of formula (I) and their pharmaceutically acceptable salt, solvate or polymorph thereof have activity as pharmaceuticals, in particular as modulators of Toll-Like Receptor (especially TLR7 and/or TLR8) activity.
  • the present invention provides a pharmaceutical composition comprising a compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof together with one or more pharmaceutically acceptable excipients, diluents or carriers.
  • a compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof according to the current invention, or a pharmaceutical composition comprising said compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof can be used as a medicament.
  • a compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof, or said pharmaceutical composition comprising said compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof can be used accordingly in the treatment of any disorder in which the modulation of TLR7 and /or TLR8 is involved.
  • alkyl refers to a straight-chain or branched-chain saturated aliphatic hydrocarbon containing the specified number of carbon atoms.
  • halogen refers to fluorine, chlorine, bromine or iodine.
  • alkenyl refers to an alkyl as defined above consisting of at least two carbon atoms and at least one carbon-carbon double bond.
  • alkynyl refers to an alkyl as defined above consisting of at least two carbon atoms and at least one carbon-carbon triple bond.
  • cycloalkyl refers to a carbocyclic ring containing the specified number of carbon atoms.
  • alkoxy refers to an alkyl (carbon and hydrogen chain) group singular bonded to oxygen like for instance a methoxy group or ethoxy group.
  • aryl means an aromatic ring structure optionally comprising one or two heteroatoms selected from N, O and S, in particular from N and O.
  • Said aromatic ring structure may have 5, 6 or 7 ring atoms.
  • said aromatic ring structure may have 5 or 6 ring atoms.
  • aryloxy refers to an aromatic ring structure. Said aromatic group is singularly bonded to oxygen, like for instance phenol.
  • heteroaryloxy refers to an aromatic ring structure optionally comprising one or two heteroatoms selected from N, O and S. Said aromatic group, containing 5 to 7 ring atoms, one of which is singularly bonded to oxygen like for instance
  • bicyclic heterocycle means an aromatic ring structure, as defined for the term ā€œarylā€ comprised of two fused aromatic rings. Each ring is optionally comprised of heteroatoms selected from N, O and S, in particular from N and O.
  • arylalkyl means an aromatic ring structure as defined for the term ā€œarylā€ optionally substituted with an alkyl group.
  • heteroarylalkyl means an aromatic ring structure as defined for the term ā€œheteroarylā€ optionally substituted by an alkyl group.
  • Heterocycle refers to molecules that are saturated or partially saturated and include but are not limited to tetrahydrofuran, dioxane or other cyclic ethers. Heterocycles containing nitrogen include, for example azetidine, morpholine, piperidine, piperazine, pyrrolidine, and the like. Other heterocycles include, for example, thiomorpholine, morpholine, and cyclic sulfones. "Heteroarylā€ groups are heterocyclic groups which are aromatic in nature. These are monocyclic, bicyclic, or polycyclic containing one or more heteroatoms selected from N, O or S.
  • Heteroaryl groups can be, for example, imidazolyl, isoxazolyl, furyl, oxazolyl, pyrrolyl, pyridonyl, pyridyl, pyridazinyl, pyrazinyl, thiophene or quinoline.
  • Pharmaceutically acceptable salts of the compounds of formula (I) include the acid addition and base salts thereof. Suitable acid addition salts are formed from acids which form non-toxic salts. Suitable base salts are formed from bases which form nontoxic salts.
  • the compounds of the invention may also exist in unsolvated and solvated forms.
  • solvate is used herein to describe a molecular complex comprising the compound of the invention and one or more pharmaceutically acceptable solvent molecules, for example, ethanol.
  • polymorph refers to the ability of the compound of the invention to exist in more than one form or crystal structure.
  • the compounds of the present invention may be administered as crystalline or amorphous products. They may be obtained for example as solid plugs, powders, or films by methods such as precipitation, crystallization, freeze drying, spray drying, or evaporative drying. They may be administered alone or in combination with one or more other compounds of the invention or in combination with one or more other drugs. Generally, they will be administered as a formulation in association with one or more pharmaceutically acceptable excipients.
  • excipient is used herein to describe any ingredient other than the compound(s) of the invention.
  • compositions of the present invention may be formulated into various pharmaceutical forms for administration purposes. As appropriate compositions there may be cited all compositions usually employed for systemically administering drugs.
  • a pharmaceutically acceptable carrier which carrier may take a wide variety of forms depending on the form of preparation desired for administration.
  • These pharmaceutical compositions are desirably in unitary dosage form suitable, for example, for oral, rectal, or percutaneous administration.
  • any of the usual pharmaceutical media may be employed such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as suspensions, syrups, elixirs, emulsions, and solutions; or solid carriers such as starches, sugars, kaolin, diluents, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules, and tablets. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit forms, in which case solid pharmaceutical carriers are obviously employed. Also included are solid form preparations that can be converted, shortly before use, to liquid forms.
  • the carrier optionally comprises a penetration enhancing agent and/or a suitable wetting agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not introduce a significant deleterious effect on the skin. Said additives may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions.
  • These compositions may be administered in various ways, e.g., as a transdermal patch, as a spot-on, as an ointment.
  • the compounds of the present invention may also be administered via inhalation or insufflation by means of methods and formulations employed in the art for administration via this way.
  • the compounds of the present invention may be administered to the lungs in the form of a solution, a suspension or a dry powder. It is especially advantageous to formulate the aforementioned pharmaceutical compositions in unit dosage form for ease of administration and uniformity of dosage.
  • Unit dosage form as used herein refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required
  • unit dosage forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, suppositories, injectable solutions or suspensions and the like, and segregated multiples thereof.
  • an effective daily amount would be from 0.01 mg/kg to 50 mg/kg body weight, more preferably from 0.1 mg/kg to 10 mg/kg body weight. It may be appropriate to administer the required dose as two, three, four or more sub-doses at appropriate intervals throughout the day. Said sub-doses may be formulated as unit dosage forms, for example, containing 1 to 1000 mg, and in particular 5 to 200 mg of active ingredient per unit dosage form. The exact dosage and frequency of administration depends on the particular compound of formula (I) used, the particular condition being treated, the severity of the condition being treated, the age, weight and general physical condition of the particular patient as well as other medication the individual may be taking, as is well known to those skilled in the art.
  • the effective amount may be lowered or increased depending on the response of the treated subject and/or depending on the evaluation of the physician prescribing the compounds of the instant invention.
  • the effective amount ranges mentioned above are therefore only guidelines and are not intended to limit the scope or use of the invention to any extent.
  • TLR7 human TLR7
  • hTLR8 TLR8
  • TLR expression construct expresses the respective wild type sequence or a mutant sequence comprising a deletion in the second leucine-rich repeat of the TLR.
  • mutant TLR proteins have previously been shown to be more susceptible to agonist activation (US 7498409).
  • HEK293 cells were grown in culture medium (DMEM supplemented with 10% FCS and 2 mM Glutamine).
  • culture medium DMEM supplemented with 10% FCS and 2 mM Glutamine.
  • cells were detached with Trypsin-EDTA, transfected with a mix of CMV-TLR7 or TLR8 plasmid (750 ng), N FKB-IUC plasmid (375 ng) and a transfection reagent and incubated overnight at 37Ā°C in a humidified 5% C0 2 atmosphere.
  • Transfected cells were then detached with Trypsin-EDTA, washed in PBS and resuspended in medium to a density of 1 .67 x 10 5 cells/mL.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Virology (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

This invention relates to alkylpyrimidine derivatives of formula (I), processes for their preparation, phamaceutical compositions, and their use in therapy for the treatment of viral infections.

Description

ALKYLPYRIMIDINE DERIVATIVES FOR THE TREATMENT OF VIRAL INFECTIONS AND FURTHER DISEASES.
This invention relates to alkylpyrimidine derivatives, processes for their preparation, pharmaceutical compositions, and their use in treatment and /or therapy of diseases. The present invention relates to the use of alkylpyrimidine derivatives in the treatment of viral infections, immune or inflammatory disorders, whereby the modulation, or agonism, of toll-like-receptors (TLRs) is involved. Toll-Like Receptors are primary transmembrane proteins characterized by an extracellular leucine rich domain and a cytoplasmic extension that contains a conserved region. The innate immune system can recognize pathogen-associated molecular patterns via these TLRs expressed on the cell surface of certain types of immune cells. Recognition of foreign pathogens activates the production of cytokines and upregulation of co-stimulatory molecules on phagocytes. This leads to the modulation of T cell behaviour.
A majority of mammalian species have between ten and fifteen types of Toll-like receptors. Thirteen TLRs (named simply TLR1 to TLR13) have been identified in humans and mice together, and equivalent forms of many of these have been found in other mammalian species. However, equivalents of certain TLR found in humans are not present in all mammals. For example, a gene coding for a protein analogous to TLR10 in humans is present in mice, but appears to have been damaged at some point in the past by a retrovirus. On the other hand, mice express TLRs 1 1 , 12, and 13, none of which are represented in humans. Other mammals may express TLRs which are not found in humans. Other non-mammalian species may have TLRs distinct from mammals, as demonstrated by TLR14, which is found in the Takifugu pufferfish. This may complicate the process of using experimental animals as models of human innate immunity.
For reviews on toll-like receptors see the following journal articles. Hoffmann, J.A., Nature, 426, p33-38, 2003; Akira, S., Takeda, K., and Kaisho, T., Annual Rev.
Immunology, 21 , p335-376, 2003; Ulevitch, R. J., Nature Reviews: Immunology, 4, P512-520, 2004. Compounds indicating activity on Toll-Like receptors have been previously described such as heterocyclic derivatives in WO2000006577, adenine derivatives in
WO 98/01448 and WO 99/28321 , and pyrimidines in WO 2009/067081 . ln the treatment of certain viral infections, regular injections of interferon (IFNalfa) can be administered, as is the case for hepatitis C virus (HCV), (Fried et. al. Peginterferon- alfa plus ribavirin for chronic hepatitis C virus infection, N Engl J Med 2002; 347: 975-82). Orally available small molecule IFN inducers offer the potential advantages of reduced immunogenicity and convenience of administration. Thus, novel IFN inducers are potentially effective new class of drugs for treating virus infections. For an example in the literature of a small molecule IFN inducer having antiviral effect see De Clercq, E.; Descamps, J.; De Somer, P. Science 1978, 200, 563-565. Interferon a is also given in combination with other drugs in the treatment of certain types of cancer (Eur. J. Cancer 46, 2849-57, and Cancer Res. 1992, 52, 1056). TLR 7/8 agonists are also of interest as vaccine adjuvants because of their ability to induce pronounced Th1 response (Hum. Vaccines 2010, 6, 322-335, and Hum. Vaccines 2009, 5, 381-394). However, there exists a strong need for novel Toll-Like receptor modulators having preferred selectivity, and an improved safety profile compared to the compounds of the prior art.
In accordance with the present invention a compound of formula (I) is provided
Figure imgf000003_0001
or a pharmaceutically acceptable salt, solvate or polymorph thereof, wherein
Ri is hydrogen, fluorine, hydroxyl, amine, Chalky], C1-ealkylamino,
Figure imgf000003_0002
alkoxy, Ca-y cycloalkyl, C4.7 heterocycle, aryl, bicyclic heterocycle, arylalkyl, heteroaryl, heteroarylalkyl, aryloxy, heteroaryloxy, carboxylic acid, carboxylic ester, carboxylic amide each of which is optionally substituted by one or more substituents
independently selected from halogen, hydroxyl, amino, C1-3 alkyl, di-(Ci.6)alkylamino, (Ci-4)alkoxy-(C1-4)alkyl, C1j3 alkylamino, C^ alkyl, C^ alkoxy, C^ cycloalkyl, carboxylic acid, carboxylic ester, carboxylic amide, heterocycle, aryl, alkenyl, alkynyl, arylalkyl, heteroaryl, heteroarylalkyl, or nitrile,
R2 is C1-3 alkyl, each of which is optionally substituted by one or more substituents independently selected from halogen, hydroxyl, amino, nitrile, carboxylic acid, carboxylic ester, carboxylic amide, C1-3 alkyl, C1-3 alkoxy or C3-6 cycloalkyl, sulfone, sulfoxide, or nitrile, with the proviso that N-(2-amino-5-phenethylpyrimidine-4-yl)-N-pentylamine is excluded. In a first embodiment the current invention relates to compounds of formula (I) wherein R-i is a heterocycle and R2 is C1-6 alkyl substituted with, for example, a hydroxyl group.
In a second embodiment the present invention provides compounds of formula (I) wherein R-i is hydrogen and wherein R2 is C1-6 alkyl, each of which is optionally substituted by one or more substituents independently selected from halogen, hydroxyl, amino, nitrile, carboxylic acid, carboxylic ester, carboxylic amide, C1-3 alkyl, C1-3 alkoxy or C3-6 cycloalkyl, sulfone, sulfoxide, or nitrile.
.The compounds of formula (I) and their pharmaceutically acceptable salt, solvate or polymorph thereof have activity as pharmaceuticals, in particular as modulators of Toll-Like Receptor (especially TLR7 and/or TLR8) activity. In a further aspect the present invention provides a pharmaceutical composition comprising a compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof together with one or more pharmaceutically acceptable excipients, diluents or carriers.
Furthermore a compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof according to the current invention, or a pharmaceutical composition comprising said compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof can be used as a medicament.
Another aspect of the invention is that a compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof, or said pharmaceutical composition comprising said compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof can be used accordingly in the treatment of any disorder in which the modulation of TLR7 and /or TLR8 is involved.
The term "alkyl" refers to a straight-chain or branched-chain saturated aliphatic hydrocarbon containing the specified number of carbon atoms. The term "halogen" refers to fluorine, chlorine, bromine or iodine. The term "alkenyl" refers to an alkyl as defined above consisting of at least two carbon atoms and at least one carbon-carbon double bond.
The term " alkynyl" refers to an alkyl as defined above consisting of at least two carbon atoms and at least one carbon-carbon triple bond. The term "cycloalkyl" refers to a carbocyclic ring containing the specified number of carbon atoms.
The term "alkoxy" refers to an alkyl (carbon and hydrogen chain) group singular bonded to oxygen like for instance a methoxy group or ethoxy group.
The term "aryl" means an aromatic ring structure optionally comprising one or two heteroatoms selected from N, O and S, in particular from N and O. Said aromatic ring structure may have 5, 6 or 7 ring atoms. In particular, said aromatic ring structure may have 5 or 6 ring atoms.
The term "aryloxy" refers to an aromatic ring structure. Said aromatic group is singularly bonded to oxygen, like for instance phenol. The term "heteroaryloxy" refers to an aromatic ring structure optionally comprising one or two heteroatoms selected from N, O and S. Said aromatic group, containing 5 to 7 ring atoms, one of which is singularly bonded to oxygen like for instance
hydroxypyridine.
The term "bicyclic heterocycle" means an aromatic ring structure, as defined for the term "aryl" comprised of two fused aromatic rings. Each ring is optionally comprised of heteroatoms selected from N, O and S, in particular from N and O.
The term arylalkyl" means an aromatic ring structure as defined for the term "aryl" optionally substituted with an alkyl group.
The term "heteroarylalkyl" means an aromatic ring structure as defined for the term "heteroaryl" optionally substituted by an alkyl group.
"Heterocycle" refers to molecules that are saturated or partially saturated and include but are not limited to tetrahydrofuran, dioxane or other cyclic ethers. Heterocycles containing nitrogen include, for example azetidine, morpholine, piperidine, piperazine, pyrrolidine, and the like. Other heterocycles include, for example, thiomorpholine, morpholine, and cyclic sulfones. "Heteroaryl" groups are heterocyclic groups which are aromatic in nature. These are monocyclic, bicyclic, or polycyclic containing one or more heteroatoms selected from N, O or S. Heteroaryl groups can be, for example, imidazolyl, isoxazolyl, furyl, oxazolyl, pyrrolyl, pyridonyl, pyridyl, pyridazinyl, pyrazinyl, thiophene or quinoline. Pharmaceutically acceptable salts of the compounds of formula (I) include the acid addition and base salts thereof. Suitable acid addition salts are formed from acids which form non-toxic salts. Suitable base salts are formed from bases which form nontoxic salts.
The compounds of the invention may also exist in unsolvated and solvated forms. The term "solvate" is used herein to describe a molecular complex comprising the compound of the invention and one or more pharmaceutically acceptable solvent molecules, for example, ethanol.
The term "polymorph" refers to the ability of the compound of the invention to exist in more than one form or crystal structure. The compounds of the present invention may be administered as crystalline or amorphous products. They may be obtained for example as solid plugs, powders, or films by methods such as precipitation, crystallization, freeze drying, spray drying, or evaporative drying. They may be administered alone or in combination with one or more other compounds of the invention or in combination with one or more other drugs. Generally, they will be administered as a formulation in association with one or more pharmaceutically acceptable excipients. The term "excipient" is used herein to describe any ingredient other than the compound(s) of the invention. The choice of excipient depends largely on factors such as the particular mode of administration, the effect of the excipient on solubility and stability, and the nature of the dosage form. The compounds of the present invention or any subgroup thereof may be formulated into various pharmaceutical forms for administration purposes. As appropriate compositions there may be cited all compositions usually employed for systemically administering drugs. To prepare the pharmaceutical compositions of this invention, an effective amount of the particular compound, optionally in addition salt form, as the active ingredient is combined in intimate admixture with a pharmaceutically acceptable carrier, which carrier may take a wide variety of forms depending on the form of preparation desired for administration. These pharmaceutical compositions are desirably in unitary dosage form suitable, for example, for oral, rectal, or percutaneous administration. For example, in preparing the compositions in oral dosage form, any of the usual pharmaceutical media may be employed such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as suspensions, syrups, elixirs, emulsions, and solutions; or solid carriers such as starches, sugars, kaolin, diluents, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules, and tablets. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit forms, in which case solid pharmaceutical carriers are obviously employed. Also included are solid form preparations that can be converted, shortly before use, to liquid forms. In the compositions suitable for percutaneous administration, the carrier optionally comprises a penetration enhancing agent and/or a suitable wetting agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not introduce a significant deleterious effect on the skin. Said additives may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions. These compositions may be administered in various ways, e.g., as a transdermal patch, as a spot-on, as an ointment. The compounds of the present invention may also be administered via inhalation or insufflation by means of methods and formulations employed in the art for administration via this way. Thus, in general the compounds of the present invention may be administered to the lungs in the form of a solution, a suspension or a dry powder. It is especially advantageous to formulate the aforementioned pharmaceutical compositions in unit dosage form for ease of administration and uniformity of dosage. Unit dosage form as used herein refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required
pharmaceutical carrier. Examples of such unit dosage forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, suppositories, injectable solutions or suspensions and the like, and segregated multiples thereof.
Those of skill in the treatment of infectious diseases will be able to determine the effective amount from the test results presented hereinafter. In general it is
contemplated that an effective daily amount would be from 0.01 mg/kg to 50 mg/kg body weight, more preferably from 0.1 mg/kg to 10 mg/kg body weight. It may be appropriate to administer the required dose as two, three, four or more sub-doses at appropriate intervals throughout the day. Said sub-doses may be formulated as unit dosage forms, for example, containing 1 to 1000 mg, and in particular 5 to 200 mg of active ingredient per unit dosage form. The exact dosage and frequency of administration depends on the particular compound of formula (I) used, the particular condition being treated, the severity of the condition being treated, the age, weight and general physical condition of the particular patient as well as other medication the individual may be taking, as is well known to those skilled in the art. Furthermore, it is evident that the effective amount may be lowered or increased depending on the response of the treated subject and/or depending on the evaluation of the physician prescribing the compounds of the instant invention. The effective amount ranges mentioned above are therefore only guidelines and are not intended to limit the scope or use of the invention to any extent.
Preparation of compounds
Compounds of formula (I) are prepared according to scheme 1.
Preparation of example 1
Scheme 1 :
Figure imgf000008_0001
B-1
Synthesis of A-1
Figure imgf000008_0002
5604-46-6
A-1 CH3PPh3Br (27.91 g, 78.1 mmol, 1 .5 eq.) was suspended in THF (70 mL) and stirred at -78 Ā°C under a N2 atmosphere, n-butyllithium (30 mL, 75 mmol, 1 .44 eq., 2.5 M in hexane) was added dropwise over 20 minutes and stirred for an additional 0.5 hours, followed by the addition of 2-amino-4,6-dichloro-5-formylpyrimidine [5604-46-6] (10.0 g, 52 mmol, 1 .0 eq.) as a suspension in THF (180 ml_). The cooling bath was removed and the mixture was stirred at room temperature for 2 hours. The reaction was cooled to -78 Ā°C then NH4CI (sat., aq.) was added slowly. The cooling bath was removed and the mixture was stirred for 1 .5 hours. The organic layer was separated, washed with water, dried (Na2S04), the solids were removed by filtration, and the solvents of the filtrate were removed under reduced pressure. The crude was purified by silica column chromatography using an petroleum ether to ethyl acetate gradient to afford a colorless oil, A-1 (1 .2 g).
1H NMR (400 MHz, chloroform-d) Ī“ ppm 5.30 (br. s., 2 H), 5.65 (d, 1 H), 5.82 (d, 1 H),6.58 (q, 1 H)
Preparation of B-1
Figure imgf000009_0001
A"1 B-1
A-1 (1.0 g, 5.26 mmol), n-butylamine (0.39 g, 5.26 mmol) and Et3N (0.53 g,
5.26 mmol, 1.0 eq.) in ethanol (10 mL) were refluxed for 12 hours. The solvent was removed under reduced pressure. The crude was purified by silica gel column chromatography using a petroleum ether to ethyl acetate gradient. The best fractions were pooled and concentrated under reduced pressure to give B-1 (300 mg).
LC-MS m/z = 227 (M+H)
1H NMR (400 MHz, CHLOROFORM-d) Ī“ ppm 0.95 (t, J=7.3 Hz, 3 H), 1 .38 (dq, J=14.9, 7.4 Hz, 2 H), 1 .55 (quin, J=7.4 Hz, 2 H), 3.38 (q, J=7.3 Hz, 2 H), 4.75 (br. s., 2 H), 5.39 (br. s., 1 H), 5.5 (m, 2H), 6.55 (m, 1 H) Preparation of example 1
Figure imgf000010_0001
B-1 1
To a solution of B-1 (200 mg, 0.88 mmol, 1.0 eq.) in methanol (5 mL) was added 10% Pd/C (20 mg) and mixed with H2 gas (50 Psi) at 50Ā°C for 17 hours. The crude product was purified by preparative high-performance liquid chromatography (C18 column, eluent: CH3CN/H20 from 10/90 to 95/5, 0.05% HCI). The desired fractions were pooled and concentrated under reduced pressure to afford 1 (74 mg).
LC-MS m/z = 195 (M+H) 1H NMR (400 MHz, CHLOROFORM-d) Ī“ ppm 0.95 (t, J=7.3 Hz, 3 H), 1 .20 (t, J=7.3 Hz, 3 H), 1.38 (dq, J=14.9, 7.4 Hz, 2 H), 1.62 (quin, J=7.4 Hz, 2 H), 1 .93 (br. s., 1 H), 2.37 (q, J=7.3 Hz, 2 H), 3.40 - 3.63 (m, 2 H), 6.18 (br. s., 1 H), 7.24 (br. s., 1 H), 13.43 (br. s., 1 H) Table 1 . Compounds of formula (I). All compounds were synthesized according to the method to prepare example 1.
Figure imgf000010_0002
Figure imgf000011_0001
Figure imgf000012_0001
Analytical Methods. All compounds were characterized by LC-MS using the following methods:
Method 1. An Agilent 1 100 LC-MS in positive ion mode was equipped with a YMC- PACK ODS-AQ, 50 x 2.0 mm, 5 Ī¼Ī·Ī¹ column held at 50Ā°C. The following mobile phase and gradient was used over a 10 minute total run time at 0.8 mL/min, monitoring at 220 nm :
Figure imgf000012_0003
Method 2. An Agilent 1 100 LC-MS in positive ion mode was equipped
with a YMC-PACK ODS-AQ, 50 x 2.0 mm, 5 Ī¼Ī·Ī¹ column held at 50Ā°C.
The following mobile phase and gradient was used over a 10 minute total run time at 0.8 mL/min, monitoring at 220 nm :
Figure imgf000012_0002
Biological Activity of compounds of formula (I)
Description of Biological Assays
Assessment of TLR 7 and TLR 8 activity
The ability of compounds to activate human TLR7 (hTLR7) and/or TLR8 (hTLR8) was assessed in a cellular reporter assay using HEK293 cells transiently transfected with a TLR7 or TLR8 expression vector and N FKB-IUC reporter construct. In one instance the TLR expression construct expresses the respective wild type sequence or a mutant sequence comprising a deletion in the second leucine-rich repeat of the TLR. Such mutant TLR proteins have previously been shown to be more susceptible to agonist activation (US 7498409).
Briefly, HEK293 cells were grown in culture medium (DMEM supplemented with 10% FCS and 2 mM Glutamine). For transfection of cells in 10 cm dishes, cells were detached with Trypsin-EDTA, transfected with a mix of CMV-TLR7 or TLR8 plasmid (750 ng), N FKB-IUC plasmid (375 ng) and a transfection reagent and incubated overnight at 37Ā°C in a humidified 5% C02 atmosphere. Transfected cells were then detached with Trypsin-EDTA, washed in PBS and resuspended in medium to a density of 1 .67 x 105 cells/mL. Thirty microliters of cells were then dispensed into each well in 384-well plates, where 10 Ī¼ĪÆ of compound in 4% DMSO was already present. Following 48 hours incubation at 37Ā°C, 5% C02, the luciferase activity was determined by adding 15 Ī¼ I of Steady Lite Plus substrate (Perkin Elmer) to each well and readout performed on a ViewLux ultraHTS microplate imager (Perkin Elmer). Dose response curves were generated from measurements performed in quadruplicates. Lowest effective concentrations (LEC) values, defined as the concentration that induces an effect which is at least two fold above the standard deviation of the assay, were determined for each compound.
In parallel, a similar dilution series of compound was used (10 Ī¼ĪÆ of compound in 4% DMSO) with 30 Ī¼ĪÆ per well of cells transfected with N FKB-IUC reporter construct alone (1 .67 x 105 cells/mL). Six hours after incubation at 37Ā°C, 5% C02, the luciferase activity was determined by adding 15 Ī¼ I of Steady Lite Plus substrate (Perkin Elmer) to each well and readout performed on a ViewLux ultraHTS microplate imager (Perkin Elmer). Counterscreen data is reported as LEC.
All compounds showed CC50 of >24Ī¼Īœ in the HEK 293 TOX assay described above.
Figure imgf000014_0001

Claims

Claims
1. A compound of formula (I)
Figure imgf000015_0001
or a pharmaceutically acceptable salt, solvate or polymorph thereof, wherein
Ri is hydrogen, fluorine, hydroxyl, amine, Ci_6 alkyl, Ci-6 alkylamino, Ci-6 alkoxy, C3-7 cycloalkyl, C4-7 heterocycle, aryl, bicyclic heterocycle, arylalkyl, heteroaryl, heteroarylalkyi, aryloxy, heteroaryloxy, carboxylic acid, carboxylic ester, carboxylic amide each of which is optionally substituted by one or more substituents independently selected from halogen, hydroxyl, amino, Ci-6 alkyl, di-(Ci-6)alkyl- amino, (Ci-4)alkoxy-(Ci-4)alkyl, Ci-6 alkylamino, Ci-6 alkyl, Ci-6 alkoxy, C3-6 cyclo- alkyl, carboxylic acid, carboxylic ester, carboxylic amide, heterocycle, aryl, alkenyl, alkynyl, arylalkyl, heteroaryl, heteroarylalkyi, or nitrile,
R2 is C1-6 alkyl, each of which is optionally substituted by one or more substituents independently selected from halogen, hydroxyl, amino, nitrile, carboxylic acid, carboxylic ester, carboxylic amide, Ci-3 alkyl, Ci-3 alkoxy or C3-6 cycloalkyl, sulfone, sulfoxide, or nitrile, with the proviso that N-(2-amino-5-phenethylpyrimidine-4-yl)-N-pentylamine is excluded.
A compound according to claim 1 wherein R-i is a heterocycle and R2 is Ci-6 alkyl substituted with a hydroxyl group.
A compound according to claim 1 wherein R-i is hydrogen and wherein R2 is C1-6 alkyl, each of which is optionally substituted by one or more substituents independently selected from halogen, hydroxyl, amino, nitrile, carboxylic acid, carboxylic ester, carboxylic amide, Ci-3 alkyl, Ci-3 alkoxy or C3-6 cycloalkyl, sulfone, sulfoxide, or nitrile .
A pharmaceutical composition comprising a compound of formula (I) or a
Figure imgf000015_0002
pharmaceutically acceptable salt, solvate or polymorph thereof according to claim
1 -3 together with one or more pharmaceutically acceptable excipients, diluents or carriers.
A compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof according to claim 1 -3, or a pharmaceutical composition according to claim 4 for use as a medicament.
A compound of formula (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof according to claim 1 -3, or a pharmaceutical composition according to claim 4 for use in the treatment of a disorder in which the modulation of TLR 7 and/or the modulation of TLR8 is involved.
PCT/EP2013/066673 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases WO2014023813A1 (en)

Priority Applications (22)

Application Number Priority Date Filing Date Title
UAA201500301A UA115558C2 (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
KR1020217004007A KR102280589B1 (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
JP2015525892A JP6302906B2 (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for treating viral infections and other diseases
ES13748289T ES2707885T3 (en) 2012-08-10 2013-08-09 Alkylpyrimidines for the treatment of viral infections and other diseases
IN478MUN2015 IN2015MN00478A (en) 2012-08-10 2013-08-09
CN201380042284.4A CN104781239B (en) 2012-08-10 2013-08-09 For treating the alkyl derivative of virus infection and other disease
EP13748289.9A EP2882721B1 (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
US14/420,066 US9284304B2 (en) 2012-08-10 2013-08-09 Substituted pyrimidines as toll-like receptor modulators
NZ703731A NZ703731A (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
MX2015001829A MX369417B (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases.
MYPI2015000167A MY183534A (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
BR112015002524-2A BR112015002524B1 (en) 2012-08-10 2013-08-09 ALKYLPYRIMIDINE DERIVATIVES, PHARMACEUTICAL COMPOSITION INCLUDING THEM AND THE USE OF THE SAME
AU2013301450A AU2013301450B2 (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
SG11201500814UA SG11201500814UA (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
DK13748289.9T DK2882721T3 (en) 2012-08-10 2013-08-09 ALKYLPYRIMIDINE DERIVATIVES FOR TREATING VIRAL INFECTIONS AND ADDITIONAL DISEASES
CA2879617A CA2879617C (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
KR1020157003081A KR102216479B1 (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
EA201590343A EA029266B1 (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections
IL236700A IL236700A (en) 2012-08-10 2015-01-13 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
PH12015500274A PH12015500274A1 (en) 2012-08-10 2015-02-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases
ZA2015/00921A ZA201500921B (en) 2012-08-10 2015-02-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diaseases
HK15108264.5A HK1207636A1 (en) 2012-08-10 2015-08-26 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP12180167 2012-08-10
EP12180167.4 2012-08-10

Publications (1)

Publication Number Publication Date
WO2014023813A1 true WO2014023813A1 (en) 2014-02-13

Family

ID=48985736

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2013/066673 WO2014023813A1 (en) 2012-08-10 2013-08-09 Alkylpyrimidine derivatives for the treatment of viral infections and further diseases

Country Status (23)

Country Link
US (1) US9284304B2 (en)
EP (1) EP2882721B1 (en)
JP (1) JP6302906B2 (en)
KR (2) KR102216479B1 (en)
CN (2) CN104781239B (en)
AU (1) AU2013301450B2 (en)
BR (1) BR112015002524B1 (en)
CA (1) CA2879617C (en)
CL (1) CL2015000295A1 (en)
DK (1) DK2882721T3 (en)
EA (1) EA029266B1 (en)
ES (1) ES2707885T3 (en)
HK (1) HK1207636A1 (en)
IL (1) IL236700A (en)
IN (1) IN2015MN00478A (en)
MX (1) MX369417B (en)
MY (1) MY183534A (en)
NZ (1) NZ703731A (en)
PH (1) PH12015500274A1 (en)
SG (1) SG11201500814UA (en)
UA (1) UA115558C2 (en)
WO (1) WO2014023813A1 (en)
ZA (1) ZA201500921B (en)

Cited By (109)

* Cited by examiner, ā€  Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016141092A1 (en) 2015-03-04 2016-09-09 Gilead Sciences, Inc. Toll-like receptor modulating 4,6-diamino-pyrido[3,2-d]pyrimidine compounds
WO2017035230A1 (en) 2015-08-26 2017-03-02 Gilead Sciences, Inc. Deuterated toll-like receptor modulators
WO2017048727A1 (en) 2015-09-15 2017-03-23 Gilead Sciences, Inc. Modulators of toll-like recptors for the treatment of hiv
WO2017106346A2 (en) 2015-12-15 2017-06-22 Gilead Sciences, Inc. Human immunodeficiency virus neutralizing antibodies
WO2017205078A1 (en) 2016-05-27 2017-11-30 Gilead Sciences, Inc. Methods for treating hepatitis b virus infections using ns5a, ns5b or ns3 inhibitors
WO2017205115A1 (en) 2016-05-27 2017-11-30 Gilead Sciences, Inc. Compounds for the treatment of hepatitis b virus infection
WO2018039531A1 (en) 2016-08-26 2018-03-01 Gilead Sciences, Inc. Substituted pyrrolizine compounds and uses thereof
WO2018045150A1 (en) 2016-09-02 2018-03-08 Gilead Sciences, Inc. 4,6-diamino-pyrido[3,2-d]pyrimidine derivaties as toll like receptor modulators
WO2018045144A1 (en) 2016-09-02 2018-03-08 Gilead Sciences, Inc. Toll like receptor modulator compounds
WO2018144605A1 (en) 2017-02-02 2018-08-09 Gilead Sciences, Inc. Compounds for the treatment of hepatitis b virus infection
WO2018144390A1 (en) 2017-01-31 2018-08-09 Gilead Sciences, Inc. Crystalline forms of tenofovir alafenamide
WO2018195321A1 (en) 2017-04-20 2018-10-25 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
WO2019040102A1 (en) 2017-08-22 2019-02-28 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
WO2019084060A1 (en) 2017-10-24 2019-05-02 Silverback Therapeutics, Inc. Conjugates and methods of use thereof for selective delivery of immune-modulatory agents
WO2019118884A1 (en) 2017-12-15 2019-06-20 Silverback Therapeutics, Inc. Antibody construct-drug conjugate for the treatment of hepatitis
WO2019160882A1 (en) 2018-02-13 2019-08-22 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
WO2019165374A1 (en) 2018-02-26 2019-08-29 Gilead Sciences, Inc. Substituted pyrrolizine compounds as hbv replication inhibitors
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
WO2019193533A1 (en) 2018-04-06 2019-10-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'2'-cyclic dinucleotides
WO2019195181A1 (en) 2018-04-05 2019-10-10 Gilead Sciences, Inc. Antibodies and fragments thereof that bind hepatitis b virus protein x
WO2019200247A1 (en) 2018-04-12 2019-10-17 Precision Biosciences, Inc. Optimized engineered meganucleases having specificity for a recognition sequence in the hepatitis b virus genome
WO2019204609A1 (en) 2018-04-19 2019-10-24 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
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
WO2020010107A1 (en) 2018-07-03 2020-01-09 Gilead Sciences, Inc. Antibodies that target hiv gp120 and methods of use
WO2020010223A1 (en) 2018-07-06 2020-01-09 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
WO2020010200A1 (en) 2018-07-06 2020-01-09 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
WO2020014643A1 (en) 2018-07-13 2020-01-16 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
WO2020028097A1 (en) 2018-08-01 2020-02-06 Gilead Sciences, Inc. Solid forms of (r)-11-(methoxymethyl)-12-(3-methoxypropoxy)-3,3-dimethyl-8-0x0-2,3,8,13b-tetrahydro-1h-pyrido[2,1-a]pyrrolo[1,2-c] phthalazine-7-c arboxylic acid
WO2020056008A1 (en) 2018-09-12 2020-03-19 Silverback Therapeutics, Inc. Compositions for the treatment of disease with immune stimulatory conjugates
WO2020072656A1 (en) 2018-10-03 2020-04-09 Gilead Sciences, Inc. Imidozopyrimidine derivatives
CN111051296A (en) * 2017-08-17 2020-04-21 吉利德ē§‘学公åø Solid forms of HIV capsid inhibitors
CN111051297A (en) * 2017-08-17 2020-04-21 吉利德ē§‘学公åø Choline salt forms of HIV capsid inhibitors
WO2020086556A1 (en) 2018-10-24 2020-04-30 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
WO2020092621A1 (en) 2018-10-31 2020-05-07 Gilead Sciences, Inc. Substituted 6-azabenzimidazole compounds as hpk1 inhibitors
WO2020092528A1 (en) 2018-10-31 2020-05-07 Gilead Sciences, Inc. Substituted 6-azabenzimidazole compounds having hpk1 inhibitory activity
US10662416B2 (en) 2016-10-14 2020-05-26 Precision Biosciences, Inc. Engineered meganucleases specific for recognition sequences in the hepatitis B virus genome
WO2020176510A1 (en) 2019-02-25 2020-09-03 Gilead Sciences, Inc. Protein kinase c agonists
WO2020176505A1 (en) 2019-02-25 2020-09-03 Gilead Sciences, Inc. Protein kinase c agonists
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
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
WO2020214663A1 (en) 2019-04-17 2020-10-22 Gilead Sciences, Inc. Solid forms of a toll-like receptor modulator
WO2020214652A1 (en) 2019-04-17 2020-10-22 Gilead Sciences, Inc. Solid forms of a toll-like receptor modulator
WO2020237025A1 (en) 2019-05-23 2020-11-26 Gilead Sciences, Inc. Substituted exo-methylene-oxindoles which are hpk1/map4k1 inhibitors
WO2020236753A1 (en) 2019-05-21 2020-11-26 Gilead Sciences, Inc. Methods of identifying hiv patients sensitive to therapy with gp120 v3 glycan-directed antibodies
WO2020255038A1 (en) 2019-06-18 2020-12-24 Janssen Sciences Ireland Unlimited Company Combination of hepatitis b virus (hbv) vaccines and pyridopyrimidine derivatives
WO2020257407A1 (en) 2019-06-19 2020-12-24 Silverback Therapeutics, Inc. Anti-mesothelin antibodies and immunoconjugates thereof
WO2020263830A1 (en) 2019-06-25 2020-12-30 Gilead Sciences, Inc. Flt3l-fc fusion proteins and methods of use
WO2021011544A1 (en) 2019-07-16 2021-01-21 Gilead Sciences, Inc. Hiv vaccines and methods of making and using
WO2021011891A1 (en) 2019-07-18 2021-01-21 Gilead Sciences, Inc. Long-acting formulations of tenofovir alafenamide
WO2021034804A1 (en) 2019-08-19 2021-02-25 Gilead Sciences, Inc. Pharmaceutical formulations of tenofovir alafenamide
US10966999B2 (en) 2017-12-20 2021-04-06 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3ā€²3ā€² 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
WO2021067181A1 (en) 2019-09-30 2021-04-08 Gilead Sciences, Inc. Hbv vaccines and methods treating hbv
WO2021076908A1 (en) 2019-10-18 2021-04-22 Forty Seven, Inc. Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia
WO2021087064A1 (en) 2019-10-31 2021-05-06 Forty Seven, Inc. Anti-cd47 and anti-cd20 based treatment of blood cancer
WO2021096860A1 (en) 2019-11-12 2021-05-20 Gilead Sciences, Inc. Mcl1 inhibitors
WO2021113765A1 (en) 2019-12-06 2021-06-10 Precision Biosciences, Inc. Optimized engineered meganucleases having specificity for a recognition sequence in the hepatitis b virus genome
WO2021130638A1 (en) 2019-12-24 2021-07-01 Carna Biosciences, Inc. Diacylglycerol kinase modulating compounds
WO2021163064A2 (en) 2020-02-14 2021-08-19 Jounce Therapeutics, Inc. Antibodies and fusion proteins that bind to ccr8 and uses thereof
WO2021168274A1 (en) 2020-02-21 2021-08-26 Silverback Therapeutics, Inc. Nectin-4 antibody conjugates and uses thereof
WO2021188959A1 (en) 2020-03-20 2021-09-23 Gilead Sciences, Inc. Prodrugs of 4'-c-substituted-2-halo-2'-deoxyadenosine nucleosides and methods of making and using the same
WO2021222522A1 (en) 2020-05-01 2021-11-04 Gilead Sciences, Inc. Cd73 inhibiting 2,4-dioxopyrimidine compounds
WO2021236944A1 (en) 2020-05-21 2021-11-25 Gilead Sciences, Inc. Pharmaceutical compositions comprising bictegravir
US11203610B2 (en) 2017-12-20 2021-12-21 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2ā€²3ā€² cyclic dinucleotides with phosphonate bond activating the sting adaptor protein
WO2021262990A1 (en) 2020-06-25 2021-12-30 Gilead Sciences, Inc. Capsid inhibitors for the treatment of hiv
WO2022006327A1 (en) 2020-07-01 2022-01-06 Silverback Therapeutics, Inc. Anti-asgr1 antibody conjugates and uses thereof
WO2022031894A1 (en) 2020-08-07 2022-02-10 Gilead Sciences, Inc. Prodrugs of phosphonamide nucleotide analogues and their pharmaceutical use
US11267801B2 (en) 2018-02-15 2022-03-08 Gilead Sciences, Inc. Therapeutic compounds
US11286257B2 (en) 2019-06-28 2022-03-29 Gilead Sciences, Inc. Processes for preparing toll-like receptor modulator compounds
WO2022087149A2 (en) 2020-10-22 2022-04-28 Gilead Sciences, Inc. Interleukin-2-fc fusion proteins and methods of use
WO2022103758A1 (en) 2020-11-11 2022-05-19 Gilead Sciences, Inc. METHODS OF IDENTIFYING HIV PATIENTS SENSITIVE TO THERAPY WITH gp120 CD4 BINDING SITE-DIRECTED ANTIBODIES
WO2022217022A1 (en) 2021-04-10 2022-10-13 Profoundbio Us Co. Folr1 binding agents, conjugates thereof and methods of using the same
WO2022221304A1 (en) 2021-04-14 2022-10-20 Gilead Sciences, Inc. CO-INHIBITION OF CD47/SIRPĪ± BINDING AND NEDD8-ACTIVATING ENZYME E1 REGULATORY SUBUNIT FOR THE TREATMENT OF CANCER
WO2022226317A1 (en) 2021-04-23 2022-10-27 Profoundbio Us Co. Anti-cd70 antibodies, conjugates thereof and methods of using the same
WO2022241134A1 (en) 2021-05-13 2022-11-17 Gilead Sciences, Inc. COMBINATION OF A TLR8 MODULATING COMPOUND AND ANTI-HBV siRNA THERAPEUTICS
WO2022245671A1 (en) 2021-05-18 2022-11-24 Gilead Sciences, Inc. Methods of using flt3l-fc fusion proteins
WO2022271684A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
WO2022271659A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
WO2022271650A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
WO2022271677A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
WO2023280227A2 (en) 2021-07-06 2023-01-12 Profoundbio Us Co. Linkers, drug linkers and conjugates thereof and methods of using the same
WO2023076983A1 (en) 2021-10-28 2023-05-04 Gilead Sciences, Inc. Pyridizin-3(2h)-one derivatives
WO2023077030A1 (en) 2021-10-29 2023-05-04 Gilead Sciences, Inc. Cd73 compounds
WO2023102523A1 (en) 2021-12-03 2023-06-08 Gilead Sciences, Inc. Therapeutic compounds for hiv virus infection
WO2023102529A1 (en) 2021-12-03 2023-06-08 Gilead Sciences, Inc. Therapeutic compounds for hiv virus infection
WO2023102239A1 (en) 2021-12-03 2023-06-08 Gilead Sciences, Inc. Therapeutic compounds for hiv virus infection
WO2023107954A1 (en) 2021-12-08 2023-06-15 Dragonfly Therapeutics, Inc. Antibodies targeting 5t4 and uses thereof
WO2023107956A1 (en) 2021-12-08 2023-06-15 Dragonfly Therapeutics, Inc. Proteins binding nkg2d, cd16 and 5t4
WO2023122581A2 (en) 2021-12-22 2023-06-29 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
WO2023122615A1 (en) 2021-12-22 2023-06-29 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
WO2023147418A1 (en) 2022-01-28 2023-08-03 Gilead Sciences, Inc. Parp7 inhibitors
US11760746B2 (en) 2018-02-16 2023-09-19 Gilead Sciences, Inc. Methods and intermediates for preparing therapeutic compounds
EP4245756A1 (en) 2022-03-17 2023-09-20 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
WO2023183817A1 (en) 2022-03-24 2023-09-28 Gilead Sciences, Inc. Combination therapy for treating trop-2 expressing cancers
WO2023196875A1 (en) 2022-04-06 2023-10-12 Gilead Sciences, Inc. Bridged tricyclic carbamoylpyridone compounds and uses thereof
WO2023196784A1 (en) 2022-04-05 2023-10-12 Gilead Sciences, Inc. Combinations of antibody therapies for treating colorectal cancer
WO2023205719A1 (en) 2022-04-21 2023-10-26 Gilead Sciences, Inc. Kras g12d modulating compounds
US11807625B2 (en) 2019-11-26 2023-11-07 Gilead Sciences, Inc. Capsid inhibitors for the prevention of HIV
WO2024006982A1 (en) 2022-07-01 2024-01-04 Gilead Sciences, Inc. Therapeutic compounds useful for the prophylactic or therapeutic treatment of an hiv virus infection
WO2024006929A1 (en) 2022-07-01 2024-01-04 Gilead Sciences, Inc. Cd73 compounds
WO2024015741A1 (en) 2022-07-12 2024-01-18 Gilead Sciences, Inc. Hiv immunogenic polypeptides and vaccines and uses thereof
WO2024044477A1 (en) 2022-08-26 2024-02-29 Gilead Sciences, Inc. Dosing and scheduling regimen for broadly neutralizing antibodies
WO2024064668A1 (en) 2022-09-21 2024-03-28 Gilead Sciences, Inc. FOCAL IONIZING RADIATION AND CD47/SIRPĪ± DISRUPTION ANTICANCER COMBINATION THERAPY
US11944611B2 (en) 2018-07-16 2024-04-02 Gilead Sciences, Inc. Capsid inhibitors for the treatment of HIV
WO2024076915A1 (en) 2022-10-04 2024-04-11 Gilead Sciences, Inc. 4'-thionucleoside analogues and their pharmaceutical use
WO2024137852A1 (en) 2022-12-22 2024-06-27 Gilead Sciences, Inc. Prmt5 inhibitors and uses thereof
US12077537B2 (en) 2023-02-15 2024-09-03 Gilead Sciences, Inc. Capsid inhibitors for the treatment of HIV

Families Citing this family (18)

* Cited by examiner, ā€  Cited by third party
Publication number Priority date Publication date Assignee Title
LT2694484T (en) 2011-04-08 2018-10-10 Janssen Sciences Ireland Uc Pyrimidine derivatives for the treatment of viral infections
JP6349256B2 (en) 2011-11-09 2018-06-27 ćƒ¤ćƒ³ć‚»ćƒ³ćƒ»ć‚µć‚¤ć‚Øćƒ³ć‚·ć‚ŗćƒ»ć‚¢ć‚¤ćƒ«ćƒ©ćƒ³ćƒ‰ćƒ»ćƒ¦ćƒ¼ć‚·ćƒ¼ Purine derivatives for the treatment of viral infections
EP2872515B1 (en) 2012-07-13 2016-06-08 Janssen Sciences Ireland UC Macrocyclic purines for the treatment of viral infections
CA2884478C (en) 2012-10-10 2021-02-16 Janssen Sciences Ireland Uc Pyrrolo[3,2-d]pyrimidine derivatives for the treatment of viral infections and other diseases
ES2655843T3 (en) 2012-11-16 2018-02-21 Janssen Sciences Ireland Uc Heterocyclic substituted 2-aminoquinazoline derivatives for the treatment of viral infections
DK2958900T3 (en) 2013-02-21 2019-07-01 Janssen Sciences Ireland Unlimited Co 2-AMINOPYRIMIDIN DERIVATIVES FOR TREATMENT OF VIRUS INFECTIONS
DK2978429T3 (en) 2013-03-29 2017-05-15 Janssen Sciences Ireland Uc MACROCYCLIC DEAZA PURINONES FOR TREATING VIRUS INFECTIONS
US10377738B2 (en) 2013-05-24 2019-08-13 Janssen Sciences Ireland Unlimited Company Pyridone derivatives for the treatment of viral infections and further diseases
WO2014207082A1 (en) 2013-06-27 2014-12-31 Janssen R&D Ireland Pyrrolo[3,2-d]pyrimidine derivatives for the treatment of viral infections and other diseases
UA117253C2 (en) 2013-07-30 2018-07-10 ŠÆŠŠ”Š”Š•Š Š”ŠŠ™Š„ŠŠ”Š•Š— ŠŠ™Š Š›Š•ŠŠ” Š®Š”і THIENO[3,2-d]PYRIMIDINES DERIVATIVES FOR THE TREATMENT OF VIRAL INFECTIONS
CA3027471A1 (en) 2016-07-01 2018-01-04 Janssen Sciences Ireland Unlimited Company Dihydropyranopyrimidines for the treatment of viral infections
DE102016212303A1 (en) 2016-07-06 2018-01-11 Thyssenkrupp Ag Rack and a method for producing a rack for a steering gear of a motor vehicle
DE102016212308B4 (en) 2016-07-06 2018-02-22 Thyssenkrupp Ag A method for producing a rack for a steering gear of a motor vehicle, and rack
DE102016212304B4 (en) 2016-07-06 2018-02-22 Thyssenkrupp Ag A method for producing a rack for a steering gear of a motor vehicle, and rack
DE102016212307B4 (en) 2016-07-06 2018-02-22 Thyssenkrupp Ag Method for producing a rack for a motor vehicle, and rack for a steering gear
WO2018060317A1 (en) 2016-09-29 2018-04-05 Janssen Sciences Ireland Uc Pyrimidine prodrugs for the treatment of viral infections and further diseases
US10662161B2 (en) 2017-01-30 2020-05-26 Regents Of The University Of Minnesota Pyrimidines and uses thereof
TW201945003A (en) 2018-03-01 2019-12-01 ꄛēˆ¾č˜­å•†å„ē”Ÿē§‘å­øꄛēˆ¾č˜­ē„”限公åø 2,4-diaminoquinazoline derivatives and medical uses thereof

Citations (3)

* Cited by examiner, ā€  Cited by third party
Publication number Priority date Publication date Assignee Title
EP1110951A1 (en) * 1998-08-27 2001-06-27 Sumitomo Pharmaceuticals Company, Limited Pyrimidine derivatives
WO2009067081A1 (en) * 2007-11-22 2009-05-28 Astrazeneca Ab Pyrimidine derivatives for the treatment of asthma, copd, allergic rhinitis, allergic conjunctivitis, atopic dermatitis, cancer, hepatitis b, hepatitis c, hiv, hpv, bacterial infections and dermatosis
WO2012066335A1 (en) * 2010-11-19 2012-05-24 Astrazeneca Ab Phenol compounds als toll -like receptor 7 agonists

Family Cites Families (7)

* Cited by examiner, ā€  Cited by third party
Publication number Priority date Publication date Assignee Title
ES2232871T3 (en) 1996-07-03 2005-06-01 Sumitomo Pharmaceuticals Company, Limited NEW DERIVATIVES OF PURINA.
ATE247654T1 (en) 1997-11-28 2003-09-15 Sumitomo Pharma NEW HETEROCYCLIC COMPOUNDS
US6110929A (en) 1998-07-28 2000-08-29 3M Innovative Properties Company Oxazolo, thiazolo and selenazolo [4,5-c]-quinolin-4-amines and analogs thereof
US6583148B1 (en) * 1999-04-08 2003-06-24 Krenitsky Pharmaceuticals, Inc. Neurotrophic substituted pyrimidines
AU2006242920A1 (en) 2005-05-04 2006-11-09 Pfizer Limited 2-amido-6-amino-8-oxopurine derivatives as Toll-Like receptor modulators for the treatment of cancer and viral infections, such as hepatitis C
NZ582090A (en) 2007-06-29 2012-05-25 Gilead Sciences Inc Purine derivatives and their use as modulators of toll-like receptor 7
WO2009134624A1 (en) 2008-04-28 2009-11-05 Merck & Co., Inc. Hcv ns3 protease inhibitors

Patent Citations (3)

* Cited by examiner, ā€  Cited by third party
Publication number Priority date Publication date Assignee Title
EP1110951A1 (en) * 1998-08-27 2001-06-27 Sumitomo Pharmaceuticals Company, Limited Pyrimidine derivatives
WO2009067081A1 (en) * 2007-11-22 2009-05-28 Astrazeneca Ab Pyrimidine derivatives for the treatment of asthma, copd, allergic rhinitis, allergic conjunctivitis, atopic dermatitis, cancer, hepatitis b, hepatitis c, hiv, hpv, bacterial infections and dermatosis
WO2012066335A1 (en) * 2010-11-19 2012-05-24 Astrazeneca Ab Phenol compounds als toll -like receptor 7 agonists

Cited By (148)

* Cited by examiner, ā€  Cited by third party
Publication number Priority date Publication date Assignee Title
EP3321265A1 (en) 2015-03-04 2018-05-16 Gilead Sciences, Inc. 4,6-diamino-pyrido[3,2-d]pyrimidine compounds and their utilisation as modulators of toll-like receptors
US9670205B2 (en) 2015-03-04 2017-06-06 Gilead Sciences, Inc. Toll like receptor modulator compounds
US10285990B2 (en) 2015-03-04 2019-05-14 Gilead Sciences, Inc. Toll like receptor modulator compounds
WO2016141092A1 (en) 2015-03-04 2016-09-09 Gilead Sciences, Inc. Toll-like receptor modulating 4,6-diamino-pyrido[3,2-d]pyrimidine compounds
EP3722297A1 (en) 2015-03-04 2020-10-14 Gilead Sciences, Inc. Toll-like receptor modulating 4,6-diamino-pyrido[3,2-d]pyrimidine compounds
WO2017035230A1 (en) 2015-08-26 2017-03-02 Gilead Sciences, Inc. Deuterated toll-like receptor modulators
WO2017048727A1 (en) 2015-09-15 2017-03-23 Gilead Sciences, Inc. Modulators of toll-like recptors for the treatment of hiv
WO2017106346A2 (en) 2015-12-15 2017-06-22 Gilead Sciences, Inc. Human immunodeficiency virus neutralizing antibodies
EP3992206A1 (en) 2015-12-15 2022-05-04 Gilead Sciences, Inc. Human immunodeficiency virus neutralizing antibodies
WO2017205115A1 (en) 2016-05-27 2017-11-30 Gilead Sciences, Inc. Compounds for the treatment of hepatitis b virus infection
WO2017205078A1 (en) 2016-05-27 2017-11-30 Gilead Sciences, Inc. Methods for treating hepatitis b virus infections using ns5a, ns5b or ns3 inhibitors
EP3922634A1 (en) 2016-08-26 2021-12-15 Gilead Sciences, Inc. Substituted pyrrolizine compounds and uses thereof
WO2018039531A1 (en) 2016-08-26 2018-03-01 Gilead Sciences, Inc. Substituted pyrrolizine compounds and uses thereof
US10370342B2 (en) 2016-09-02 2019-08-06 Gilead Sciences, Inc. Toll like receptor modulator compounds
US11124487B2 (en) 2016-09-02 2021-09-21 Gilead Sciences, Inc. Toll like receptor modulator compounds
US10640499B2 (en) 2016-09-02 2020-05-05 Gilead Sciences, Inc. Toll like receptor modulator compounds
WO2018045144A1 (en) 2016-09-02 2018-03-08 Gilead Sciences, Inc. Toll like receptor modulator compounds
US11827609B2 (en) 2016-09-02 2023-11-28 Gilead Sciences, Inc. Toll like receptor modulator compounds
WO2018045150A1 (en) 2016-09-02 2018-03-08 Gilead Sciences, Inc. 4,6-diamino-pyrido[3,2-d]pyrimidine derivaties as toll like receptor modulators
US10662416B2 (en) 2016-10-14 2020-05-26 Precision Biosciences, Inc. Engineered meganucleases specific for recognition sequences in the hepatitis B virus genome
US11274285B2 (en) 2016-10-14 2022-03-15 Precision Biosciences, Inc. Engineered meganucleases specific for recognition sequences in the Hepatitis B virus genome
WO2018144390A1 (en) 2017-01-31 2018-08-09 Gilead Sciences, Inc. Crystalline forms of tenofovir alafenamide
WO2018144605A1 (en) 2017-02-02 2018-08-09 Gilead Sciences, Inc. Compounds for the treatment of hepatitis b virus infection
US10442804B2 (en) 2017-02-02 2019-10-15 Gilead Sciences, Inc. Compounds for the treatment of hepatitis B virus infection
WO2018195321A1 (en) 2017-04-20 2018-10-25 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
EP4026835A2 (en) 2017-04-20 2022-07-13 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
US11267799B2 (en) 2017-08-17 2022-03-08 Gilead Sciences, Inc. Solid forms of an HIV capsid inhibitor
US11845739B2 (en) 2017-08-17 2023-12-19 Gilead Sciences, Inc. Solid forms of an HIV capsid inhibitor
US11266638B2 (en) 2017-08-17 2022-03-08 Gilead Sciences, Inc. Choline salt forms of an HIV capsid inhibitor
CN111051297A (en) * 2017-08-17 2020-04-21 吉利德ē§‘学公åø Choline salt forms of HIV capsid inhibitors
US11833143B2 (en) 2017-08-17 2023-12-05 Gilead Sciences, Inc. Choline salt forms of an HIV capsid inhibitor
CN111051296A (en) * 2017-08-17 2020-04-21 吉利德ē§‘学公åø Solid forms of HIV capsid inhibitors
WO2019040102A1 (en) 2017-08-22 2019-02-28 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
WO2019084060A1 (en) 2017-10-24 2019-05-02 Silverback Therapeutics, Inc. Conjugates and methods of use thereof for selective delivery of immune-modulatory agents
WO2019118884A1 (en) 2017-12-15 2019-06-20 Silverback Therapeutics, Inc. Antibody construct-drug conjugate for the treatment of hepatitis
US11203610B2 (en) 2017-12-20 2021-12-21 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2ā€²3ā€² 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. 3ā€²3ā€² cyclic dinucleotides with phosphonate bond activating the sting adaptor protein
EP4227302A1 (en) 2018-02-13 2023-08-16 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
WO2019160882A1 (en) 2018-02-13 2019-08-22 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
US11753399B2 (en) 2018-02-15 2023-09-12 Gilead Sciences, Inc. Therapeutic compounds
US11267801B2 (en) 2018-02-15 2022-03-08 Gilead Sciences, Inc. Therapeutic compounds
US11760746B2 (en) 2018-02-16 2023-09-19 Gilead Sciences, Inc. Methods and intermediates for preparing therapeutic compounds
WO2019165374A1 (en) 2018-02-26 2019-08-29 Gilead Sciences, Inc. Substituted pyrrolizine compounds as hbv replication inhibitors
WO2019195181A1 (en) 2018-04-05 2019-10-10 Gilead Sciences, Inc. Antibodies and fragments thereof that bind hepatitis b virus protein x
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
WO2019193533A1 (en) 2018-04-06 2019-10-10 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2'2'-cyclic dinucleotides
US11292812B2 (en) 2018-04-06 2022-04-05 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3ā€²3ā€²-cyclic dinucleotides
US11149052B2 (en) 2018-04-06 2021-10-19 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 2ā€²3ā€²-cyclic dinucleotides
US11142750B2 (en) 2018-04-12 2021-10-12 Precision Biosciences, Inc. Optimized engineered meganucleases having specificity for a recognition sequence in the Hepatitis B virus genome
WO2019200247A1 (en) 2018-04-12 2019-10-17 Precision Biosciences, Inc. Optimized engineered meganucleases having specificity for a recognition sequence in the hepatitis b virus genome
US11788077B2 (en) 2018-04-12 2023-10-17 Precision Biosciences, Inc. Polynucleotides encoding optimized engineered meganucleases having specificity for a recognition sequence in the Hepatitis B virus genome
WO2019204609A1 (en) 2018-04-19 2019-10-24 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
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
WO2020010107A1 (en) 2018-07-03 2020-01-09 Gilead Sciences, Inc. Antibodies that target hiv gp120 and methods of use
EP4257600A2 (en) 2018-07-03 2023-10-11 Gilead Sciences, Inc. Antibodies that target hiv gp120 and methods of use
US11098027B2 (en) 2018-07-06 2021-08-24 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
WO2020010223A1 (en) 2018-07-06 2020-01-09 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
WO2020010200A1 (en) 2018-07-06 2020-01-09 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
US11186579B2 (en) 2018-07-06 2021-11-30 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
EP4234030A2 (en) 2018-07-13 2023-08-30 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
WO2020014643A1 (en) 2018-07-13 2020-01-16 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
US11944611B2 (en) 2018-07-16 2024-04-02 Gilead Sciences, Inc. Capsid inhibitors for the treatment of HIV
WO2020028097A1 (en) 2018-08-01 2020-02-06 Gilead Sciences, Inc. Solid forms of (r)-11-(methoxymethyl)-12-(3-methoxypropoxy)-3,3-dimethyl-8-0x0-2,3,8,13b-tetrahydro-1h-pyrido[2,1-a]pyrrolo[1,2-c] phthalazine-7-c arboxylic acid
WO2020056008A1 (en) 2018-09-12 2020-03-19 Silverback Therapeutics, Inc. Compositions for the treatment of disease with immune stimulatory conjugates
WO2020072656A1 (en) 2018-10-03 2020-04-09 Gilead Sciences, Inc. Imidozopyrimidine derivatives
WO2020086556A1 (en) 2018-10-24 2020-04-30 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
WO2020092528A1 (en) 2018-10-31 2020-05-07 Gilead Sciences, Inc. Substituted 6-azabenzimidazole compounds having hpk1 inhibitory activity
EP4371987A1 (en) 2018-10-31 2024-05-22 Gilead Sciences, Inc. Substituted 6-azabenzimidazole compounds as hpk1 inhibitors
WO2020092621A1 (en) 2018-10-31 2020-05-07 Gilead Sciences, Inc. Substituted 6-azabenzimidazole compounds as hpk1 inhibitors
WO2020176510A1 (en) 2019-02-25 2020-09-03 Gilead Sciences, Inc. Protein kinase c agonists
WO2020176505A1 (en) 2019-02-25 2020-09-03 Gilead Sciences, Inc. Protein kinase c agonists
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
US11766447B2 (en) 2019-03-07 2023-09-26 Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. 3ā€²3ā€²-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
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
US11583531B2 (en) 2019-04-17 2023-02-21 Gilead Sciences, Inc. Solid forms of a toll-like receptor modulator
US11396509B2 (en) 2019-04-17 2022-07-26 Gilead Sciences, Inc. Solid forms of a toll-like receptor modulator
WO2020214652A1 (en) 2019-04-17 2020-10-22 Gilead Sciences, Inc. Solid forms of a toll-like receptor modulator
WO2020214663A1 (en) 2019-04-17 2020-10-22 Gilead Sciences, Inc. Solid forms of a toll-like receptor modulator
WO2020236753A1 (en) 2019-05-21 2020-11-26 Gilead Sciences, Inc. Methods of identifying hiv patients sensitive to therapy with gp120 v3 glycan-directed antibodies
WO2020237025A1 (en) 2019-05-23 2020-11-26 Gilead Sciences, Inc. Substituted exo-methylene-oxindoles which are hpk1/map4k1 inhibitors
WO2020255038A1 (en) 2019-06-18 2020-12-24 Janssen Sciences Ireland Unlimited Company Combination of hepatitis b virus (hbv) vaccines and pyridopyrimidine derivatives
WO2020257407A1 (en) 2019-06-19 2020-12-24 Silverback Therapeutics, Inc. Anti-mesothelin antibodies and immunoconjugates thereof
WO2020263830A1 (en) 2019-06-25 2020-12-30 Gilead Sciences, Inc. Flt3l-fc fusion proteins and methods of use
US11286257B2 (en) 2019-06-28 2022-03-29 Gilead Sciences, Inc. Processes for preparing toll-like receptor modulator compounds
WO2021011544A1 (en) 2019-07-16 2021-01-21 Gilead Sciences, Inc. Hiv vaccines and methods of making and using
WO2021011891A1 (en) 2019-07-18 2021-01-21 Gilead Sciences, Inc. Long-acting formulations of tenofovir alafenamide
WO2021034804A1 (en) 2019-08-19 2021-02-25 Gilead Sciences, Inc. Pharmaceutical formulations of tenofovir alafenamide
WO2021067181A1 (en) 2019-09-30 2021-04-08 Gilead Sciences, Inc. Hbv vaccines and methods treating hbv
WO2021067644A1 (en) 2019-10-01 2021-04-08 Silverback Therapeutics, Inc. Combination therapy with immune stimulatory conjugates
WO2021076908A1 (en) 2019-10-18 2021-04-22 Forty Seven, Inc. Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia
EP4349413A2 (en) 2019-10-18 2024-04-10 Forty Seven, Inc. Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia
WO2021087064A1 (en) 2019-10-31 2021-05-06 Forty Seven, Inc. Anti-cd47 and anti-cd20 based treatment of blood cancer
WO2021096860A1 (en) 2019-11-12 2021-05-20 Gilead Sciences, Inc. Mcl1 inhibitors
US11807625B2 (en) 2019-11-26 2023-11-07 Gilead Sciences, Inc. Capsid inhibitors for the prevention of HIV
WO2021113765A1 (en) 2019-12-06 2021-06-10 Precision Biosciences, Inc. Optimized engineered meganucleases having specificity for a recognition sequence in the hepatitis b virus genome
WO2021130638A1 (en) 2019-12-24 2021-07-01 Carna Biosciences, Inc. Diacylglycerol kinase modulating compounds
WO2021163064A2 (en) 2020-02-14 2021-08-19 Jounce Therapeutics, Inc. Antibodies and fusion proteins that bind to ccr8 and uses thereof
US11692038B2 (en) 2020-02-14 2023-07-04 Gilead Sciences, Inc. Antibodies that bind chemokine (C-C motif) receptor 8 (CCR8)
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
WO2021188959A1 (en) 2020-03-20 2021-09-23 Gilead Sciences, Inc. Prodrugs of 4'-c-substituted-2-halo-2'-deoxyadenosine nucleosides and methods of making and using the same
WO2021222522A1 (en) 2020-05-01 2021-11-04 Gilead Sciences, Inc. Cd73 inhibiting 2,4-dioxopyrimidine compounds
WO2021236944A1 (en) 2020-05-21 2021-11-25 Gilead Sciences, Inc. Pharmaceutical compositions comprising bictegravir
US11680064B2 (en) 2020-06-25 2023-06-20 Gilead Sciences, Inc. Capsid inhibitors for the treatment of HIV
WO2021262990A1 (en) 2020-06-25 2021-12-30 Gilead Sciences, Inc. Capsid inhibitors for the treatment of hiv
US11541126B1 (en) 2020-07-01 2023-01-03 Silverback Therapeutics, Inc. Anti-ASGR1 antibody TLR8 agonist comprising conjugates and uses thereof
WO2022006327A1 (en) 2020-07-01 2022-01-06 Silverback Therapeutics, Inc. Anti-asgr1 antibody conjugates and uses thereof
WO2022031894A1 (en) 2020-08-07 2022-02-10 Gilead Sciences, Inc. Prodrugs of phosphonamide nucleotide analogues and their pharmaceutical use
WO2022087149A2 (en) 2020-10-22 2022-04-28 Gilead Sciences, Inc. Interleukin-2-fc fusion proteins and methods of use
WO2022103758A1 (en) 2020-11-11 2022-05-19 Gilead Sciences, Inc. METHODS OF IDENTIFYING HIV PATIENTS SENSITIVE TO THERAPY WITH gp120 CD4 BINDING SITE-DIRECTED ANTIBODIES
WO2022217022A1 (en) 2021-04-10 2022-10-13 Profoundbio Us Co. Folr1 binding agents, conjugates thereof and methods of using the same
WO2022221304A1 (en) 2021-04-14 2022-10-20 Gilead Sciences, Inc. CO-INHIBITION OF CD47/SIRPĪ± BINDING AND NEDD8-ACTIVATING ENZYME E1 REGULATORY SUBUNIT FOR THE TREATMENT OF CANCER
WO2022226317A1 (en) 2021-04-23 2022-10-27 Profoundbio Us Co. Anti-cd70 antibodies, conjugates thereof and methods of using the same
WO2022241134A1 (en) 2021-05-13 2022-11-17 Gilead Sciences, Inc. COMBINATION OF A TLR8 MODULATING COMPOUND AND ANTI-HBV siRNA THERAPEUTICS
WO2022245671A1 (en) 2021-05-18 2022-11-24 Gilead Sciences, Inc. Methods of using flt3l-fc fusion proteins
WO2022271684A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
WO2022271650A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
WO2022271659A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
WO2022271677A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
WO2023280227A2 (en) 2021-07-06 2023-01-12 Profoundbio Us Co. Linkers, drug linkers and conjugates thereof and methods of using the same
WO2023076983A1 (en) 2021-10-28 2023-05-04 Gilead Sciences, Inc. Pyridizin-3(2h)-one derivatives
WO2023077030A1 (en) 2021-10-29 2023-05-04 Gilead Sciences, Inc. Cd73 compounds
WO2023102239A1 (en) 2021-12-03 2023-06-08 Gilead Sciences, Inc. Therapeutic compounds for hiv virus infection
WO2023102529A1 (en) 2021-12-03 2023-06-08 Gilead Sciences, Inc. Therapeutic compounds for hiv virus infection
WO2023102523A1 (en) 2021-12-03 2023-06-08 Gilead Sciences, Inc. Therapeutic compounds for hiv virus infection
US11787825B2 (en) 2021-12-03 2023-10-17 Gilead Sciences, Inc. Therapeutic compounds for HIV virus infection
WO2023107956A1 (en) 2021-12-08 2023-06-15 Dragonfly Therapeutics, Inc. Proteins binding nkg2d, cd16 and 5t4
WO2023107954A1 (en) 2021-12-08 2023-06-15 Dragonfly Therapeutics, Inc. Antibodies targeting 5t4 and uses thereof
WO2023122615A1 (en) 2021-12-22 2023-06-29 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
WO2023122581A2 (en) 2021-12-22 2023-06-29 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
WO2023147418A1 (en) 2022-01-28 2023-08-03 Gilead Sciences, Inc. Parp7 inhibitors
WO2023178181A1 (en) 2022-03-17 2023-09-21 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
EP4245756A1 (en) 2022-03-17 2023-09-20 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
WO2023183817A1 (en) 2022-03-24 2023-09-28 Gilead Sciences, Inc. Combination therapy for treating trop-2 expressing cancers
WO2023196784A1 (en) 2022-04-05 2023-10-12 Gilead Sciences, Inc. Combinations of antibody therapies for treating colorectal cancer
WO2023196875A1 (en) 2022-04-06 2023-10-12 Gilead Sciences, Inc. Bridged tricyclic carbamoylpyridone compounds and uses thereof
EP4310087A1 (en) 2022-04-06 2024-01-24 Gilead Sciences, Inc. Bridged tricyclic carbamoylpyridone compounds and uses thereof
WO2023205719A1 (en) 2022-04-21 2023-10-26 Gilead Sciences, Inc. Kras g12d modulating compounds
WO2024006929A1 (en) 2022-07-01 2024-01-04 Gilead Sciences, Inc. Cd73 compounds
WO2024006982A1 (en) 2022-07-01 2024-01-04 Gilead Sciences, Inc. Therapeutic compounds useful for the prophylactic or therapeutic treatment of an hiv virus infection
WO2024015741A1 (en) 2022-07-12 2024-01-18 Gilead Sciences, Inc. Hiv immunogenic polypeptides and vaccines and uses thereof
WO2024044477A1 (en) 2022-08-26 2024-02-29 Gilead Sciences, Inc. Dosing and scheduling regimen for broadly neutralizing antibodies
WO2024064668A1 (en) 2022-09-21 2024-03-28 Gilead Sciences, Inc. FOCAL IONIZING RADIATION AND CD47/SIRPĪ± DISRUPTION ANTICANCER COMBINATION THERAPY
WO2024076915A1 (en) 2022-10-04 2024-04-11 Gilead Sciences, Inc. 4'-thionucleoside analogues and their pharmaceutical use
WO2024137852A1 (en) 2022-12-22 2024-06-27 Gilead Sciences, Inc. Prmt5 inhibitors and uses thereof
US12077537B2 (en) 2023-02-15 2024-09-03 Gilead Sciences, Inc. Capsid inhibitors for the treatment of HIV

Also Published As

Publication number Publication date
CN104781239B (en) 2019-03-01
EP2882721B1 (en) 2018-12-05
CN109232439A (en) 2019-01-18
ES2707885T3 (en) 2019-04-05
US9284304B2 (en) 2016-03-15
EA029266B1 (en) 2018-02-28
CN104781239A (en) 2015-07-15
MX369417B (en) 2019-11-07
KR102216479B1 (en) 2021-02-17
US20150239872A1 (en) 2015-08-27
IN2015MN00478A (en) 2015-09-04
PH12015500274B1 (en) 2015-04-27
SG11201500814UA (en) 2015-03-30
CA2879617C (en) 2021-05-04
BR112015002524A2 (en) 2017-07-04
MY183534A (en) 2021-02-25
KR20210018974A (en) 2021-02-18
ZA201500921B (en) 2021-10-27
MX2015001829A (en) 2015-09-23
PH12015500274A1 (en) 2015-04-27
AU2013301450B2 (en) 2018-01-18
BR112015002524B1 (en) 2021-11-03
CL2015000295A1 (en) 2015-04-24
EA201590343A1 (en) 2015-05-29
NZ703731A (en) 2018-03-23
EP2882721A1 (en) 2015-06-17
DK2882721T3 (en) 2019-03-18
IL236700A0 (en) 2015-02-26
IL236700A (en) 2017-02-28
CA2879617A1 (en) 2014-02-13
KR20150040910A (en) 2015-04-15
UA115558C2 (en) 2017-11-27
KR102280589B1 (en) 2021-07-22
JP2015524462A (en) 2015-08-24
AU2013301450A1 (en) 2015-02-05
JP6302906B2 (en) 2018-03-28
HK1207636A1 (en) 2016-02-05

Similar Documents

Publication Publication Date Title
US9284304B2 (en) Substituted pyrimidines as toll-like receptor modulators
DK2812331T3 (en) PIPERIDINOPYRIMIDINE DERIVATIVES FOR TREATING VIRUS INFECTIONS
EP2958900B1 (en) 2-aminopyrimidine derivatives for the treatment of viral infections
JP6401788B2 (en) Thieno [3,2-d] pyrimidine derivatives for viral infection treatment
AU2013328732B2 (en) Pyrrolo[3,2-d]pyrimidine derivatives for the treatment of viral infections and other diseases
AU2013326579B2 (en) 1,2,4-triazine derivatives for the treatment of viral infections.
IL228317A (en) Pyrimidine derivatives and pharmaceutical compositions comprising them
AU2014270418B2 (en) Pyridone derivatives for the treatment of viral infections and further diseases
NZ714267A (en) Pyrrolo[3,2-d]pyrimidine derivatives for the treatment of viral infections and other diseases
NZ709769B2 (en) 2-aminopyrimidine derivatives for the treatment of viral infections

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: 13748289

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 236700

Country of ref document: IL

ENP Entry into the national phase

Ref document number: 2879617

Country of ref document: CA

ENP Entry into the national phase

Ref document number: 20157003081

Country of ref document: KR

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2013301450

Country of ref document: AU

Date of ref document: 20130809

Kind code of ref document: A

Ref document number: 2015525892

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 2015000295

Country of ref document: CL

Ref document number: 14420066

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: 12015500274

Country of ref document: PH

Ref document number: MX/A/2015/001829

Country of ref document: MX

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: A201500301

Country of ref document: UA

WWE Wipo information: entry into national phase

Ref document number: 2013748289

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 201590343

Country of ref document: EA

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112015002524

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 112015002524

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20150205