WO2015124941A1 - Pyrazolo[1,5-a]pyrimidine-5,7-diamine compounds as cdk inhibitors and their therapeutic use - Google Patents

Pyrazolo[1,5-a]pyrimidine-5,7-diamine compounds as cdk inhibitors and their therapeutic use Download PDF

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Publication number
WO2015124941A1
WO2015124941A1 PCT/GB2015/050494 GB2015050494W WO2015124941A1 WO 2015124941 A1 WO2015124941 A1 WO 2015124941A1 GB 2015050494 W GB2015050494 W GB 2015050494W WO 2015124941 A1 WO2015124941 A1 WO 2015124941A1
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compound according
independently
present
compound
substituted
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PCT/GB2015/050494
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English (en)
French (fr)
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Alexander BONDKE
Sebastian KROLL
Anthony Barrett
Matthew FUCHTER
Brian SLAFER
Simak Ali
Charles COOMBES
James Patrick Snyder
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Cancer Research Technology Limited
Imperial Innovations Limited
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Priority to US15/117,982 priority Critical patent/US9932344B2/en
Priority to LTEP15706282.9T priority patent/LT3107914T/lt
Priority to SM20190266T priority patent/SMT201900266T1/it
Priority to RS20190487A priority patent/RS58704B1/sr
Priority to DK15706282.9T priority patent/DK3107914T3/en
Priority to CN201580011502.7A priority patent/CN106103445B/zh
Priority to EP15706282.9A priority patent/EP3107914B8/en
Priority to CA2939786A priority patent/CA2939786C/en
Priority to BR112016018633-8A priority patent/BR112016018633B1/pt
Priority to SI201530714T priority patent/SI3107914T1/sl
Priority to AU2015220560A priority patent/AU2015220560B2/en
Application filed by Cancer Research Technology Limited, Imperial Innovations Limited filed Critical Cancer Research Technology Limited
Priority to NZ724323A priority patent/NZ724323A/en
Priority to MEP-2019-119A priority patent/ME03427B/me
Priority to PL15706282T priority patent/PL3107914T3/pl
Priority to JP2016553387A priority patent/JP6498212B2/ja
Priority to HRP20190685TT priority patent/HRP20190685T1/hr
Priority to ES15706282T priority patent/ES2721268T3/es
Publication of WO2015124941A1 publication Critical patent/WO2015124941A1/en
Priority to US15/941,063 priority patent/US10414772B2/en
Priority to CY20191100425T priority patent/CY1121588T1/el
Priority to US16/559,735 priority patent/US10927119B2/en
Priority to US17/175,780 priority patent/US11566029B2/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • 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
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis

Definitions

  • the present invention pertains generally to the field of therapeutic compounds.
  • the present invention pertains to certain pyrazolo[1 ,5-a]pyrimidine-5,7- diamine compounds (referred to herein as "PPDA compounds”) that, inter alia, inhibit (e.g., selectively inhibit) CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.).
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.
  • the present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit CDK; and to treat disorders including: disorders that are associated with CDK; disorders that result from an inappropriate activity of a cyclin-dependent kinase (CDK); disorders that are associated with CDK mutation; disorders that are associated with CDK overexpression; disorders that are associated with upstream pathway activation of CDK; disorders that are ameliorated by the inhibition of CDK; proliferative disorders; cancer; viral infections (including HIV); neurodegenerative disorders (including Alzheimer's disease and
  • the treatment further comprises treatment (e.g., a)
  • a further active agent which is, e.g., an aromatase inhibitor, an anti-estrogen, a Her2 blocker, a cytotoxic chemotherapeutic agent, etc.
  • Cyclin-dependent protein kinases are the catalytic subunits of a family of
  • CDK4 and CDK6 are required for progression through the growth (G1) phase, CDK2 in the DNA synthesis (S phase) and CDK1 for mitosis and cell division (M phase).
  • CDK inhibitors CDKI
  • CIP/KIP and INK-type CDKIs see, e.g., Sherr et al., 1995
  • phosphorylation and dephosphorylation at specific residues see, e.g., Sherr et al., 1995
  • T-loop The phosphorylation status of a specific threonine residue in the activation loop, the so-called T-loop, is a key modification for the activity of cell cycle CDKs (see, e.g., Fisher et al., 1994).
  • CDK activity is an important component of many disease states, generally through elevated and/or inappropriate activation, as CDKs themselves are infrequently mutated.
  • CDKs themselves are infrequently mutated.
  • Rare examples of mutations in cell cycle CDKs include CDK4 families with hereditary melanoma that result in insensitivity to the INK4 CDKIs (see, e.g., Zuo et al, 1996).
  • CDKN2A gene which encodes for p16INK4 and p14ARF CDKIs
  • CDKN2A gene which encodes for p16INK4 and p14ARF CDKIs
  • these mutations also being associated with greater incidence of breast and pancreatic cancer in affected families (see, e.g., Borg et al., 2000).
  • CDK4 and CDK6 can be amplified and/or overexpressed in cancer, their cyclin effectors, D-type cyclins, are also often amplified and/or over-expressed, whilst the CDK4/CDK6 inhibitors (INK4 genes) are frequently deleted in many cancer types and/or undergo epigenetic silencing (see, e.g., Ortega et al., 2002).
  • E-type cyclins interact with CDK2 for its activity and are frequently over-expressed in cancer, whilst the p21 and p27 inhibitory proteins that act on CDK2, as well as CDK1 , are epigenetically silenced in cancer (see, e.g., Malumbres et al., 2001 ; Jones et al., 2007). Up-regulation of the activities of cell cycle CDKs is therefore integral to cancer development and progression.
  • CDK7 another member of the CDK family, which complexes with cyclin H and MAT1 , phosphorylates the cell cycle CDKs in the activation of T-loop, to promote their activities (see, e.g., Fisher et al., 1994).
  • CDK7 would provide a potent means of inhibiting cell cycle progression, which may be especially relevant given that there is compelling evidence from gene knockout studies in mice for lack of an absolute requirement for CDK2, CDK4 and CDK6 for the cell cycle, at least in most cell types (see, e.g., Malumbres et al., 2009), whilst different tumors appear to require some, but be independent of other interphase CDKs (CDK2, CDK4, CDK6). Recent genetic and biochemical studies have confirmed the importance of CDK7 for cell cycle progression (see, e.g., Larochelle et al., 2007; Ganuza et al., 2012).
  • CDK7/cyclin H/MAT1 In addition to its role as the CDK Activating Kinase (CAK), CDK7/cyclin H/MAT1 , in complex with the basal transcription factor TFIIH, phosphorylates RNA polymerase II (Pol II) in its C-terminal domain (CTD) (see, e.g., Lu et al., 1995; Serizawa et al., 1995). CDK9, another member of the family, is also required for Poll I CTD phosphorylation.
  • CAK7/cyclin H/MAT1 in complex with the basal transcription factor TFIIH, phosphorylates RNA polymerase II (Pol II) in its C-terminal domain (CTD) (see, e.g., Lu et al., 1995; Serizawa et al., 1995).
  • CDK9 another member of the family, is also required for Poll I CTD phosphorylation.
  • the Poll I CTD is comprised of a seven amino acid repeat having the sequence Tyrosine- Serine-Proline-Threonine-Serine-Proline-Serine (YSPTSPS), 52 YSPTSPS heptad repeats being present in the mammalian Poll I CTD.
  • Phosphorylation of serine-2 (S2) and serine-5 (S5) by CDK7 and CDK9 is required for release of Poll I from the gene promoter at initiation of transcription.
  • CDK7 appears to act upstream of CDK9, phosphorylation of S5 phosphorylation by CDK7 preceding S2 phosphorylation by CDK9 (see, e.g.,
  • Transcriptional inhibitors such as flavopiridol, as well as CDK inhibitors that inhibit CDK7 and CDK9 demonstrate the potential utility of CDK7 and CDK9 inhibition in cancer (see, e.g., Wang et al., 2008).
  • CDK7 and CDK9 have been implicated in regulating the activities of a number of transcription factors, including the breast cancer associated estrogen receptor (ER) (see, e.g., Chen et al., 2000), retinoid receptors (see, e.g., Rochette-Egly et al., 1997; Bastien et al., 2000), the androgen receptor (see, e.g., Chymkowitch et al., 2011 ; Gordon et al., 2010), as well as the tumor suppressor p53 (Lu et al., 1997; Ko et al., 1997; Radhakrishnan et al., 2006; Claudio et al., 2006).
  • ER breast cancer associated estrogen receptor
  • retinoid receptors see, e.g., Rochette-Egly et al., 1997; Bastien et al., 2000
  • the androgen receptor see, e.g., Chymkowitch et al
  • CDK8 a component of the mediator complex that regulates gene transcription, through a mechanism involving interaction between transcription factors and the Poll I basal transcription machinery, also phosphorylates transcription factors to regulate their activities (see, e.g., Alarcon et al., 2009).
  • CDK8 also appears to be important for regulating transcription reinitiation. The importance of CDK8 in cancer is highlighted by the finding that the CDK8 gene is amplified in 40-60% of colorectal cancers, whilst its cyclin partner, cyclin c, is upregulated in many cancer types, whilst functional studies are supportive of an oncogenic role for CDK8 in cancer (see, e.g., Xu et al., 2011).
  • CDK1 1 A potential role for CDK1 1 in regulating mediator activity has been described, indicating a role for CDK1 1 in transcription regulation (see, e.g., Drogat et al., 2012), whilst their ability to phosphorylate S2 the Poll I CTD also implicates CDK12 and CDK13 in transcription; CDK12 is also implicated in maintenance of genome stability (see, e.g., Bartkowiak et al., 2010; Blazek et al., 201 1 ; Cheng et al., 2012).
  • CDKs are also important in viral infections including HIV (see, e.g., Knockeart et al., 2002), neurodegenerative disorders including Alzheimer's and Parkinson's disease (of particular note here is CDK5, see, e.g., Monaco et al., 2005; Faterna et al., 2008), ischaemia, and proliferative disorders, including renal diseases (see, e.g., Marshall et al., 2006) and cardiovascular disorders including atherosclerosis.
  • HIV see, e.g., Knockeart et al., 2002
  • neurodegenerative disorders including Alzheimer's and Parkinson's disease
  • CDK5 see, e.g., Monaco et al., 2005; Faterna et al., 2008
  • ischaemia see, e.g., renal diseases (see, e.g., Marshall et al., 2006) and cardiovascular disorders including atherosclerosis.
  • CDK inhibitors provide a potentially powerful approach in the treatment of many human diseases, in particular cancer.
  • inhibition of cell cycle progression may be achieved through the development of selective CDK1 inhibitors (as CDK1 appears to be indispensible for the cell cycle) or selective CDK7 inhibitors (as CDK7 regulates the cell cycle CDKs) or with inhibitors with activity against all of the cell cycle CDKs.
  • CDK4/CDK6 or CDK2 inhibitors may have utility for specific conditions (e.g., CDK4/CDK6 in haematological malignancies and CDK2 in glioblastomas or osteosarcomas), and so development of selective inhibitors for these CDKs may be of utility, the selectivity perhaps aiding toxicity issues.
  • Figure 1 is a graph of percentage growth inhibition as a function of the base-10 logarithm of the molar concentration of the test compound, PPDA-001 , as determined by the NCI60 cancer cell line screen. Each line represents one cell line.
  • Figure 2 is a graph of relative tumour volume as a function of time in the HCT116 tumour xenograft study, for vehicle control (squares), 50 mg/kg/bi-daily (triangles), and
  • Figure 3 is a graph of percent body weight as a function of time in the HCT1 16 tumour xenograft study, for vehicle control (squares), 50 mg/kg/bi-daily (triangles), and
  • Figure 4 which is a graph of relative growth (mean growth ⁇ standard errors of the mean) as function of time for treatment with: (a) vehicle; (b) PPDA-001 / ICEC0942;
  • Figure 6 shows immunoblot gels for the bands for phospho-ER S118 , ER, and ⁇ -actin, as a function of time, for cell lysates from MCF-7 cells treated with 1 ⁇ / ⁇ _ PPDA-001 / ICEC0942. As shown in the figure, PPDA-001 / ICEC0942 inhibits phosphorylation of ER at serine-1 18 (phospho-ER S118 ).
  • Figure 7 shows immunoblot gels for cell lysates from MCF-7 cells treated for 24 hours with 10 ⁇ / ⁇ _ PPDA-001 / ICEC0942.
  • One aspect of the invention pertains to certain certain pyrazolo[1 ,5-a]pyrimidine-5,7- diamine compounds (referred to herein as "PPDA compounds”), as described herein.
  • compositions e.g., a pharmaceutical composition
  • a composition comprising a PPDA compound, as described herein, and a pharmaceutically acceptable carrier or diluent.
  • a method of preparing a composition comprising the step of mixing a PPDA compound, as described herein, and a pharmaceutically acceptable carrier or diluent.
  • Another aspect of the present invention pertains to a method of inhibiting CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12,
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12,
  • CDK13, etc. function (e.g., in a cell), in vitro or in vivo, comprising contacting the cell with an effective amount of a PPDA compound, as described herein.
  • Another aspect of the present invention pertains to a method of regulating (e.g., inhibiting) cell proliferation (e.g., proliferation of a cell), inhibiting cell cycle progression, promoting apoptosis, or a combination of one or more these, in vitro or in vivo, comprising contacting a cell with an effective amount of a PPDA compound, as described herein.
  • Another aspect of the present invention pertains to a PPDA compound as described herein for use in a method of treatment of the human or animal body by therapy, for example, for use a method of treatment of a disorder (e.g., a disease) as described herein.
  • a disorder e.g., a disease
  • Another aspect of the present invention pertains to use of a PPDA compound, as described herein, in the manufacture of a medicament, for example, for use in a method of treatment, for example, for use a method of treatment of a disorder (e.g., a disease) as described herein.
  • a PPDA compound as described herein, in the manufacture of a medicament, for example, for use in a method of treatment, for example, for use a method of treatment of a disorder (e.g., a disease) as described herein.
  • Another aspect of the present invention pertains to a method of treatment, for example, a method of treatment of a disorder (e.g., a disease) as described herein, comprising administering to a subject in need of treatment a therapeutically-effective amount of a PPDA compound, as described herein, preferably in the form of a pharmaceutical composition.
  • the treatment further comprises treatment (e.g., simultaneous or sequential treatment) with a further active agent which is, e.g., an aromatase inhibitor, an anti-estrogen, a Her2 blocker, a cytotoxic chemotherapeutic agent, etc., as described herein.
  • kits comprising (a) a PPDA compound, as described herein, preferably provided as a pharmaceutical composition and in a suitable container and/or with suitable packaging; and (b) instructions for use, for example, written instructions on how to administer the compound.
  • Another aspect of the present invention pertains to a PPDA compound obtainable by a method of synthesis as described herein, or a method comprising a method of synthesis as described herein.
  • Another aspect of the present invention pertains to a PPDA compound obtained by a method of synthesis as described herein, or a method comprising a method of synthesis as described herein.
  • Another aspect of the present invention pertains to novel intermediates, as described herein, which are suitable for use in the methods of synthesis described herein.
  • Another aspect of the present invention pertains to the use of such novel intermediates, as described herein, in the methods of synthesis described herein.
  • one aspect of the present invention is a compound of the following formula, or a pharmaceutically acceptable salt, hydrate, or solvate thereof, wherein -R 2 , -R 3 , -R 5X , -R 5Y , -R 6 , and -R 7 are as defined herein (for convenience, collectively referred to herein as "pyrazolo[1 ,5-a]pyrimidine-5,7-diamine compounds" and "PPDA compounds”):
  • Some embodiments of the invention include the following: (1) A compound of the following formula:
  • -L 5X - is independently a covalent single bond or -L 5XA -;
  • _ 5XA - is independently linear or branched saturated Ci-6alkylene, and is optionally substituted with one or more groups selected from -OH and -OR L5X , wherein each -R L5X is independently linear or branched saturated Ci-6alkyl or saturated C3-6cycloalkyl;
  • -Q is a non-aromatic heterocyclic ring having from 5 to 7 ring atoms, including at least one nitrogen ring atom, and is substituted with "n" groups -J, and is substituted with "m” groups -R Q ;
  • n is 1 , 2, or 3;
  • m is 0, 1 , 2, or 3;
  • each -J is independently -OH, -OR J , -L J -OH, or -L J -OR J ;
  • each -R J is independently linear or branched saturated Ci-ealkyl or saturated Cs-ecycloalkyl;
  • each -L J - is independently linear or branched saturated Ci- 6 alkylene
  • each -R Q is independently -F, -CI, -Br, -I, -R QA , -CF 3 , -OCF 3 , -NH 2 , -NHR QA , -NR QA 2 , pyrrolidino, piperidino, morpholino, piperazino, N-(R QA )-piperazino, -SH, -SR QA , or -CN;
  • each -R 0 ⁇ is independently linear or branched saturated Ci- 6 alkyl or saturated
  • -R 5Y is independently -H or -R 5YA ;
  • -R 5YA is independently linear or branched saturated Ci-ealkyl
  • each -R 7X is independently:
  • each -L 7 - is independently linear or branched saturated Ci-6alkylene; each -R 7A is independently linear or branched saturated Ci-ealkyl, and is optionally substituted with one or more substituents -W 1 ;
  • each -R 7B is saturated C3-6cycloalkyl, and is optionally substituted with one or more substituents -W 2 ;
  • each -R 7C is non-aromatic C3-7heterocyclyl, and is optionally substituted with one or more substituents -W 2 ;
  • each -R 7D is independently phenyl or naphthyl, and is optionally substituted with one or more substituents -W 3 ;
  • each -R 7E is C5-i2heteroaryl, and is optionally substituted with one or more substituents -W 3 ; each -W is independently:
  • each -R W is independently linear or branched saturated Ci-ealkyl, phenyl, or -CH 2 -phenyl, wherein each phenyl is optionally substituted with one or more groups selected from -F, -CI, -Br, -I, -R W ⁇ -CF 3 , -OH, -0R W ⁇ and -OCF 3 , wherein each -R W 1 is independently linear or branched saturated Ci-ealkyl; each -W 2 is independently:
  • each -R W2 is independently linear or branched saturated Ci-ealkyl, phenyl, or -CH 2 -phenyl, wherein each phenyl is optionally substituted with one or more groups selected from -F, -CI, -Br, -I, -R W22 , -CF 3 , -OH, -OR W22 , and -OCF 3 , wherein each -R W22 is independently linear or branched saturated Ci-ealkyl; each -W 3 is independently:
  • each -R W3 is independently linear or branched saturated Ci-ealkyl, phenyl, or -CH 2 -phenyl, wherein each phenyl is optionally substituted with one or more groups selected from -F, -CI, -Br, -I, -R W33 , -CF 3 , -OH, -OR W33 , and -OCF 3 , wherein each -R W33 is independently linear or branched saturated Ci-ealkyl; -R 3 is independently -R 3A or -R 3B ;
  • -R 3A is independently linear or branched saturated Ci-ealkyl
  • -R 2 is independently -H or -R 2A ;
  • -R 2A is independently -F, -CI, -Br, -I, -R 2AA , -CF 3 , -OH, -OR 2AA , -OCF 3 , -NH 2 ,
  • -R 6A is independently -F, -CI, -Br, -I, -R 6AA , -CF 3 , -OH, -OR 6AA , -OCF 3 , -NH 2 , -NHR 6AA , -NR 6AA 2 , pyrrolidino, piperidino, morpholino, piperazino, N-(R 6AA )-piperazino, -SH, -SR 6AA , or -CN; and
  • each -R 6AA is independently linear or branched saturated Ci-ealkyl.
  • C x . y in terms such as “Cs-ioheteroaryl”, “C 3 -7heterocyclyl”, and the like, refers to the number of ring atoms, which may be carbon atoms or heteroatoms (e.g., N, O, S).
  • pyridyl is an example of a Ceheteroaryl group
  • piperidino is an example of a Ceheterocyclyl group.
  • heteroaryl refers to a group that is attached to the rest of the molecule by an atom that is part of an aromatic ring, wherein the aromatic ring is part of an aromatic ring system, and the aromatic ring system has one or more heteroatoms (e.g., N, O, S).
  • heteroatoms e.g., N, O, S.
  • pyridyl is an example of a Ceheteroaryl group
  • quinolyl is an example of a Cioheteroaryl group.
  • heterocyclyl refers to a group that is attached to the rest of the molecule by a ring atom that is not part of an aromatic ring (i.e., the ring is partially or fully saturated), and the ring contains one or more heteroatoms (e.g. , N, O, S).
  • heteroatoms e.g. , N, O, S.
  • piperidino is an example of a Ceheterocyclyl group.
  • stereoisomers are disclosed and encompassed, both individually (e.g. , as isolated from the other stereoisomer(s)) and as mixtures (e.g. , as equimolar or non-equimolar mixtures of two or more stereoisomers).
  • mixtures e.g. , as equimolar or non-equimolar mixtures of two or more stereoisomers.
  • each of the (R) and (S) enantiomers are disclosed and encompassed, both individually (e.g., as isolated from the other enantiomer) and as a mixture (e.g.
  • the initial carbon atom of a pendant sec-butyl group, -CH(CH3)CH2CH3 is usually chiral, and so gives rise to stereoisomers, e.g. , (R) and (S) enantiomers if it is the only chiral centre, each of which is disclosed and encompassed.
  • each -R L5X if present, is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu.
  • each -R L5X if present, is independently -Me, -Et, -nPr, or -iPr.
  • -Q is pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, azepanyl, or diazepanyl, and is substituted with "n” groups -J, and is substituted with "m” groups -R Q .
  • (21) A compound according to any one of (1) to (17), wherein -Q is pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, azepanyl, or diazepanyl, wherein the point of attachment is via a ring carbon atom, and is substituted with "n" groups -J, and is substituted with "m” groups -R Q .
  • -Q is piperazinyl, and is substituted with "n” groups -J, and is substituted with "m” groups -R Q .
  • each -J is -L J -OR J .
  • the Group -R J (105) A compound according to any one of (1) to (104), wherein each -R J , if present, is independently linear or branched saturated or saturated C 3 - 6 cycloalkyl.
  • each -R J is independently linear or branched saturated Ci ⁇ alkyl.
  • each -R J is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu.
  • each -R J is independently -Me, -Et, -nPr, or -iPr.
  • each -L J - is independently -CH 2 -, -CH(CH 3 )-, -C(CH 3 ) 2 -, -CH 2 CH 2 -, -CH(CH 3 )CH 2 -, -CH 2 CH(CH 3 )-, or
  • each -L J - is independently -CH 2 -, -CH(CH 3 )-, -C(CH 3 ) 2 -, or -CH 2 CH 2 -.
  • each -R Q is independently -F, -CI, -Br, -I, -R QA , -CF 3 , -OH, -OR QA , -OCF 3 , -NH 2 , -NHR QA , -NR QA 2 , pyrrolidino, piperidino, morpholino, piperazino, or N- R ⁇ -piperazino.
  • each -R Q if present, is independently -F, -CI, -Br, -I, -R QA , -OH, or -OR QA .
  • each -R QA if present, is independently linear or branched saturated or saturated C3- 6 cycloalkyl.
  • each -R QA if present, is independently linear or branched (122) A compound according to any one of (1) to (119), wherein each -R QA , if present, is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu.
  • each -R QA if present, is independently -Me, -Et, -nPr, or -iPr.
  • -R 5YA if present, is independently -Me, -Et, -nPr, or -iPr.
  • each -R 7X is -L 7 -R 7B .
  • each -R 7X is -L 7 -R 7C .
  • each -L 7 -, if present, is independently -CH 2 -, -CH(CH 3 )-, -C(CH 3 ) 2 -, -CH 2 CH 2 -, -CH(CH 3 )CH 2 -, -CH 2 CH(CH 3 )-, or -CH 2 CH 2 CH 2 -.
  • each -L 7 -, if present, is independently -CH 2 -, -CH(CH 3 )-, -C(CH 3 ) 2 -, or -CH 2 CH 2 -.
  • each -L 7 - is independently -CH 2 -, -CH(CH 3 )-, or -C(CH 3 ) 2 -.
  • each -R 7A is independently linear or branched saturated Ci-ealkyl.
  • each -R 7A is independently linear or branched saturated and is optionally substituted with one or more substituents -W 1 .
  • each -R 7A is independently linear or branched saturated
  • each -R 7A is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu, and is optionally substituted with one or more substituents -W 1 .
  • each -R 7A is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu.
  • each -R 7A if present, is independently -Me, -Et, -nPr, or -iPr, and is optionally substituted with one or more substituents -W 1 .
  • each -R 7A if present, is independently -Me, -Et, -nPr, or -iPr.
  • each -R 7A if present, is independently -Me or -Et, and is optionally substituted with one or more substituents - W.
  • each -R 7B is independently cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, and is optionally substituted with one or more substituents -W 2 .
  • each -R 7B is independently cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl.
  • each -R 7B is independently cyclopentyl or cyclohexyl, and is optionally substituted with one or more substituents -W 2 .
  • each -R 7B is independently cyclopentyl or cyclohexyl.
  • 169) A compound according to any one of (1) to (164), wherein each -R 7B , if present, is cyclohexyl, and is optionally substituted with one or more substituents -W 2 .
  • each -R 7C is independently pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, tetrahydrofuranyl, tetrahydropyranyl, dixoanyl, azepanyl, or diazepanyl, and is optionally substituted with one or more substituents -W 2 .
  • each -R 7C is independently pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, tetrahydrofuranyl, tetrahydropyranyl, or dixoanyl, and is optionally substituted with one or more substituents -W 2 .
  • each -R 7C is independently pyrrolidinyl, piperidinyl, morpholinyl, or piperazinyl, and is optionally substituted with one or more substituents -W 2 .
  • each -R 7C is independently piperidinyl, and is optionally substituted with one or more substituents -W 2 .
  • the Group -R 7D is independently piperidinyl, and is optionally substituted with one or more substituents -W 2 .
  • each -R 7D if present, is phenyl, and is optionally substituted with one or more substituents -W 3 .
  • each -R 7D if present, is naphthyl, and is optionally substituted with one or more substituents -W 3 .
  • each -R 7E if present, is Cg-ioheteroaryl.
  • each -R 7E is independently furanyl, thienyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyridyl, pyrimidinyl, pyrazinyl, or pyridazinyl, and is optionally substituted, for example, with one or more substituents -W 3 .
  • each -R 7E is independently furanyl, thienyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, or isothiazolyl, and is optionally substituted, for example, with one or more substituents -W 3 .
  • each -R 7E is independently pyridyl, pyrimidinyl, pyrazinyl, or pyridazinyl, and is optionally substituted, for example, with one or more substituents -W 3 .
  • each -R 7E is independently indolyl, indazolyl, benzofuranyl, benzothienyl, benzimidazolyl,
  • benzothiazolyl benzoxazolyl, benzoisoxazolyl, quinolinyl, isoquinolinyl, cinnolinyl, quinazolinyl, phthalazinyl, or quinoxalinyl, and is optionally substituted, for example, with one or more substituents -W 3 .
  • each -W if present, is independently: -F, -CI, -Br, -I, -CF 3 , -OH, -OR w , -OCF 3 , -NH 2 , -NHR W , -NR W 2 , pyrrolidino, piperidino, morpholino, piperazino, or N-(R w )-piperazino.
  • each -W if present, is independently: -F, -CI, -Br, -I, -CF 3 , -OH, -OR w , or -OCF 3 .
  • each -R W if present, is independently linear or branched saturated phenyl, or -CH2-phenyl, wherein each phenyl is optionally substituted with one or more groups selected from -F, -CI, -Br, -I, -R W ⁇ -CF 3 , -OH, -0R W ⁇ and -OCF 3 , wherein each -R W 1 is independently linear or branched saturated phenyl, or -CH2-phenyl, wherein each phenyl is optionally substituted with one or more groups selected from -F, -CI, -Br, -I, -R W ⁇ -CF 3 , -OH, -0R W ⁇ and -OCF 3 , wherein each -R W 1 is independently linear or branched saturated
  • each -R W1 if present, is independently linear or branched saturated phenyl, or -CH2-phenyl.
  • each -R W if present, is independently linear or branched saturated Ci ⁇ alkyl.
  • each -R W if present, is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu.
  • each -R W if present, is independently -Me, -Et, -nPr, or -iPr.
  • each -R W 1 is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu.
  • each -R W 1 is independently -Me, -Et, -nPr, or -iPr.
  • each -R W 1 is independently -Me or -Et.
  • each -W 2 is independently: -F, -CI, -Br, -I, -CF 3 , -OH, -OR W2 , -OCF 3 , -NH 2 , -NHR W2 , -NR W2 2 , pyrrolidino, piperidino, morpholino, piperazino, or N-(R W2 )-piperazino.
  • each -W 2 is independently: -F, -CI, -Br, -I, -CF 3 , -OH, -OR W2 , or -OCF 3 .
  • the Group -R W2 is independently: -F, -CI, -Br, -I, -CF 3 , -OH, -OR W2 , or -OCF 3 .
  • each -R W2 if present, is independently linear or branched saturated phenyl, or -CH 2 -phenyl, wherein each phenyl is optionally substituted with one or more groups selected from -F, -CI, -Br, -I, -R W22 , -CF 3 , -OH, -ORTM 22 , and -OCF 3 , wherein each -RTM 22 is independently linear or branched saturated
  • each -R W2 if present, is independently linear or branched saturated phenyl, or -CH 2 -phenyl.
  • each -R W2 if present, is independently linear or branched saturated (210)
  • each -R W2 is independently -Me, -Et, -nPr, or -iPr.
  • each -R W22 if present, is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu.
  • each -R W22 if present, is independently -Me, -Et, -nPr, or -iPr.
  • each -W 3 is independently: -F, -CI, -Br, -I, -CF 3 , -OH, -OR W3 , -OCF 3 , -NH 2 , -NHR W3 , -NR W3 2 , pyrrolidino, piperidino, morpholino, piperazino, or N-(R W3 )-piperazino.
  • each -W 3 is independently: -F, -CI, -Br, -I, -CF 3 , -OH, -OR W3 , or -OCF 3 .
  • each -R W3 is independently linear or branched saturated phenyl, or -CH2-phenyl, wherein each phenyl is optionally substituted with one or more groups selected from -F, -CI, -Br, -I, -R W33 , -CF 3 , -OH, -OR TO3 , and -OCF 3 , wherein each -R TO3 is independently linear or branched saturated phenyl, or -CH2-phenyl, wherein each phenyl is optionally substituted with one or more groups selected from -F, -CI, -Br, -I, -R W33 , -CF 3 , -OH, -OR TO3 , and -OCF 3 , wherein each -R TO3 is independently linear or branched saturated
  • each -R W3 is independently linear or branched saturated phenyl, or -CH2-phenyl.
  • the Group -R W33 (226) A compound according to any one of (1) to (225), wherein each -R W33 , if present, is independently linear or branched saturated
  • each -R W33 if present, is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu.
  • each -R W33 if present, is independently -Me, -Et, -nPr, or -iPr.
  • (233) A compound according to any one of (1) to (232), wherein -R 3A , if present, is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu, n-pentyl, t-pentyl, neo-pentyl, iso-pentyl, sec-pentyl, 3-pentyl, 1-hexyl, 2-hexyl, 3-hexyl, 3-methyl-1-pentyl,
  • -R 2A is independently -F, -CI, -Br, -I, -R 2AA , -CF 3 , -OH, -OR 2AA , -OCF 3 , -NH 2 , -NHR 2AA , -NR 2AA 2 , pyrrolidino, piperidino, morpholino, piperazino, or N-(R 2AA )-piperazino.
  • the Group -R 2AA (247) A compound according to any one of (1) to (246), wherein each -R 2AA , if present, is independently linear or branched saturated
  • each -R 2AA is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu.
  • -R 6A is independently -F, -CI, -Br, -I, -R 6AA , -CF 3 , -OH, -OR 6AA , -OCF 3 , -NH 2 , -NHR 6AA , -NR 6AA 2 , pyrrolidino, piperidino, morpholino, piperazino, or N-(R 6AA )-piperazino.
  • each -R 6AA if present, is independently -Me, -Et, -nPr, -iPr, -nBu, -iBu, -sBu, or -tBu.
  • each -R 6AA if present, is independently -Me, -Et, -nPr, or -iPr.
  • One aspect of the present invention pertains to PPDA compounds, as described herein, in substantially purified form and/or in a form substantially free from contaminants.
  • the substantially purified form is at least 50% by weight, e.g., at least 60% by weight, e.g., at least 70% by weight, e.g., at least 80% by weight, e.g., at least 90% by weight, e.g., at least 95% by weight, e.g., at least 97% by weight, e.g., at least 98% by weight, e.g., at least 99% by weight.
  • the substantially purified form refers to the compound in any stereoisomeric or enantiomeric form.
  • the substantially purified form refers to a mixture of stereoisomers, i.e., purified with respect to other compounds.
  • the substantially purified form refers to one
  • the substantially purified form refers to a mixture of enantiomers. In one embodiment, the substantially purified form refers to a equimolar mixture of enantiomers (i.e., a racemic mixture, a racemate). In one embodiment, the substantially purified form refers to one enantiomer, e.g., optically pure enantiomer.
  • the contaminants represent no more than 50% by weight, e.g., no more than 40% by weight, e.g., no more than 30% by weight, e.g., no more than 20% by weight, e.g., no more than 10% by weight, e.g., no more than 5% by weight, e.g., no more than 3% by weight, e.g., no more than 2% by weight, e.g., no more than 1 % by weight.
  • the contaminants refer to other compounds, that is, other than stereoisomers or enantiomers. In one embodiment, the contaminants refer to other compounds and other stereoisomers. In one embodiment, the contaminants refer to other compounds and the other enantiomer.
  • the substantially purified form is at least 60% optically pure (i.e., 60% of the compound, on a molar basis, is the desired stereoisomer or enantiomer, and 40% is the undesired stereoisomer or enantiomer), e.g., at least 70% optically pure, e.g., at least 80% optically pure, e.g., at least 90% optically pure, e.g., at least 95% optically pure, e.g., at least 97% optically pure, e.g., at least 98% optically pure, e.g., at least 99% optically pure.
  • 60% optically pure i.e., 60% of the compound, on a molar basis, is the desired stereoisomer or enantiomer, and 40% is the undesired stereoisomer or enantiomer
  • at least 70% optically pure e.g., at least 80% optically pure, e.g., at least 90% optically pure, e
  • Certain compounds may exist in one or more particular geometric, optical, enantiomeric, diastereoisomeric, epimeric, atropic, stereoisomeric, tautomeric, conformational, or anomeric forms, including but not limited to, cis- and trans-forms; E- and Z-forms; c-, t-, and r- forms; endo- and exo-forms; R-, S-, and meso-forms; D- and L-forms; d- and l-forms; (+) and (-) forms; keto-, enol-, and enolate-forms; syn- and anti-forms; synclinal- and anticlinal-forms; a- and ⁇ -forms; axial and equatorial forms; boat-, chair-, twist-, envelope-, and halfchair-forms; and combinations thereof, hereinafter collectively referred to as "isomers" (or "isomeric forms").
  • a reference to a class of structures may well include structurally isomeric forms falling within that class (e.g., Ci- 7 alkyl includes n-propyl and iso-propyl; butyl includes n-, iso-, sec-, and tert-butyl; methoxyphenyl includes ortho-, meta-, and para-methoxyphenyl).
  • reference to a specific group or substitution pattern is not intended to include other structural (or constitutional isomers) which differ with respect to the connections between atoms rather than by positions in space.
  • a reference to a methoxy group, -OCH 3 is not to be construed as a reference to its structural isomer, a
  • keto/enol (illustrated below), imine/enamine, amide/imino alcohol, amidine/amidine, nitroso/oxime, thioketone/enethiol, N-nitroso/hydroxyazo, and nitro/aci-nitro.
  • keto/enol illustrated below
  • imine/enamine imine/enamine
  • amide/imino alcohol amidine/amidine
  • nitroso/oxime nitroso/oxime
  • thioketone/enethiol N-nitroso/hydroxyazo
  • nitro/aci-nitro nitro/aci-nitro
  • keto enol enolate For example, 1 H-pyridin-2-one-5-yl and 2-hydroxyl-pyridin-5-yl (shown below) are tautomers of one another. A reference herein to one is intended to encompass both.
  • a reference to a particular compound includes all such isomeric forms, including mixtures (e.g., racemic mixtures) thereof.
  • a salt may be formed with a suitable cation.
  • suitable inorganic cations include, but are not limited to, alkali metal ions such as Na + and K + , alkaline earth cations such as Ca 2+ and Mg 2+ , and other cations such as Al 3+ as well as the ammonium ion (i.e., NH 4 + ).
  • suitable organic cations include, but are not limited to substituted ammonium ions (e.g. , NHsR + , Nh ⁇ F , NHR3 + , NR 4 + ), for example, where each R is independently linear or branched saturated
  • suitable substituted ammonium ions are those derived from: ethylamine, diethylamine, dicyclohexylamine, triethylamine, butylamine, ethylenediamine, ethanolamine, diethanolamine, piperazine, benzylamine, phenylbenzylamine, choline, meglumine, and tromethamine, as well as amino acids, such as lysine and arginine.
  • An example of a common quaternary ammonium ion is N(CH3) 4 + .
  • a salt may be formed with a suitable anion.
  • a parent structure contains a cationic group (e.g., - ⁇ 2 + ), or has a functional group, which upon protonation may become cationic (e.g., -NH2 may become -NhV), then a salt may be formed with a suitable anion.
  • a quaternary ammonium compound a counter-anion is generally always present in order to balance the positive charge.
  • the compound in addition to a cationic group (e.g., - ⁇ 2 + , -Nh ), the compound also contains a group capable of forming an anion (e.g., -COOH), then an inner salt (also referred to as a zwitterion) may be formed.
  • suitable inorganic anions include, but are not limited to, those derived from the following inorganic acids: hydrochloric, hydrobromic, hydroiodic, sulfuric, sulfurous, nitric, nitrous, phosphoric, and phosphorous.
  • Suitable organic anions include, but are not limited to, those derived from the following organic acids: 2-acetyloxybenzoic, acetic, trifluoroacetic, ascorbic, aspartic, benzoic, camphorsulfonic, cinnamic, citric, edetic, 1 ,2-ethanedisulfonic, ethanesulfonic, fumaric, glucoheptonic, gluconic, glutamic, glycolic, hydroxymaleic, hydroxynaphthalene carboxylic, isethionic, lactic, lactobionic, lauric, maleic, malic, methanesulfonic, mucic, oleic, oxalic, palmitic, pamoic, pantothenic, phenylacetic, phenylsulfonic, propionic, pyruvic, salicylic, stearic, succinic, sulfanilic, tartaric, toluenesulfonic,
  • Suitable polymeric organic anions include, but are not limited to, those derived from the following polymeric acids: tannic acid, carboxymethyl cellulose.
  • suitable counter-ions which are especially suitable for quaternary ammonium compounds (e.g., those with a - ⁇ 2 + group) include 1-adamantanesulfonate, benzenesulfonate, bisulfate, bromide, chloride, iodide, methanesulfonate, methylsulfate, 1 ,5-napthalene-bis-sulfonate, 4-nitrobenzenesulfonate, formate, tartrate, tosylate, trifluoroacetate, trifluoromethylsulfonate, sulphate.
  • the compound also contains a group capable of forming an anion (e.g., -COOH)
  • an inner salt may be formed.
  • a reference to a particular compound also includes salt forms thereof.
  • solvate is used herein in the conventional sense to refer to a complex of solute (e.g., compound, salt of compound) and solvent. If the solvent is water, the solvate may be conveniently referred to as a hydrate, for example, a mono-hydrate, a di-hydrate, a tri-hydrate, etc.
  • chemically protected form is used herein in the conventional chemical sense and pertains to a compound in which one or more reactive functional groups are protected from undesirable chemical reactions under specified conditions (e.g., pH, temperature, radiation, solvent, and the like).
  • specified conditions e.g., pH, temperature, radiation, solvent, and the like.
  • well-known chemical methods are employed to reversibly render unreactive a functional group, which otherwise would be reactive, under specified conditions.
  • one or more reactive functional groups are in the form of a protected or protecting group (alternatively as a masked or masking group or a blocked or blocking group).
  • a compound which has two nonequivalent reactive functional groups may be derivatized to render one of the functional groups "protected,” and therefore unreactive, under the specified conditions; so protected, the compound may be used as a reactant which has effectively only one reactive functional group.
  • the protected group may be "deprotected” to return it to its original functionality.
  • a hydroxy group may be protected as an ether (-OR) or an ester
  • the aldehyde or ketone group is readily regenerated, for example, by hydrolysis using water in the presence of acid.
  • an amine group may be protected, for example, as an amide (-NRCO-R) or a urethane (-NRCO-OR), for example, as: an acetamide (-NHCO-CH3); a benzyloxy amide (-NHCO-OCH 2 C 6 H 5 , -NH-Cbz); as a t-butoxy amide (-NHCO-OC(CH 3 ) 3 , -NH-Boc); a 2-biphenyl-2-propoxy amide (-NHCO-OCCCHs ⁇ CeFUCeHs, -NH-Bpoc), as a 9- fluorenylmethoxy amide (-NH-Fmoc), as a 6-nitroveratryloxy amide (-NH-Nvoc), as a 2-trimethylsilylethyloxy amide (-NH-Teoc), as a 2,2,2-trichloroethyloxy amide (-NH-Troc), as an allyloxy
  • a carboxylic acid group may be protected as an ester for example, as: an Ci- 7 alkyl ester (e.g. , a methyl ester; a t-butyl ester); a Ci- 7 haloalkyl ester (e.g.
  • a 2,2,2- trihaloethyl ester a 2-tri(Ci- 7 alkyl)silyl-ethyl ester; or a C5-2oaryl-Ci- 7 alkyl ester (e.g., a benzyl ester; a nitrobenzyl ester); or as an amide or hydrazide, for example, as acetamide or a ⁇ /, ⁇ /, ⁇ /'-trimethylhydrazide.
  • prodrug refers to a compound, which yields the desired active compound in vivo. Typically, the prodrug is inactive, or less active than the desired active compound, but may provide advantageous handling, administration, or metabolic properties.
  • prodrugs are activated enzymatically to yield the active compound, or a compound, which, upon further chemical reaction, yields the active compound (for example, as in antibody directed enzyme prodrug therapy (ADEPT), gene directed enzyme prodrug therapy (GDEPT), lipid directed enzyme prodrug therapy (LIDEPT), etc.).
  • the prodrug may be a sugar derivative or other glycoside conjugate, or may be an amino acid ester derivative.
  • compositions e.g., a pharmaceutical composition
  • a composition comprising a PPDA compound, as described herein, and a pharmaceutically acceptable carrier, diluent, or excipient.
  • compositions e.g., a pharmaceutical composition
  • a composition comprising mixing a PPDA compound, as described herein, and a pharmaceutically acceptable carrier, diluent, or excipient.
  • the PPDA compounds described herein are useful in the treatment of, for example, proliferative disorders (as “anti-proliferative agents”), cancer (as “anti-cancer agents”), viral infections (as “anti-viral agents”), neurodegenerative diseases (as
  • anti-neurodegenerative agents etc.
  • One aspect of the present invention pertains to a method of inhibiting CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.) function (e.g., in a cell), in vitro or in vivo, comprising contacting the cell with an effective amount of a PPDA compound, as described herein.
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.
  • suitable assays are described herein or are known in the art.
  • the method is performed in vitro.
  • the method is performed in vivo.
  • the PPDA compound is provided in the form of a pharmaceutically acceptable composition. Any type of cell may be treated, including adipose, lung, gastrointestinal (including, e.g., bowel, colon), breast (mammary), ovarian, prostate, liver (hepatic), kidney (renal), bladder, pancreas, brain, and skin.
  • a sample of cells may be grown in vitro and a compound brought into contact with said cells, and the effect of the compound on those cells observed.
  • effect the morphological status of the cells (e.g., alive or dead, etc.) may be determined. Where the compound is found to exert an influence on the cells, this may be used as a prognostic or diagnostic marker of the efficacy of the compound in methods of treating a patient carrying cells of the same cellular type.
  • the PPDA compounds described herein e.g., (a) regulate (e.g., inhibit) cell proliferation; (b) inhibit cell cycle progression; (c) promote apoptosis; or (d) a combination of one or more of these.
  • One aspect of the present invention pertains to a method of regulating (e.g., inhibiting) cell proliferation (e.g., proliferation of a cell), inhibiting cell cycle progression, promoting apoptosis, or a combination of one or more these, in vitro or in vivo, comprising contacting a cell with an effective amount of a PPDA compound, as described herein.
  • the method is a method of regulating (e.g., inhibiting) cell proliferation (e.g., proliferation of a cell), in vitro or in vivo, comprising contacting a cell with an effective amount of a PPDA compound, as described herein.
  • the method is performed in vitro.
  • the method is performed in vivo.
  • the PPDA compound is provided in the form of a pharmaceutically acceptable composition.
  • Any type of cell may be treated, including lung, gastrointestinal (including, e.g., bowel, colon), breast (mammary), ovarian, prostate, liver (hepatic), kidney (renal), bladder, pancreas, brain, and skin.
  • gastrointestinal including, e.g., bowel, colon
  • breast mammary
  • ovarian prostate
  • liver hepatic
  • kidney renal
  • bladder pancreas
  • brain skin
  • a candidate compound regulates (e.g., inhibits) cell proliferation, etc.
  • assays which may conveniently be used to assess the activity offered by a particular compound are described herein.
  • a sample of cells e.g., from a tumour
  • a compound brought into contact with said cells, and the effect of the compound on those cells observed.
  • effect the morphological status of the cells (e.g., alive or dead, etc.) may be determined.
  • this may be used as a prognostic or diagnostic marker of the efficacy of the compound in methods of treating a patient carrying cells of the same cellular type.
  • Another aspect of the present invention pertains to a PPDA compound, as described herein, for use in a method of treatment of the human or animal body by therapy, for example, for use a method of treatment of a disorder (e.g., a disease) as described herein.
  • a disorder e.g., a disease
  • Another aspect of the present invention pertains to use of a PPDA compound, as described herein, in the manufacture of a medicament, for example, for use in a method of treatment, for example, for use a method of treatment of a disorder (e.g., a disease) as described herein.
  • a PPDA compound as described herein, in the manufacture of a medicament, for example, for use in a method of treatment, for example, for use a method of treatment of a disorder (e.g., a disease) as described herein.
  • the medicament comprises the PPDA compound.
  • Another aspect of the present invention pertains to a method of treatment, for example, a method of treatment of a disorder (e.g., a disease) as described herein, comprising administering to a subject in need of treatment a therapeutical ly-effective amount of a PPDA compound, as described herein, preferably in the form of a pharmaceutical composition.
  • a disorder e.g., a disease
  • a PPDA compound as described herein
  • the treatment is treatment of: a disorder (e.g., a disease) that is associated with CDK; a disorder (e.g., a disease) resulting from an inappropriate activity of a CDK; a disorder (e.g., a disease) that is associated with CDK mutation; a disorder (e.g., a disease) that is associated with CDK overexpression;
  • a disorder e.g., a disease
  • a disorder e.g., a disease
  • a disorder e.g., a disease
  • an inhibition e.g., selective inhibition
  • the treatment is treatment of: a proliferative disorder; cancer; a viral infection (e.g., HIV); a neurodegenerative disorder (e.g.,
  • Alzheimer's disease Parkinson's disease
  • ischaemia a renal disease
  • renal disease a renal disease
  • cardiovascular disorder e.g., atherosclerosis.
  • the treatment is treatment of a disorder (e.g., a disease) that is associated with CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12, CDK13, etc.).
  • a disorder e.g., a disease
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12, CDK13, etc.
  • the treatment is treatment of: a disorder (e.g., a disease) resulting from an inappropriate activity of a CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12, CDK13, etc.).
  • a disorder e.g., a disease
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12, CDK13, etc.
  • the treatment is treatment of: a disorder (e.g., a disease) that is associated with CDK mutation; CDK overexpression (e.g., as compared to corresponding normal cells; e.g., wherein the overexpression is by a factor of 1.5, 2, 3, 5, 10, 20 or 50); or upstream pathway activation of CDK.
  • a disorder e.g., a disease
  • CDK overexpression e.g., as compared to corresponding normal cells; e.g., wherein the overexpression is by a factor of 1.5, 2, 3, 5, 10, 20 or 50
  • upstream pathway activation of CDK e.g., a disorder that is associated with CDK mutation
  • the treatment is treatment of a disorder (e.g., a disease) that is ameliorated by the inhibition (e.g., selective inhibition) of CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12, CDK13, etc.).
  • a disorder e.g., a disease
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12, CDK13, etc.
  • the treatment is treatment of a proliferative disorder.
  • proliferative disorder pertains to an unwanted or uncontrolled cellular proliferation of excessive or abnormal cells which is undesired, such as neoplastic or hyperplastic growth.
  • the treatment is treatment of: a proliferative disorder characterised by benign, pre-malignant, or malignant cellular proliferation.
  • the treatment is treatment of: hyperplasia; a neoplasm; a tumour (e.g., a histocytoma, a glioma, an astrocyoma, an osteoma); cancer; psoriasis; a bone disease; a fibroproliferative disorder (e.g., of connective tissues); pulmonary fibrosis; atherosclerosis; or smooth muscle cell proliferation in the blood vessels (e.g., stenosis or restenosis following angioplasty).
  • a tumour e.g., a histocytoma, a glioma, an astrocyoma, an osteoma
  • cancer e.g., a fibroproliferative disorder (e.g., of connective tissues); pulmonary fibrosis; atherosclerosis; or smooth muscle cell proliferation in the blood vessels (e.g., stenosis or restenosis following angioplasty).
  • the treatment is treatment of cancer.
  • the treatment is treatment of cancer metastasis.
  • Carcinomas including tumours derived from stratified squamous epithelia (squamous cell carcinomas) and tumours arising within organs or glands (adenocarcinomas).
  • Examples include breast, colon, lung, prostate, ovary.
  • chondrosarcoma (cartilage); leiomyosarcoma (smooth muscle); rhabdomyosarcoma (skeletal muscle); mesothelial sarcoma and mesothelioma (membranous lining of body cavities); fibrosarcoma (fibrous tissue); angiosarcoma and haemangioendothelioma (blood vessels); liposarcoma (adipose tissue); glioma and astrocytoma (neurogenic connective tissue found in the brain); myxosarcoma (primitive embryonic connective tissue); mesenchymous and mixed mesodermal tumour (mixed connective tissue types).
  • Haematopoietic tumours including: myelogenous and granulocytic leukaemia (malignancy of the myeloid and granulocytic white blood cell series); lymphatic, lymphocytic, and lymphoblastic leukaemia (malignancy of the lymphoid and lymphocytic blood cell series); polycythaemia vera (malignancy of various blood cell products, but with red cells predominating).
  • Lymphomas including: Hodgkin and Non-Hodgkin lymphomas.
  • Mixed Types including, e.g., adenosquamous carcinoma; mixed mesodermal tumour; carcinosarcoma; teratocarcinoma.
  • the treatment is treatment of breast cancer.
  • the cancer is characterised by, or further characterised by, cancer stem cells.
  • the cancer is associated with CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12, CDK13, etc.), especially CDK7.
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12, CDK13, etc.
  • the cancer is characterised by, or further characterised by, inappropriate activity of CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12, CDK13, etc.), especially CDK7.
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK1 1 , CDK12, CDK13, etc.
  • the cancer is characterised by, or further characterised by, overexpression of CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.), especially CDK7.
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.
  • the anti-cancer effect may arise through one or more mechanisms, including but not limited to, the regulation of cell proliferation, the inhibition of cell cycle progression, the inhibition of angiogenesis (the formation of new blood vessels), the inhibition of metastasis (the spread of a tumour from its origin), the inhibition of cell migration (the spread of cancer cells to other parts of the body), the inhibition of invasion (the spread of tumour cells into neighbouring normal structures), the promotion of apoptosis
  • the treatment is treatment of a viral infection.
  • the treatment is treatment of a viral infection by:
  • a dsDNA virus e.g., an adenovirus, a herpesvirus, a poxvirus
  • ssDNA virus e.g., a parvovirus
  • a dsRNA virus e.g., a reovirus
  • a (+)ssRNA virus e.g., a picornavirus, a togavirus
  • a (-)ssRNA virus e.g., an orthomyxovirus, a rhabdovirus
  • a ssRNA-RT virus e.g., a retrovirus
  • a dsDNA-RT virus e.g., a hepadnavirus.
  • ds double strand
  • ss +strand
  • (+)ssRNA +strand RNA
  • (+)ssRNA +strand RNA
  • (+)ssRNA - strand RNA
  • ssRNA-RT (+ strand)RNA with DNA intermediate in life-cycle.
  • the treatment is treatment of: human immunodeficiency virus (HIV); hepatitis B virus (HBV); hepatitis C virus (HCV); human papilloma virus (HPV);
  • HAV human immunodeficiency virus
  • HBV hepatitis B virus
  • HCV hepatitis C virus
  • HPV human papilloma virus
  • CMV cytomegalovirus
  • EBV Epstein-Barr virus
  • HHV human herpesvirus 8 associated with Kaposi sarcoma
  • Coxsackievirus B3 Coxsackievirus B3
  • Borna virus influenza virus.
  • treatment refers generally to treatment of a human or an animal (e.g., in veterinary applications), in which some desired therapeutic effect is achieved, for example, the inhibition of the progress of the disorder, and includes a reduction in the rate of progress, a halt in the rate of progress, alleviation of symptoms of the disorder, amelioration of the disorder, and cure of the disorder.
  • Treatment as a prophylactic measure i.e., prophylaxis
  • use with patients who have not yet developed the disorder, but who are at risk of developing the disorder is encompassed by the term "treatment.”
  • treatment includes the prophylaxis of cancer, reducing the incidence of cancer, alleviating the symptoms of cancer, etc.
  • terapéuticaally-effective amount refers to that amount of a compound, or a material, composition or dosage form comprising a compound, which is effective for producing some desired therapeutic effect, commensurate with a reasonable benefit/risk ratio, when administered in accordance with a desired treatment regimen.
  • treatment includes combination treatments and therapies, in which two or more treatments or therapies are combined, for example, sequentially or simultaneously.
  • the compounds described herein may also be used in combination therapies, e.g., in conjunction with other agents.
  • treatments and therapies include chemotherapy (the administration of active agents, including, e.g., drugs, antibodies (e.g., as in immunotherapy), prodrugs (e.g., as in photodynamic therapy, GDEPT, ADEPT, etc.); surgery; radiation therapy; photodynamic therapy; gene therapy; and controlled diets.
  • One aspect of the present invention pertains to a compound as described herein, in combination with one or more (e.g., 1 , 2, 3, 4, etc.) additional therapeutic agents, as described below. The particular combination would be at the discretion of the physician who would select dosages using his common general knowledge and dosing regimens known to a skilled practitioner.
  • the agents may be administered simultaneously or sequentially, and may be administered in individually varying dose schedules and via different routes.
  • the agents can be administered at closely spaced intervals (e.g., over a period of 5-10 minutes) or at longer intervals (e.g., 1 , 2, 3, 4 or more hours apart, or even longer periods apart where required), the precise dosage regimen being commensurate with the properties of the therapeutic agent(s).
  • agents i.e., the compound described here, plus one or more other agents
  • the agents may be formulated together in a single dosage form, or alternatively, the individual agents may be formulated separately and presented together in the form of a kit, optionally with instructions for their use.
  • agents/therapies that may be co-administered/combined with treatment with the PPDA compounds described herein include the following:
  • aromatase inhibitor for example, exemestane (also known as Aromasin), letrozole (also known as Femara), anastrozole (also known as Arimidex), etc.;
  • an anti-estrogen for example, faslodex (also known as Fulvestrant and
  • tamoxifen also known as Nolvadex
  • hydroxytamoxifen etc.
  • Her2 blocker for example, herceptin, pertuzumab, lapatinib, etc.;
  • a cytotoxic chemotherapeutic agent for example, a taxane (e.g., paclitaxel also known as Taxol; docetaxel also known as Taxotere), cyclophosphamide, an cytotoxic chemotherapeutic agent, for example, a taxane (e.g., paclitaxel also known as Taxol; docetaxel also known as Taxotere), cyclophosphamide, an cytotoxic chemotherapeutic agent, for example, a taxane (e.g., paclitaxel also known as Taxol; docetaxel also known as Taxotere), cyclophosphamide, an cytotoxic chemotherapeutic agent, for example, a taxane (e.g., paclitaxel also known as Taxol; docetaxel also known as Taxotere), cyclophosphamide, an cytotoxic chemotherapeutic agent, for example, a taxane (e.
  • antimetabolite e.g., carboplatin, capecitabine, gemcitabine, doxorubicin, epirubicin, 5-fluorouracil, etc.
  • the treatment further comprises treatment (e.g., simultaneous or sequential treatment) with a further active agent which is, e.g., an aromatase inhibitor, an anti-estrogen, a Her2 blocker, a cytotoxic chemotherapeutic agent, etc.
  • a further active agent which is, e.g., an aromatase inhibitor, an anti-estrogen, a Her2 blocker, a cytotoxic chemotherapeutic agent, etc.
  • Combination Therapy with an Aromatase Inhibitor and/or an Anti-Estrogen Estrogen receptor a is expressed in 70% of breast tumours and is recognised as the major driver of breast cancer development and progression in these cases. Consequently, ERa is the predominant target for adjuvant therapies in ERa-positive breast cancer. Inhibition of its activity with anti-estrogens and by inhibition of estrogen biosynthesis (e.g., using aromatase inhibitors), reduces relapse and improves patient survival (see, e.g., Osborne, 1998; Cuzick et al., 2010). Tamoxifen (Nolvadex) is an anti- estrogen that acts by competing with estrogen for binding to the estrogen receptor, to inhibit ERa activity.
  • Tamoxifen is an exemplifier of the class of anti-estrogen known as selective estrogen receptor modulators (SERMs), which are anti-estrogenic in the breast, but often have estrogen-like activities in other tissues, such as the cardiovascular system, and bone.
  • SERMs selective estrogen receptor modulators
  • Fulvestrant is an anti-estrogen that competes with estrogen for binding to ERa to prevent its activation, but also promotes down-regulation of the ERa protein.
  • fulvestrant is an exempifier of the class of anti-estrogens known as selective estrogen recepto downregulators (SERD).
  • SESD selective estrogen recepto downregulators
  • Aromatase is a cytochrome P450 enzyme that catalyses the limiting step in conversion of androgens to estrogens.
  • anastrozole Arimidex
  • letrozole Femara
  • Aromatse inhibitors act by inhibiting estrogan biosynthesis and thereby levels of circulating estrogens and consequently by limiting estrogen availability they prevent ERa activation.
  • Estrogen binding to ERa protein occurs in the ligand (hormone) binding domain (LBD), which is C-terminal to the DNA binding domain (DBD), to promote ERa dimerisation, nuclear localisation and binding to DNA in regulatory regions of target genes, to regulate the expression of said target genes.
  • Phosphorylation of ERa provides a key mechanism for regulating ERa activity, including DNA binding and transcription activation.
  • ERa phosphorylation at serine-118 in a region N-terminal to the DBD that is important for transcription activation by ERa is one of the earlies events in ERa activation.
  • Serine-118 phophorylation is mediated by estrogen stimulated recruitment of the transcription factor complex, TFIIH, which includes CDK7.
  • TFIIH transcription factor complex
  • Estrogen-stimulated TFIIH recruitment to the estrogen-bound LBD allows CDK7-mediated phosphorylation of serine-118, to promote ERa activity.
  • CDK7 over-expression can promote ERa activity under conditions of low estrogen levels, as engendered by aromatse inhibitors, and lead to activation of the tamoxifen-bound ERa (see, e.g., AN et al., 1993; Chen et al., 2000; Chen et al., 2002).
  • PPDA-001 also referred to herein as ICEC0942
  • an anti-estrogen (4-hydroxytamoxifen or Faslodex) in the estrogen-responsive ERa-positive MCF-7 breast cancer cell line.
  • the agents acts co-operatively to inhibit the growth of breast cancer cells.
  • MCF-7 cells purchased from ATCC (USA) were routinely passaged in DM EM,
  • fetal calf serum FCS
  • FCS fetal calf serum
  • Vehicle refers to the addition of an equal volume of the solvent (ethanol) in which 4-hydroxytamoxifen (100 nmol/L) and Faslodex (100 nmol/L) were prepared.
  • 4-hydroxytamoxifen and Faslodex were prepared at a concentration of 100 ⁇ /L in ethanol, and so were diluted in culture medium at 1 per 1 mL of medium (1 : 1000 dilution), to give a final concentration of 100 nmol/L.
  • plates were removed for an SRB assay. For this assay, cells were fixed by the addition of 100 ⁇ _ ⁇ / ⁇ of ice-cold 40% trichloroacetic acid (TCA).
  • Figure 4 is a graph of relative growth (mean growth ⁇ standard errors of the mean) as function of time for treatment with: (a) vehicle; (b) PPDA-001 / ICEC0942; (c) 4-hydroxytamoxifen; and (d) PPDA-001 / ICEC0942 with 4-hydroxytamoxifen.
  • co-treatment greatly enhances the growth inhibition observed for each drug alone.
  • Faslodex is illustrated in Figure 5, which is a graph of relative growth (mean growth ⁇ standard errors of the mean) as function of time for treatment with: (a) vehicle; (b) PPDA-001/ ICEC0942; (c) Faslodex; and (d) PPDA-001 / ICEC0942 with Faslodex.
  • co-treatment greatly enhances the growth inhibition observed for each drug alone.
  • MCF-7 cells cultured in DM EM supplemented with 10% FCS were treated with 1 ⁇ / ⁇ PPDA-001 / ICEC0942 for the time period shown.
  • PPDA-001 / ICEC0942 was solubilized in DMSO, an equal volume of DMSO was added as a control.
  • Cell lysates were prepared by the addition of RIPA buffer (Sigma-Aldrich, cat no: R0278).
  • Immunoblotting was carried out using standard methods (see, e.g., Harlow & Lane, 1988, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory Press, USA), with antibodies for the protein or phosphorylation mark indicated, ⁇ -actin was used as control for protein loading.
  • the various primary antibodies and their dilutions are shown in the following table.
  • the second antibody was HRP-coupled Goat anti Mouse or Rabbit IgG.
  • RNA Poll II (phospho-Ser2) 1 :500 1 :2500
  • CDK2 (phospho-T160) 1 :500 1 :2500
  • CDK1 (phospho-T161) 1 :500 1 :2500
  • Figure 6 shows immunoblot gels for the bands for phospho-ER S118 , ER, and ⁇ -actin, as a function of time, for cell lysates from MCF-7 cells treated with 1 ⁇ / ⁇ _ PPDA-001 / ICEC0942. As shown in the figure, PPDA-001 / ICEC0942 inhibits phosphorylation of ER at serine-1 18 (phospho-ER S118 ).
  • Figure 7 shows immunoblot gels for cell lysates from MCF-7 cells treated for 24 hours with 10 ⁇ / ⁇ _ PPDA-001 / ICEC0942.
  • the treatment further comprises treatment (e.g., simultaneous or sequential treatment) with a further active agent which is an aromatase inhibitor, for example, exemestane (also known as Aromasin), letrozole (also known as Femara), or anastrozole (also known as Arimidex).
  • the disorder is breast cancer (e.g., breast cancer which is resistant to said aromatase inhibitor).
  • the treatment further comprises treatment (e.g., simultaneous or sequential treatment) with a further active agent which is an anti-estrogen, for example, faslodex (also known as Fulvestrant and IC1182780), tamoxifen (also known as
  • the disorder is breast cancer (e.g., breast cancer which is resistant to said anti-estrogen).
  • the PPDA compounds described herein may also be used as cell culture additives to inhibit CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.).
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.
  • the PPDA compounds described herein may also be used as part of an in vitro assay, for example, in order to determine whether a candidate host is likely to benefit from treatment with the compound in question.
  • the PPDA compounds described herein may also be used as a standard, for example, in an assay, in order to identify other active compounds, other CDK (e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.) inhibitors, etc.
  • CDK e.g., CDK1 , CDK2, CDK4, CDK5, CDK6, CDK7, CDK8, CDK9, CDK10, CDK11 , CDK12, CDK13, etc.
  • kits comprising (a) a PPDA compound as described herein, or a composition comprising a PPDA compound as described herein, e.g., preferably provided in a suitable container and/or with suitable packaging; and (b) instructions for use, e.g., written instructions on how to administer the compound or composition.
  • the written instructions may also include a list of indications for which the active ingredient is a suitable treatment.
  • the PPDA compound or pharmaceutical composition comprising the PPDA compound may be administered to a subject by any convenient route of administration, whether systemically/peripherally or topically (i.e., at the site of desired action).
  • routes of administration examples include oral (e.g., by ingestion); buccal; sublingual; transdermal (including, e.g., by a patch, plaster, etc.); transmucosal (including, e.g., by a patch, plaster, etc.); intranasal (e.g., by nasal spray); ocular (e.g., by eyedrops);
  • pulmonary e.g., by inhalation or insufflation therapy using, e.g., via an aerosol, e.g., through the mouth or nose
  • rectal e.g., by suppository or enema
  • vaginal e.g., by pessary
  • parenteral for example, by injection, including subcutaneous, intradermal, intramuscular, intravenous, intraarterial, intracardiac, intrathecal, intraspinal,
  • the subject/patient may be a chordate, a vertebrate, a mammal, a placental mammal, a marsupial (e.g., kangaroo, wombat), a rodent (e.g., a guinea pig, a hamster, a rat, a mouse), murine (e.g., a mouse), a lagomorph (e.g., a rabbit), avian (e.g., a bird), canine (e.g., a dog), feline (e.g., a cat), equine (e.g., a horse), porcine (e.g., a pig), ovine (e.g., a sheep), bovine (e.g., a cow), a primate, simian (e.g., a monkey or ape), a monkey (e.g., marmoset, baboon), an ape (e.g
  • the subject/patient is a human.
  • a PPDA compound While it is possible for a PPDA compound to be administered alone, it is preferable to present it as a pharmaceutical formulation (e.g., composition, preparation, medicament) comprising at least one PPDA compound, as described herein, together with one or more other pharmaceutically acceptable ingredients well known to those skilled in the art, including pharmaceutically acceptable carriers, diluents, excipients, adjuvants, fillers, buffers, preservatives, anti-oxidants, lubricants, stabilisers, solubilisers, surfactants (e.g., wetting agents), masking agents, colouring agents, flavouring agents, and sweetening agents.
  • the formulation may further comprise other active agents, for example, other therapeutic or prophylactic agents.
  • the present invention further provides pharmaceutical compositions, as defined above, and methods of making a pharmaceutical composition comprising mixing at least one PPDA compound, as described herein, together with one or more other
  • pharmaceutically acceptable ingredients well known to those skilled in the art, e.g., carriers, diluents, excipients, etc. If formulated as discrete units (e.g., tablets, etc.), each unit contains a predetermined amount (dosage) of the compound.
  • pharmaceutically acceptable pertains to compounds, ingredients, materials, compositions, dosage forms, etc., which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of the subject in question (e.g., human) without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
  • Each carrier, diluent, excipient, etc. must also be “acceptable” in the sense of being compatible with the other ingredients of the formulation.
  • Suitable carriers, diluents, excipients, etc. can be found in standard pharmaceutical texts, for example, Remington's Pharmaceutical Sciences, 18th edition, Mack Publishing Company, Easton, Pa., 1990; and Handbook of Pharmaceutical Excipients, 5th edition, 2005.
  • the formulations may be prepared by any methods well known in the art of pharmacy. Such methods include the step of bringing into association the compound with a carrier, which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing into association the compound with carriers (e.g., liquid carriers, finely divided solid carrier, etc.), and then shaping the product, if necessary.
  • carriers e.g., liquid carriers, finely divided solid carrier, etc.
  • the formulation may be prepared to provide for rapid or slow release; immediate, delayed, timed, or sustained release; or a combination thereof.
  • Formulations may suitably be in the form of liquids, solutions (e.g., aqueous, nonaqueous), suspensions (e.g., aqueous, non-aqueous), emulsions (e.g., oil-in-water, water-in-oil), elixirs, syrups, electuaries, mouthwashes, drops, tablets (including, e.g., coated tablets), granules, powders, losenges, pastilles, capsules (including, e.g., hard and soft gelatin capsules), cachets, pills, ampoules, boluses, suppositories, pessaries, tinctures, gels, pastes, ointments, creams, lotions, oils, foams, sprays, mists, or aerosols.
  • solutions e.g., aqueous, nonaqueous
  • suspensions e.g., aqueous, non-aqueous
  • emulsions
  • Formulations may suitably be provided as a patch, adhesive plaster, bandage, dressing, or the like which is impregnated with one or more compounds and optionally one or more other pharmaceutically acceptable ingredients, including, for example, penetration, permeation, and absorption enhancers. Formulations may also suitably be provided in the form of a depot or reservoir. The compound may be dissolved in, suspended in, or mixed with one or more other pharmaceutically acceptable ingredients. The compound may be presented in a liposome or other microparticulate which is designed to target the compound, for example, to blood components or one or more organs.
  • Formulations suitable for oral administration include liquids, solutions (e.g., aqueous, non-aqueous), suspensions (e.g., aqueous, non-aqueous), emulsions (e.g., oil-in-water, water-in-oil), elixirs, syrups, electuaries, tablets, granules, powders, capsules, cachets, pills, ampoules, boluses.
  • Formulations suitable for buccal administration include mouthwashes, losenges, pastilles, as well as patches, adhesive plasters, depots, and reservoirs.
  • Losenges typically comprise the compound in a flavored basis, usually sucrose and acacia or tragacanth.
  • Pastilles typically comprise the compound in an inert matrix, such as gelatin and glycerin, or sucrose and acacia.
  • Mouthwashes typically comprise the compound in a suitable liquid carrier.
  • Formulations suitable for sublingual administration include tablets, losenges, pastilles, capsules, and pills.
  • Formulations suitable for oral transmucosal administration include liquids, solutions (e.g., aqueous, non-aqueous), suspensions (e.g., aqueous, non-aqueous), emulsions (e.g., oil- in-water, water-in-oil), mouthwashes, losenges, pastilles, as well as patches, adhesive plasters, depots, and reservoirs.
  • Formulations suitable for non-oral transmucosal administration include liquids, solutions (e.g. , aqueous, non-aqueous), suspensions (e.g. , aqueous, non-aqueous), emulsions (e.g. , oil-in-water, water-in-oil), suppositories, pessaries, gels, pastes, ointments, creams, lotions, oils, as well as patches, adhesive plasters, depots, and reservoirs.
  • solutions e.g. , aqueous, non-aqueous
  • suspensions e.g. , aqueous, non-aqueous
  • emulsions e.g. , oil-in-water, water-in-oil
  • suppositories e.g. , oil-in-water, water-in-oil
  • pessaries e.g. , oil-in-water, water-in-oil
  • Formulations suitable for transdermal administration include gels, pastes, ointments, creams, lotions, and oils, as well as patches, adhesive plasters, bandages, dressings, depots, and reservoirs.
  • Tablets may be made by conventional means, e.g. , compression or moulding, optionally with one or more accessory ingredients.
  • Compressed tablets may be prepared by compressing in a suitable machine the compound in a free-flowing form such as a powder or granules, optionally mixed with one or more binders (e.g. , povidone, gelatin, acacia, sorbitol, tragacanth, hydroxypropylmethyl cellulose); fillers or diluents (e.g. , lactose, microcrystalline cellulose, calcium hydrogen phosphate); lubricants (e.g.
  • disintegrants e.g., sodium starch glycolate, cross-linked povidone, cross-linked sodium carboxymethyl cellulose
  • surface-active or dispersing or wetting agents e.g. , sodium lauryl sulfate
  • preservatives e.g. , methyl p-hydroxybenzoate, propyl p-hydroxybenzoate, sorbic acid
  • flavours enhancing agents, and sweeteners.
  • Tablets may be made by moulding in a suitable machine a mixture of the powdered compound moistened with an inert liquid diluent.
  • the tablets may optionally be coated or scored and may be formulated so as to provide slow or controlled release of the compound therein using, for example, hydroxypropylmethyl cellulose in varying proportions to provide the desired release profile. Tablets may optionally be provided with a coating, for example, to affect release, for example an enteric coating, to provide release in parts of the gut other than the stomach.
  • Ointments are typically prepared from the compound and a paraffinic or a water-miscible ointment base.
  • Creams are typically prepared from the compound and an oil-in-water cream base.
  • the aqueous phase of the cream base may include, for example, at least about 30% w/w of a polyhydric alcohol, i.e. , an alcohol having two or more hydroxyl groups such as propylene glycol, butane-1 ,3-diol, mannitol, sorbitol, glycerol and polyethylene glycol and mixtures thereof.
  • the topical formulations may desirably include a compound which enhances absorption or penetration of the compound through the skin or other affected areas. Examples of such dermal penetration enhancers include dimethylsulfoxide and related analogues.
  • Emulsions are typically prepared from the compound and an oily phase, which may optionally comprise merely an emulsifier (otherwise known as an emulgent), or it may comprise a mixture of at least one emulsifier with a fat or an oil or with both a fat and an oil.
  • an emulsifier also known as an emulgent
  • a hydrophilic emulsifier is included together with a lipophilic emulsifier which acts as a stabiliser. It is also preferred to include both an oil and a fat.
  • the emulsifier(s) with or without stabiliser(s) make up the so-called emulsifying wax
  • the wax together with the oil and/or fat make up the so-called emulsifying ointment base which forms the oily dispersed phase of the cream formulations.
  • Suitable emulgents and emulsion stabilisers include Tween 60, Span 80, cetostearyl alcohol, myristyl alcohol, glyceryl monostearate and sodium lauryl sulfate.
  • suitable oils or fats for the formulation is based on achieving the desired cosmetic properties, since the solubility of the compound in most oils likely to be used in pharmaceutical emulsion formulations may be very low.
  • the cream should preferably be a non-greasy, non-staining and washable product with suitable consistency to avoid leakage from tubes or other containers.
  • Straight or branched chain, mono- or dibasic alkyl esters such as di-isoadipate, isocetyl stearate, propylene glycol diester of coconut fatty acids, isopropyl myristate, decyl oleate, isopropyl palmitate, butyl stearate, 2-ethylhexyl palmitate or a blend of branched chain esters known as Crodamol CAP may be used, the last three being preferred esters. These may be used alone or in combination depending on the properties required. Alternatively, high melting point lipids such as white soft paraffin and/or liquid paraffin or other mineral oils can be used.
  • Formulations suitable for intranasal administration, where the carrier is a liquid include, for example, nasal spray, nasal drops, or by aerosol administration by nebuliser, include aqueous or oily solutions of the compound.
  • Formulations suitable for intranasal administration include, for example, those presented as a coarse powder having a particle size, for example, in the range of about 20 to about 500 microns which is administered in the manner in which snuff is taken, i.e., by rapid inhalation through the nasal passage from a container of the powder held close up to the nose.
  • Formulations suitable for pulmonary administration include those presented as an aerosol spray from a pressurised pack, with the use of a suitable propellant, such as dichlorodifluoromethane, trichlorofluoromethane, dichoro-tetrafluoroethane, carbon dioxide, or other suitable gases.
  • Formulations suitable for ocular administration include eye drops wherein the compound is dissolved or suspended in a suitable carrier, especially an aqueous solvent for the compound.
  • Formulations suitable for rectal administration may be presented as a suppository with a suitable base comprising, for example, natural or hardened oils, waxes, fats, semi-liquid or liquid polyols, for example, cocoa butter or a salicylate; or as a solution or suspension for treatment by enema.
  • Formulations suitable for vaginal administration may be presented as pessaries, tampons, creams, gels, pastes, foams or spray formulations containing in addition to the compound, such carriers as are known in the art to be appropriate.
  • Formulations suitable for parenteral administration include aqueous or non-aqueous, isotonic, pyrogen-free, sterile liquids (e.g., solutions, suspensions), in which the compound is dissolved, suspended, or otherwise provided (e.g., in a liposome or other micro particulate).
  • Such liquids may additionally contain other pharmaceutically acceptable ingredients, such as anti-oxidants, buffers, preservatives, stabilisers, bacteriostats, suspending agents, thickening agents, and solutes, which render the formulation isotonic with the blood (or other relevant bodily fluid) of the intended recipient.
  • excipients include, for example, water, alcohols, polyols, glycerol, vegetable oils, and the like.
  • suitable isotonic carriers for use in such formulations include Sodium Chloride Injection, Ringer's Solution, or Lactated Ringer's Injection.
  • the concentration of the compound in the liquid is from about 1 ng/mL to about 10 ⁇ g/mL, for example from about 10 ng/mL to about 1 ⁇ g/mL.
  • the formulations may be presented in unit-dose or multi-dose sealed containers, for example, ampoules and vials, and may be stored in a freeze-dried (lyophilised) condition requiring only the addition of the sterile liquid carrier, for example water for injections, immediately prior to use.
  • Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules, and tablets.
  • appropriate dosages of the PPDA compounds, and compositions comprising the PPDA compounds can vary from patient to patient. Determining the optimal dosage will generally involve the balancing of the level of therapeutic benefit against any risk or deleterious side effects.
  • the selected dosage level will depend on a variety of factors including the activity of the particular PPDA compound, the route of administration, the time of administration, the rate of excretion of the PPDA compound, the duration of the treatment, other drugs, compounds, and/or materials used in combination, the severity of the disorder, and the species, sex, age, weight, condition, general health, and prior medical history of the patient.
  • the amount of PPDA compound and route of administration will ultimately be at the discretion of the physician, veterinarian, or clinician, although generally the dosage will be selected to achieve local concentrations at the site of action which achieve the desired effect without causing substantial harmful or deleterious side-effects.
  • Administration can be effected in one dose, continuously or intermittently (e.g., in divided doses at appropriate intervals) throughout the course of treatment. Methods of determining the most effective means and dosage of administration are well known to those of skill in the art and will vary with the formulation used for therapy, the purpose of the therapy, the target cell(s) being treated, and the subject being treated. Single or multiple administrations can be carried out with the dose level and pattern being selected by the treating physician, veterinarian, or clinician.
  • a suitable dose of the PPDA compound is in the range of about 10 ⁇ g to about 250 mg (more typically about 100 ⁇ g to about 25 mg) per kilogram body weight of the subject per day. Where the compound is a salt, an ester, an amide, a prodrug, or the like, the amount administered is calculated on the basis of the parent compound and so the actual weight to be used is increased proportionately.
  • the general synthetic route towards the target compounds is illustrated in the following scheme.
  • the three main side chains (R 1 , R 2 and R 3 ) can be greatly varied.
  • Ci 6 H 17 CIN 4 (M+H + ): 301.1220, found: 301.1230; Anal. calc. for C 16 Hi 7 CIN 4 : C 63.89, H 5.70, N 18.63, found: C 63.95, H 5.78, N 18.59.
  • reaction mixture was filtered through Celite, washed with hot THF (50 mL) and the filtrate was concentrated in vacuo to give crude (S/ ⁇ / ⁇ -l-benzyl-S ⁇ -dihydroxypyrrolidine as a pale yellow solid, which was used for the next step without further purification.
  • the crude oil was dissolved in dry DMF (20 mL), sodium azide (1.2 g, 18.6 mmol) was added and the resulting suspension was heated at 100 °C for 48 h, cooled to room temperature and diluted with water (10 mL) and Et20 (10 mL). The aqueous layer was extracted with Et20 (3 x 10 mL) and the combined organic layers were washed with water and brine, dried over MgS0 4 , filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography (hexane:Et202:3) to yield azide 21 (825 mg, 81%) as a colorless oil.
  • Triol 25 (440 mg, 1.85 mmol) was dissolved in MeOH (3 ml) and treated with Pd/C (15% wt., 22 mg) and stirred under an atmosphere of hydrogen for 10 h at 50 °C. The mixture was filtered through Celite and the filtrate was concentrated under reduced pressure giving amine 26 (270 mg, 99%).
  • Boc 2 0 (370 mg, 1.70 mmol) and MeOH (0.5 mL) were added with stirring to a solution of amine 26 (250 mg, 1.70 mmol) in CH2CI2 (2 mL) and the reaction mixture was stirred for 3 h at room temperature.
  • the solvent was removed under reduced pressure and purification by flash column chromatography (CH2CI2: MeOH gradient 19: 1 to 9: 1) afforded 27 (342 mg, 81 %) of carbamate 27 as a white solid.
  • Azide 29 (130 mg, 0.48 mmol) was dissolved in acetone and dimethoxypropane (1 : 1 ; 6 mL) and pTsOH (9 mg, 0.05 mmol) was added. The reaction mixture was stirred at room temperature for 2 h and concentrated under reduced pressure. The residue was purified by flash column chromatography (hexane:EtOAc 1 :1) giving azide 30 (130 mg, 87%) as a colorless oil.
  • Tetrahydropyridine 24 (2.00 g, 9.85 mmol) was dissolved in THF (19 ml) and cooled to -30 °C. Borane.THF complex (1 M in THF, 19.0 ml, 19.0 mmol) was added dropwise and the mixture allowed to warm to room temperature overnight. The solution was cooled to -10 °C and quenched by addition of water (0.5 ml_). Hydrogen peroxide (30% in water, 1.24 ml) and sodium hydroxide (3 M in water, 1.37 ml) were simultaneously added dropwise. Sodium hydroxide (50% in water, 2.5 ml) was added and the mixture heated at reflux for 4 h. The reaction mixture was cooled to room temperature and the white precipitate removed by filtration.
  • Piperidine 32 (2.62 g, 1 1.9 mmol) and Pd/C (10% wt., 263 mg) were suspended in MeOH (25.0 ml) and Boc 2 0 (3.89 g, 17.8 mmol) was added. The atmosphere was replaced by hydrogen and the mixture heated to 50 °C overnight. The suspension was cooled to room temperature, filtered first through Celite and subsequently through a plug of silica to yield the title compound (2.74 g, 99%), which was used in the next step without further purification.
  • ferf-Butyl-4-oxopiperidine-1-carboxylate 39 (10.0 g, 50.2 mmol) was added portion-wise with stirring to a solution of nitromethane (100 mL) and ⁇ (42.8 mL, 301 mmol) and the mixture was stirred for 4 days at room temperature.
  • the reaction mixture was diluted with EtOAc (80 mL) and washed with water, saturated aqueous NH4CI and brine, dried over MgSCU and concentrated under reduced pressure to give the title compound (12.1 g, 93%) as a white solid. See, e.g., Bosmans et al., 2005.
  • Diol 43 (750 mg, 3.2 mmol) was dissolved in CH2CI2 and pyridine (3.6 ml_, 1 : 1). The mixture was cooled to 0 °C and treated with pTsCI (0.648 mg, 3.4 mmol) and DMAP (2 mg, 0.02 mmol). The mixture was stirred for 24 h at room temperature. The mixture was concentrated under reduced pressure, dissolved in DMF (15 ml), treated with NalS (1.85 mg, 22.4 mmol) and the mixture was heated to 85 °C for 24 h. The mixture was re-cooled to room temperature, filtered and the filtrate was extracted with EtOAc and washed with brine. The combined organic layers were dried (Na 2 SC>4) and concentrated under reduced pressure. The title azide was obtained as a colorless oil (434 mg, 53%) after flash column chromatography (hexane:EtOAc gradient 9:1 to 7:3).
  • aqueous phase was extracted with ethyl acetate (3 x 10 mL) and the combined organic phases were dried over MgSCU and concentrated under reduced pressure. Purification by flash column chromatography (hexane:EtOAc) gave the corresponding product. See, e.g., Hong et al., 1997.

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AU2015220560A AU2015220560B2 (en) 2014-02-21 2015-02-20 Pyrazolo[1,5-a]pyrimidine-5,7-diamine compounds as CDK inhibitors and their therapeutic use
SM20190266T SMT201900266T1 (it) 2014-02-21 2015-02-20 Composti di pirazolo[1,5-a]piramidin-5,7-diammina come inibitori di cdk e loro uso terapeutico
RS20190487A RS58704B1 (sr) 2014-02-21 2015-02-20 Pirazolo[1,5-a]pirimidin-5,7-diamin jedinjenja kao cdk inhibitori i njihova terapeutska primena
DK15706282.9T DK3107914T3 (en) 2014-02-21 2015-02-20 PYRAZOLO [1,5-A] PYRIMIDINE-5,7-DIAMINE COMPOUNDS AS CDK INHIBITORS AND THERAPEUTIC APPLICATION THEREOF
CN201580011502.7A CN106103445B (zh) 2014-02-21 2015-02-20 作为cdk抑制剂的吡唑并[1,5-a]嘧啶-5,7-二胺化合物和它们的治疗用途
EP15706282.9A EP3107914B8 (en) 2014-02-21 2015-02-20 Pyrazolo[1,5-a]pyrimidine-5,7-diamine compounds as cdk inhibitors and their therapeutic use
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LTEP15706282.9T LT3107914T (lt) 2014-02-21 2015-02-20 Pirazolo[1,5-a]pirimidin-5,7-diamino junginiai kaip cdk inhibitoriai ir jų terapinis panaudojimas
SI201530714T SI3107914T1 (sl) 2014-02-21 2015-02-20 Pirazolo(1,5-A)pirimidin-5,7-diaminske spojine kot inhibitorji CDK in njihova terapevtska uporaba
US15/117,982 US9932344B2 (en) 2014-02-21 2015-02-20 Pyrazolo[1,5-A]pyrimidine-5,7-diamine compounds as CDK inhibitors and their therapeutic use
BR112016018633-8A BR112016018633B1 (pt) 2014-02-21 2015-02-20 Pirazolopirimidina-5,7-diaminas como inibidores de cdk, seus usos, composição farmacêutica e seu método de preparação, e método in vitro para inibir a função de quinase dependente de ciclina em uma célula
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PL15706282T PL3107914T3 (pl) 2014-02-21 2015-02-20 Związki pirazolo[1,5-a]pirymidyno-5,7-diaminowe jako inhibitory CDK i ich zastosowanie terapeutyczne
JP2016553387A JP6498212B2 (ja) 2014-02-21 2015-02-20 Ｃｄｋ阻害剤としてのピラゾロ［１，５‐ａ］ピリミジン‐５，７‐ジアミン化合物及びその治療用途
HRP20190685TT HRP20190685T1 (hr) 2014-02-21 2015-02-20 Spojevi pirazolo[1,5-a]pirimidin-5,7-diamina kao inhibitori za cdk i njihove terapeutske uporabe
ES15706282T ES2721268T3 (es) 2014-02-21 2015-02-20 Compuestos de pirazolo[1,5-a]pirimidina-5,7-diamina como inhibidores de CDK y su uso terapéutico
US15/941,063 US10414772B2 (en) 2014-02-21 2018-03-30 Pyrazolo[1,5-A]pyrimidine-5,7-diamine compounds as CDK inhibitors and their therapeutic use
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US16/559,735 US10927119B2 (en) 2014-02-21 2019-09-04 Pyrazolo[1,5-a]pyrimidine-5,7-diamine compounds as CDK inhibitors and their therapeutic use
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Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017096326A1 (en) 2015-12-02 2017-06-08 Massachusetts Institute Of Technology Method for efficient generation of neurons from non-neuronal cells
KR20170077168A (ko) 2014-10-31 2017-07-05 우베 고산 가부시키가이샤 치환 디히드로피롤로피라졸 화합물
KR20180018661A (ko) 2015-06-15 2018-02-21 우베 고산 가부시키가이샤 치환 디히드로피롤로피라졸 유도체
WO2019057825A1 (en) * 2017-09-20 2019-03-28 Carrick Therapeutics Limited 4 - [[(7-AMINOPYRAZOLO [1,5-A] PYRIMIDIN-5-YL) AMINO] METHYL] PIPERIDIN-3-OL COMPOUNDS AS CDK INHIBITORS
WO2019213403A1 (en) 2018-05-02 2019-11-07 Kinnate Biopharma Inc. Inhibitors of cyclin-dependent kinases
WO2020092314A1 (en) * 2018-10-30 2020-05-07 Kronos Bio, Inc. Compounds, compositions, and methods for modulating cdk9 activity
WO2020100944A1 (ja) 2018-11-14 2020-05-22 宇部興産株式会社 ジヒドロピロロピラゾール誘導体
WO2020186196A1 (en) * 2019-03-13 2020-09-17 The Translational Genomics Research Institute Trisubstituted pyrazolo [1,5-a] pyrimidine compounds as cdk7 inhibitors
US10800782B2 (en) 2016-08-31 2020-10-13 Agios Pharmaceutical, Inc. Inhibitors of cellular metabolic processes
US10894788B2 (en) 2018-06-29 2021-01-19 Kinnate Biopharma Inc. Inhibitors of cyclin-dependent kinases
WO2021122745A1 (en) 2019-12-16 2021-06-24 Carrick Therapeutics Limited 4-[[(7-aminopyrazolo[1,5-a]pyrimidin-5-yl)amino]methyl]piperidin-3-ol compounds and their therapeutic use
WO2021216828A1 (en) * 2020-04-24 2021-10-28 Massachusetts Institute Of Technology Chimeric degraders of cyclin-dependent kinase 9 and uses thereof
CN114269742A (zh) * 2019-07-10 2022-04-01 常州千红生化制药股份有限公司 作为治疗剂的4-(咪唑并[1,2-a]吡啶-3-基)-N-(吡啶基)嘧啶-2-胺的衍生物
CN115485030A (zh) * 2020-03-06 2022-12-16 拜耳公司 咪唑并三嗪通过抑制cdk12作用于癌症
WO2023001061A1 (en) * 2021-07-17 2023-01-26 Jingrui Biopharma Co., Ltd. Cdk7 selective inhibitors as anticancer agents
WO2023096922A1 (en) * 2021-11-24 2023-06-01 Kronos Bio, Inc. Polymorphic and salt forms of (ls,3s)-n1-(5-(pentan-3- yl)pyrazolo[l,5-a]pyrimidin-7-yl)cyclopentane-l,3-diamine
EP4051282A4 (en) * 2019-10-29 2023-12-13 Syros Pharmaceuticals, Inc. METHODS OF TREATING CANCER IN BIOMARKER-IDENTIFIED PATIENTS WITH CYCLIN-DEPENDENT KINASE 7 (CDK7) INHIBITORS
WO2024174949A1 (zh) * 2023-02-20 2024-08-29 江苏正大丰海制药有限公司 作为cdk7激酶抑制剂的杂芳环化合物及其制备和应用
US12097261B2 (en) 2021-05-07 2024-09-24 Kymera Therapeutics, Inc. CDK2 degraders and uses thereof
WO2025006569A1 (en) 2023-06-27 2025-01-02 Arvinas Operations, Inc. Combinations of estrogen receptor degraders and cdk7 inhibitors for the treatment of cancer
WO2025057087A1 (en) 2023-09-11 2025-03-20 Assia Chemical Industries Ltd. Solid state forms of samuraciclib

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201403093D0 (en) 2014-02-21 2014-04-09 Cancer Rec Tech Ltd Therapeutic compounds and their use
CA2970574C (en) 2014-12-17 2023-09-19 King's College London Bicycloheteroaryl-heteroaryl-benzoic acid compounds as retinoic acid receptor beta (rar.beta.) agonists
CA2976109A1 (en) * 2015-02-13 2016-08-18 Dana-Farber Cancer Institute, Inc. Substituted pyrrolopyrimidine, pyrazolopyrimidine and purine derivatives and use thereof as lrrk2 inhibitors
EP4438117A3 (en) 2017-07-28 2024-12-18 Takeda Pharmaceutical Company Limited Tyk2 inhibitors and uses thereof
MX2020001531A (es) * 2017-08-07 2020-03-20 Biocad Joint Stock Co Nuevos compuestos hetorociclicos como inhibidores de cdk8/19.
US20200197392A1 (en) * 2017-08-15 2020-06-25 The Brigham & Women's Hospital, Inc. Compositions and methods for treating tuberous sclerosis complex
TWI703149B (zh) * 2017-11-16 2020-09-01 美商美國禮來大藥廠 用於抑制cdk7之化合物
IL277770B2 (en) * 2018-04-11 2024-01-01 Qurient Co Ltd Pyrazolo-triazine and/or pyrazolo-pyrimidine derivatives as selective inhibitor of cyclin dependent kinase
CN109860354B (zh) 2018-12-28 2020-05-19 南京邮电大学 同质集成红外光子芯片及其制备方法
WO2022156779A1 (zh) * 2021-01-22 2022-07-28 上海海雁医药科技有限公司 取代的吡唑并[1,5-a]嘧啶-7-胺衍生物、其组合物及医药上的用途
GB202108572D0 (en) * 2021-06-16 2021-07-28 Carrick Therapeutics Ltd Therapeutic compounds and their use
WO2024102447A1 (en) * 2022-11-10 2024-05-16 Emory University Uses of hydroimidazopyridopyrimidinone derivatives for managing aneurysms or other vascular conditions or diseases
WO2024175024A1 (zh) * 2023-02-21 2024-08-29 杭州德睿智药科技有限公司 作为CDKs抑制剂的新型并杂环类新化合物及其应用

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004087707A1 (en) * 2003-03-31 2004-10-14 Vernalis (Cambridge) Limited Pyrazolopyrimidine compounds and their use in medicine
WO2008151304A1 (en) * 2007-06-05 2008-12-11 Emory University Selective inhibitors for cyclin-dependent kinases
WO2011068667A1 (en) * 2009-12-04 2011-06-09 Cylene Pharmaceuticals, Inc. Pyrazolopyrimidines and related heterocycles as ck2 inhibitors

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2457201A (en) 1999-12-28 2001-07-09 Bristol-Myers Squibb Company Cytokine, especially tnf-alpha, inhibitors
JP4881558B2 (ja) 2002-09-04 2012-02-22 シェーリング コーポレイション サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン
US7388019B2 (en) 2003-01-31 2008-06-17 Merck & Co., Inc. 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes
EP1599482A4 (en) 2003-02-28 2008-10-01 Teijin Pharma Ltd PYRAZOLO1,5-A PYRIMIDINE DERIVATIVES
JO2478B1 (en) 2003-06-19 2009-01-20 جانسين فارماسوتيكا ان. في. (Aminomethyl) -biperidine benzamides as 5 HT4 antagonists
CA2627623C (en) * 2005-10-06 2014-04-22 Schering Corporation Methods for inhibiting protein kinases
WO2012059932A1 (en) 2010-11-01 2012-05-10 Aurigene Discovery Technologies Limited 2, 4 -diaminopyrimidine derivatives as protein kinase inhibitors
EP3812387A1 (en) * 2011-07-21 2021-04-28 Sumitomo Dainippon Pharma Oncology, Inc. Heterocyclic protein kinase inhibitors
EP2634189A1 (en) 2012-03-01 2013-09-04 Lead Discovery Center GmbH Pyrazolo-triazine derivatives as selective cyclin-dependent kinase inhibitors
EP2634190A1 (en) 2012-03-01 2013-09-04 Lead Discovery Center GmbH Pyrazolo-triazine derivatives as selective cyclin-dependent kinase inhinitors
GB201403093D0 (en) 2014-02-21 2014-04-09 Cancer Rec Tech Ltd Therapeutic compounds and their use

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004087707A1 (en) * 2003-03-31 2004-10-14 Vernalis (Cambridge) Limited Pyrazolopyrimidine compounds and their use in medicine
WO2008151304A1 (en) * 2007-06-05 2008-12-11 Emory University Selective inhibitors for cyclin-dependent kinases
WO2011068667A1 (en) * 2009-12-04 2011-06-09 Cylene Pharmaceuticals, Inc. Pyrazolopyrimidines and related heterocycles as ck2 inhibitors

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US10131679B2 (en) 2014-10-31 2018-11-20 Ube Industries, Ltd. Substituted dihydropyrrolopyrazole compound
US10968238B2 (en) 2014-10-31 2021-04-06 Ube Industries, Ltd. Substituted dihydropyrrolopyrazole compound
US10894798B2 (en) 2015-06-15 2021-01-19 Ube Industries, Ltd. Substituted dihydropyrrolopyrazole derivative
KR20180018661A (ko) 2015-06-15 2018-02-21 우베 고산 가부시키가이샤 치환 디히드로피롤로피라졸 유도체
US10273252B2 (en) 2015-06-15 2019-04-30 Ube Industries, Ltd. Substituted dihydropyrrolopyrazole derivative
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US11325914B1 (en) 2016-08-31 2022-05-10 Servier Pharmaceuticals Llc Inhibitors of cellular metabolic processes
US10800782B2 (en) 2016-08-31 2020-10-13 Agios Pharmaceutical, Inc. Inhibitors of cellular metabolic processes
USRE49934E1 (en) 2016-08-31 2024-04-23 Servier Pharmaceuticals Llc Inhibitors of cellular metabolic processes
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US11447493B2 (en) 2018-05-02 2022-09-20 Kinnate Biopharma Inc. Inhibitors of cyclin-dependent kinases
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US11390618B2 (en) 2018-06-29 2022-07-19 Kinnate Biopharma Inc. Inhibitors of cyclin-dependent kinases
US10894788B2 (en) 2018-06-29 2021-01-19 Kinnate Biopharma Inc. Inhibitors of cyclin-dependent kinases
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US12097261B2 (en) 2021-05-07 2024-09-24 Kymera Therapeutics, Inc. CDK2 degraders and uses thereof
WO2023001061A1 (en) * 2021-07-17 2023-01-26 Jingrui Biopharma Co., Ltd. Cdk7 selective inhibitors as anticancer agents
WO2023096922A1 (en) * 2021-11-24 2023-06-01 Kronos Bio, Inc. Polymorphic and salt forms of (ls,3s)-n1-(5-(pentan-3- yl)pyrazolo[l,5-a]pyrimidin-7-yl)cyclopentane-l,3-diamine
WO2024174949A1 (zh) * 2023-02-20 2024-08-29 江苏正大丰海制药有限公司 作为cdk7激酶抑制剂的杂芳环化合物及其制备和应用
WO2025006569A1 (en) 2023-06-27 2025-01-02 Arvinas Operations, Inc. Combinations of estrogen receptor degraders and cdk7 inhibitors for the treatment of cancer
WO2025057087A1 (en) 2023-09-11 2025-03-20 Assia Chemical Industries Ltd. Solid state forms of samuraciclib

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US11566029B2 (en) 2023-01-31
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US20210253583A1 (en) 2021-08-19
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US20160362410A1 (en) 2016-12-15
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BR112016018633A2 (en, 2012) 2017-08-08
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