PE20180530A1 - Derivados de amidas policiclicas como inhibidores de cdk9 - Google Patents

Derivados de amidas policiclicas como inhibidores de cdk9

Info

Publication number
PE20180530A1
PE20180530A1 PE2017002874A PE2017002874A PE20180530A1 PE 20180530 A1 PE20180530 A1 PE 20180530A1 PE 2017002874 A PE2017002874 A PE 2017002874A PE 2017002874 A PE2017002874 A PE 2017002874A PE 20180530 A1 PE20180530 A1 PE 20180530A1
Authority
PE
Peru
Prior art keywords
pyridin
lymphoma
tetrahydroimidazo
carboxamide
chloro
Prior art date
Application number
PE2017002874A
Other languages
English (en)
Spanish (es)
Inventor
Kurt Gordon Pike
Bernard Christophe Barlaam
Janet Hawkins
Savi Christopher De
Melissa Marie Vasbinder
Alexander Hird
Michelle Lamb
Original Assignee
Astrazeneca Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of PE20180530A1 publication Critical patent/PE20180530A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Detergent Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
PE2017002874A 2015-06-29 2016-06-27 Derivados de amidas policiclicas como inhibidores de cdk9 PE20180530A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201562185852P 2015-06-29 2015-06-29

Publications (1)

Publication Number Publication Date
PE20180530A1 true PE20180530A1 (es) 2018-03-19

Family

ID=56292699

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2017002874A PE20180530A1 (es) 2015-06-29 2016-06-27 Derivados de amidas policiclicas como inhibidores de cdk9

Country Status (38)

Country Link
US (4) US9845331B2 (cg-RX-API-DMAC7.html)
EP (2) EP3313838B1 (cg-RX-API-DMAC7.html)
JP (1) JP6997627B2 (cg-RX-API-DMAC7.html)
KR (1) KR102663113B1 (cg-RX-API-DMAC7.html)
CN (1) CN107873028B (cg-RX-API-DMAC7.html)
AR (1) AR105179A1 (cg-RX-API-DMAC7.html)
AU (1) AU2016286200B2 (cg-RX-API-DMAC7.html)
BR (1) BR122019013677B1 (cg-RX-API-DMAC7.html)
CA (1) CA2989499C (cg-RX-API-DMAC7.html)
CL (1) CL2017003306A1 (cg-RX-API-DMAC7.html)
CO (1) CO2017013713A2 (cg-RX-API-DMAC7.html)
CR (2) CR20210297A (cg-RX-API-DMAC7.html)
CY (2) CY1122111T1 (cg-RX-API-DMAC7.html)
DK (2) DK3313838T3 (cg-RX-API-DMAC7.html)
DO (2) DOP2017000295A (cg-RX-API-DMAC7.html)
EA (1) EA035383B1 (cg-RX-API-DMAC7.html)
ES (2) ES2728356T3 (cg-RX-API-DMAC7.html)
HR (2) HRP20211970T1 (cg-RX-API-DMAC7.html)
HU (2) HUE057343T2 (cg-RX-API-DMAC7.html)
IL (1) IL256393B (cg-RX-API-DMAC7.html)
LT (2) LT3313838T (cg-RX-API-DMAC7.html)
ME (1) ME03404B (cg-RX-API-DMAC7.html)
MX (1) MX371034B (cg-RX-API-DMAC7.html)
MY (1) MY201673A (cg-RX-API-DMAC7.html)
NI (1) NI201700174A (cg-RX-API-DMAC7.html)
PE (1) PE20180530A1 (cg-RX-API-DMAC7.html)
PH (1) PH12017502334B1 (cg-RX-API-DMAC7.html)
PL (2) PL3313838T3 (cg-RX-API-DMAC7.html)
PT (2) PT3313838T (cg-RX-API-DMAC7.html)
RS (2) RS58712B1 (cg-RX-API-DMAC7.html)
SI (2) SI3539961T1 (cg-RX-API-DMAC7.html)
SM (2) SMT201900298T1 (cg-RX-API-DMAC7.html)
SV (1) SV2017005598A (cg-RX-API-DMAC7.html)
TN (1) TN2017000486A1 (cg-RX-API-DMAC7.html)
TR (1) TR201909286T4 (cg-RX-API-DMAC7.html)
TW (1) TWI723028B (cg-RX-API-DMAC7.html)
WO (1) WO2017001354A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA201800563B (cg-RX-API-DMAC7.html)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20200289506A1 (en) 2017-09-25 2020-09-17 Astrazeneca Ab Combination of a btk inhibitor and an inhibitor or cdk9 to treat cancer
WO2019074748A1 (en) * 2017-10-09 2019-04-18 Merck Sharp & Dohme Corp. NOVEL SUBSTITUTED PHENYL-OXETANE AND PHENYLTETRAHYDROFURAN COMPOUNDS AS INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE (IDO)
CN108129288B (zh) * 2017-12-27 2021-01-22 上海毕得医药科技股份有限公司 一种反式-3-羟基环丁基甲酸的合成方法
TWI810397B (zh) 2018-11-14 2023-08-01 瑞典商阿斯特捷利康公司 治療癌症之方法
WO2020259556A1 (zh) * 2019-06-27 2020-12-30 南京明德新药研发有限公司 作为cdk9抑制剂的氮杂吲哚连吡唑类化合物
CN114786673A (zh) * 2019-09-11 2022-07-22 普莱鲁德疗法有限公司 Cdk抑制剂及其作为药物的用途
EP4074699A4 (en) * 2019-12-09 2024-01-03 CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. COMPOUND USEFUL AS CYCLIN-DEPENDENT KINASE 9 INHIBITOR AND USE THEREOF
EP4140997A4 (en) 2020-05-12 2023-09-06 Suzhou Alphama Biotechnology Co., Ltd. PYRIDINE ACETAMIDE DERIVATIVE AS CDK INHIBITOR, PREPARATION METHOD AND USE THEREOF
WO2021227904A1 (zh) 2020-05-12 2021-11-18 苏州阿尔脉生物科技有限公司 一种作为cdk9抑制剂的多环酰胺类衍生物、其制备方法及用途
TW202216207A (zh) * 2020-06-24 2022-05-01 英商阿斯特捷利康英國股份有限公司 抗體-藥物結合物及cdk9抑制劑之組合
JP7537002B2 (ja) 2020-08-07 2024-08-20 南京薬石科技股▲フン▼有限公司 Cdk9阻害剤およびその使用
TWI809330B (zh) * 2020-11-20 2023-07-21 大陸商勁方醫藥科技(上海)有限公司 Cdk9抑制劑的多晶型物及其製法和用途
WO2022247785A1 (zh) * 2021-05-24 2022-12-01 石药集团中奇制药技术(石家庄)有限公司 一种周期蛋白依赖性激酶9抑制剂的用途
WO2022247796A1 (zh) * 2021-05-24 2022-12-01 石药集团中奇制药技术(石家庄)有限公司 周期蛋白依赖性激酶9抑制剂的用途
CN117813289A (zh) * 2021-07-14 2024-04-02 上海海雁医药科技有限公司 吡唑衍生物及其中间体和制备方法
CN115703738B (zh) * 2021-08-16 2024-06-21 中国科学院上海药物研究所 含2-芳杂环取代的脲类化合物、其制备方法和用途
EP4452254A4 (en) * 2021-12-23 2025-12-31 The Katholieke Univ Leuven TETRAHYDROPYRAZOLOPYRIMIDINES AND ASSOCIATED ANALOGUES TO INHIBIT YAP/TAZ-TEAD
CN120051473A (zh) 2022-08-17 2025-05-27 韩国化学研究院 抑制或降解cdk2和/或cdk9的化合物及其医学用途
CN117659022A (zh) * 2022-09-06 2024-03-08 苏州阿尔脉生物科技有限公司 脲基取代吡啶类化合物、包含其的药物组合物及其医药用途
WO2024220876A1 (en) * 2023-04-19 2024-10-24 Alcon Inc. N-substituted c6 cyclyl carboxamide compounds and uses thereof
WO2025076115A1 (en) * 2023-10-02 2025-04-10 Prelude Therapeutics Incorporated Cdk inhibitors and their use as pharmaceuticals

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008133192A1 (ja) * 2007-04-19 2008-11-06 Takeda Pharmaceutical Company Limited 縮合イミダゾール化合物およびその用途
JP5566879B2 (ja) 2007-04-24 2014-08-06 インゲニウム ファーマシューティカルズ ジーエムビーエイチ プロテインキナーゼの阻害剤
JP5379787B2 (ja) 2007-04-24 2013-12-25 インゲニウム ファーマシューティカルズ ジーエムビーエイチ プロテインキナーゼの阻害剤
JP5693951B2 (ja) 2007-04-24 2015-04-01 アストラゼネカ エービー プロテインキナーゼの阻害剤
EP2137166B1 (en) 2007-04-24 2012-05-30 Ingenium Pharmaceuticals GmbH 4, 6-disubstituted aminopyrimidine derivatives as inhibitors of protein kinases
WO2008132138A1 (en) * 2007-04-25 2008-11-06 Ingenium Pharmaceuticals Gmbh Derivatives of 4,6-disubstituted aminopyrimidines
HRP20110470T1 (hr) 2007-10-12 2011-07-31 Ingenium Pharmaceuticals Gmbh Inhibitori proteinskih kinaza
BR112012008147A2 (pt) 2009-09-04 2016-03-01 Novartis Ag compostos heteroarílicos como inibidores da quinase
US20110113038A1 (en) 2009-11-12 2011-05-12 International Business Machines Corporation Search term security
GB201002911D0 (en) * 2010-02-19 2010-04-07 Medical Res Council Compound
NZ601924A (en) 2010-03-10 2014-10-31 Astrazeneca Ab 4-phenyl pyridine analogues as protein kinase inhibitors
AR081810A1 (es) * 2010-04-07 2012-10-24 Bayer Cropscience Ag Piridinilpirazoles biciclicos
WO2012066065A1 (en) 2010-11-17 2012-05-24 Novartis Ag Phenyl-heteroaryl amine compounds and their uses
WO2012101064A1 (en) * 2011-01-28 2012-08-02 Novartis Ag N-acyl pyrimidine biaryl compounds as protein kinase inhibitors
US20130303507A1 (en) * 2011-01-28 2013-11-14 Novartis Ag Substituted hetero-biaryl compounds and their uses
WO2012101063A1 (en) * 2011-01-28 2012-08-02 Novartis Ag N-acyl pyridine biaryl compounds and their uses
EP2763993B1 (en) * 2011-10-06 2017-04-19 Bayer Intellectual Property GmbH Heterocyclylpyri(mi)dinylpyrazole
MX2015012386A (es) 2013-03-13 2016-02-03 Abbvie Inc Inhibidores de la cinasa cdk9.
EP2970200A1 (en) * 2013-03-13 2016-01-20 Abbvie Inc. Pyridine cdk9 kinase inhibitors
WO2014139328A1 (en) 2013-03-14 2014-09-18 Abbvie Inc. Pyrrolo[2,3-b]pyridine cdk9 kinase inhibitors
BR112015023078A2 (pt) 2013-03-14 2017-07-18 Abbvie Inc inibidores de pirrolopirimindina cdk9 quinase

Also Published As

Publication number Publication date
CY1125066T1 (el) 2023-03-24
SMT201900298T1 (it) 2019-07-11
EP3539961B1 (en) 2021-10-06
MY201673A (en) 2024-03-12
ES2728356T3 (es) 2019-10-23
LT3313838T (lt) 2019-06-10
ES2902148T3 (es) 2022-03-25
CO2017013713A2 (es) 2018-03-28
TWI723028B (zh) 2021-04-01
HUE043440T2 (hu) 2019-08-28
US20160376287A1 (en) 2016-12-29
SI3539961T1 (sl) 2022-02-28
PH12017502334A1 (en) 2018-06-25
DOP2017000295A (es) 2017-12-31
PL3313838T3 (pl) 2019-08-30
TN2017000486A1 (en) 2019-04-12
TW201718573A (zh) 2017-06-01
WO2017001354A1 (en) 2017-01-05
EA035383B1 (ru) 2020-06-04
EP3313838A1 (en) 2018-05-02
IL256393B (en) 2021-12-01
SMT202200005T1 (it) 2022-03-21
PT3313838T (pt) 2019-06-24
CY1122111T1 (el) 2020-11-25
KR102663113B1 (ko) 2024-05-02
MX2017016244A (es) 2018-04-20
KR20180021830A (ko) 2018-03-05
DK3313838T3 (da) 2019-06-11
DK3539961T3 (da) 2022-01-03
US10717746B2 (en) 2020-07-21
US20180093998A1 (en) 2018-04-05
US9845331B2 (en) 2017-12-19
CR20170596A (es) 2018-07-04
PL3539961T3 (pl) 2022-02-14
JP2018522869A (ja) 2018-08-16
US20210171541A1 (en) 2021-06-10
EP3313838B1 (en) 2019-04-03
US11352369B2 (en) 2022-06-07
AU2016286200A1 (en) 2018-02-08
BR122019013677B1 (pt) 2024-01-02
US20220340592A1 (en) 2022-10-27
SV2017005598A (es) 2018-02-23
HRP20190748T1 (hr) 2019-06-14
CN107873028A (zh) 2018-04-03
EA201890094A1 (ru) 2018-07-31
TR201909286T4 (tr) 2019-07-22
RS58712B1 (sr) 2019-06-28
AR105179A1 (es) 2017-09-13
HUE057343T2 (hu) 2022-05-28
JP6997627B2 (ja) 2022-01-17
BR112017027394A2 (pt) 2018-11-06
ME03404B (me) 2020-01-20
CN107873028B (zh) 2021-02-02
AU2016286200B2 (en) 2018-10-04
NI201700174A (es) 2018-10-19
MX371034B (es) 2020-01-13
CA2989499C (en) 2023-10-31
RS62781B1 (sr) 2022-01-31
HRP20211970T1 (hr) 2022-03-18
DOP2018000207A (es) 2018-10-15
PH12017502334B1 (en) 2023-05-26
ZA201800563B (en) 2022-08-31
IL256393A (en) 2018-02-28
LT3539961T (lt) 2021-12-27
SI3313838T1 (sl) 2019-06-28
EP3539961A1 (en) 2019-09-18
CL2017003306A1 (es) 2018-06-29
PT3539961T (pt) 2021-12-20
CA2989499A1 (en) 2017-01-05
CR20210297A (es) 2021-09-29

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