PE20190475A1 - Inhibidores de cdk2/4/6 - Google Patents

Inhibidores de cdk2/4/6

Info

Publication number
PE20190475A1
PE20190475A1 PE2019000359A PE2019000359A PE20190475A1 PE 20190475 A1 PE20190475 A1 PE 20190475A1 PE 2019000359 A PE2019000359 A PE 2019000359A PE 2019000359 A PE2019000359 A PE 2019000359A PE 20190475 A1 PE20190475 A1 PE 20190475A1
Authority
PE
Peru
Prior art keywords
alkyl
fluoroalkyl
cdk2
compounds
pyrimidin
Prior art date
Application number
PE2019000359A
Other languages
English (en)
Inventor
Douglas Carl Behenna
Ping Chen
Kevin Daniel Freeman-Cook
Robert Louis Hoffman
Mehran Jalaie
Asako Nagata
Sajiv Krishnan Nair
Sacha Ninkovic
Martha Alicia Ornelas
Cynthia Louise Palmer
Eugene Yuanjin Rui
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of PE20190475A1 publication Critical patent/PE20190475A1/es

Links

Classifications

    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Se refiere a compuestos de las formulas (I) o una sal farmaceuticamente aceptable del mismo, en donde: R1 es heterociclilo de 3 a 10 miembros sustituido; R2 es independientemente F, OH, alquilo de C1-C4, entre otros; R3 es H, F, Cl, NH2, alquilo de C1-C4 o fluoroalquilo de C1-C4, en donde el alquilo de C1-C4 y fluoroalquilo de C1-C4 se sustituyen opcionalemente por OH; CN, alcoxi de C1-C4, entre otros; R4 es H, alquilo de C1-C2 o fluoroalquilo de C1-C2; R2A y R2B son independientemente H, OH o alquilo de C1-C4; p es 0,1, 2, 3 o 4; q es 0,1, 2 o 3; r es 0, 1 o 2. Son compuestos preferidos 8-ciclopentil-2-{[1-(metilsulfonil) piperidin-4-il] amino}pirido[2,3-d]pirimidin-7(8H)-ona; 4-({6-(2-hidroxietil)-8-[(1R,2S)-2-metilciclopentil]-7-oxo-7,8-dihidropirido[2,3-d]pirimidin-2-il}amino)-N-metilpiperidin-1-sulfonamida. Dichos compuestos pueden inhibir la actividad de CDK2, incluyendo CDK2, CDK4 y/o CDK6. Tambien se refiere a una composicion farmaceutica que es util para el tratamiento de crecimiento celular anormal, en particular el cancer de mama y ovario.
PE2019000359A 2016-08-15 2017-07-31 Inhibidores de cdk2/4/6 PE20190475A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662371602P 2016-08-15 2016-08-15
US201762533347P 2017-07-17 2017-07-17

Publications (1)

Publication Number Publication Date
PE20190475A1 true PE20190475A1 (es) 2019-04-04

Family

ID=59631834

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2019000359A PE20190475A1 (es) 2016-08-15 2017-07-31 Inhibidores de cdk2/4/6

Country Status (41)

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US (4) US10233188B2 (es)
EP (1) EP3497103B1 (es)
JP (1) JP6563623B1 (es)
KR (1) KR102236605B1 (es)
CN (2) CN109803968A (es)
AU (1) AU2017311645B2 (es)
BR (1) BR112019002610A2 (es)
CA (1) CA2975033C (es)
CL (1) CL2019000368A1 (es)
CO (1) CO2019001240A2 (es)
CR (1) CR20190062A (es)
CU (1) CU24522B1 (es)
CY (1) CY1124206T1 (es)
DK (1) DK3497103T3 (es)
DO (1) DOP2019000030A (es)
EC (1) ECSP19011216A (es)
ES (1) ES2876411T3 (es)
GE (1) GEP20217234B (es)
HR (1) HRP20210871T1 (es)
HU (1) HUE055978T2 (es)
IL (1) IL264687B (es)
LT (1) LT3497103T (es)
MA (1) MA45920B1 (es)
MD (1) MD3497103T2 (es)
MX (1) MX2019001849A (es)
NI (1) NI201900013A (es)
PE (1) PE20190475A1 (es)
PH (1) PH12019500329A1 (es)
PL (1) PL3497103T3 (es)
PT (1) PT3497103T (es)
RS (1) RS61934B1 (es)
RU (1) RU2726115C1 (es)
SG (1) SG11201900799XA (es)
SI (1) SI3497103T1 (es)
SV (1) SV2019005836A (es)
TN (1) TN2019000039A1 (es)
TW (1) TWI663169B (es)
UA (1) UA124804C2 (es)
UY (1) UY37352A (es)
WO (1) WO2018033815A1 (es)
ZA (1) ZA201900716B (es)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CR20190062A (es) * 2016-08-15 2019-05-22 Pfizer Inhibidores de cdk2/4/6
JP6952747B2 (ja) * 2018-09-18 2021-10-20 ファイザー・インク がん処置のためのTGFβ阻害剤およびCDK阻害剤の組合せ
JP2020097562A (ja) * 2018-09-25 2020-06-25 ファイザー・インク ピリド[2,3−d]ピリミジン−7(8h)−オンの合成
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
JPWO2020130125A1 (ja) 2018-12-21 2021-11-04 第一三共株式会社 抗体−薬物コンジュゲートとキナーゼ阻害剤の組み合わせ
EP3911650A1 (en) 2019-01-17 2021-11-24 Pfizer Inc. Crystalline form of a cdk inhibitor
MX2021009682A (es) * 2019-02-15 2021-11-12 Incyte Corp Biomarcadores de cinasa 2 dependientes de ciclinas y sus usos.
US11384083B2 (en) 2019-02-15 2022-07-12 Incyte Corporation Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors
WO2020180959A1 (en) 2019-03-05 2020-09-10 Incyte Corporation Pyrazolyl pyrimidinylamine compounds as cdk2 inhibitors
WO2020205560A1 (en) 2019-03-29 2020-10-08 Incyte Corporation Sulfonylamide compounds as cdk2 inhibitors
KR20220003565A (ko) * 2019-04-19 2022-01-10 화이자 인코포레이티드 Pah를 치료하기 위한 항증식제
US11440914B2 (en) 2019-05-01 2022-09-13 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
WO2020223558A1 (en) 2019-05-01 2020-11-05 Incyte Corporation Tricyclic amine compounds as cdk2 inhibitors
EP3976090A1 (en) 2019-05-24 2022-04-06 Pfizer Inc. Combination therapies using cdk inhibitors
WO2020240360A1 (en) 2019-05-24 2020-12-03 Pfizer Inc. Combination therapies using cdk inhibitors
WO2021014360A1 (en) 2019-07-23 2021-01-28 Pfizer Inc. Oral modified release dosage forms
KR20220064369A (ko) 2019-08-14 2022-05-18 인사이트 코포레이션 Cdk2 저해제로서의 이미다졸릴 피리디미딘일아민 화합물
WO2021072232A1 (en) * 2019-10-11 2021-04-15 Incyte Corporation Bicyclic amines as cdk2 inhibitors
JP2023501110A (ja) * 2019-10-17 2023-01-18 シーセン ファーマシューティカル カンパニー リミテッド Cdk2/4/6三重阻害剤としてのアミノピリミジン化合物
IL293926A (en) 2019-12-17 2022-08-01 Pfizer Antibodies unique to d47, pd-l1 and their uses
CN115551856A (zh) * 2020-02-28 2022-12-30 重庆复尚源创医药技术有限公司 作为cdk2/4/6抑制剂的化合物
TW202146017A (zh) 2020-03-05 2021-12-16 美商輝瑞股份有限公司 間變性淋巴瘤激酶抑制劑及周期蛋白依賴型激酶抑制劑之組合
JP2021167301A (ja) 2020-04-08 2021-10-21 ファイザー・インク Cdk2阻害剤に対する腫瘍適応を抑制するためのcdk4/6およびcdk2阻害剤による同時処置
CN113773315A (zh) * 2020-06-10 2021-12-10 无锡佰翱得生物科学有限公司 细胞周期蛋白依赖性激酶2(cdk2)高选择性氘代抑制剂
CN115702155A (zh) * 2020-06-17 2023-02-14 微境生物医药科技(上海)有限公司 新型吡啶并[2,3-d]嘧啶-7(8H)-酮衍生物
WO2022015670A1 (en) * 2020-07-14 2022-01-20 Nikang Therapeutics, Inc. Pyrido[2,3-d]pyrimidin-7(8h)-one derivatives as cyclin-dependent kinase 2 inhibitors
WO2022018667A1 (en) 2020-07-24 2022-01-27 Pfizer Inc. Combination therapies using cdk2 and cdc25a inhibitors
US20230357211A1 (en) 2020-09-15 2023-11-09 Pfizer Inc. Solid forms of a cdk4 inhibitor
AR124154A1 (es) 2020-11-27 2023-02-22 Rhizen Pharmaceuticals Ag Inhibidores de cdk
IL303661A (en) * 2020-12-22 2023-08-01 Nikang Therapeutics Inc COMPOUNDS FOR BREAKING CYCLIN-DEPENDENT KINASE 2 THROUGH THE UBIQUITIN PROTEOSOME PATHWAY
WO2022149057A1 (en) 2021-01-05 2022-07-14 Rhizen Pharmaceuticals Ag Cdk inhibitors
WO2022152259A1 (zh) * 2021-01-15 2022-07-21 江苏先声药业有限公司 Cdk2/4/6抑制剂及其制备方法和应用
TWI823420B (zh) * 2021-06-09 2023-11-21 大陸商鄭州同源康醫藥有限公司 用作cdk激酶抑制劑的化合物及其應用
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
WO2023281413A1 (en) 2021-07-09 2023-01-12 Pfizer Inc. Methods and dosing regimens comprising pf-06873600 for the treatment of cancer
CN116390921A (zh) * 2021-09-29 2023-07-04 中国医药研究开发中心有限公司 具有细胞周期蛋白依赖性激酶抑制活性的杂环化合物及其制备方法和医药用途
CA3238551A1 (en) * 2021-11-18 2023-05-25 Steven FRUCHTMAN Methods and compositions for treating cancer
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors
WO2023111810A1 (en) 2021-12-14 2023-06-22 Pfizer Inc. Combination therapies and uses for treating cancer
WO2023141522A2 (en) * 2022-01-21 2023-07-27 Slap Pharmaceuticals Llc Multicyclic compounds
WO2023249968A1 (en) * 2022-06-22 2023-12-28 Nikang Therapeutics, Inc. Bifunctional compounds containing pyrido[2,3-djpyrimidin-7(8h)-one derivatives for degrading cyclin-dependent kinase 2 via ubiquitin proteasome pathway
US20240174665A1 (en) * 2022-08-19 2024-05-30 Kymera Therapeutics, Inc. Cdk2 inhibitors and uses thereof
WO2024084364A1 (en) 2022-10-18 2024-04-25 Pfizer Inc. Compounds for the treatment of cancer

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
GB9518953D0 (en) 1995-09-15 1995-11-15 Pfizer Ltd Pharmaceutical formulations
TW477787B (en) 1996-08-27 2002-03-01 Pfizer Pyrido six-membered nitrogen-containing cyclic ring derivatives having corticotropin releasing factor antagonist activity and pharmaceutical composition containing same
EP0946554A1 (en) 1996-11-27 1999-10-06 Pfizer Inc. Fused bicyclic pyrimidine derivatives
WO2000035296A1 (en) 1996-11-27 2000-06-22 Wm. Wrigley Jr. Company Improved release of medicament active agents from a chewing gum coating
AU749750B2 (en) 1997-02-05 2002-07-04 Warner-Lambert Company Pyrido {2,3-d} pyrimidines and 4-aminopyrimidines as inhibitors of cellular proliferation
US6498163B1 (en) * 1997-02-05 2002-12-24 Warner-Lambert Company Pyrido[2,3-D]pyrimidines and 4-aminopyrimidines as inhibitors of cellular proliferation
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
JP2003523358A (ja) * 2000-01-27 2003-08-05 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー 神経変性疾患の治療のためのピリドピリミジノン誘導体
AP2002002643A0 (en) 2000-03-06 2002-12-31 Warner Lambert Co 5-alkylpyrido[2,3-d]pyrimidines tyrosine kinase inhibitors
DK1361880T3 (da) 2001-02-12 2006-01-23 Hoffmann La Roche 6-substituerede pyrido-pyrimidiner
KR20060111716A (ko) * 2002-01-22 2006-10-27 워너-램버트 캄파니 엘엘씨 2-(피리딘-2-일아미노)-피리도[2,3-d]피리미딘-7-온
US7196090B2 (en) * 2002-07-25 2007-03-27 Warner-Lambert Company Kinase inhibitors
US6951769B2 (en) 2003-06-04 2005-10-04 Texas Instruments Incorporated Method for stripping sacrificial layer in MEMS assembly
EP1648889B1 (en) 2003-07-11 2008-10-29 Warner-Lambert Company LLC Isethionate salt of a selective cdk4 inhibitor
CA2555724A1 (en) 2004-02-18 2005-09-09 Warner-Lambert Company Llc 2-(pyridin-3-ylamino)-pyrido[2,3-d]pyrimidin-7-ones
US20060142312A1 (en) * 2004-12-23 2006-06-29 Pfizer Inc C6-aryl and heteroaryl substituted pyrido[2,3-D] pyrimidin-7-ones
CN102746298A (zh) * 2005-10-07 2012-10-24 埃克塞里艾克西斯公司 PI3Kα的吡啶并嘧啶酮抑制剂
US8044062B2 (en) * 2005-10-07 2011-10-25 Exelixis, Inc. Substituted pyrido[2,3-d]pyrimidin-7(8H)-one inhibitors of phospatidylinositol 3-kinase alpha
RU2009108006A (ru) 2006-09-08 2010-10-20 Пфайзер Продактс Инк. (Us) Синтез 2-(пиридин-2-иламино)-пиридо[2, 3-d]пиримидин-7-онов
KR101099926B1 (ko) * 2006-09-15 2011-12-28 화이자 프로덕츠 인코포레이티드 피리도 (2,3-d) 피리미디논 화합물 및 이의 pi3 억제제로서의 용도
EP1914234A1 (en) * 2006-10-16 2008-04-23 GPC Biotech Inc. Pyrido[2,3-d]pyrimidines and their use as kinase inhibitors
WO2008124161A1 (en) * 2007-04-10 2008-10-16 Exelixis, Inc. Methods of treating cancer using pyridopyrimidinone inhibitors of pi3k alpha
CN102015704A (zh) * 2008-04-29 2011-04-13 霍夫曼-拉罗奇有限公司 Jnk的嘧啶基吡啶酮抑制剂
WO2010022081A1 (en) 2008-08-19 2010-02-25 Array Biopharma Inc. Triazolopyridine compounds as pim kinase inhibitors
CN102177161A (zh) 2008-10-22 2011-09-07 霍夫曼-拉罗奇有限公司 Jnk的嘧啶基吡啶酮抑制剂
JP2014513079A (ja) * 2011-04-08 2014-05-29 アフラクシス・ホールディングス・インコーポレイテッド 神経系疾患及び癌の治療のための8−エチル−6−(アリール)ピリド[2,3−d]ピリミジン−7(8h)−オン
KR20140040726A (ko) * 2011-04-29 2014-04-03 엑셀리시스, 인코포레이티드 PI3K/mTOR의 피리도피리미디논 억제제를 사용하는 림프종을 치료하는 방법
TW201306842A (zh) * 2011-06-15 2013-02-16 Exelixis Inc 使用pi3k/mtor吡啶並嘧啶酮抑制劑及苯達莫司汀及/或利妥昔單抗治療惡性血液疾病之組合療法
AR088082A1 (es) 2011-10-13 2014-05-07 Lilly Co Eli Moduladores selectivos del receptor androgeno
JP2015511245A (ja) * 2012-02-23 2015-04-16 アッヴィ・インコーポレイテッド ピリドピリミジノン系キナーゼ阻害薬
DK2958916T3 (en) 2013-02-21 2018-11-12 Pfizer Solid forms of a selective CDK4 / 6 inhibitor
US9321786B2 (en) 2013-03-15 2016-04-26 Celgene Avilomics Research, Inc. Heteroaryl compounds and uses thereof
US20160304466A1 (en) * 2013-12-04 2016-10-20 The Scripps Research Institute Novel compounds as jnk kinase inhibitors
US9760610B2 (en) 2014-07-31 2017-09-12 Linkedin Corporation Personalized search using searcher features
CZ201589A3 (cs) * 2015-02-11 2016-08-24 Zentiva, K.S. Pevné formy soli Palbociclibu
CR20190062A (es) * 2016-08-15 2019-05-22 Pfizer Inhibidores de cdk2/4/6

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AU2017311645B2 (en) 2021-05-27
TWI663169B (zh) 2019-06-21
US20180044344A1 (en) 2018-02-15
CA2975033C (en) 2023-01-24
DOP2019000030A (es) 2019-06-30
TN2019000039A1 (en) 2020-07-15
RS61934B1 (sr) 2021-07-30
TW201819383A (zh) 2018-06-01
RU2726115C1 (ru) 2020-07-09
US10233188B2 (en) 2019-03-19
AU2017311645A1 (en) 2019-02-28
CO2019001240A2 (es) 2019-02-19
HUE055978T2 (hu) 2022-01-28
ES2876411T3 (es) 2021-11-12
KR102236605B1 (ko) 2021-04-05
MD3497103T2 (ro) 2021-08-31
MA45920A (fr) 2019-06-19
CN114394966A (zh) 2022-04-26
CL2019000368A1 (es) 2019-05-10
JP2019527722A (ja) 2019-10-03
NI201900013A (es) 2019-04-08
UA124804C2 (uk) 2021-11-24
EP3497103B1 (en) 2021-05-05
US10800783B2 (en) 2020-10-13
LT3497103T (lt) 2021-07-26
CY1124206T1 (el) 2022-05-27
US20190135817A1 (en) 2019-05-09
IL264687B (en) 2021-04-29
BR112019002610A2 (pt) 2019-07-02
CU24522B1 (es) 2021-06-08
SV2019005836A (es) 2019-03-19
JP6563623B1 (ja) 2019-08-21
US20200392142A1 (en) 2020-12-17
PL3497103T3 (pl) 2021-10-25
HRP20210871T1 (hr) 2021-07-09
KR20190038915A (ko) 2019-04-09
CU20190010A7 (es) 2019-10-04
PH12019500329A1 (en) 2019-10-28
GEP20217234B (en) 2021-03-25
DK3497103T3 (da) 2021-06-14
CN109803968A (zh) 2019-05-24
MX2019001849A (es) 2019-05-09
SI3497103T1 (sl) 2021-07-30
CR20190062A (es) 2019-05-22
CA2975033A1 (en) 2018-02-15
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SG11201900799XA (en) 2019-02-27
US20220324872A1 (en) 2022-10-13
UY37352A (es) 2018-03-23
US11396512B2 (en) 2022-07-26
WO2018033815A1 (en) 2018-02-22
ECSP19011216A (es) 2019-03-29
ZA201900716B (en) 2022-03-30
EP3497103A1 (en) 2019-06-19
MA45920B1 (fr) 2021-08-31

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