MX2020011294A - Derivados de 2-amino-piridina o 2-amino-pirimidina como inhibidores de cinasa dependientes de ciclina. - Google Patents

Derivados de 2-amino-piridina o 2-amino-pirimidina como inhibidores de cinasa dependientes de ciclina.

Info

Publication number
MX2020011294A
MX2020011294A MX2020011294A MX2020011294A MX2020011294A MX 2020011294 A MX2020011294 A MX 2020011294A MX 2020011294 A MX2020011294 A MX 2020011294A MX 2020011294 A MX2020011294 A MX 2020011294A MX 2020011294 A MX2020011294 A MX 2020011294A
Authority
MX
Mexico
Prior art keywords
amino
pyridine
kinase inhibitors
dependent kinase
pyrimidine derivatives
Prior art date
Application number
MX2020011294A
Other languages
English (en)
Inventor
Sajiv Krishnan Nair
Sujin Cho-Schultz
Robert Steven Kania
Ping Chen
Sacha Ninkovic
Mehran Jalaie
Cynthia Louise Palmer
Judith Gail Deal
Gary Michael Gallego
Suvi Tuula Marjukka Orr
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 MX2020011294A publication Critical patent/MX2020011294A/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
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53831,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • 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
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • 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
    • 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

Abstract

Esta invención se relaciona con compuestos de la Fórmula (I) (ver Fórmula), o una sal farmacéuticamente aceptable del mismo, en la cual los grupos-R R1 a R23, A, Q, U, V, W, X, Y, Z, n, p y q son como se definen en la presente, con composiciones farmacéuticas que comprenden tales compuestos y sales, y con métodos para utilizar tales compuestos, sales y composiciones para el tratamiento de crecimiento celular anormal, que incluye cáncer, en un sujeto.
MX2020011294A 2018-04-26 2019-04-22 Derivados de 2-amino-piridina o 2-amino-pirimidina como inhibidores de cinasa dependientes de ciclina. MX2020011294A (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201862663096P 2018-04-26 2018-04-26
US201862750454P 2018-10-25 2018-10-25
US201962826609P 2019-03-29 2019-03-29
PCT/IB2019/053314 WO2019207463A1 (en) 2018-04-26 2019-04-22 2-amino-pyridine or 2-amino-pyrimidine derivatives as cyclin dependent kinase inhibitors

Publications (1)

Publication Number Publication Date
MX2020011294A true MX2020011294A (es) 2020-11-18

Family

ID=66676856

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2020011294A MX2020011294A (es) 2018-04-26 2019-04-22 Derivados de 2-amino-piridina o 2-amino-pirimidina como inhibidores de cinasa dependientes de ciclina.

Country Status (27)

Country Link
US (3) US10766884B2 (es)
EP (1) EP3784664A1 (es)
JP (2) JP7089061B2 (es)
KR (1) KR102596598B1 (es)
AU (1) AU2019259653B2 (es)
BR (1) BR112020021689B1 (es)
CA (1) CA3098283C (es)
CL (1) CL2020002748A1 (es)
CO (1) CO2020013149A2 (es)
CR (1) CR20200503A (es)
CU (1) CU20200070A7 (es)
DO (1) DOP2020000191A (es)
EC (1) ECSP20067394A (es)
GE (1) GEP20227433B (es)
IL (1) IL278075B2 (es)
MA (1) MA52360A (es)
MX (1) MX2020011294A (es)
NI (1) NI202000072A (es)
PE (1) PE20201202A1 (es)
PH (1) PH12020551692A1 (es)
RU (1) RU2762557C1 (es)
SG (1) SG11202009992VA (es)
TW (1) TWI740135B (es)
UA (1) UA126177C2 (es)
UY (1) UY38196A (es)
WO (1) WO2019207463A1 (es)
ZA (1) ZA202006944B (es)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4119558A1 (en) 2016-09-09 2023-01-18 Incyte Corporation Pyrazolopyridine compounds and uses thereof
TW201811799A (zh) 2016-09-09 2018-04-01 美商英塞特公司 吡唑并嘧啶化合物及其用途
WO2018049214A1 (en) 2016-09-09 2018-03-15 Incyte Corporation Pyrazolopyridine derivatives as hpk1 modulators and uses thereof for the treatment of cancer
LT3755703T (lt) 2018-02-20 2022-10-10 Incyte Corporation N-(fenil)-2-(fenil)pirimidin-4-karboksamido dariniai ir susiję junginiai, kaip hpk1 inhibitoriai, skirti vėžio gydymui
WO2019164847A1 (en) 2018-02-20 2019-08-29 Incyte Corporation Indazole compounds and uses thereof
UA126177C2 (uk) 2018-04-26 2022-08-25 Пфайзер Інк. Похідні 2-амінопіридину або 2-амінопіримідину як інгібітори циклінзалежної кінази
US10899755B2 (en) 2018-08-08 2021-01-26 Incyte Corporation Benzothiazole compounds and uses thereof
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
WO2020168197A1 (en) 2019-02-15 2020-08-20 Incyte Corporation Pyrrolo[2,3-d]pyrimidinone compounds as cdk2 inhibitors
WO2020180959A1 (en) 2019-03-05 2020-09-10 Incyte Corporation Pyrazolyl pyrimidinylamine compounds as cdk2 inhibitors
US11919904B2 (en) 2019-03-29 2024-03-05 Incyte Corporation Sulfonylamide compounds as CDK2 inhibitors
US11447494B2 (en) 2019-05-01 2022-09-20 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
WO2020223469A1 (en) 2019-05-01 2020-11-05 Incyte Corporation N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer
JP2022543155A (ja) 2019-08-06 2022-10-07 インサイト・コーポレイション Hpk1阻害剤の固体形態
CN116348458A (zh) 2019-08-14 2023-06-27 因赛特公司 作为cdk2抑制剂的咪唑基嘧啶基胺化合物
US11038699B2 (en) 2019-08-29 2021-06-15 Advanced New Technologies Co., Ltd. Method and apparatus for performing multi-party secure computing based-on issuing certificate
US11851426B2 (en) 2019-10-11 2023-12-26 Incyte Corporation Bicyclic amines as CDK2 inhibitors
BR112023000687A2 (pt) 2020-07-15 2023-02-07 Pfizer Métodos e combinações de inibidores de kat6 para o tratamento de câncer
CA3188821A1 (en) 2020-08-13 2022-02-17 Lars ANDERS Combination therapy
CN112028834B (zh) * 2020-09-11 2022-03-29 济南悟通生物科技有限公司 一种阿贝西利的中间体的合成方法
JP7260606B2 (ja) * 2020-09-15 2023-04-18 ファイザー・インク 固体形態のcdk4阻害薬
CN112679522B (zh) * 2020-12-29 2023-02-14 南京正济医药研究有限公司 一种巴洛沙韦中间体的制备方法
WO2022149057A1 (en) * 2021-01-05 2022-07-14 Rhizen Pharmaceuticals Ag Cdk inhibitors
JP2024504452A (ja) 2021-02-03 2024-01-31 上海拓界生物医薬科技有限公司 縮合三環系サイクリン依存性キナーゼ阻害剤及びその調製方法並びに医薬用途
WO2023100070A1 (en) 2021-12-02 2023-06-08 Pfizer Inc. Cdk4 inhibitor for the treatment of cancer
WO2023100134A1 (en) 2021-12-02 2023-06-08 Pfizer Inc. Methods and dosing regimens comprising a cdk2 inhibitor and a cdk4 inhibitor for treating cancer
WO2024023703A1 (en) 2022-07-29 2024-02-01 Pfizer Inc. Dosing regimens comprising a kat6 inhibitor for the treatment of cancer
WO2024022487A1 (en) * 2022-07-29 2024-02-01 Allorion Therapeutics Inc Aminoheteroaryl kinase inhibitors

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
WO2000035298A1 (en) 1996-11-27 2000-06-22 Wm. Wrigley Jr. Company Chewing gum containing medicament active agents
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
IL148698A0 (en) 1999-09-17 2002-09-12 Cor Therapeutics Inc INHIBITORS OF FACTOR Xa
US6376515B2 (en) 2000-02-29 2002-04-23 Cor Therapeutics, Inc. Benzamides and related inhibitors of factor Xa
WO2002102783A1 (en) 2001-06-19 2002-12-27 Merck & Co., Inc. Tyrosine kinase inhibitors
GB0308466D0 (en) 2003-04-11 2003-05-21 Novartis Ag Organic compounds
GB0317127D0 (en) * 2003-07-22 2003-08-27 Astex Technology Ltd Pharmaceutical compounds
PL1651612T3 (pl) 2003-07-22 2012-09-28 Astex Therapeutics Ltd Związki 3,4-pochodne 1h-pirazolu i ich zastosowanie jako kinazy zależne od cyklin (cdk) i modulatory kinazy syntazy glikogenu-3 (gsk-3)
WO2006038001A1 (en) 2004-10-06 2006-04-13 Celltech R & D Limited Aminopyrimidine derivatives as jnk inhibitors
AU2007288245A1 (en) * 2006-08-24 2008-02-28 Novartis Ag 2- (pyrazin-2-yl) -thiazole and 2- (1h-pyrazol-3-yl) -thiazole derivatives as well as related compounds as stearoyl-CoA desaturase (SCD) inhibitors for the treatment of metabolic, cardiovascular and other disorders
BRPI0914682B8 (pt) 2008-06-27 2021-05-25 Avila Therapeutics Inc compostos de heteroarila e composições compreendendo os referidos compostos
US8338439B2 (en) 2008-06-27 2012-12-25 Celgene Avilomics Research, Inc. 2,4-disubstituted pyrimidines useful as kinase inhibitors
CA2745297A1 (en) 2008-12-19 2010-06-24 F. Hoffmann-La Roche Ag Pyrimidin-2-ylamino derivatives and their use to treat inflammation
JO2885B1 (en) 2008-12-22 2015-03-15 ايلي ليلي اند كومباني Protein kinase inhibitors
JP5658756B2 (ja) 2009-09-10 2015-01-28 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Jakの阻害剤
EP2569302A1 (en) 2010-05-13 2013-03-20 Amgen, Inc Heteroaryloxyheterocyclyl compounds as pde10 inhibitors
US9464065B2 (en) 2011-03-24 2016-10-11 The Scripps Research Institute Compounds and methods for inducing chondrogenesis
JO3300B1 (ar) * 2012-06-06 2018-09-16 Novartis Ag مركبات وتركيبات لتعديل نشاط egfr
BR112015021549A2 (pt) 2013-03-13 2017-07-18 Abbvie Inc inibidores de piridina cinase cdk9
US10370371B2 (en) 2013-08-30 2019-08-06 Ptc Therapeutics, Inc. Substituted pyrimidine Bmi-1 inhibitors
WO2015058163A2 (en) 2013-10-18 2015-04-23 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
MX370906B (es) 2013-12-30 2020-01-09 Genentech Inc Inhibidores de serina/treonina cinasa.
CN106458990B (zh) 2014-04-04 2019-06-07 希洛斯医药品股份有限公司 细胞周期蛋白依赖性激酶7(cdk7)的抑制剂
US9878994B2 (en) 2014-07-24 2018-01-30 Beta Pharma Inc. 2-H-indazole derivatives as cyclin-dependent kinase (CDK) inhibitors and therapeutic uses thereof
CN105294655B (zh) 2014-07-26 2019-03-15 广东东阳光药业有限公司 Cdk类小分子抑制剂的化合物及其用途
CN107567443B (zh) 2014-12-24 2023-04-28 株式会社Lg化学 作为gpr120激动剂的联芳基衍生物
CN106188038A (zh) 2015-06-01 2016-12-07 中国科学院上海药物研究所 一类具有激酶抑制活性的化合物、制备方法和用途
AU2016283105C1 (en) 2015-06-26 2023-02-02 Dana-Farber Cancer Institute, Inc. 4,6-pyrimidinylene derivatives and uses thereof
CN105111191B (zh) * 2015-07-21 2018-06-08 上海皓元生物医药科技有限公司 一种用于合成cdk9抑制剂的关键中间体及其制备方法和用途
CN106928216A (zh) 2015-12-31 2017-07-07 中国科学院上海药物研究所 具有erk激酶抑制活性的化合物、其制备方法和用途
WO2017133701A1 (en) 2016-02-06 2017-08-10 Shanghai Fochon Pharmaceutical Co., Ltd. Certain protein kinase inhibitors
CN110036004A (zh) * 2016-07-13 2019-07-19 希洛斯医药品股份有限公司 细胞周期蛋白依赖性激酶7(cdk7)的抑制剂
WO2018161033A1 (en) 2017-03-02 2018-09-07 Wright, Adrian Small molecule ire1-alpha inhibitors
CN109843872B (zh) 2017-09-20 2022-08-30 杭州英创医药科技有限公司 作为ido抑制剂和/或ido-hdac双重抑制剂的多环化合物
UA126177C2 (uk) 2018-04-26 2022-08-25 Пфайзер Інк. Похідні 2-амінопіридину або 2-амінопіримідину як інгібітори циклінзалежної кінази

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Publication number Publication date
RU2021136543A (ru) 2021-12-16
SG11202009992VA (en) 2020-11-27
CA3098283A1 (en) 2019-10-31
CA3098283C (en) 2023-05-23
GEP20227433B (en) 2022-10-25
MA52360A (fr) 2021-03-03
ZA202006944B (en) 2023-07-26
AU2019259653B2 (en) 2023-01-19
PE20201202A1 (es) 2020-11-11
RU2762557C1 (ru) 2021-12-21
NI202000072A (es) 2021-03-23
DOP2020000191A (es) 2021-02-28
CO2020013149A2 (es) 2020-11-10
JP2021522275A (ja) 2021-08-30
KR102596598B1 (ko) 2023-11-03
US10766884B2 (en) 2020-09-08
TWI740135B (zh) 2021-09-21
US11220494B2 (en) 2022-01-11
BR112020021689A2 (pt) 2021-01-26
JP7089061B2 (ja) 2022-06-21
UY38196A (es) 2019-11-29
UA126177C2 (uk) 2022-08-25
ECSP20067394A (es) 2020-12-31
KR20210002642A (ko) 2021-01-08
IL278075A (en) 2020-11-30
KR20230152182A (ko) 2023-11-02
BR112020021689B1 (pt) 2023-02-28
WO2019207463A1 (en) 2019-10-31
IL278075B2 (en) 2023-05-01
EP3784664A1 (en) 2021-03-03
IL278075B1 (en) 2023-01-01
CR20200503A (es) 2020-12-17
CN112313219A (zh) 2021-02-02
CU20200070A7 (es) 2021-05-12
CL2020002748A1 (es) 2021-02-12
PH12020551692A1 (en) 2021-07-19
JP2022120096A (ja) 2022-08-17
US20220089580A1 (en) 2022-03-24
AU2019259653A1 (en) 2020-10-29
TW202000661A (zh) 2020-01-01
US20190330196A1 (en) 2019-10-31
US20200354350A1 (en) 2020-11-12

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