CR20200503A - Inhibidores de cinasa dependientes de ciclina - Google Patents

Inhibidores de cinasa dependientes de ciclina

Info

Publication number
CR20200503A
CR20200503A CR20200503A CR20200503A CR20200503A CR 20200503 A CR20200503 A CR 20200503A CR 20200503 A CR20200503 A CR 20200503A CR 20200503 A CR20200503 A CR 20200503A CR 20200503 A CR20200503 A CR 20200503A
Authority
CR
Costa Rica
Prior art keywords
amino
pyridine
kinase inhibitors
dependent kinase
pyrimidine derivatives
Prior art date
Application number
CR20200503A
Other languages
English (en)
Inventor
Robert Steven Kania
Sacha Ninkovic
Sujin Cho-Schultz
Gary Michael Gallego
Mehran Jalaie
Cynthia Louise Palmer
Sajiv Krishnan Nair
Judith Gail Deal
Suvi Tuula Marjukka Orr
Ping Chen
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 CR20200503A publication Critical patent/CR20200503A/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
    • 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
    • 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
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Peptides Or Proteins (AREA)

Abstract

<p>Esta invención se relaciona con compuestos de la Fórmula (I) o una sal farmacéuticamente aceptable del mismo, en 10 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 15 cáncer, en un sujeto.</p>
CR20200503A 2018-04-26 2019-04-22 Inhibidores de cinasa dependientes de ciclina CR20200503A (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
CR20200503A true CR20200503A (es) 2020-12-17

Family

ID=66676856

Family Applications (1)

Application Number Title Priority Date Filing Date
CR20200503A CR20200503A (es) 2018-04-26 2019-04-22 Inhibidores de cinasa dependientes de ciclina

Country Status (28)

Country Link
US (3) US10766884B2 (es)
EP (1) EP3784664A1 (es)
JP (2) JP7089061B2 (es)
KR (2) KR102661053B1 (es)
CN (1) CN112313219B (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 (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180072741A1 (en) 2016-09-09 2018-03-15 Incyte Corporation Pyrazolopyrimidine compounds and uses thereof
WO2018049214A1 (en) 2016-09-09 2018-03-15 Incyte Corporation Pyrazolopyridine derivatives as hpk1 modulators and uses thereof for the treatment of cancer
CN115819417A (zh) 2016-09-09 2023-03-21 因赛特公司 作为hpk1调节剂的吡唑并吡啶衍生物及其用于治疗癌症的用途
WO2019164847A1 (en) 2018-02-20 2019-08-29 Incyte Corporation Indazole compounds and uses thereof
PL3755703T3 (pl) 2018-02-20 2022-11-07 Incyte Corporation Pochodne n-(fenylo)-2-(fenylo)pirymidyno-4-karboksyamidu i związki pokrewne jako inhibitory hpk1 do leczenia nowotworu
MX2020011294A (es) 2018-04-26 2020-11-18 Pfizer Derivados de 2-amino-piridina o 2-amino-pirimidina como inhibidores de cinasa dependientes de ciclina.
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
TW202100520A (zh) 2019-03-05 2021-01-01 美商英塞特公司 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物
US11919904B2 (en) 2019-03-29 2024-03-05 Incyte Corporation Sulfonylamide compounds as CDK2 inhibitors
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
AU2020326703A1 (en) 2019-08-06 2022-02-17 Incyte Corporation Solid forms of an HPK1 inhibitor
KR20220064369A (ko) 2019-08-14 2022-05-18 인사이트 코포레이션 Cdk2 저해제로서의 이미다졸릴 피리디미딘일아민 화합물
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
BR112022006977A2 (pt) 2019-10-11 2022-09-20 Incyte Corp Aminas bicíclicas como inibidores de cdk2
IL299871A (en) 2020-07-15 2023-03-01 Pfizer Methods and combinations of KAT6 inhibitors for the treatment of cancer
KR20230057384A (ko) 2020-08-13 2023-04-28 화이자 인코포레이티드 조합 요법
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
MX2023003054A (es) * 2020-09-15 2023-04-05 Pfizer Formas solidas de un inhibidor de cdk4.
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
KR20230142735A (ko) 2021-02-03 2023-10-11 투오지에 바이오텍 (상하이) 컴퍼니 리미티드 융합된 삼환식 사이클린-의존적 키나제 저해제, 및이의 제조 방법 및 이의 약학적 용도
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
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
AU2022400308A1 (en) 2021-12-02 2024-05-16 Pfizer Inc. Cdk4 inhibitor for the treatment of cancer
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors
WO2023116862A1 (zh) * 2021-12-24 2023-06-29 江苏恒瑞医药股份有限公司 氢化吲哚类化合物、其制备方法及其在医药上的应用
WO2024022487A1 (en) * 2022-07-29 2024-02-01 Allorion Therapeutics Inc Aminoheteroaryl kinase inhibitors
WO2024023703A1 (en) 2022-07-29 2024-02-01 Pfizer Inc. Dosing regimens comprising a kat6 inhibitor for the treatment of cancer
TW202406912A (zh) * 2022-08-01 2024-02-16 大陸商江蘇恒瑞醫藥股份有限公司 稠三環類衍生物的晶型及製備方法
CN117645604A (zh) * 2022-09-05 2024-03-05 浙江同源康医药股份有限公司 用作cdk4激酶抑制剂的化合物及其应用
WO2024066986A1 (zh) * 2022-09-30 2024-04-04 楚浦创制(武汉)医药科技有限公司 2-氨基嘧啶类化合物及其应用、药用组合物

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
WO2000035296A1 (en) 1996-11-27 2000-06-22 Wm. Wrigley Jr. Company Improved release of medicament active agents from a chewing gum coating
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
CN1390206A (zh) 1999-09-17 2003-01-08 千嬉药品公司 因子Xa的抑制剂
EP1259485B1 (en) 2000-02-29 2005-11-30 Millennium Pharmaceuticals, Inc. BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa
US20040171630A1 (en) 2001-06-19 2004-09-02 Yuntae Kim 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
WO2005012256A1 (en) 2003-07-22 2005-02-10 Astex Therapeutics Limited 3, 4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases (cdk) and glycogen synthase kinase-3 (gsk-3) modulators
WO2006038001A1 (en) 2004-10-06 2006-04-13 Celltech R & D Limited Aminopyrimidine derivatives as jnk inhibitors
EP2086970B1 (en) * 2006-08-24 2014-02-26 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
KR101892989B1 (ko) 2008-06-27 2018-08-30 셀젠 카르 엘엘씨 헤테로아릴 화합물 및 이의 용도
US8338439B2 (en) 2008-06-27 2012-12-25 Celgene Avilomics Research, Inc. 2,4-disubstituted pyrimidines useful as kinase inhibitors
EP2379527A1 (en) 2008-12-19 2011-10-26 F. Hoffmann-La Roche AG Pyrimidin- 2 -ylamino derivatives and their use to treat inflammation
PA8852901A1 (es) 2008-12-22 2010-07-27 Lilly Co Eli Inhibidores de proteina cinasa
BR112012005382A2 (pt) 2009-09-10 2016-03-29 Hoffmann La Roche inibidores de jak
CA2798325A1 (en) 2010-05-13 2011-11-17 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
US9650358B2 (en) * 2013-03-13 2017-05-16 Abbvie Inc. Pyridine CDK9 kinase inhibitors
TWI692477B (zh) 2013-08-30 2020-05-01 美商Ptc治療公司 經取代嘧啶bmi-1抑制劑
AU2014337067B2 (en) 2013-10-18 2019-01-24 Syros Pharmaceuticals, Inc. Heteroaromatic compounds useful for the treatment of proliferative diseases
MX370906B (es) 2013-12-30 2020-01-09 Genentech Inc Inhibidores de serina/treonina cinasa.
EP3489232A3 (en) 2014-04-04 2019-07-31 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
SG11201700037QA (en) 2014-07-24 2017-02-27 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
CA3121986C (en) 2014-12-24 2024-04-09 Lg Chem, Ltd. Biaryl derivative as gpr120 agonist
WO2016192630A1 (zh) 2015-06-01 2016-12-08 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
US10695346B2 (en) * 2015-06-26 2020-06-30 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
WO2018013867A1 (en) * 2016-07-13 2018-01-18 Marineau Jason J Inhibitors of cyclin dependnt kinase 7 (cdk7)
WO2018161033A1 (en) 2017-03-02 2018-09-07 Wright, Adrian Small molecule ire1-alpha inhibitors
US11266640B2 (en) 2017-09-20 2022-03-08 Hangzhou Innogate Pharma Co., Ltd. Polycyclic compound acting as IDO inhibitor and/or IDO-HDAC dual inhibitor
MX2020011294A (es) 2018-04-26 2020-11-18 Pfizer Derivados de 2-amino-piridina o 2-amino-pirimidina como inhibidores de cinasa dependientes de ciclina.

Also Published As

Publication number Publication date
CA3098283C (en) 2023-05-23
BR112020021689B1 (pt) 2023-02-28
GEP20227433B (en) 2022-10-25
KR102661053B1 (ko) 2024-04-26
DOP2020000191A (es) 2021-02-28
KR102596598B1 (ko) 2023-11-03
IL278075A (en) 2020-11-30
SG11202009992VA (en) 2020-11-27
RU2762557C1 (ru) 2021-12-21
MX2020011294A (es) 2020-11-18
RU2021136543A (ru) 2021-12-16
IL278075B2 (en) 2023-05-01
US20220089580A1 (en) 2022-03-24
WO2019207463A1 (en) 2019-10-31
US10766884B2 (en) 2020-09-08
ECSP20067394A (es) 2020-12-31
JP2021522275A (ja) 2021-08-30
CL2020002748A1 (es) 2021-02-12
CO2020013149A2 (es) 2020-11-10
NI202000072A (es) 2021-03-23
EP3784664A1 (en) 2021-03-03
MA52360A (fr) 2021-03-03
US20190330196A1 (en) 2019-10-31
AU2019259653B2 (en) 2023-01-19
CA3098283A1 (en) 2019-10-31
UA126177C2 (uk) 2022-08-25
KR20230152182A (ko) 2023-11-02
PE20201202A1 (es) 2020-11-11
IL278075B1 (en) 2023-01-01
ZA202006944B (en) 2023-07-26
BR112020021689A2 (pt) 2021-01-26
CN112313219B (zh) 2024-04-26
CN112313219A (zh) 2021-02-02
US20200354350A1 (en) 2020-11-12
UY38196A (es) 2019-11-29
JP2022120096A (ja) 2022-08-17
PH12020551692A1 (en) 2021-07-19
CU20200070A7 (es) 2021-05-12
AU2019259653A1 (en) 2020-10-29
KR20210002642A (ko) 2021-01-08
JP7089061B2 (ja) 2022-06-21
TWI740135B (zh) 2021-09-21
TW202000661A (zh) 2020-01-01
US11220494B2 (en) 2022-01-11

Similar Documents

Publication Publication Date Title
CR20200503A (es) Inhibidores de cinasa dependientes de ciclina
PH12019500329A1 (en) Pyridopyrimdinone cdk2/4/6 inhibitors
PH12020551717A1 (en) Dual atm and dna-pk inhibitors for use in anti-tumor therapy
PH12021551529A1 (en) 3-carbonylamino-5-cyclopentyl-1h-pyrazole compounds having inhibitory activity on cdk2
MX2021000887A (es) Compuestos espiroheterociclicos y metodos de uso de los mismos para el tratamiento de cancer.
PH12020552004A1 (en) Heterocyclic compounds as kinase inhibitors, compositions comprising the heterocyclic compound, and methods of use thereof
TN2016000529A1 (en) Substituted dihydroisoquinolinone compounds
MX2020002924A (es) Lactamas fusionadas de arilo y heteroarilo.
CR20210627A (es) Derivados de benzisoxazol sulfonimada
EP3693369A3 (en) Bromodomain inhibitors
EA202090413A1 (ru) Пиразоло- и триазолобициклические соединения в качестве ингибиторов jak киназы
MX2016009403A (es) Compuestos heterociclicos.
MX2023004309A (es) Inhibidores de quinasa alk2 que contienen imidazol.
MX2020009530A (es) Inhibidores de la o-glicoproteína-2-acetamido-2-desoxi-3-dglicopir anosidasa.
MX2016016538A (es) Derivados de quinazolinona como inhibidores de fosfatidilinositol 3-cinasa.
TW200745066A (en) Novel PTP1B inhibitors
MX2016016530A (es) Inhibidores de fosfatidilinositol 3-quinasa.
MX2020001717A (es) Inhibidores macrociclicos de mcl-1 y metodos de uso.
TN2019000170A1 (en) Tetracyclic heterocycle compounds useful as hiv integrase inhibitors
PH12021550825A1 (en) Quinoline derivatives as alpha4beta7 integrin inhibitors
MX2020010942A (es) Inhibidores dobles de atm y adn-pk para uso en terapias antitumorales.
EP4249071A3 (en) Benzoazepine analogs as inhibiting agents for bruton&#39;s tyrosine kinase
MX2022013401A (es) Compuestos de azalactama como inhibidores de hpk1.
MX2011012629A (es) Inhibidores de actividad de cinasa tipo pirimidina.
TN2016000459A1 (en) Cycloalkyl-linked diheterocycle derivatives.