MX367158B - Benzotienilo-pirrolotriazinas disustituidas y su uso como inhibidores de quinasa fgfr. - Google Patents

Benzotienilo-pirrolotriazinas disustituidas y su uso como inhibidores de quinasa fgfr.

Info

Publication number
MX367158B
MX367158B MX2014006905A MX2014006905A MX367158B MX 367158 B MX367158 B MX 367158B MX 2014006905 A MX2014006905 A MX 2014006905A MX 2014006905 A MX2014006905 A MX 2014006905A MX 367158 B MX367158 B MX 367158B
Authority
MX
Mexico
Prior art keywords
hydrogen
compounds
pyrrolotriazines
kinase inhibitors
methoxy
Prior art date
Application number
MX2014006905A
Other languages
English (en)
Spanish (es)
Other versions
MX2014006905A (es
Inventor
Walter Hübsch
Klemens Lustig
Mario Lobell
Dirk Brohm
Melanie Heroult
Marie-Pierre Collin
Sylvia Grünewald
Ulf Bömer
Verena VÖHRINGER
Original Assignee
Bayer Pharma AG
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 Bayer Pharma AG filed Critical Bayer Pharma AG
Publication of MX2014006905A publication Critical patent/MX2014006905A/es
Publication of MX367158B publication Critical patent/MX367158B/es

Links

Classifications

    • 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
    • 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
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • 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
    • A61K31/5355Non-condensed oxazines and containing further heterocyclic 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
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541Non-condensed thiazines containing further heterocyclic rings
    • 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
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (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)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
MX2014006905A 2011-12-15 2012-12-10 Benzotienilo-pirrolotriazinas disustituidas y su uso como inhibidores de quinasa fgfr. MX367158B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP11193841 2011-12-15
PCT/EP2012/074977 WO2013087578A1 (en) 2011-12-15 2012-12-10 Disubstituted benzothienyl-pyrrolotriazines and their use as fgfr kinase inhibitors

Publications (2)

Publication Number Publication Date
MX2014006905A MX2014006905A (es) 2014-09-08
MX367158B true MX367158B (es) 2019-08-07

Family

ID=47326168

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2014006905A MX367158B (es) 2011-12-15 2012-12-10 Benzotienilo-pirrolotriazinas disustituidas y su uso como inhibidores de quinasa fgfr.

Country Status (42)

Country Link
US (4) US20140336173A1 (enExample)
EP (1) EP2791140B1 (enExample)
JP (1) JP6050829B2 (enExample)
KR (1) KR102057444B1 (enExample)
CN (1) CN104245700B (enExample)
AR (1) AR089207A1 (enExample)
AU (3) AU2012350750B2 (enExample)
BR (1) BR112014014531B1 (enExample)
CA (1) CA2859133C (enExample)
CL (1) CL2014001547A1 (enExample)
CO (1) CO7030961A2 (enExample)
CR (1) CR20140288A (enExample)
CU (2) CU24426B1 (enExample)
CY (1) CY1118112T1 (enExample)
DK (1) DK2791140T3 (enExample)
DO (1) DOP2014000127A (enExample)
EA (1) EA029556B1 (enExample)
EC (1) ECSP14004722A (enExample)
ES (1) ES2591203T3 (enExample)
GT (1) GT201400113A (enExample)
HR (1) HRP20161130T1 (enExample)
HU (1) HUE029582T2 (enExample)
IL (1) IL232611A (enExample)
IN (1) IN2014CN04310A (enExample)
JO (1) JO3295B1 (enExample)
LT (1) LT2791140T (enExample)
ME (1) ME02517B (enExample)
MX (1) MX367158B (enExample)
MY (1) MY178660A (enExample)
PE (1) PE20141855A1 (enExample)
PH (1) PH12014501355B1 (enExample)
PL (1) PL2791140T3 (enExample)
PT (1) PT2791140T (enExample)
RS (1) RS55144B1 (enExample)
SG (1) SG11201402325QA (enExample)
SI (1) SI2791140T1 (enExample)
TN (1) TN2014000255A1 (enExample)
TW (1) TWI567076B (enExample)
UA (1) UA116768C2 (enExample)
UY (1) UY34484A (enExample)
WO (1) WO2013087578A1 (enExample)
ZA (1) ZA201405140B (enExample)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10388493B2 (en) 2011-09-16 2019-08-20 Lam Research Corporation Component of a substrate support assembly producing localized magnetic fields
UY34484A (es) * 2011-12-15 2013-07-31 Bayer Ip Gmbh Benzotienilo-pirrolotriazinas disustituidas y sus usos
US10124003B2 (en) 2013-07-18 2018-11-13 Taiho Pharmaceutical Co., Ltd. Therapeutic agent for FGFR inhibitor-resistant cancer
AU2014291161B2 (en) 2013-07-18 2018-04-26 Taiho Pharmaceutical Co., Ltd. Antitumor drug for intermittent administration of FGFR inhibitor
PL3060562T3 (pl) * 2013-10-21 2022-01-10 Genosco Podstawione związki pirymidynowe i ich zastosowanie jako inhibitory syk
KR20170090431A (ko) * 2014-12-11 2017-08-07 바이엘 파마 악티엔게젤샤프트 범 fgfr 억제제의 용도 및 범 fgfr 억제제를 사용하는 치료에 대하여 적격인 암 환자를 확인하는 방법
WO2016142312A1 (en) * 2015-03-09 2016-09-15 Bayer Pharma Aktiengesellschaft Substituted 2,3-dihydroimidazo[1,2-c]quinazoline-containing combinations
SG11201804901WA (en) 2015-12-22 2018-07-30 SHY Therapeutics LLC Compounds for the treatment of cancer and inflammatory disease
EP3424505A4 (en) 2016-03-04 2019-10-16 Taiho Pharmaceutical Co., Ltd. PREPARATION AND COMPOSITION FOR THE TREATMENT OF MALIGNANT TUMORS
US11883404B2 (en) 2016-03-04 2024-01-30 Taiho Pharmaceuticals Co., Ltd. Preparation and composition for treatment of malignant tumors
KR102483020B1 (ko) 2016-03-28 2023-01-04 인사이트 코포레이션 Tam 저해제로서의 피롤로트리아진 화합물
CN107513068A (zh) * 2016-06-16 2017-12-26 中国科学院上海药物研究所 一种具有fgfr抑制活性的新型化合物及其制备和应用
AU2017362350B2 (en) 2016-11-18 2021-12-23 Cystic Fibrosis Foundation Pyrrolopyrimidines as CFTR potentiators
US10131670B2 (en) 2016-12-16 2018-11-20 Cystic Fibrosis Foundation Therapeutics, Inc. Bicyclic heteroaryl derivatives as CFTR potentiators
EA201992780A1 (ru) 2017-06-21 2020-06-02 ШАЙ ТЕРАПЬЮТИКС ЭлЭлСи Соединения, которые взаимодействуют с суперсемейством ras, для лечения рака, воспалительных заболеваний, ras-опатий и фиброзного заболевания
WO2019034076A1 (zh) * 2017-08-15 2019-02-21 南京明德新药研发股份有限公司 Fgfr抑制剂及其医药用途
WO2019034075A1 (zh) * 2017-08-15 2019-02-21 南京明德新药研发股份有限公司 Fgfr和egfr抑制剂
MA50655B1 (fr) 2017-09-27 2021-11-30 Incyte Corp Sels de dérivés de pyrrolotriazine utiles en tant qu'inhibiteurs de tam
PE20211268A1 (es) * 2017-10-25 2021-07-19 Bayer Pharma AG Proceso para preparar el benzotiofen-2-il boronato
WO2019105734A1 (en) 2017-11-28 2019-06-06 Bayer Consumer Care Ag Combinations of copanlisib
JP6918204B2 (ja) 2018-03-19 2021-08-11 大鵬薬品工業株式会社 アルキル硫酸ナトリウムを含む医薬組成物
WO2019180141A1 (en) 2018-03-23 2019-09-26 Bayer Aktiengesellschaft Combinations of rogaratinib
AR117600A1 (es) 2018-06-29 2021-08-18 Incyte Corp Formulaciones de un inhibidor de axl / mer
US12391705B2 (en) 2018-12-19 2025-08-19 Shy Therapeutics, Llc Compounds that interact with the Ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease
JOP20210204A1 (ar) * 2019-01-31 2023-01-30 Bayer Ag أحادي هيدرات هيدروكلوريد روجاراتينيب وأشكال صلبة منه
AU2020220512B2 (en) * 2019-02-15 2023-08-24 Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. FGFR inhibitor compound in solid form and preparation method therefor
WO2020170355A1 (ja) * 2019-02-20 2020-08-27 大鵬薬品工業株式会社 Fgfr1変異腫瘍の治療方法
CN109928976A (zh) * 2019-02-26 2019-06-25 泰州亿腾景昂药业有限公司 一种工业化生产eoc317的方法
BR112021020441A2 (pt) 2019-04-12 2021-12-14 Blueprint Medicines Corp Derivados de pirrolotriazina para tratar doenças mediadas por kit e pdgfra
WO2020231990A1 (en) 2019-05-13 2020-11-19 Relay Therapeutics, Inc. Fgfr inhibitors and methods of use thereof
CN114641293B (zh) * 2019-11-08 2024-05-31 石药集团中奇制药技术(石家庄)有限公司 一种fgfr抑制剂的用途
CN111004234A (zh) * 2019-11-28 2020-04-14 湖南农业大学 一种2-苯基咪唑并[1,2-α]吡啶类化合物的C3位卤化方法
WO2021178779A1 (en) 2020-03-06 2021-09-10 Incyte Corporation Combination therapy comprising axl/mer and pd-1/pd-l1 inhibitors
CN117402161A (zh) * 2022-07-06 2024-01-16 上海科恩泰生物医药科技有限公司 一种具有fgfr抑制作用的亚砜亚胺类化合物、包含其的药物组合物及其用途
AU2024241633A1 (en) 2023-03-30 2025-11-06 Revolution Medicines, Inc. Compositions for inducing ras gtp hydrolysis and uses thereof
TW202508595A (zh) 2023-05-04 2025-03-01 美商銳新醫藥公司 用於ras相關疾病或病症之組合療法
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
AU2024360465A1 (en) 2023-10-12 2026-04-09 Revolution Medicines, Inc. Macrocyclic ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
TW202547461A (zh) 2024-05-17 2025-12-16 美商銳新醫藥公司 Ras抑制劑
WO2025255438A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Ras inhibitors
WO2026015796A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015801A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015790A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015825A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Use of ras inhibitor for treating pancreatic cancer
WO2026050446A1 (en) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Ras inhibitors
WO2026072904A2 (en) 2024-09-26 2026-04-02 Revolution Medicines, Inc. Compositions and methods for treating lung cancer

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4649046B2 (ja) * 1999-05-21 2011-03-09 ブリストル−マイヤーズ スクイブ カンパニー キナーゼのピロロトリアジン阻害剤
MXPA02002938A (es) 1999-09-17 2004-12-06 Abbott Gmbh & Co Kg Inhibidores de cinasa como agentes agentes terapeuticos.
JPWO2004096806A1 (ja) * 2003-04-30 2006-07-13 大日本住友製薬株式会社 縮合イミダゾール誘導体
DE10327439A1 (de) * 2003-06-18 2005-01-05 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Imidazopyridazinon- und Imidazopyridonderivate, deren Herstellung und deren Verwendung als Arzneimittel
EP2168968B1 (en) 2004-04-02 2017-08-23 OSI Pharmaceuticals, LLC 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors
UY28931A1 (es) 2004-06-03 2005-12-30 Bayer Pharmaceuticals Corp Derivados de pirrolotriazina utiles para tratar trastornos hiper-proliferativos y enfermedades asociadas con angiogenesis
TW200635927A (en) * 2004-12-22 2006-10-16 Bristol Myers Squibb Co Synthetic process
JP5116687B2 (ja) 2005-11-02 2013-01-09 バイエル・ファルマ・アクチェンゲゼルシャフト がんおよび他の過剰増殖性疾患の処置のためのピロロ[2,1−f][1,2,4]トリアジン−4−イルアミンIGF−1Rキナーゼ阻害剤
ES2365869T3 (es) * 2005-11-17 2011-10-11 OSI Pharmaceuticals, LLC COMPUESTOS BICÍCLICOS FUSIONADOS INHIBIDORES DE LA mTOR.
US7514435B2 (en) 2005-11-18 2009-04-07 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
PE20070855A1 (es) 2005-12-02 2007-10-14 Bayer Pharmaceuticals Corp Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
WO2007064931A2 (en) 2005-12-02 2007-06-07 Bayer Healthcare Llc Substituted 4-amino-pyrrolotriazine derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis
WO2007064932A2 (en) 2005-12-02 2007-06-07 Bayer Healthcare Llc. Pyrrolotriazine derivatives useful for treating cancer through inhibition of aurora kinase
ES2545907T3 (es) * 2005-12-29 2015-09-16 Abbvie Inc. Inhibidores de proteína quinasa
US8124759B2 (en) 2007-05-09 2012-02-28 Abbott Laboratories Inhibitors of protein kinases
US8476431B2 (en) 2008-11-03 2013-07-02 Itellikine LLC Benzoxazole kinase inhibitors and methods of use
US8765754B2 (en) 2009-04-29 2014-07-01 Locus Pharmaceuticals, Inc. Pyrrolotriazine compounds
UY34484A (es) * 2011-12-15 2013-07-31 Bayer Ip Gmbh Benzotienilo-pirrolotriazinas disustituidas y sus usos

Also Published As

Publication number Publication date
ZA201405140B (en) 2017-04-26
ME02517B (me) 2017-02-20
MY178660A (en) 2020-10-20
RS55144B1 (sr) 2016-12-30
TWI567076B (zh) 2017-01-21
TN2014000255A1 (en) 2015-09-30
HK1205123A1 (en) 2015-12-11
CA2859133A1 (en) 2013-06-20
PL2791140T3 (pl) 2017-08-31
HRP20161130T1 (hr) 2016-11-18
BR112014014531A2 (pt) 2019-08-06
PH12014501355A1 (en) 2014-09-22
IN2014CN04310A (enExample) 2015-09-04
EP2791140A1 (en) 2014-10-22
PT2791140T (pt) 2016-09-20
IL232611A (en) 2017-05-29
CU24426B1 (es) 2019-06-04
PH12014501355B1 (en) 2014-09-22
CU20160039A7 (es) 2016-08-31
US20130158000A1 (en) 2013-06-20
AU2012350750B2 (en) 2017-08-03
KR20140103328A (ko) 2014-08-26
CO7030961A2 (es) 2014-08-21
EA201400707A1 (ru) 2014-11-28
PE20141855A1 (es) 2014-11-26
JO3295B1 (ar) 2018-09-16
LT2791140T (lt) 2016-10-10
CU20140065A7 (es) 2014-11-27
HUE029582T2 (en) 2017-03-28
EP2791140B1 (en) 2016-06-15
AU2012350750A1 (en) 2014-06-12
US20190016724A1 (en) 2019-01-17
CN104245700A (zh) 2014-12-24
SG11201402325QA (en) 2014-09-26
US20220153745A1 (en) 2022-05-19
CY1118112T1 (el) 2017-06-28
KR102057444B1 (ko) 2019-12-19
IL232611A0 (en) 2014-06-30
MX2014006905A (es) 2014-09-08
AR089207A1 (es) 2014-08-06
CL2014001547A1 (es) 2014-10-24
ECSP14004722A (es) 2015-11-30
TW201339162A (zh) 2013-10-01
AU2019204255A1 (en) 2019-07-04
JP6050829B2 (ja) 2016-12-21
SI2791140T1 (sl) 2016-10-28
AU2017206140A1 (en) 2017-08-03
ES2591203T3 (es) 2016-11-25
GT201400113A (es) 2015-08-25
CA2859133C (en) 2020-03-24
UA116768C2 (uk) 2018-05-10
US9206184B2 (en) 2015-12-08
DOP2014000127A (es) 2014-08-15
US20140336173A1 (en) 2014-11-13
JP2015500307A (ja) 2015-01-05
NZ625073A (en) 2016-07-29
CR20140288A (es) 2014-07-14
CN104245700B (zh) 2016-11-16
BR112014014531B1 (pt) 2022-02-08
WO2013087578A1 (en) 2013-06-20
EA029556B1 (ru) 2018-04-30
DK2791140T3 (en) 2016-09-19
UY34484A (es) 2013-07-31

Similar Documents

Publication Publication Date Title
PH12014501355A1 (en) Disubstituted benzothienyl-pyrrolotriazines and their use as fgfr kinase inhibitors
GEP20135785B (en) Pyrrolopyrimidine compounds as cdk inhibitors
MX2021013110A (es) Compuestos heterociclicos como inhibidores de la cinasa ret.
TN2014000128A1 (en) 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
PH12015502018A1 (en) 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
EA201070618A1 (ru) 4-пиразолил-n-арилпиримидин-2-амины и 4-пиразолил-n-гетероарилпиримидин-2-амины в качестве ингибиторов киназ janus
EA201591753A1 (ru) 3-пиримидин-4-илоксазолидин-2-оны в качестве ингибиторов мутантного idh
EA201100580A1 (ru) Имидазопиридазинкарбонитрилы, используемые в качестве ингибиторов киназы
MX336051B (es) Diarilacetileno hidracido que contiene inhibidores de tirosina quinasa.
ZA202205900B (en) 5-(2-(2,5-difluorophenyl)pyrrolidin-1 -yl)-3-(1h-pyrazol-1-yl)pyrazolo[1,5-a]pyrimidine derivatives and related compounds as trk kinase inhibitors for treating cancer
PH12012502391A1 (en) 2,4- diaryl - substituted [1,8] naphthyridines as kinase inhibitors for use against cancer
GEP20156285B (en) Compounds and compositions as trk inhibitors
MX370390B (es) Compuesto de 2-amino-6-fluoro-n-[5-fluoro-piridin-3-il]pirazolo[1, 5-a]pirimidin-3-carboxamida util como inhibidor de cinasa de ataxia telangiectasia mutada (atm) y rad3 relacionados (atr), su preparacion, diferentes formas solidas y sus derivados radiomarcados.
PH12012502070A1 (en) Inhibitors of protein tyrosine kinase activity and use thereof to treat ophthalmic disorders
MX2012002327A (es) Inhibidores de cinasa, formas de profarmaco de los mismos y su uso en terapia.
MX2014011326A (es) Derivados de 6-(4-(1-amino-3-hidroxiciclobutil) fenil)-5-fenil (furo, tieno o pirrolo) [2, 3-d] pirimidin 4-ona para el tratamiento de cancer.
PH12016500735B1 (en) Substituted pyrimidine compounds and their use as syk inhibitors
MX2011012522A (es) Inhibidores de pirazol sustituido de proteina cinasa c-met.
MX2011012524A (es) Inhibidores de proteina cinasa c-met.
MX2009012079A (es) Compuestos heterociclicos condensados como inhibidores de proteina cinasas.
EA202091617A1 (ru) Гетероарил-замещенные пирроло[2,3-b]пиридины и пирроло[2,3-b]пиримидины в качестве ингибиторов янус-киназы

Legal Events

Date Code Title Description
FG Grant or registration