MA37316B1 - Dérivés de 2-amino, 6-phenyl à substitution pyrido [2, 3 - d] pyrimidine utilisés en tant qu'inhibiteurs de la raf kinase - Google Patents

Dérivés de 2-amino, 6-phenyl à substitution pyrido [2, 3 - d] pyrimidine utilisés en tant qu'inhibiteurs de la raf kinase

Info

Publication number
MA37316B1
MA37316B1 MA37316A MA37316A MA37316B1 MA 37316 B1 MA37316 B1 MA 37316B1 MA 37316 A MA37316 A MA 37316A MA 37316 A MA37316 A MA 37316A MA 37316 B1 MA37316 B1 MA 37316B1
Authority
MA
Morocco
Prior art keywords
pyrido
pyrimidine
inhibitors
amino
substituted
Prior art date
Application number
MA37316A
Other languages
English (en)
French (fr)
Other versions
MA37316A1 (fr
Inventor
Matthew Carl Allgeier
Daniel L Flynn
Michael D Kaufman
Phenil J Patel
Craig D Wolfangel
Original Assignee
Lilly Co Eli
Deciphera Pharmaceuticals Llc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=47884613&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA37316(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lilly Co Eli, Deciphera Pharmaceuticals Llc filed Critical Lilly Co Eli
Publication of MA37316A1 publication Critical patent/MA37316A1/fr
Publication of MA37316B1 publication Critical patent/MA37316B1/fr

Links

Classifications

    • 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
    • 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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
    • 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
    • C07D471/12Heterocyclic 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 three hetero rings

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)
  • Oncology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)
MA37316A 2012-03-07 2013-03-05 Dérivés de 2-amino, 6-phenyl à substitution pyrido [2, 3 - d] pyrimidine utilisés en tant qu'inhibiteurs de la raf kinase MA37316B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261607702P 2012-03-07 2012-03-07
PCT/US2013/029084 WO2013134243A1 (en) 2012-03-07 2013-03-05 2-amino, 6-phenyl substituted pyrido [2, 3 - d] pyrimidine derivatives useful as raf kinase inhibitors

Publications (2)

Publication Number Publication Date
MA37316A1 MA37316A1 (fr) 2016-06-30
MA37316B1 true MA37316B1 (fr) 2017-03-31

Family

ID=47884613

Family Applications (1)

Application Number Title Priority Date Filing Date
MA37316A MA37316B1 (fr) 2012-03-07 2013-03-05 Dérivés de 2-amino, 6-phenyl à substitution pyrido [2, 3 - d] pyrimidine utilisés en tant qu'inhibiteurs de la raf kinase

Country Status (39)

Country Link
US (2) US9334267B2 (cg-RX-API-DMAC7.html)
EP (1) EP2850082B1 (cg-RX-API-DMAC7.html)
JP (1) JP2015509536A (cg-RX-API-DMAC7.html)
KR (1) KR20140129087A (cg-RX-API-DMAC7.html)
CN (1) CN104302646B (cg-RX-API-DMAC7.html)
AP (1) AP2014007899A0 (cg-RX-API-DMAC7.html)
AR (1) AR090151A1 (cg-RX-API-DMAC7.html)
AU (1) AU2013230146B2 (cg-RX-API-DMAC7.html)
BR (1) BR112014018528A8 (cg-RX-API-DMAC7.html)
CA (1) CA2863673A1 (cg-RX-API-DMAC7.html)
CL (1) CL2014002220A1 (cg-RX-API-DMAC7.html)
CO (1) CO7010837A2 (cg-RX-API-DMAC7.html)
CR (1) CR20140378A (cg-RX-API-DMAC7.html)
CY (1) CY1117846T1 (cg-RX-API-DMAC7.html)
DK (1) DK2850082T3 (cg-RX-API-DMAC7.html)
DO (1) DOP2014000200A (cg-RX-API-DMAC7.html)
EA (1) EA024824B1 (cg-RX-API-DMAC7.html)
EC (1) ECSP14017584A (cg-RX-API-DMAC7.html)
ES (1) ES2584387T3 (cg-RX-API-DMAC7.html)
HK (1) HK1202541A1 (cg-RX-API-DMAC7.html)
HR (1) HRP20160654T1 (cg-RX-API-DMAC7.html)
HU (1) HUE028095T2 (cg-RX-API-DMAC7.html)
IL (1) IL234052A (cg-RX-API-DMAC7.html)
IN (1) IN2014MN01575A (cg-RX-API-DMAC7.html)
LT (1) LT2850082T (cg-RX-API-DMAC7.html)
MA (1) MA37316B1 (cg-RX-API-DMAC7.html)
ME (1) ME02423B (cg-RX-API-DMAC7.html)
MX (1) MX2014010701A (cg-RX-API-DMAC7.html)
NZ (1) NZ627454A (cg-RX-API-DMAC7.html)
PE (1) PE20142338A1 (cg-RX-API-DMAC7.html)
PH (1) PH12014501986B1 (cg-RX-API-DMAC7.html)
PT (1) PT2850082T (cg-RX-API-DMAC7.html)
RS (1) RS54840B1 (cg-RX-API-DMAC7.html)
SG (1) SG11201404969YA (cg-RX-API-DMAC7.html)
SI (1) SI2850082T1 (cg-RX-API-DMAC7.html)
TN (1) TN2014000375A1 (cg-RX-API-DMAC7.html)
TW (1) TW201348233A (cg-RX-API-DMAC7.html)
UA (1) UA112340C2 (cg-RX-API-DMAC7.html)
WO (2) WO2013134252A1 (cg-RX-API-DMAC7.html)

Families Citing this family (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR090151A1 (es) * 2012-03-07 2014-10-22 Lilly Co Eli Compuestos inhibidores de raf
US8461179B1 (en) 2012-06-07 2013-06-11 Deciphera Pharmaceuticals, Llc Dihydronaphthyridines and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
TWI704151B (zh) 2014-12-22 2020-09-11 美商美國禮來大藥廠 Erk抑制劑
JP2019517549A (ja) * 2016-06-10 2019-06-24 ノバルティス アーゲー C−raf阻害薬の治療的使用
EP3878850A1 (en) 2016-12-22 2021-09-15 Boehringer Ingelheim International GmbH Novel benzylamino substituted quinazolines and derivatives as sos1 inhibitors
JP2020518660A (ja) * 2017-04-28 2020-06-25 クォーツ セラピューティクス,インコーポレイティド Raf分解性結合体化合物
PH12020550786A1 (en) 2017-12-21 2021-04-12 Boehringer Ingelheim Int Novel benzylamino substituted pyridopyrimidinones and derivatives as sos1 inhibitors
JP7161849B2 (ja) * 2018-01-24 2022-10-27 株式会社クラレ 第一級アミンの製造方法
SG11202007287XA (en) 2018-01-31 2020-08-28 Deciphera Pharmaceuticals Llc Combination therapy for the treatment of mastocytosis
BR112020015581A2 (pt) 2018-01-31 2021-02-02 Deciphera Pharmaceuticals, Llc terapia de combinação para o tratamento de tumores estromais gastrointestinais
EP3849536A4 (en) 2018-09-10 2022-06-29 Mirati Therapeutics, Inc. Combination therapies
CN118453608A (zh) 2018-12-28 2024-08-09 德西费拉制药有限责任公司 用于治疗癌症的csf1r抑制剂
SMT202400003T1 (it) 2019-02-06 2024-03-13 Lilly Co Eli Derivati di 1-((2-(2,2,2-trifluoroetossi)piridin-4-il)metil)urea come potenziatori di kcnq
TWI756636B (zh) * 2019-02-18 2022-03-01 美商建南德克公司 嘧啶并嘧啶化合物及使用方法
CN114072148A (zh) * 2019-05-03 2022-02-18 金耐特生物制药公司 Raf激酶的抑制剂
KR20220008873A (ko) 2019-05-10 2022-01-21 데시페라 파마슈티칼스, 엘엘씨. 페닐아미노피리미딘 아미드 자가포식 억제제 및 이의 사용 방법
BR112021022576A2 (pt) 2019-05-10 2022-01-25 Deciphera Pharmaceuticals Llc Inibidores de autofagia de heteroarilaminopirimidina amida e métodos de uso dos mesmos
JP7626722B2 (ja) 2019-06-17 2025-02-04 デシフェラ・ファーマシューティカルズ,エルエルシー アミノピリミジンアミドオートファジー阻害剤およびその使用方法
KR20220045189A (ko) 2019-08-12 2022-04-12 데시페라 파마슈티칼스, 엘엘씨. 위장관 기질 종양을 치료하는 방법
WO2021030405A1 (en) 2019-08-12 2021-02-18 Deciphera Pharmaceuticals, Llc Ripretinib for treating gastrointestinal stromal tumors
CN114845711B (zh) 2019-10-24 2024-10-01 皮埃尔法布雷医药公司 Raf激酶的抑制剂
PL4084779T3 (pl) 2019-12-30 2025-02-24 Deciphera Pharmaceuticals, Llc Kompozycje 1-(4-bromo-5-(1-etylo-7-(metyloamino)-2-okso-1,2-dihydro-1,6-naftyrydyn-3-ylo)-2-fluorofenylo)-3-fenylomocznika
CN119950433A (zh) 2019-12-30 2025-05-09 德西费拉制药有限责任公司 非晶型激酶抑制剂制剂及其使用方法
EP4157837B1 (en) 2020-06-02 2024-12-18 Boehringer Ingelheim International GmbH Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
US11407737B2 (en) 2020-09-18 2022-08-09 Kinnate Biopharma Inc. Inhibitors of RAF kinases
WO2022081469A1 (en) 2020-10-12 2022-04-21 Kinnate Biopharma Inc. Inhibitors of raf kinases
CN116507627A (zh) 2020-11-02 2023-07-28 勃林格殷格翰国际有限公司 作为egfr抑制剂的经取代1h-吡唑并[4,3-c]吡啶及衍生物
JP2023549540A (ja) 2020-11-18 2023-11-27 デシフェラ・ファーマシューティカルズ,エルエルシー Gcn2およびperkキナーゼ阻害剤およびその使用方法
CN117396472A (zh) 2020-12-22 2024-01-12 上海齐鲁锐格医药研发有限公司 Sos1抑制剂及其用途
MX2023012515A (es) 2021-04-23 2023-12-15 Kinnate Biopharma Inc Tratamiento del cancer con un inhibidor de raf.
US12065427B2 (en) 2021-04-29 2024-08-20 Boehringer Ingelheim International Gmbh Heterocyclic compounds capable of activating STING
TW202337432A (zh) 2021-12-01 2023-10-01 德商百靈佳殷格翰國際股份有限公司 用於治療癌症之環狀2-胺基-3-氰基噻吩及衍生物
US20250313553A1 (en) 2021-12-01 2025-10-09 Boehringer Ingelheim Int'l GmbH Corp. Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
EP4441053A1 (en) 2021-12-01 2024-10-09 Boehringer Ingelheim International GmbH Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
US20250129096A1 (en) 2021-12-01 2025-04-24 Boehringer Ingelheim Int'l GmbH Corp. Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
WO2023099620A1 (en) 2021-12-01 2023-06-08 Boehringer Ingelheim International Gmbh Kras degrading compounds comprising annulated 2-amino-3-cyano thiophenes
IL312905A (en) 2021-12-01 2024-07-01 Boehringer Ingelheim Int Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
WO2023108108A1 (en) 2021-12-09 2023-06-15 Deciphera Pharmaceuticals, Llc Raf kinase inhibitors and methods of use thereof
JP2024546107A (ja) 2021-12-09 2024-12-17 デシフェラ・ファーマシューティカルズ,エルエルシー Rafキナーゼ阻害剤及びその使用方法
WO2023118250A1 (en) 2021-12-23 2023-06-29 Boehringer Ingelheim International Gmbh 8-aza quinazolines as brain-penetrant sos1-inhibitors
WO2023173017A1 (en) * 2022-03-09 2023-09-14 Blossomhill Therapeutics, Inc. Kras inhibitors for treating disease
US11779572B1 (en) 2022-09-02 2023-10-10 Deciphera Pharmaceuticals, Llc Methods of treating gastrointestinal stromal tumors
CA3266173A1 (en) 2022-10-26 2024-05-02 Boehringer Ingelheim International Gmbh HETEROCYCLIC COMPOUNDS CAPABLE OF ACTIVATING STING
CA3267008A1 (en) 2022-10-26 2024-05-02 Boehringer Ingelheim International Gmbh HETEROCYCLIC COMPOUNDS CAPABLE OF ACTIVATING STING
WO2024089008A1 (en) 2022-10-26 2024-05-02 Boehringer Ingelheim International Gmbh Heterocyclic compounds capable of activating sting
AU2024265078A1 (en) 2023-05-04 2025-12-11 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
TW202511268A (zh) 2023-05-30 2025-03-16 德商百靈佳殷格翰國際股份有限公司 用於治療癌症之螺環狀2-胺基-3-氰基噻吩及衍生物
GB2631397A (en) 2023-06-28 2025-01-08 Sevenless Therapeutics Ltd New treatments for pain
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
GB2633813A (en) 2023-09-21 2025-03-26 Sevenless Therapeutics Ltd New treatments for pain
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors
WO2025083426A1 (en) 2023-10-20 2025-04-24 Sevenless Therapeutics Limited New treatments for pain
WO2025122952A1 (en) 2023-12-08 2025-06-12 Deciphera Pharmaceuticals, Llc Formulations of vimseltinib
WO2025137507A1 (en) 2023-12-22 2025-06-26 Regor Pharmaceuticals, Inc. Sos1 inhibitors and uses thereof
WO2025146548A1 (en) 2024-01-04 2025-07-10 Sevenless Therapeutics Limited Sos1 inhibitors useful to treat pain and cancer
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
US20250313560A1 (en) 2024-04-03 2025-10-09 Boehringer Ingelheim International Gmbh Novel bicyclic benzylamido pyridine derivatives as SOS1 inhibitors
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors
WO2025255438A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003033472A1 (en) * 2001-10-17 2003-04-24 Kirin Beer Kabushiki Kaisha Quinoline or quinazoline derivatives inhibiting auto- phosphorylation of fibroblast growth factor receptors
AU2003280599A1 (en) * 2002-10-29 2004-05-25 Kirin Beer Kabushiki Kaisha QUINOLINE DERIVATIVES AND QUINAZOLINE DERIVATIVES INHIBITING AUTOPHOSPHORYLATION OF Flt3 AND MEDICINAL COMPOSITIONS CONTAINING THE SAME
US20070054916A1 (en) 2004-10-01 2007-03-08 Amgen Inc. Aryl nitrogen-containing bicyclic compounds and methods of use
US7897762B2 (en) 2006-09-14 2011-03-01 Deciphera Pharmaceuticals, Llc Kinase inhibitors useful for the treatment of proliferative diseases
US8188113B2 (en) * 2006-09-14 2012-05-29 Deciphera Pharmaceuticals, Inc. Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
WO2011100319A1 (en) * 2010-02-09 2011-08-18 Exelixis, Inc. Methods of treating cancer using pyridopyrimidinone inhibitors of pi3k and mtor in combination with autophagy inhibitors
AR090151A1 (es) * 2012-03-07 2014-10-22 Lilly Co Eli Compuestos inhibidores de raf

Also Published As

Publication number Publication date
ES2584387T3 (es) 2016-09-27
AP2014007899A0 (en) 2014-08-31
PH12014501986A1 (en) 2014-11-24
CY1117846T1 (el) 2017-05-17
EP2850082A1 (en) 2015-03-25
IN2014MN01575A (cg-RX-API-DMAC7.html) 2015-05-08
CN104302646B (zh) 2016-05-04
UA112340C2 (uk) 2016-08-25
CO7010837A2 (es) 2014-07-31
PH12014501986B1 (en) 2014-11-24
HRP20160654T1 (hr) 2016-07-01
CN104302646A (zh) 2015-01-21
AU2013230146A1 (en) 2014-08-14
CA2863673A1 (en) 2013-09-12
KR20140129087A (ko) 2014-11-06
EA024824B1 (ru) 2016-10-31
MA37316A1 (fr) 2016-06-30
BR112014018528A2 (cg-RX-API-DMAC7.html) 2017-06-20
BR112014018528A8 (pt) 2017-07-11
SI2850082T1 (sl) 2016-07-29
NZ627454A (en) 2016-09-30
CL2014002220A1 (es) 2015-06-05
WO2013134243A1 (en) 2013-09-12
US8741911B2 (en) 2014-06-03
US9334267B2 (en) 2016-05-10
AU2013230146B2 (en) 2015-09-10
ECSP14017584A (es) 2016-01-29
ME02423B (me) 2016-09-20
LT2850082T (lt) 2016-09-12
US20130252977A1 (en) 2013-09-26
AR090151A1 (es) 2014-10-22
DOP2014000200A (es) 2014-10-15
PE20142338A1 (es) 2015-01-10
SG11201404969YA (en) 2014-10-30
DK2850082T3 (en) 2016-08-15
TN2014000375A1 (en) 2015-12-21
RS54840B1 (sr) 2016-10-31
CR20140378A (es) 2014-11-27
IL234052A (en) 2016-05-31
WO2013134252A1 (en) 2013-09-12
HUE028095T2 (en) 2016-11-28
HK1202541A1 (en) 2015-10-02
US20150119392A1 (en) 2015-04-30
MX2014010701A (es) 2015-03-10
EP2850082B1 (en) 2016-05-18
EA201491456A1 (ru) 2014-12-30
TW201348233A (zh) 2013-12-01
JP2015509536A (ja) 2015-03-30
PT2850082T (pt) 2016-07-15

Similar Documents

Publication Publication Date Title
MA37316B1 (fr) Dérivés de 2-amino, 6-phenyl à substitution pyrido [2, 3 - d] pyrimidine utilisés en tant qu'inhibiteurs de la raf kinase
CL2019000942A1 (es) Compuestos de pirazolo[1,5-a]piridina sustituidos como inhibidores de la quinasa ret.
PH12018500792A1 (en) Benzolactam compounds as protein kinase inhibitors
PH12016501535A1 (en) Uracil derivatives as axl and c-met kinase inhibitors
MA53675A (fr) Composés substitués de pyrazolo[1,5-a]pyridine en tant qu'inhibiteurs de la kinase ret
EP3492462A4 (en) AMINOPYRIMIDIN COMPOUND FOR INHIBITING PROTEINTYROSINKINASE ACTIVITY
MX2016007371A (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.
MA52987A (fr) Dérivés de pyrazolo[1,5-a]pyrazin-4-yl en tant qu'inhibiteurs de jak
CL2017001566A1 (es) Derivados de azabiciclootano como agonistas de fxr para el uso en el tratamiento de enfermedades hepáticas y gastrointestinales.
MX2020003458A (es) Derivados radiomarcados de un compuesto de 2-amino-6-fluoro-n-[ 5-fluoro-piridin-3-il]-pirazolo[1,5-a]pirimidin-3- carboxamida util como inhibidor de ataxia telangiectasia mutada y rad3 relacionado (atr) cinasa, preparacion de tal compuesto y diferentes formas solidas del mismo.
HK1246286A1 (zh) Lrrk2抑制剂及其制备和使用方法
CL2013003051A1 (es) Compuestos derivados de pirazolo (4.3-d) pirimidinas, inhibidores de quinasa; composicion farmaceutica; y uso para el tratamiento de enfermedades y trastornos del aparato respiratorio
NZ722624A (en) Fused pyrimidines as inhibitors of p97 complex
MX2017016772A (es) Metodo para producir un derivado de 7h-pirrolo[2,3-d]pirimidina e intermediario del mismo.
PH12019501022A1 (en) Pyrazolopyrimidine compounds and methods of use thereof
PH12017501123A1 (en) Solid state forms of fused heteroaromatic pyrrolidinones
EA202091475A1 (ru) ПРОИЗВОДНЫЕ 5-(2-(2,5-ДИФТОРФЕНИЛ)ПИРРОЛИДИН-1-ИЛ)-3-(1H-ПИРАЗОЛ-1-ИЛ)ПИРАЗОЛО[1,5-а]ПИРИМИДИНА И РОДСТВЕННЫЕ СОЕДИНЕНИЯ В КАЧЕСТВЕ ИНГИБИТОРОВ Trk КИНАЗЫ ДЛЯ ЛЕЧЕНИЯ РАКА
MA38884A1 (fr) Composé de triazolopyridine, compositions et procédés d'utilisation associés
JOP20190233A1 (ar) نظائر بنزوازيبين بوصفها عوامل مثبطة لتيروزين كيناز بروتون
MX366839B (es) Pirimidinas novedosas 2,5-sustituidas como inhibidores de pde4.
EP3508487A4 (en) PYRAZOLO [1,5-A] PYRIMIDINE COMPOUND
MA46690A (fr) Composés de [1,2,4]triazolo [1,5-a]pyrimidine en tant qu'inhibiteurs de pde2
MX2017000522A (es) Pirimidinas novedosas 2,5-sustituidas como inhibidores de pde.
EP3679042A4 (en) IMIDAZO [1,5-A] PYRAZINE DERIVATIVES AS PI3KDELTA INHIBITORS
EA201791743A1 (ru) Производные имидазо[2,1-в]тиазола и 5,6-дигидроимидазо[2,1-в]тиазола, применяемые в качестве s100-ингибиторов