MX2013001247A - 6- (1-metil-1h-pirazol-4-il) -3- )2-metil-2h-indazol-5-iltio)- [1, 2, 4] triazolo [4, 3-b] piridazina como inhibidor de c-met. - Google Patents

6- (1-metil-1h-pirazol-4-il) -3- )2-metil-2h-indazol-5-iltio)- [1, 2, 4] triazolo [4, 3-b] piridazina como inhibidor de c-met.

Info

Publication number
MX2013001247A
MX2013001247A MX2013001247A MX2013001247A MX2013001247A MX 2013001247 A MX2013001247 A MX 2013001247A MX 2013001247 A MX2013001247 A MX 2013001247A MX 2013001247 A MX2013001247 A MX 2013001247A MX 2013001247 A MX2013001247 A MX 2013001247A
Authority
MX
Mexico
Prior art keywords
compound
salt
cancer
met
methyl
Prior art date
Application number
MX2013001247A
Other languages
English (en)
Spanish (es)
Inventor
Zhipei Wu
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of MX2013001247A publication Critical patent/MX2013001247A/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
    • A61K31/495Heterocyclic 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
MX2013001247A 2010-07-30 2011-07-22 6- (1-metil-1h-pirazol-4-il) -3- )2-metil-2h-indazol-5-iltio)- [1, 2, 4] triazolo [4, 3-b] piridazina como inhibidor de c-met. MX2013001247A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US36933510P 2010-07-30 2010-07-30
PCT/US2011/044926 WO2012015677A1 (en) 2010-07-30 2011-07-22 6- (1-methyl-1h-pyrazol-4-yl)-3-(2-methyl-2h-indazol-5-

Publications (1)

Publication Number Publication Date
MX2013001247A true MX2013001247A (es) 2013-03-18

Family

ID=44513148

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2013001247A MX2013001247A (es) 2010-07-30 2011-07-22 6- (1-metil-1h-pirazol-4-il) -3- )2-metil-2h-indazol-5-iltio)- [1, 2, 4] triazolo [4, 3-b] piridazina como inhibidor de c-met.

Country Status (15)

Country Link
US (1) US8268836B2 (OSRAM)
EP (1) EP2598144B1 (OSRAM)
JP (1) JP5738412B2 (OSRAM)
KR (1) KR20130052740A (OSRAM)
CN (1) CN103002898A (OSRAM)
AR (1) AR085183A1 (OSRAM)
AU (1) AU2011282973B2 (OSRAM)
BR (1) BR112013002211A2 (OSRAM)
CA (1) CA2805494A1 (OSRAM)
EA (1) EA201270818A1 (OSRAM)
ES (1) ES2516940T3 (OSRAM)
IN (1) IN2012MN02924A (OSRAM)
MX (1) MX2013001247A (OSRAM)
TW (1) TWI431008B (OSRAM)
WO (1) WO2012015677A1 (OSRAM)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6129956B2 (ja) * 2012-05-09 2017-05-17 イーライ リリー アンド カンパニー 抗c−Met抗体
CN103122000B (zh) 2012-09-03 2013-12-25 中美冠科生物技术(太仓)有限公司 用作抗肿瘤药物的高选择性的c-Met激酶抑制剂
TWI667233B (zh) 2013-12-19 2019-08-01 德商拜耳製藥公司 新穎吲唑羧醯胺,其製備方法、含彼等之醫藥製劑及其製造醫藥之用途
US10386376B2 (en) 2015-11-09 2019-08-20 Jeimei, Llc Sample container with integrated test strip
CN106924260B (zh) * 2015-12-31 2018-05-25 北京浦润奥生物科技有限责任公司 化合物在制备用于治疗脑胶质瘤的药物中的用途
KR20210142154A (ko) 2019-03-21 2021-11-24 옹쎄오 암 치료를 위한 키나제 억제제와 조합된 dbait 분자
CN114761006A (zh) 2019-11-08 2022-07-15 Inserm(法国国家健康医学研究院) 对激酶抑制剂产生耐药性的癌症的治疗方法
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
AU2024241633A1 (en) 2023-03-30 2025-11-06 Revolution Medicines, Inc. Compositions for inducing ras gtp hydrolysis and uses thereof
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
WO2025034702A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Rmc-6291 for use in the treatment of ras protein-related disease or disorder
TW202530228A (zh) 2023-10-12 2025-08-01 美商銳新醫藥公司 Ras抑制劑
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras 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 (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2008007049A (es) * 2005-11-30 2008-10-23 Vertex Pharma Inhibidores de c-met y usos de los mismos.
PE20121506A1 (es) * 2006-07-14 2012-11-26 Amgen Inc Compuestos triazolopiridinas como inhibidores de c-met
US8217177B2 (en) 2006-07-14 2012-07-10 Amgen Inc. Fused heterocyclic derivatives and methods of use
PL2081937T3 (pl) 2006-10-23 2013-01-31 Sgx Pharmaceuticals Inc Triazolopirydazynowe modulatory kinaz białkowych
KR20090071612A (ko) * 2006-10-23 2009-07-01 에스지엑스 파마슈티컬스, 인코포레이티드 단백질 키나제 조정제로서의 바이시클릭 트리아졸
SI2081937T1 (sl) * 2006-10-23 2012-11-30 Sgx Pharmaceuticals Inc Triazolopiridazinski modulatorji proteinskih kinaz
PA8792501A1 (es) * 2007-08-09 2009-04-23 Sanofi Aventis Nuevos derivados de 6-triazolopiridacina-sulfanil benzotiazol y bencimidazol,su procedimiento de preparación,su aplicación como medicamentos,composiciones farmacéuticas y nueva utilización principalmente como inhibidores de met.
UY31676A1 (es) 2008-02-28 2009-09-30 "derivados de 3-metil-imidiazo-[1,2-b]-piridazina"

Also Published As

Publication number Publication date
AR085183A1 (es) 2013-09-18
EP2598144A1 (en) 2013-06-05
US8268836B2 (en) 2012-09-18
WO2012015677A1 (en) 2012-02-02
KR20130052740A (ko) 2013-05-23
EA201270818A1 (ru) 2013-05-30
TWI431008B (zh) 2014-03-21
ES2516940T3 (es) 2014-10-31
AU2011282973B2 (en) 2014-03-20
CA2805494A1 (en) 2012-02-02
US20120028984A1 (en) 2012-02-02
TW201219393A (en) 2012-05-16
AU2011282973A1 (en) 2013-01-10
JP2013532687A (ja) 2013-08-19
EP2598144B1 (en) 2014-08-13
JP5738412B2 (ja) 2015-06-24
WO2012015677A9 (en) 2012-12-13
BR112013002211A2 (pt) 2016-05-24
CN103002898A (zh) 2013-03-27
IN2012MN02924A (OSRAM) 2015-06-12

Similar Documents

Publication Publication Date Title
AU2011282973B2 (en) 6-(1-methyl-1H-pyrazol-4-yl)-3-(2-methyl-2H-indazol -5-ylthio)-[1,2,4] triazolo [4,3-b]pyridazine as a c-Met inhibitor
US10227329B2 (en) Compounds useful for treating disorders related to RET
EP2850082B1 (en) 1-(3,3-dimethylbutyl)-3-(2-fluoro-4-methyl-5-(7-methyl-2-(methylamino)pyrido(2,3-d)pyrimidin-6-yl)phenyl)urea as Raf kinase inhibitor for the treatment of cancer
US7129351B2 (en) Pyrimido compounds having antiproliferative activity
EP4592289A1 (en) Novel prmt5 inhibitor and use thereof
CA2952230C (en) Pyrimidine compounds and methods using the same
CN107567503B (zh) 用于ttk抑制剂化疗的预后生物标记
Zhao et al. Discovery of thieno [3, 2-c] pyridin-4-amines as novel Bruton’s tyrosine kinase (BTK) inhibitors
EP3661936B1 (en) [1,2,4]triazolo[4,3-a]pyrazin-6(5h)-one derivatives
CN104447706B (zh) 4‑苯基‑2‑氨基嘧啶类化合物及其制备方法与应用
KR20200011990A (ko) 단백질 키나제 저해제로서 유용한 피리도퀴나졸린 유도체
HK1175778A1 (en) Process for preparing a 5h-pyrimido[5,4-d][2]benzazepine
HK1175778B (en) Process for preparing a 5h-pyrimido[5,4-d][2]benzazepine

Legal Events

Date Code Title Description
FA Abandonment or withdrawal