MX2014010701A - Inhibidores de pirido [2,3-d] 2-amino, 6-fenil substituidos utiles como inhibidores de cinasa raf. - Google Patents

Inhibidores de pirido [2,3-d] 2-amino, 6-fenil substituidos utiles como inhibidores de cinasa raf.

Info

Publication number
MX2014010701A
MX2014010701A MX2014010701A MX2014010701A MX2014010701A MX 2014010701 A MX2014010701 A MX 2014010701A MX 2014010701 A MX2014010701 A MX 2014010701A MX 2014010701 A MX2014010701 A MX 2014010701A MX 2014010701 A MX2014010701 A MX 2014010701A
Authority
MX
Mexico
Prior art keywords
amino
kinase inhibitors
phenyl substituted
pyrimidine derivatives
raf kinase
Prior art date
Application number
MX2014010701A
Other languages
English (en)
Spanish (es)
Inventor
Daniel L Flynn
Matthew Carl Allgeier
Michael D Kaufman
Phenil J Patel
Craig D Wolfangel
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
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=MX2014010701(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of MX2014010701A publication Critical patent/MX2014010701A/es

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)
MX2014010701A 2012-03-07 2013-03-05 Inhibidores de pirido [2,3-d] 2-amino, 6-fenil substituidos utiles como inhibidores de cinasa raf. MX2014010701A (es)

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 (1)

Publication Number Publication Date
MX2014010701A true MX2014010701A (es) 2015-03-10

Family

ID=47884613

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2014010701A MX2014010701A (es) 2012-03-07 2013-03-05 Inhibidores de pirido [2,3-d] 2-amino, 6-fenil substituidos utiles como inhibidores de cinasa raf.

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)

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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
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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
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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.
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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
MA37316B1 (fr) 2017-03-31
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
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

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