MX2010003927A - Derivados de pirrolo [2,3-d] pirimidina como inhibidores de proteinas cinasas b. - Google Patents
Derivados de pirrolo [2,3-d] pirimidina como inhibidores de proteinas cinasas b.Info
- Publication number
- MX2010003927A MX2010003927A MX2010003927A MX2010003927A MX2010003927A MX 2010003927 A MX2010003927 A MX 2010003927A MX 2010003927 A MX2010003927 A MX 2010003927A MX 2010003927 A MX2010003927 A MX 2010003927A MX 2010003927 A MX2010003927 A MX 2010003927A
- Authority
- MX
- Mexico
- Prior art keywords
- sup
- protein kinase
- pyrrolo
- inhibitors
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
Abstract
La invenci?n se refiere a un grupo nuevo de compuestos de F?rmula (I) o sales de lo mismo: en donde Y, Z1, Z2, R1, R4, R5 y n son como se describen en la especificaci?n, en el cual pueden utilizarse en el tratamiento o prevenci?n de una enfermedad o afecci?n m?dica mediada por la prote?na cinasa B (PKB) tal como c?ncer. La invenci?n tambi?n se refiere a composiciones farmac?uticas que comprenden tales compuestos, m?todos de tratamiento de enfermedades mediadas por PKB que usan tales compuestos y m?todos para preparar compuestos de F?rmula (I).
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US97919207P | 2007-10-11 | 2007-10-11 | |
US4786208P | 2008-04-25 | 2008-04-25 | |
PCT/GB2008/050925 WO2009047563A1 (en) | 2007-10-11 | 2008-10-09 | Pyrrolo [2, 3 -d] pyrimidin derivatives as protein kinase b inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2010003927A true MX2010003927A (es) | 2010-04-30 |
Family
ID=40251789
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2010003927A MX2010003927A (es) | 2007-10-11 | 2008-10-09 | Derivados de pirrolo [2,3-d] pirimidina como inhibidores de proteinas cinasas b. |
Country Status (38)
Country | Link |
---|---|
US (8) | US8101623B2 (es) |
EP (1) | EP2201012B1 (es) |
JP (2) | JP4705695B2 (es) |
KR (1) | KR101494734B1 (es) |
CN (1) | CN101861321B (es) |
AR (1) | AR068846A1 (es) |
AU (1) | AU2008309383B2 (es) |
BR (1) | BRPI0818533B8 (es) |
CA (1) | CA2701057C (es) |
CL (1) | CL2008003023A1 (es) |
CO (1) | CO6270328A2 (es) |
CR (1) | CR11359A (es) |
CU (1) | CU23886B1 (es) |
CY (1) | CY1116929T1 (es) |
DK (1) | DK2201012T3 (es) |
DO (1) | DOP2010000103A (es) |
EA (1) | EA018512B1 (es) |
ES (1) | ES2522365T3 (es) |
GT (1) | GT201000082A (es) |
HK (1) | HK1143154A1 (es) |
HN (1) | HN2010000653A (es) |
HR (1) | HRP20140807T1 (es) |
IL (1) | IL204721A (es) |
ME (1) | ME01999B (es) |
MX (1) | MX2010003927A (es) |
MY (1) | MY150059A (es) |
NI (1) | NI201000050A (es) |
NZ (1) | NZ585261A (es) |
PE (2) | PE20130152A1 (es) |
PL (1) | PL2201012T3 (es) |
PT (1) | PT2201012E (es) |
RS (1) | RS53552B1 (es) |
SA (1) | SA08290625B1 (es) |
SI (1) | SI2201012T1 (es) |
TW (1) | TWI453021B (es) |
UY (1) | UY31384A1 (es) |
WO (1) | WO2009047563A1 (es) |
ZA (1) | ZA201002318B (es) |
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MY179032A (en) | 2004-10-25 | 2020-10-26 | Cancer Research Tech Ltd | Ortho-condensed pyridine and pyrimidine derivatives (e.g.purines) as protein kinase inhibitors |
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KR20090064378A (ko) | 2006-08-10 | 2009-06-18 | 온코세라피 사이언스 가부시키가이샤 | 유방암 관련 유전자 및 폴리펩티드 |
MY150059A (en) | 2007-10-11 | 2013-11-29 | Astrazeneca Ab | Pyrrolo [2,3-d] pyrimidin derivatives as protein kinase b inhibitors |
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EP2651417B1 (en) | 2010-12-16 | 2016-11-30 | Calchan Limited | Ask1 inhibiting pyrrolopyrimidine derivatives |
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KR102421235B1 (ko) | 2014-02-13 | 2022-07-15 | 인사이트 코포레이션 | Lsd1 저해제로서 사이클로프로필아민 |
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US9695168B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted imidazo[1,5-α]pyridines and imidazo[1,5-α]pyrazines as LSD1 inhibitors |
US9695180B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted imidazo[1,2-a]pyrazines as LSD1 inhibitors |
US9758523B2 (en) | 2014-07-10 | 2017-09-12 | Incyte Corporation | Triazolopyridines and triazolopyrazines as LSD1 inhibitors |
EP3277689B1 (en) | 2015-04-03 | 2019-09-04 | Incyte Corporation | Heterocyclic compounds as lsd1 inhibitors |
BR112018002553A8 (pt) | 2015-08-12 | 2023-01-24 | Incyte Corp | Sais de um inibidor de lsd1 |
TW201726140A (zh) | 2015-09-17 | 2017-08-01 | 瑞典商阿斯特捷利康公司 | 治療癌症之新型生物標記及方法 |
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2008
- 2008-10-09 MY MYPI2010001617A patent/MY150059A/en unknown
- 2008-10-09 PT PT88067418T patent/PT2201012E/pt unknown
- 2008-10-09 MX MX2010003927A patent/MX2010003927A/es active IP Right Grant
- 2008-10-09 ME MEP-2014-102A patent/ME01999B/me unknown
- 2008-10-09 UY UY31384A patent/UY31384A1/es not_active Application Discontinuation
- 2008-10-09 PL PL08806741T patent/PL2201012T3/pl unknown
- 2008-10-09 CA CA2701057A patent/CA2701057C/en active Active
- 2008-10-09 EA EA201000552A patent/EA018512B1/ru not_active IP Right Cessation
- 2008-10-09 BR BRPI0818533A patent/BRPI0818533B8/pt active IP Right Grant
- 2008-10-09 NZ NZ585261A patent/NZ585261A/en unknown
- 2008-10-09 SI SI200831281T patent/SI2201012T1/sl unknown
- 2008-10-09 ES ES08806741.8T patent/ES2522365T3/es active Active
- 2008-10-09 JP JP2010528485A patent/JP4705695B2/ja active Active
- 2008-10-09 DK DK08806741.8T patent/DK2201012T3/da active
- 2008-10-09 WO PCT/GB2008/050925 patent/WO2009047563A1/en active Application Filing
- 2008-10-09 RS RS20140457A patent/RS53552B1/en unknown
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