PE20040805A1 - Indazolilpirrolotriazinas c-6 modificadas - Google Patents
Indazolilpirrolotriazinas c-6 modificadasInfo
- Publication number
- PE20040805A1 PE20040805A1 PE2003001275A PE2003001275A PE20040805A1 PE 20040805 A1 PE20040805 A1 PE 20040805A1 PE 2003001275 A PE2003001275 A PE 2003001275A PE 2003001275 A PE2003001275 A PE 2003001275A PE 20040805 A1 PE20040805 A1 PE 20040805A1
- Authority
- PE
- Peru
- Prior art keywords
- substituted
- indazol
- carbamic
- triazine
- ethyl
- 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
- A61K31/53—Heterocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
Abstract
SE REFIERE A COMPUESTOS DE FORMULA (I), DONDE R ES ARILO O HETEROCICLO SUSTITUIDOS O NO; R1 ES ALQUILO SUSTITUIDO O NO; R2 ES H, ALQUILO, CICLOALQUILO, ARILO,SUSTITUIDOS O NO, ARALQUILO, O HETEROCICLO SUSTITUIDO O NO, O BIEN R2 PUEDE ESTAR AUSENTE; X ES O, S, C(R3)2, C(R3)3, NR3 o N(R3)2; R3 ES H, ALQUILO O ARILO SUSTITUIDOS O NO, ARALQUILO, O HETEROCICLO SUSTITUIDOS O NO. SON COMPUESTOS PREFERIDOS: ESTER (3S)-3-MORFOLINILMETILICO DEL ACIDO [5-ETIL-4-[[(1-FENILMETIL)-1H-INDAZOL-5-IL]AMINO]PIRROLO[2,1-f][1,2,4]TRIAZINA-6-IL]-CARBAMICO, ESTER (2R)-2-PIRROLIDINILMETILICO DEL ACIDO [5-ETIL-4-[[(1-FENILMETIL)-1H-INDAZOL-5-IL]AMINO]PIRROLO[2,1-f][1,2,4]TRIAZINA-6-IL]-CARBAMICO, ESTER 3-[(3S)-3-HIDROXI-1-PIPERIDINIL]PROPILICO DEL ACIDO [5-ETIL-4-[[(1-FNILMETIL)-1H-INDAZOL-5-IL]AMINO]PIRROLO[2,1-f][1,2,4]TRIAZINA-6-IL]-CARBAMICO, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA QUE LO CONTIENE Y QUE PUEDE ESTAR COMBINADO CON AL MENOS OTRO AGENTE ANTI-CANCER O CITOTOXICO. ESTOS COMPUESTOS SON INHIBEN LA ACTIVIDAD DE LA TIROCINA CINASA DE LOS RECEPTORES DEL FACTOR DE CRECIMIENTO TALES COMO HER1, HER2, Y HER4, POR LO QUE SON UTILES PARA TRATAR ENFERMEDADES PROLIFERATIVAS, Y ENFERMEDADES ASOCIADAS CON LAS TRAYECTORIAS DE TRANSDUCCION DE SENAL QUE OPERAN A TRAVES DE LOS RECEPTORES DE CRECIMIENTO, COMO EL CANCER, PSORIASIS Y ATRITIS REUMATOIDE
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US43319002P | 2002-12-13 | 2002-12-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20040805A1 true PE20040805A1 (es) | 2004-11-20 |
Family
ID=32595133
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2003001275A PE20040805A1 (es) | 2002-12-13 | 2003-12-12 | Indazolilpirrolotriazinas c-6 modificadas |
Country Status (27)
Country | Link |
---|---|
US (2) | US6916815B2 (es) |
EP (1) | EP1569937B1 (es) |
JP (1) | JP4511367B2 (es) |
KR (1) | KR101073801B1 (es) |
CN (2) | CN1726216A (es) |
AR (1) | AR042450A1 (es) |
AT (1) | ATE534648T1 (es) |
AU (1) | AU2003300877B2 (es) |
BR (1) | BR0316755A (es) |
CA (1) | CA2509650C (es) |
CO (1) | CO5570660A2 (es) |
DK (1) | DK1569937T3 (es) |
ES (1) | ES2374393T3 (es) |
HR (1) | HRP20050535A2 (es) |
IS (1) | IS7890A (es) |
MX (1) | MXPA05006164A (es) |
NO (1) | NO20052733L (es) |
NZ (1) | NZ540338A (es) |
PE (1) | PE20040805A1 (es) |
PL (1) | PL377517A1 (es) |
PT (1) | PT1569937E (es) |
RS (1) | RS20050441A (es) |
RU (1) | RU2356903C2 (es) |
TW (1) | TW200420565A (es) |
UA (1) | UA80591C2 (es) |
WO (1) | WO2004054514A2 (es) |
ZA (1) | ZA200504507B (es) |
Families Citing this family (56)
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CA2273083C (en) * | 1996-12-03 | 2012-09-18 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto, analogues and uses thereof |
US7625859B1 (en) * | 2000-02-16 | 2009-12-01 | Oregon Health & Science University | HER-2 binding antagonists |
US7393823B1 (en) | 1999-01-20 | 2008-07-01 | Oregon Health And Science University | HER-2 binding antagonists |
US6867300B2 (en) | 2000-11-17 | 2005-03-15 | Bristol-Myers Squibb Company | Methods for the preparation of pyrrolotriazine compounds useful as kinase inhibitors |
US20090197852A9 (en) * | 2001-08-06 | 2009-08-06 | Johnson Robert G Jr | Method of treating breast cancer using 17-AAG or 17-AG or a prodrug of either in combination with a HER2 inhibitor |
AU2003221753A1 (en) | 2002-04-23 | 2003-11-10 | Bristol-Myers Squibb Company | Aryl ketone pyrrolo-triazine compounds useful as kinase inhibitors |
MXPA04010379A (es) | 2002-04-23 | 2005-02-17 | Squibb Bristol Myers Co | Compuestos de pirrolo-triazina anilina utiles como inhibidores de cinasa. |
TWI329112B (en) * | 2002-07-19 | 2010-08-21 | Bristol Myers Squibb Co | Novel inhibitors of kinases |
MXPA05002113A (es) | 2002-08-23 | 2005-06-03 | Sloan Kettering Inst Cancer | Sintesis de epotilonas, intermediarios para ellas, analogos y usos de los mismos. |
US7649006B2 (en) | 2002-08-23 | 2010-01-19 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
TW200420565A (en) * | 2002-12-13 | 2004-10-16 | Bristol Myers Squibb Co | C-6 modified indazolylpyrrolotriazines |
MXPA05008183A (es) | 2003-02-05 | 2005-10-05 | Bristol Myers Squibb Co | Proceso para preparar pirrolotriazina como inhibidores de cinasa. |
EP2633866A3 (en) * | 2003-10-17 | 2013-12-18 | Novo Nordisk A/S | Combination therapy |
US7102001B2 (en) | 2003-12-12 | 2006-09-05 | Bristol-Myers Squibb Company | Process for preparing pyrrolotriazine |
US20060014741A1 (en) * | 2003-12-12 | 2006-01-19 | Dimarco John D | Synthetic process, and crystalline forms of a pyrrolotriazine compound |
US7064203B2 (en) * | 2003-12-29 | 2006-06-20 | Bristol Myers Squibb Company | Di-substituted pyrrolotriazine compounds |
MY145634A (en) | 2003-12-29 | 2012-03-15 | Bristol Myers Squibb Co | Pyrrolotriazine compounds as kinase inhibitors |
US7102002B2 (en) * | 2004-06-16 | 2006-09-05 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
TW200600513A (en) * | 2004-06-30 | 2006-01-01 | Bristol Myers Squibb Co | A method for preparing pyrrolotriazine compounds |
US7253167B2 (en) * | 2004-06-30 | 2007-08-07 | Bristol-Myers Squibb Company | Tricyclic-heteroaryl compounds useful as kinase inhibitors |
US7102003B2 (en) * | 2004-07-01 | 2006-09-05 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds |
US7504521B2 (en) | 2004-08-05 | 2009-03-17 | Bristol-Myers Squibb Co. | Methods for the preparation of pyrrolotriazine compounds |
PE20060421A1 (es) | 2004-08-12 | 2006-06-01 | Bristol Myers Squibb Co | Procedimiento para preparar un compuesto de pirrolotriazina anilina como inhibidores de cinasa |
EP1807106A2 (en) * | 2004-10-05 | 2007-07-18 | Oregon Health and Science University | Compositions and methods for treating disease |
US7151176B2 (en) * | 2004-10-21 | 2006-12-19 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds |
EP1877439B1 (en) * | 2005-04-18 | 2011-02-09 | Novo Nordisk A/S | Il-21 variants |
US7405213B2 (en) * | 2005-07-01 | 2008-07-29 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds useful as kinase inhibitors and methods of treating kinase-associated conditions therewith |
US7402582B2 (en) * | 2005-07-01 | 2008-07-22 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds useful as kinase inhibitors and methods of treating kinase-associated conditions therewith |
WO2007035428A1 (en) | 2005-09-15 | 2007-03-29 | Bristol-Myers Squibb Company | Met kinase inhibitors |
US7547782B2 (en) | 2005-09-30 | 2009-06-16 | Bristol-Myers Squibb Company | Met kinase inhibitors |
US7514435B2 (en) * | 2005-11-18 | 2009-04-07 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
US7348325B2 (en) | 2005-11-30 | 2008-03-25 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
US8063208B2 (en) | 2006-02-16 | 2011-11-22 | Bristol-Myers Squibb Company | Crystalline forms of (3R,4R)-4-amino-1-[[4-[(3-methoxyphenyl)amino]pyrrolo[2,1-f][1,2,4]triazin-5-yl]methyl]piperidin-3-ol |
CN101395158A (zh) | 2006-03-07 | 2009-03-25 | 百时美施贵宝公司 | 可作为激酶抑制剂的吡咯并三嗪苯胺前体药物化合物 |
AU2007310777A1 (en) | 2006-10-26 | 2008-05-02 | Novo Nordisk A/S | IL-21 variants |
WO2008074863A1 (en) * | 2006-12-21 | 2008-06-26 | Novo Nordisk A/S | Interleukin-21 variants with altered binding to the il-21 receptor |
US20090083483A1 (en) * | 2007-09-24 | 2009-03-26 | International Business Machines Corporation | Power Conservation In A RAID Array |
US8166326B2 (en) * | 2007-11-08 | 2012-04-24 | International Business Machines Corporation | Managing power consumption in a computer |
US20090132842A1 (en) * | 2007-11-15 | 2009-05-21 | International Business Machines Corporation | Managing Computer Power Consumption In A Computer Equipment Rack |
US8041521B2 (en) * | 2007-11-28 | 2011-10-18 | International Business Machines Corporation | Estimating power consumption of computing components configured in a computing system |
EP2268637A1 (en) | 2008-04-04 | 2011-01-05 | Gilead Sciences, Inc. | Triazolopyridinone derivatives for use as stearoyl coa desaturase inhibitors |
EP2274308A1 (en) * | 2008-04-04 | 2011-01-19 | Gilead Sciences, Inc. | Pyrrolotriazinone derivatives for use as stearoyl coa desaturase inhibitors |
US20110086850A1 (en) * | 2008-04-11 | 2011-04-14 | Board Of Regents, The University Of Texas System | Radiosensitization of tumors with indazolpyrrolotriazines for radiotherapy |
US8103884B2 (en) | 2008-06-25 | 2012-01-24 | International Business Machines Corporation | Managing power consumption of a computer |
US8041976B2 (en) * | 2008-10-01 | 2011-10-18 | International Business Machines Corporation | Power management for clusters of computers |
US8514215B2 (en) * | 2008-11-12 | 2013-08-20 | International Business Machines Corporation | Dynamically managing power consumption of a computer with graphics adapter configurations |
EP2376491B1 (en) | 2008-12-19 | 2015-03-04 | Cephalon, Inc. | Pyrrolotriazines as alk and jak2 inhibitors |
JP2012520314A (ja) * | 2009-03-11 | 2012-09-06 | アムビト ビオスシエンセス コルポラチオン | 癌治療のためのインダゾリルアミノピロロトリアジンとタキサンの併用 |
WO2011112689A2 (en) | 2010-03-11 | 2011-09-15 | Ambit Biosciences Corp. | Saltz of an indazolylpyrrolotriazine |
CN103450204B (zh) | 2012-05-31 | 2016-08-17 | 中国科学院上海药物研究所 | 吡咯[2,1-f][1,2,4]并三嗪类化合物,其制备方法及用途 |
US9724352B2 (en) | 2012-05-31 | 2017-08-08 | Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences | Pyrrolo[2,1-F[1,2,4]triazine compounds, preparation methods and applications thereof |
US9050345B2 (en) * | 2013-03-11 | 2015-06-09 | Bristol-Myers Squibb Company | Pyrrolotriazines as potassium ion channel inhibitors |
US9458164B2 (en) * | 2013-03-11 | 2016-10-04 | Bristol-Myers Squibb Company | Pyrrolopyridazines as potassium ion channel inhibitors |
CN105026399B (zh) * | 2013-03-11 | 2017-06-23 | 百时美施贵宝公司 | 作为钾离子通道抑制剂的吡咯并三嗪类化合物 |
WO2015081783A1 (zh) * | 2013-12-06 | 2015-06-11 | 江苏奥赛康药业股份有限公司 | 吡咯并[2,1-f][1,2,4]三嗪类衍生物及其制备方法和用途 |
CN111533708B (zh) * | 2020-06-12 | 2021-03-16 | 上海馨远医药科技有限公司 | 一种手性n-叔丁氧羰基吗啉-3-羧酸的制备方法 |
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US4908056A (en) * | 1986-04-25 | 1990-03-13 | E. I. Du Pont De Nemours And Company | Heterocyclic acyl sulfonamides |
ES2200039T3 (es) | 1995-12-08 | 2004-03-01 | Pfizer Inc. | Derivados heterociclicos sustituidos como antagonistas de crf. |
ATE340176T1 (de) | 1996-08-28 | 2006-10-15 | Pfizer | Substituierte 6,5-heterobicyclische-derivate |
WO2000071129A1 (en) * | 1999-05-21 | 2000-11-30 | Bristol-Myers Squibb Company | Pyrrolotriazine inhibitors of kinases |
JP4623483B2 (ja) | 1999-08-23 | 2011-02-02 | 塩野義製薬株式会社 | sPLA2阻害作用を有するピロロトリアジン誘導体 |
BR0115446A (pt) * | 2000-11-17 | 2005-08-09 | Bristol Myers Squibb Co | Processos para tratamento de condições associadas a quinase p38 e compostos pirrolotriazina úteis como inibidores de quinase |
US6867300B2 (en) | 2000-11-17 | 2005-03-15 | Bristol-Myers Squibb Company | Methods for the preparation of pyrrolotriazine compounds useful as kinase inhibitors |
TW200300350A (en) | 2001-11-14 | 2003-06-01 | Bristol Myers Squibb Co | C-5 modified indazolylpyrrolotriazines |
MXPA04010379A (es) | 2002-04-23 | 2005-02-17 | Squibb Bristol Myers Co | Compuestos de pirrolo-triazina anilina utiles como inhibidores de cinasa. |
AU2003221753A1 (en) | 2002-04-23 | 2003-11-10 | Bristol-Myers Squibb Company | Aryl ketone pyrrolo-triazine compounds useful as kinase inhibitors |
TW200400034A (en) | 2002-05-20 | 2004-01-01 | Bristol Myers Squibb Co | Pyrazolo-pyrimidine aniline compounds useful as kinase inhibitors |
TWI329112B (en) | 2002-07-19 | 2010-08-21 | Bristol Myers Squibb Co | Novel inhibitors of kinases |
TW200420565A (en) * | 2002-12-13 | 2004-10-16 | Bristol Myers Squibb Co | C-6 modified indazolylpyrrolotriazines |
US7102001B2 (en) * | 2003-12-12 | 2006-09-05 | Bristol-Myers Squibb Company | Process for preparing pyrrolotriazine |
-
2003
- 2003-12-08 TW TW092134601A patent/TW200420565A/zh unknown
- 2003-12-12 PE PE2003001275A patent/PE20040805A1/es not_active Application Discontinuation
- 2003-12-12 EP EP03813396A patent/EP1569937B1/en not_active Expired - Lifetime
- 2003-12-12 MX MXPA05006164A patent/MXPA05006164A/es active IP Right Grant
- 2003-12-12 CA CA002509650A patent/CA2509650C/en not_active Expired - Fee Related
- 2003-12-12 DK DK03813396.3T patent/DK1569937T3/da active
- 2003-12-12 UA UAA200506891A patent/UA80591C2/uk unknown
- 2003-12-12 KR KR1020057010549A patent/KR101073801B1/ko not_active IP Right Cessation
- 2003-12-12 PT PT03813396T patent/PT1569937E/pt unknown
- 2003-12-12 JP JP2004560804A patent/JP4511367B2/ja not_active Expired - Fee Related
- 2003-12-12 AU AU2003300877A patent/AU2003300877B2/en not_active Ceased
- 2003-12-12 RS YUP-2005/0441A patent/RS20050441A/sr unknown
- 2003-12-12 PL PL377517A patent/PL377517A1/pl not_active Application Discontinuation
- 2003-12-12 BR BR0316755-0A patent/BR0316755A/pt not_active IP Right Cessation
- 2003-12-12 WO PCT/US2003/039542 patent/WO2004054514A2/en active Application Filing
- 2003-12-12 CN CNA200380105906XA patent/CN1726216A/zh active Pending
- 2003-12-12 AR ARP030104592A patent/AR042450A1/es unknown
- 2003-12-12 NZ NZ540338A patent/NZ540338A/en not_active IP Right Cessation
- 2003-12-12 RU RU2005120650/04A patent/RU2356903C2/ru not_active IP Right Cessation
- 2003-12-12 AT AT03813396T patent/ATE534648T1/de active
- 2003-12-12 CN CN200910246410A patent/CN101723948A/zh active Pending
- 2003-12-12 ES ES03813396T patent/ES2374393T3/es not_active Expired - Lifetime
- 2003-12-15 US US10/736,476 patent/US6916815B2/en not_active Expired - Fee Related
-
2005
- 2005-06-01 ZA ZA200504507A patent/ZA200504507B/en unknown
- 2005-06-02 US US11/143,279 patent/US7148220B2/en not_active Expired - Fee Related
- 2005-06-07 NO NO20052733A patent/NO20052733L/no not_active Application Discontinuation
- 2005-06-10 HR HR20050535A patent/HRP20050535A2/hr not_active Application Discontinuation
- 2005-06-10 IS IS7890A patent/IS7890A/is unknown
- 2005-06-13 CO CO05057043A patent/CO5570660A2/es not_active Application Discontinuation
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