AR045143A1 - Compuestos de indazol 3,5- distribuidos, composiciones farmaceuticas y metodos para intervenir en o inhibir la proliferacion celular - Google Patents
Compuestos de indazol 3,5- distribuidos, composiciones farmaceuticas y metodos para intervenir en o inhibir la proliferacion celularInfo
- Publication number
- AR045143A1 AR045143A1 ARP040102681A ARP040102681A AR045143A1 AR 045143 A1 AR045143 A1 AR 045143A1 AR P040102681 A ARP040102681 A AR P040102681A AR P040102681 A ARP040102681 A AR P040102681A AR 045143 A1 AR045143 A1 AR 045143A1
- Authority
- AR
- Argentina
- Prior art keywords
- cr5r6
- cr7r8
- cycloalkyl
- compounds
- cell proliferation
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Abstract
Se describen compuestos de indazol-3,5-disustituidos que modulan y/o inhiben la proliferación celular tal como la actividad de las proteínas cinasa. Estos compuestos y composiciones farmacéuticas que los contienen son capaces de intervenir en enfermedades de la CDK para modular y/o inhibir la proliferación celular no deseada. La presente también se dirige al uso terapéutico o profiláctico de composiciones farmacéuticas que contienen tales compuestos y a métodos para tratar el cáncer así como otras condiciones patológicas asociadas con angiogénesis y/o proliferación celular, no deseada, tales como: retinopatía, diabética, glaucoma neovascular, artritis reumatoide y soriasis, por administración de cantidades eficaces de tales compuestos. Reivindicación 1: Un compuesto o sal farmacéuticamente aceptable o solvato, de la fórmula (1), en la que R1, R2, R3 y R4 se seleccionan del grupo que consta de: H, halo, ciano, nitro, trifluormetoxi, trifluormetilo, azido, hidroxi, alcoxi C1-6, alquilo C1-10, alquenilo C2-6, alquinilo C2-6, -C(O)R5, -C(O)OR5, -OC(O)R5, -NR5C(O)R6, -C(O)NR5R6, -(CR5R6)NR7R8, -CR5R6NR7R8, -NR5OR6, -SO2NR5R6, -S(O)j(alquilo C1-6), en la que j es un número entero de 0 a 2, -(CR5R6)t(arilo C6-10), -(CR5R6)t(cicloalquilo C3-10), -C(CR5R6)t(grupo heterocíclico de 4-10 miembros), -(CR5R6)qC(O)(CR7R8)t(arilo C6-10), -(CR5R6)tC(O)(CR7R8)t(cicloalquilo C3-10), -(CR5R6)qC(O)(CR7R8)t(grupo heterocíclico de 4-10 miembros), -(CR5R6)tO(CR7R8)q(arilo C6-10), -(CR5R6)tO(CR7R8)q(cicloalquilo C3-10), -(CR5R6)tO(CR7R8)q(grupo heterocíclico de 4-10 miembros), -(CR5R6)qSO2(CR7R8)t(arilo C6-10), -(CR5R6)qSO2(CR7R8)t(cicloalquilo C3-10) y -(CR5R6)qSO2(CR7R8)t(grupo heterocíclico de 4-10 miembros), en los que q y t son cada uno independientemente un número entero de 0 a 5; 1 ó 2 átomos de carbono del anillo de los restos cicloalquilo o heterocíclico de los grupos R1, R2, R3 o R4 anteriores están opcionalmente sustituidos con un resto (=O) oxo, cada R5, R6, R7 y R8 se selecciona independientemente de: H, alquilo C1-6; y, en la que R1, R2, R3 y R4 no son H al mismos tiempo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US49147403P | 2003-07-30 | 2003-07-30 | |
US49207303P | 2003-07-31 | 2003-07-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR045143A1 true AR045143A1 (es) | 2005-10-19 |
Family
ID=34108010
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP040102681A AR045143A1 (es) | 2003-07-30 | 2004-07-28 | Compuestos de indazol 3,5- distribuidos, composiciones farmaceuticas y metodos para intervenir en o inhibir la proliferacion celular |
Country Status (24)
Country | Link |
---|---|
US (2) | US7008953B2 (es) |
EP (1) | EP1658284A1 (es) |
JP (1) | JP3920914B2 (es) |
KR (1) | KR20060030914A (es) |
AR (1) | AR045143A1 (es) |
AU (1) | AU2004259531A1 (es) |
BR (1) | BRPI0413051A (es) |
CA (1) | CA2532908A1 (es) |
CO (1) | CO5650247A2 (es) |
EA (1) | EA200600123A1 (es) |
EC (1) | ECSP066335A (es) |
IL (1) | IL172924A0 (es) |
IS (1) | IS8214A (es) |
MA (1) | MA27937A1 (es) |
MX (1) | MXPA06001193A (es) |
NL (1) | NL1026761C2 (es) |
NO (1) | NO20060319L (es) |
OA (1) | OA13196A (es) |
PA (1) | PA8608201A1 (es) |
PE (1) | PE20050330A1 (es) |
TN (1) | TNSN06038A1 (es) |
TW (1) | TW200521124A (es) |
UY (1) | UY28442A1 (es) |
WO (1) | WO2005009997A1 (es) |
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US10653688B2 (en) | 2017-10-27 | 2020-05-19 | Samumed, Llc | 6-(6-membered heteroaryl and aryl)isoquinolin-3-yl carboxamides and preparation and use thereof |
WO2019084496A1 (en) | 2017-10-27 | 2019-05-02 | Samumed, Llc | 6- (HETEROARYL 5-CHAIN) ISOQUINOLIN-3-YL- (HETEROARYL 5-CHAIN) CARBOXAMIDES, PREPARATION AND USE |
WO2019089835A1 (en) | 2017-10-31 | 2019-05-09 | Samumed, Llc | Diazanaphthalen-3-yl carboxamides and preparation and use thereof |
KR20200126393A (ko) | 2018-02-23 | 2020-11-06 | 사뮤메드, 엘엘씨 | 5-헤테로아릴 치환된 인다졸-3-카복사미드 및 그의 제조 및 용도 |
WO2019241540A1 (en) | 2018-06-15 | 2019-12-19 | Samumed, Llc | Indazole containing macrocycles and therapeutic uses thereof |
WO2020150545A1 (en) | 2019-01-17 | 2020-07-23 | Samumed, Llc | Pyrazole derivatives as modulators of the wnt/b-catenin signaling pathway |
WO2021168341A1 (en) | 2020-02-21 | 2021-08-26 | Samumed, Llc | Solid forms of 1-(5-(3-(7-(3-fluorophenyl)-3h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridin-5-yl)pyridin-3-yl)-n,n-dimethylmethanamine |
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GB1376600A (en) | 1971-02-15 | 1974-12-04 | Agfa Gevaert | Photographic developer compositions |
FR2265739B1 (es) | 1974-03-29 | 1976-12-17 | Ugine Kuhlmann | |
JPS5615287A (en) | 1979-07-16 | 1981-02-14 | Chugai Pharmaceut Co Ltd | Pyrazoloindazole derivative and its preparation |
JPS57109787A (en) | 1980-12-26 | 1982-07-08 | Chugai Pharmaceut Co Ltd | Pyrazoloindazole derivative |
JPS59228248A (ja) | 1983-06-08 | 1984-12-21 | Konishiroku Photo Ind Co Ltd | 直接ポジ用ハロゲン化銀写真感光材料 |
JPS604184A (ja) | 1983-06-23 | 1985-01-10 | Chugai Pharmaceut Co Ltd | ピラゾロインダゾ−ル誘導体 |
DE3842091A1 (de) | 1987-12-14 | 1989-07-13 | Fuji Photo Film Co Ltd | Bilderzeugungsverfahren |
US5208248A (en) | 1991-01-11 | 1993-05-04 | Merck Sharpe & Dohme, Ltd. | Indazole-substituted five-membered heteroaromatic compounds |
EP0494774A1 (en) | 1991-01-11 | 1992-07-15 | MERCK SHARP & DOHME LTD. | Indazole-substituted fivemembered heteroaromatic compounds |
NZ243065A (en) | 1991-06-13 | 1995-07-26 | Lundbeck & Co As H | Piperidine derivatives and pharmaceutical compositions |
ZA951822B (en) | 1994-12-23 | 1996-09-26 | Glaxo Group Ltd | Chemical compounds |
ATE225343T1 (de) | 1995-12-20 | 2002-10-15 | Hoffmann La Roche | Matrix-metalloprotease inhibitoren |
EP0818442A3 (en) | 1996-07-12 | 1998-12-30 | Pfizer Inc. | Cyclic sulphone derivatives as inhibitors of metalloproteinases and of the production of tumour necrosis factor |
HRP970371A2 (en) | 1996-07-13 | 1998-08-31 | Kathryn Jane Smith | Heterocyclic compounds |
AU6870098A (en) | 1997-03-31 | 1998-10-22 | Du Pont Merck Pharmaceutical Company, The | Indazoles of cyclic ureas useful as hiv protease inhibitors |
FR2767475A1 (fr) | 1997-08-25 | 1999-02-26 | Oreal | Compositions de teinture des fibres keratiniques contenant des derives d'indazoles et procede |
EP1140182A2 (en) | 1998-12-23 | 2001-10-10 | G.D. Searle & Co. | Use of a matrix metalloproteinase inhibitor together with an antineoplastic agent, optionally also together with radiation, in the treatment of neoplasia |
GB2345486A (en) | 1999-01-11 | 2000-07-12 | Glaxo Group Ltd | Heteroaromatic protein tyrosine kinase inhibitors |
YU54202A (sh) | 2000-01-18 | 2006-01-16 | Agouron Pharmaceuticals Inc. | Jedinjenja indazola, farmaceutske smeše i postupci za stimulisanje i inhibiranje ćelijske proliferacije |
KR100423899B1 (ko) | 2000-05-10 | 2004-03-24 | 주식회사 엘지생명과학 | 세포 증식 억제제로 유용한 1,1-디옥소이소티아졸리딘을갖는 인다졸 |
US6897231B2 (en) | 2000-07-31 | 2005-05-24 | Signal Pharmaceuticals, Inc. | Indazole derivatives as JNK inhibitors and compositions and methods related thereto |
WO2003004488A1 (en) | 2001-07-03 | 2003-01-16 | Chiron Corporation | Indazole benzimidazole compounds as tyrosine and serine/threonine kinase inhibitors |
FR2831536A1 (fr) | 2001-10-26 | 2003-05-02 | Aventis Pharma Sa | Nouveaux derives de benzimidazoles, leur procede de preparation, leur application a titre de medicament, compositions pharmaceutiques et nouvelle utilisation notamment comme inhibiteurs de kdr |
US7008953B2 (en) * | 2003-07-30 | 2006-03-07 | Agouron Pharmaceuticals, Inc. | 3, 5 Disubstituted indazole compounds, pharmaceutical compositions, and methods for mediating or inhibiting cell proliferation |
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2004
- 2004-06-10 US US10/866,059 patent/US7008953B2/en not_active Expired - Fee Related
- 2004-07-19 OA OA1200600024A patent/OA13196A/fr unknown
- 2004-07-19 BR BRPI0413051-0A patent/BRPI0413051A/pt not_active IP Right Cessation
- 2004-07-19 CA CA002532908A patent/CA2532908A1/en not_active Abandoned
- 2004-07-19 WO PCT/IB2004/002441 patent/WO2005009997A1/en not_active Application Discontinuation
- 2004-07-19 KR KR1020067001916A patent/KR20060030914A/ko active IP Right Grant
- 2004-07-19 EP EP04744094A patent/EP1658284A1/en not_active Withdrawn
- 2004-07-19 MX MXPA06001193A patent/MXPA06001193A/es unknown
- 2004-07-19 AU AU2004259531A patent/AU2004259531A1/en not_active Abandoned
- 2004-07-19 EA EA200600123A patent/EA200600123A1/ru unknown
- 2004-07-19 JP JP2006521699A patent/JP3920914B2/ja not_active Expired - Fee Related
- 2004-07-23 PE PE2004000713A patent/PE20050330A1/es not_active Application Discontinuation
- 2004-07-27 PA PA20048608201A patent/PA8608201A1/es unknown
- 2004-07-27 UY UY28442A patent/UY28442A1/es not_active Application Discontinuation
- 2004-07-28 AR ARP040102681A patent/AR045143A1/es unknown
- 2004-07-29 TW TW093122761A patent/TW200521124A/zh unknown
- 2004-07-30 NL NL1026761A patent/NL1026761C2/nl not_active IP Right Cessation
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2005
- 2005-09-26 US US11/237,446 patent/US20060142345A1/en not_active Abandoned
- 2005-12-29 CO CO05130968A patent/CO5650247A2/es not_active Application Discontinuation
- 2005-12-29 IL IL172924A patent/IL172924A0/en unknown
- 2005-12-30 IS IS8214A patent/IS8214A/is unknown
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- 2006-01-30 EC EC2006006335A patent/ECSP066335A/es unknown
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- 2006-01-30 TN TNP2006000038A patent/TNSN06038A1/fr unknown
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EA200600123A1 (ru) | 2006-06-30 |
MA27937A1 (fr) | 2006-06-01 |
US7008953B2 (en) | 2006-03-07 |
US20050026960A1 (en) | 2005-02-03 |
OA13196A (en) | 2006-12-13 |
CO5650247A2 (es) | 2006-06-30 |
IL172924A0 (en) | 2006-06-11 |
PA8608201A1 (es) | 2005-03-03 |
TW200521124A (en) | 2005-07-01 |
ECSP066335A (es) | 2006-07-28 |
KR20060030914A (ko) | 2006-04-11 |
IS8214A (is) | 2005-12-30 |
CA2532908A1 (en) | 2005-02-03 |
JP2007500183A (ja) | 2007-01-11 |
NO20060319L (no) | 2006-02-24 |
WO2005009997A1 (en) | 2005-02-03 |
AU2004259531A1 (en) | 2005-02-03 |
UY28442A1 (es) | 2005-02-28 |
NL1026761A1 (nl) | 2005-02-01 |
EP1658284A1 (en) | 2006-05-24 |
US20060142345A1 (en) | 2006-06-29 |
TNSN06038A1 (fr) | 2007-10-03 |
NL1026761C2 (nl) | 2005-10-18 |
BRPI0413051A (pt) | 2006-10-17 |
PE20050330A1 (es) | 2005-05-16 |
MXPA06001193A (es) | 2006-04-11 |
JP3920914B2 (ja) | 2007-05-30 |
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