CU20110190A7 - Análogos de isoxazol-3(2h)-ona como agentes terapéuticos - Google Patents
Análogos de isoxazol-3(2h)-ona como agentes terapéuticosInfo
- Publication number
- CU20110190A7 CU20110190A7 CU20110190A CU20110190A CU20110190A7 CU 20110190 A7 CU20110190 A7 CU 20110190A7 CU 20110190 A CU20110190 A CU 20110190A CU 20110190 A CU20110190 A CU 20110190A CU 20110190 A7 CU20110190 A7 CU 20110190A7
- Authority
- CU
- Cuba
- Prior art keywords
- alkyl
- optionally substituted
- aryl
- heteroaryl
- atoms
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4525—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Abstract
Un compuesto de fórmula I ESPACIO PARA LA FÓRMULA o una sal farmacéuticamente aceptable de este, donde R1 y R2 son independientemente hidrógeno, deuterio, arilo, heteroarilo, alquilo C1-C8, y están opcionalmente sustituidos con uno o más sustituyentes que son independientemente R3, R3 es un arilo, heteroarilo, uno o más átomos de flúor, un alquilo C1-C6 que contiene uno o más átomos de flúor, un alquilo C1-C6 que contiene uno o más átomos de deuterio, un alquilo C1-C6 que contiene hidroxi, estando el arilo y el heteroarilo opcionalmente sustituidos con uno o más halógenos, un alcoxi fluorado, un alquilo fluorado, un sulfonilo, uno o más átomos de deuterio, un alquilo C1-C6, un alcoxi C1-C6, un nitrilo, o R3 es un alquilo C1-C6 opcionalmente sustituido con uno o más de los siguientes grupos: COOR4, OCOR4, CONR5R6, NR5COR6, OR4; donde R4 es un alquilo C1-C10 opcionalmente sustituido con uno o más átomos de flúor, deuterio, alcoxi, carboxilato de arilo, carboxilato de alquilo; R5 y R6 se seleccionan independientemente entre hidrógeno, alquilo o pueden formar conjuntamente un anillo de carbono de 4-8 miembros; o R1 y R2 forman un anillo de carbono de 3-10 miembros que comprende opcionalmente O ó N y está opcionalmente sustituido con un alquilo o arilo C1-C10, heteroarilo opcionalmente sustituido con R3.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16722409P | 2009-04-07 | 2009-04-07 | |
US17195609P | 2009-04-23 | 2009-04-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
CU20110190A7 true CU20110190A7 (es) | 2012-02-15 |
Family
ID=42934883
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CU20110190A CU20110190A7 (es) | 2009-04-07 | 2011-10-07 | Análogos de isoxazol-3(2h)-ona como agentes terapéuticos |
Country Status (21)
Country | Link |
---|---|
US (1) | US8415378B2 (es) |
EP (1) | EP2417131A4 (es) |
JP (1) | JP5711723B2 (es) |
KR (1) | KR101675607B1 (es) |
CN (1) | CN102459246B (es) |
AR (1) | AR076219A1 (es) |
AU (1) | AU2010235236B2 (es) |
BR (1) | BRPI1013984A2 (es) |
CA (1) | CA2757879C (es) |
CO (1) | CO6440580A2 (es) |
CU (1) | CU20110190A7 (es) |
EA (1) | EA020825B1 (es) |
EC (1) | ECSP11011385A (es) |
IL (1) | IL215336A0 (es) |
MX (1) | MX2011010647A (es) |
NI (1) | NI201100181A (es) |
SG (1) | SG174463A1 (es) |
TW (1) | TW201040166A (es) |
UY (1) | UY32543A (es) |
WO (1) | WO2010117323A1 (es) |
ZA (1) | ZA201108119B (es) |
Families Citing this family (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8536186B2 (en) | 2008-08-04 | 2013-09-17 | Chdi Foundation, Inc. | Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
US8883785B2 (en) | 2010-01-25 | 2014-11-11 | Chdi Foundation, Inc. | Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
WO2012047156A1 (en) * | 2010-10-04 | 2012-04-12 | Astrazeneca Ab | Isoxazol-3(2h)-one analogs as plasminogen inhibitors and their use in the treatment of fibrinolysis related diseases |
US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
PT2750677T (pt) | 2011-08-30 | 2017-07-03 | Chdi Foundation Inc | Inibidores de quinurenina-3-monooxigenase, composições farmacêuticas e métodos de utilização dos mesmos |
KR20140072037A (ko) | 2011-08-30 | 2014-06-12 | 씨에이치디아이 파운데이션, 인코포레이티드 | 키뉴레닌-3-모노옥시게나제 억제제, 약학적 조성물 및 이의 사용 방법 |
US9073881B2 (en) | 2011-09-23 | 2015-07-07 | Hoffmann-La Roche Inc. | Benzoic acid derivatives |
EP3822273B1 (en) | 2012-06-13 | 2024-04-10 | Incyte Holdings Corporation | Substituted tricyclic compounds as fgfr inhibitors |
WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
CN102977050B (zh) * | 2012-11-20 | 2015-04-22 | 浙江工业大学 | 一种2-苯并噻唑二甲缩醛和2-苯并噻唑甲醛的合成方法 |
CN102977040B (zh) * | 2012-11-20 | 2015-06-03 | 浙江工业大学 | 一种2-喹喔啉基二甲缩醛和2-喹喔啉基甲醛的合成方法 |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
SG10201708520YA (en) | 2013-04-19 | 2017-12-28 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
UY35809A (es) | 2013-11-05 | 2015-05-29 | Bayer Pharma AG | (aza)piridopirazolopirimidinonas e indazolopirimidinonas y sus usos |
KR20170026633A (ko) | 2014-07-17 | 2017-03-08 | 씨에이치디아이 파운데이션, 인코포레이티드 | Hiv-관련 장애의 치료 방법 및 치료용 조성물 |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
JP2017533235A (ja) | 2014-11-03 | 2017-11-09 | バイエル ファーマ アクチエンゲゼルシャフト | ピペリジニルピラゾロピリミジノン類及びそれらの使用 |
EP3233189A1 (en) | 2014-12-19 | 2017-10-25 | Emeriti Pharma AB | 3-(piperidin-4-yl)-isoxazol-3(2h)-ones for treatment of dermatologic disorders |
MX2017010673A (es) | 2015-02-20 | 2018-03-21 | Incyte Corp | Heterociclos biciclicos como inhibidores de receptores del factor de crecimiento fibroblastico (fgfr). |
WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
CN104725300A (zh) * | 2015-02-28 | 2015-06-24 | 宁波九胜创新医药科技有限公司 | 一种1-(6-甲基吡啶-3-基)-2-(4-甲磺酰基苯基)乙酮的制备方法 |
WO2016173948A1 (en) | 2015-04-30 | 2016-11-03 | Bayer Pharma Aktiengesellschaft | Indazolopyrimidinones as fibrinolysis inhibitors |
CN107459514B (zh) * | 2016-06-06 | 2020-10-23 | 南开大学 | 一类手性哌啶衍生物及其制备方法和用途 |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
CN107857725A (zh) * | 2017-12-19 | 2018-03-30 | 苏州艾缇克药物化学有限公司 | 一种2‑氨基吡啶‑4‑甲醇的合成方法 |
CN112867716A (zh) | 2018-05-04 | 2021-05-28 | 因赛特公司 | Fgfr抑制剂的固体形式和其制备方法 |
CN112566912A (zh) | 2018-05-04 | 2021-03-26 | 因赛特公司 | Fgfr抑制剂的盐 |
WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
AU2020366006A1 (en) | 2019-10-14 | 2022-04-21 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
EP4069696A1 (en) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
KR20220131900A (ko) | 2019-12-04 | 2022-09-29 | 인사이트 코포레이션 | Fgfr 억제제의 유도체 |
TWI803177B (zh) * | 2021-02-05 | 2023-05-21 | 大陸商賽諾哈勃藥業(成都)有限公司 | 一種纖維蛋白溶酶抑制劑、其製備方法及應用 |
US11939331B2 (en) | 2021-06-09 | 2024-03-26 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995014683A1 (en) | 1993-11-24 | 1995-06-01 | The Du Pont Merck Pharmaceutical Company | Novel isoxazoline and isoxazole fibrinogen receptor antagonists |
CA2345210A1 (en) | 1998-11-18 | 2000-05-25 | Prabhakar Kondaji Judhav | Novel isoxazoline fibrinogen receptor antagonists |
US20030207873A1 (en) * | 2002-04-10 | 2003-11-06 | Edmund Harrington | Inhibitors of Src and other protein kinases |
NZ543287A (en) * | 2003-04-15 | 2008-08-29 | Merck & Co Inc | Benzoxazinyl-amidocyclopentyl-heterocyclic modulators of chemokine receptors |
US7598243B2 (en) * | 2003-04-17 | 2009-10-06 | Merck & Co., Inc. | Heterocyclic cyclopentyl tetrahydroisoquinoline and tetrahydropyridopyridine modulators of chemokine receptor activity |
CN101328173B (zh) * | 2008-07-31 | 2010-12-15 | 石药集团欧意药业有限公司 | 一种制备6-氟-3-(4-哌啶基)-1,2-苯并异噁唑盐酸盐的方法 |
-
2010
- 2010-04-06 US US12/755,010 patent/US8415378B2/en not_active Expired - Fee Related
- 2010-04-06 CN CN201080025847.5A patent/CN102459246B/zh not_active Expired - Fee Related
- 2010-04-06 BR BRPI1013984A patent/BRPI1013984A2/pt not_active Application Discontinuation
- 2010-04-06 MX MX2011010647A patent/MX2011010647A/es active IP Right Grant
- 2010-04-06 TW TW099110636A patent/TW201040166A/zh unknown
- 2010-04-06 EP EP10761933.0A patent/EP2417131A4/en not_active Withdrawn
- 2010-04-06 EA EA201190237A patent/EA020825B1/ru not_active IP Right Cessation
- 2010-04-06 AU AU2010235236A patent/AU2010235236B2/en not_active Ceased
- 2010-04-06 SG SG2011067568A patent/SG174463A1/en unknown
- 2010-04-06 CA CA2757879A patent/CA2757879C/en not_active Expired - Fee Related
- 2010-04-06 UY UY0001032543A patent/UY32543A/es not_active Application Discontinuation
- 2010-04-06 KR KR1020117026407A patent/KR101675607B1/ko active IP Right Grant
- 2010-04-06 WO PCT/SE2010/050375 patent/WO2010117323A1/en active Application Filing
- 2010-04-06 JP JP2012504655A patent/JP5711723B2/ja not_active Expired - Fee Related
- 2010-04-07 AR ARP100101162A patent/AR076219A1/es unknown
-
2011
- 2011-09-22 IL IL215336A patent/IL215336A0/en unknown
- 2011-10-06 CO CO11132448A patent/CO6440580A2/es not_active Application Discontinuation
- 2011-10-07 CU CU20110190A patent/CU20110190A7/es unknown
- 2011-10-07 EC EC2011011385A patent/ECSP11011385A/es unknown
- 2011-10-07 NI NI201100181A patent/NI201100181A/es unknown
- 2011-11-04 ZA ZA2011/08119A patent/ZA201108119B/en unknown
Also Published As
Publication number | Publication date |
---|---|
NI201100181A (es) | 2012-06-14 |
KR20120034611A (ko) | 2012-04-12 |
EP2417131A4 (en) | 2014-08-27 |
CA2757879C (en) | 2017-06-06 |
EA201190237A1 (ru) | 2012-04-30 |
MX2011010647A (es) | 2012-02-21 |
SG174463A1 (en) | 2011-10-28 |
AU2010235236A1 (en) | 2011-10-20 |
CA2757879A1 (en) | 2010-10-14 |
WO2010117323A1 (en) | 2010-10-14 |
EP2417131A1 (en) | 2012-02-15 |
EA020825B1 (ru) | 2015-02-27 |
BRPI1013984A2 (pt) | 2018-06-19 |
KR101675607B1 (ko) | 2016-11-11 |
US8415378B2 (en) | 2013-04-09 |
ECSP11011385A (es) | 2011-11-30 |
JP2012522836A (ja) | 2012-09-27 |
CO6440580A2 (es) | 2012-05-15 |
ZA201108119B (en) | 2012-07-25 |
AR076219A1 (es) | 2011-05-26 |
TW201040166A (en) | 2010-11-16 |
CN102459246A (zh) | 2012-05-16 |
IL215336A0 (en) | 2011-12-29 |
AU2010235236B2 (en) | 2013-10-24 |
JP5711723B2 (ja) | 2015-05-07 |
US20100261755A1 (en) | 2010-10-14 |
CN102459246B (zh) | 2014-05-07 |
UY32543A (es) | 2010-11-30 |
WO2010117323A8 (en) | 2010-11-18 |
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