AR037714A1 - Derivados de tiazolidinona y oxazolidinona 2-sustituidos para la inhibicion de fosfatasas y el tratamiento de cancer - Google Patents
Derivados de tiazolidinona y oxazolidinona 2-sustituidos para la inhibicion de fosfatasas y el tratamiento de cancerInfo
- Publication number
- AR037714A1 AR037714A1 ARP020104721A ARP020104721A AR037714A1 AR 037714 A1 AR037714 A1 AR 037714A1 AR P020104721 A ARP020104721 A AR P020104721A AR P020104721 A ARP020104721 A AR P020104721A AR 037714 A1 AR037714 A1 AR 037714A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- carbon atoms
- cancer
- compounds
- treatment
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/54—Nitrogen and either oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
Abstract
La presente se refiere a ciertos heterociclos sustituidos, incluyendo a los compuestos de tiazolidinona 2-sustituida y oxazolidinona 2-sustituida. Estos compuestos son útiles para el tratamiento de enfermedades relacionadas con la proliferación celular no controlada, como por ejemplo, el cáncer o las condiciones pre-cancerígenas. Los compuestos también son útiles para modular el metabolismo de los lípidos y/o carbohidratos, y tratar la diabetes Tipo ll, hiperglicemia u obesidad, y para tratar enfermedades inflamatorias como por ejemplo, la artritis. Reivindicación (1): un compuesto que tiene la estructura de fórmula (1) o (2) donde: a) Ar1 tiene la siguiente estructura de fórmula (3): donde R10 es un radical orgánico que tiene de 1 a 12 átomos de carbono, y R11, R12, R13 y R14 se seleccionan, de manera independiente, de hidrógeno, radicales inorgánicos o radicales orgánicos que tienen de 1 a 10 átomos de carbono. B) Ar2 tiene de 4 a 30 átomos de carbono y un radical arilo, arilo sustituido, heteroarilo, o heteroarilo sustituido; c) R1 es hidrogeno, hidroxi, alcoxi, alquilo o alquilo sustituido; d) la línea punteada representa un enlace presente o ausente; e) W es -S- o -O-; f) X es -S- o -O-; y g) Y es un radical orgánico que comprende de 1 a 15 átomos de carbono; o su sal aceptable para uso farmacéutico.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US33719501P | 2001-12-06 | 2001-12-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR037714A1 true AR037714A1 (es) | 2004-12-01 |
Family
ID=23319498
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP020104721A AR037714A1 (es) | 2001-12-06 | 2002-12-05 | Derivados de tiazolidinona y oxazolidinona 2-sustituidos para la inhibicion de fosfatasas y el tratamiento de cancer |
Country Status (7)
Country | Link |
---|---|
US (1) | US20040097566A1 (es) |
EP (1) | EP1463718A1 (es) |
AR (1) | AR037714A1 (es) |
AU (1) | AU2002357098A1 (es) |
CA (1) | CA2469342A1 (es) |
TW (1) | TW200304375A (es) |
WO (1) | WO2003050098A1 (es) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MXPA02002257A (es) | 1999-08-31 | 2002-09-30 | Maxia Pharmaceuticals Inc | Bencilideno-tiazolidinadionas y analogos y su uso en el tratamiento de la diabetes. |
CA2440184A1 (en) * | 2001-03-07 | 2002-09-19 | Incyte San Diego, Inc. | Heterocyclic derivatives for the treatment of cancer and other proliferative diseases |
EP1377559A4 (en) * | 2001-03-08 | 2005-09-28 | Incyte San Diego Inc | MOLECULES ACTIVATING AN RXR RECEPTOR |
US20030083357A1 (en) * | 2001-08-17 | 2003-05-01 | Magnus Pfahl | Oxime derivatives for the treatment of dyslipidemia and hypercholesteremia |
FR2834289B1 (fr) | 2001-12-27 | 2004-03-19 | Sod Conseils Rech Applic | Derives de benzothiazole-4,7-diones et benzooxazole-4,7- diones, leur preparation et leurs applications therapeutiques |
US7196108B2 (en) * | 2002-03-08 | 2007-03-27 | Incyte San Diego Inc. | Bicyclic heterocycles for the treatment of diabetes and other diseases |
US7102000B2 (en) * | 2002-03-08 | 2006-09-05 | Incyte San Diego Inc. | Heterocyclic amide derivatives for the treatment of diabetes and other diseases |
NZ539873A (en) * | 2002-11-22 | 2008-09-26 | Smithkline Beecham Corp | Novel chemical compounds, thiazolidin-4-one, thiazol-4-one |
US20040167192A1 (en) * | 2003-01-16 | 2004-08-26 | David Solow-Cordero | Methods of treating conditions associated with an Edg-7 receptor |
US20050038098A1 (en) * | 2003-04-18 | 2005-02-17 | Catherine Tachdjian | Substituted dihydronaphthalene and isochroman compounds for the treatment of metabolic disorders, cancer and other diseases |
FR2856688B1 (fr) * | 2003-06-25 | 2008-05-30 | Sod Conseils Rech Applic | PRODUIT COMPRENANT AU MOINS UN INHIBITEUR DE PHOSPHATASE CDc25 EN ASSOCIATION AVEC AU MOINS UN AUTRE AGENT ANTI-CANCEREUX |
CN100453533C (zh) * | 2003-12-12 | 2009-01-21 | 中国科学院上海药物研究所 | 一类胰高血糖样肽-1受体激动剂及其制备方法和用途 |
CA2568186C (en) * | 2004-05-24 | 2011-11-15 | Amgen Inc. | Inhibitors of 11-beta-hydroxy steroid dehydrogenase type 1 |
US8686011B2 (en) | 2004-05-24 | 2014-04-01 | Amgen Inc. | Inhibitors of 11-β-hydroxy steroid dehydrogenase type 1 |
US7122700B2 (en) | 2004-07-30 | 2006-10-17 | Xerox Corporation | Arylamine processes |
DE102004051277A1 (de) * | 2004-10-21 | 2006-04-27 | Merck Patent Gmbh | Heterocyclische Carbonylverbindungen |
FR2877667B1 (fr) | 2004-11-05 | 2007-03-23 | Sod Conseils Rech Applic | Derives de 4,7-dioxobenzothiazole-2-carboxamides, leur preparation et leurs applications therapeutiques |
FR2879598B1 (fr) | 2004-12-17 | 2007-03-30 | Sod Conseils Rech Applic | Inhibiteurs de phosphatases cdc25 |
TW200716580A (en) * | 2005-06-08 | 2007-05-01 | Smithkline Beecham Corp | (5Z)-5-(6-quinoxalinylmethylidene)-2-[(2,6-dichlorophenyl)amino]-1,3-thiazol-4(5H)-one |
KR100814109B1 (ko) | 2006-01-09 | 2008-03-14 | 한국생명공학연구원 | 로다닌 유도체, 이의 제조방법 및 이를 유효성분으로함유하는 약학적 조성물 |
LV13736B (en) * | 2006-12-28 | 2008-09-20 | Vjaceslavs Tribulovics | Method for manufacturing 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphtoic acid |
US20100286041A1 (en) * | 2007-03-22 | 2010-11-11 | Smithkline Beecham Corporation | (5z)-5-(6-quinoxalinylmethylidene)-2-[(2,6-dichlorophenyl)amino]-1,3-thiazol-4(5h)-one |
US20100249165A1 (en) * | 2007-06-08 | 2010-09-30 | University Of Copenhagen | Pdz domain modulators |
CL2009000294A1 (es) * | 2008-02-08 | 2009-10-23 | Shlorion Pharma Inc | Compuestos derivados de heterociclos aril metilideno; composicion farmaceutica que los comprende; y uso en el tratamiento del dolor neuropatico e inflamacion. |
AU2009304598B2 (en) | 2008-10-17 | 2015-01-29 | Akaal Pharma Pty Ltd | S1P receptors modulators and their use thereof |
AU2009304596A1 (en) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | S1P receptors modulators |
CN102558088A (zh) * | 2010-12-31 | 2012-07-11 | 中国科学院上海药物研究所 | 联苯亚甲基-2-硫代-4-噻唑酮类化合物及其制备方法和用途 |
ES2769181T3 (es) | 2013-03-14 | 2020-06-24 | Dart Neuroscience Cayman Ltd | Compuestos de piridina y de pirazina sustituidos como inhibidores de PDE4 |
CN110746429B (zh) * | 2018-12-10 | 2022-11-25 | 广州华睿光电材料有限公司 | 含金刚烷的化合物、高聚物、混合物、组合物及电子器件 |
CN110698426B (zh) * | 2019-11-04 | 2022-08-23 | 陕西师范大学 | 叔丁醇钾高效催化制备1,3-苯并噻唑衍生物的方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE345332T1 (de) * | 1999-11-12 | 2006-12-15 | Fujimoto Brothers Co Ltd | 2-(n-cyanimino)thiazolidin-4-on derivate |
-
2002
- 2002-12-05 TW TW091135299A patent/TW200304375A/zh unknown
- 2002-12-05 AR ARP020104721A patent/AR037714A1/es not_active Application Discontinuation
- 2002-12-06 AU AU2002357098A patent/AU2002357098A1/en not_active Abandoned
- 2002-12-06 WO PCT/US2002/039178 patent/WO2003050098A1/en not_active Application Discontinuation
- 2002-12-06 CA CA002469342A patent/CA2469342A1/en not_active Abandoned
- 2002-12-06 US US10/313,341 patent/US20040097566A1/en not_active Abandoned
- 2002-12-06 EP EP02804747A patent/EP1463718A1/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
AU2002357098A1 (en) | 2003-06-23 |
TW200304375A (en) | 2003-10-01 |
WO2003050098A1 (en) | 2003-06-19 |
EP1463718A1 (en) | 2004-10-06 |
US20040097566A1 (en) | 2004-05-20 |
CA2469342A1 (en) | 2003-06-19 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |