CO5640137A2 - N-pirazinil-fenilsulfonamidas y su uso en el tratamiento de enfermedades mediadas por quimosina - Google Patents
N-pirazinil-fenilsulfonamidas y su uso en el tratamiento de enfermedades mediadas por quimosinaInfo
- Publication number
- CO5640137A2 CO5640137A2 CO04067437A CO04067437A CO5640137A2 CO 5640137 A2 CO5640137 A2 CO 5640137A2 CO 04067437 A CO04067437 A CO 04067437A CO 04067437 A CO04067437 A CO 04067437A CO 5640137 A2 CO5640137 A2 CO 5640137A2
- Authority
- CO
- Colombia
- Prior art keywords
- alkyl
- hydroxy
- halogen
- optionally substituted
- cyano
- Prior art date
Links
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- -1 CO2R12 Chemical group 0.000 abstract 1
- 101100240518 Caenorhabditis elegans nhr-12 gene Proteins 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 235000019000 fluorine Nutrition 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
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- Health & Medical Sciences (AREA)
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Abstract
1.- Un compuesto de la fórmula (I) o una sal o solvato farmacéuticamente aceptable del mismo: en donde:R1, R2 y R3 son, independientemente, hidrógeno, halógeno, ciano, CF3, OCF3, alquilo OC1-6 O alquilo C1-6 ;R4 es halógeno, CO2R12 ,aIcoxi C1-6 en donde el grupo alquilo puede formar un anillo saturado de 3-6 miembros o puede estar sustituido con 1-3 átomos de flúor o un grupo ciano, oxialquenilo C1-6 u oxialquinilo C1-6 en donde cualquiera puede estar opcionalmente sustituido con hidroxi o NR14R15,O-alquilo C1-6 X-alquilo C1-6 en donde los grupos alquilo pueden formar un anillo saturado de 3-6 miembros,O-alquilo1-6 R11 u O-alquilo C2-6 -X-R11 en donde el grupo alquilo puede formar un anillo saturado de 3-6 miembros y está opcionalmente sustituido con 1-3 grupos escogidos entre hidroxi, halógeno, NR14R15, SR13, S(O)2R13, S(O)R13 o COR13 ,O-alquiloC1-6 R16 ;R5 y R6 son, independientemente, hidrógeno, ciano, halógeno, CO2R12, CONR14R15 ,alquilo C1-6 opcionalmente sustituido por hidroxi, NR14R15 o 1-3 flúoros,alquinilo C1-6 o XCH(R11)alquilo C1-6 o XCH(R16)alquilo C1-6 en donde el grupo alquilo puede estar opcionalmente sustituido con 1-3 grupos escogidos entre hidroxi y NR14R15NR14R15, N(R11)R11, X-(CH2)qNR14R15, (CH2)nNR14R15, alquilo NHC(O)C1-6 opcionalmente sustituido por uno o varios grupos hidroxi,alquinilo C3-6 o alquenilo C3-6 opcionalmente ramificado y opcionalmente sustituido con 1-2 grupos escogidos entre hidroxi, ciano, halógeno y =O,R11, X-R11, X-R12; X-alquilo C1-6-R16; X-R16; X-(CH2)nCO2R12; X-(CH2)nCONR14R15;X-(CH2)nR11; X-(CH2)nCN; X-(CH2)qOR12; (CH2)nOR12; (CH2)nX¯¯R11; X-(CH2)qNHC(O)NHR12; X-(CH2)qNHC(O)R12; X-(CH2)qNHS(O)2R11; X-alquenilo C3-6; X-alquinilo C3-6;n es 1, 2, 3, 4 o 5q es 2, 3, 4, 5 o 6; ...
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0200119A SE0200119D0 (sv) | 2002-01-16 | 2002-01-16 | Novel compounds |
| SE0201857A SE0201857D0 (sv) | 2002-06-17 | 2002-06-17 | Novel compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CO5640137A2 true CO5640137A2 (es) | 2006-05-31 |
Family
ID=26655657
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CO04067437A CO5640137A2 (es) | 2002-01-16 | 2004-07-15 | N-pirazinil-fenilsulfonamidas y su uso en el tratamiento de enfermedades mediadas por quimosina |
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|---|---|
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| EP (1) | EP1467976B1 (es) |
| JP (1) | JP4504021B2 (es) |
| KR (1) | KR20040073566A (es) |
| CN (1) | CN100357275C (es) |
| AR (1) | AR038179A1 (es) |
| AT (1) | ATE534635T1 (es) |
| AU (1) | AU2003201802A1 (es) |
| BR (1) | BR0306922A (es) |
| CA (1) | CA2472204A1 (es) |
| CO (1) | CO5640137A2 (es) |
| ES (1) | ES2375107T3 (es) |
| IL (1) | IL162678A0 (es) |
| IS (1) | IS7348A (es) |
| MX (1) | MXPA04006806A (es) |
| NO (1) | NO20043370L (es) |
| NZ (1) | NZ533750A (es) |
| PL (1) | PL371432A1 (es) |
| RU (1) | RU2312105C9 (es) |
| TW (1) | TWI328007B (es) |
| WO (1) | WO2003059893A1 (es) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1541563A4 (en) * | 2002-07-10 | 2007-11-07 | Ono Pharmaceutical Co | ANTAGONIST OF CCR4 AND CORRESPONDING MEDICINAL USE |
| GB0217431D0 (en) | 2002-07-27 | 2002-09-04 | Astrazeneca Ab | Novel compounds |
| ES2295685T3 (es) | 2002-08-24 | 2008-04-16 | Astrazeneca Ab | Derivados de pirimidina como moduladores de la actividad del receptor de quimioquinas. |
| SE0301653D0 (sv) * | 2003-06-05 | 2003-06-05 | Astrazeneca Ab | Novel compounds |
| SE0302304D0 (sv) * | 2003-08-27 | 2003-08-27 | Astrazeneca Ab | Novel compounds |
| EP1661889A4 (en) * | 2003-09-05 | 2009-08-05 | Ono Pharmaceutical Co | ANTAGONIST OF THE CHEMOKINE RECEPTOR AND ITS USE FOR MEDICAL PURPOSES |
| GB0401269D0 (en) * | 2004-01-21 | 2004-02-25 | Astrazeneca Ab | Compounds |
| US7544702B2 (en) | 2004-08-12 | 2009-06-09 | Amgen Inc. | Bisaryl-sulfonamides |
| PT1809624E (pt) | 2004-08-28 | 2014-01-14 | Astrazeneca Ab | Derivados de pirimidina sulfonamida como moduladores do recetor de quimiocina |
| TW200800921A (en) * | 2005-09-19 | 2008-01-01 | Astrazeneca Ab | Novel compounds |
| US20090182142A1 (en) * | 2005-12-02 | 2009-07-16 | Shigeru Furukubo | Aromatic Compound |
| US20090182140A1 (en) * | 2005-12-02 | 2009-07-16 | Mitsubishi Tanabe Pharma Corporation | Alicyclic Heterocyclic Compound |
| TW200730512A (en) * | 2005-12-12 | 2007-08-16 | Astrazeneca Ab | Novel compounds |
| GB0526255D0 (en) | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
| CN101842361B (zh) | 2007-06-27 | 2013-06-05 | 阿斯利康(瑞典)有限公司 | 吡嗪酮衍生物及其在治疗肺病中的用途 |
| US8586748B2 (en) * | 2008-04-09 | 2013-11-19 | Boehringer Ingelheim International Gmbh | 2-sulfonylamino-4-heteroaryl butyramide antagonists of CCR10 |
| US8673908B2 (en) | 2008-11-10 | 2014-03-18 | Kyowa Hakko Kirin Co., Ltd. | Kynurenine production inhibitor |
| TW201041583A (en) * | 2009-04-22 | 2010-12-01 | Axikin Pharmaceuticals Inc | 2,5-disubstituted arylsulfonamide CCR3 antagonists |
| TWI535442B (zh) | 2010-05-10 | 2016-06-01 | Kyowa Hakko Kirin Co Ltd | A nitrogen-containing heterocyclic compound having an action of inhibiting the production of canine erythritine |
| CN108383828A (zh) * | 2010-12-16 | 2018-08-10 | 阿勒根公司 | 作为趋化因子受体调节剂的新的1,2-双-磺酰胺衍生物 |
| EP2781517B1 (en) | 2011-11-09 | 2017-10-11 | Kyowa Hakko Kirin Co., Ltd. | Nitrogen-containing heterocyclic compound |
| JP6327803B2 (ja) * | 2013-07-09 | 2018-05-23 | 久慶 ▲ふく▼楊 | 大出力高効率単相多極発電機 |
| CN106008418A (zh) * | 2016-05-20 | 2016-10-12 | 厦门大学 | 一种5-氨甲基-2-呋喃甲醇的合成方法 |
| IL276295B2 (en) * | 2018-01-26 | 2024-02-01 | Rapt Therapeutics Inc | Modulators of chemokine receptors and their uses |
| CN113069446B (zh) * | 2021-03-01 | 2022-12-02 | 中山亿维迪科技有限公司 | El102在制备治疗新型冠状病毒所致疾病的药物中的应用 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US143024A (en) * | 1873-09-23 | Improvement in clothes-pins | ||
| US5962490A (en) | 1987-09-25 | 1999-10-05 | Texas Biotechnology Corporation | Thienyl-, furyl- and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin |
| GB9504854D0 (en) * | 1994-03-31 | 1995-04-26 | Zeneca Ltd | Nitrogen derivatives |
| CA2162630C (en) | 1994-11-25 | 2007-05-01 | Volker Breu | Sulfonamides |
| GB2295616A (en) * | 1994-12-01 | 1996-06-05 | Zeneca Ltd | N-Diazine-benzenesulphonamide derivatives as endothelin receptor antagonists |
| GB9512697D0 (en) | 1995-06-22 | 1995-08-23 | Zeneca Ltd | Heterocyclic compounds |
| CN1149196C (zh) * | 1998-07-06 | 2004-05-12 | 布里斯托尔-迈尔斯斯奎布公司 | 作为血管紧张肽和内皮肽受体双重拮抗剂的联苯基磺酰胺 |
| US6638937B2 (en) | 1998-07-06 | 2003-10-28 | Bristol-Myers Squibb Co. | Biphenyl sulfonamides as dual angiotensin endothelin receptor antagonists |
| EP1741713A3 (en) * | 1999-12-15 | 2009-09-09 | Bristol-Myers Squibb Company | Biphenyl sulfonamides as dual angiotensin endothelin receptor antagonists |
| AU2002358390A1 (en) | 2001-12-18 | 2003-06-30 | Astrazeneca Ab | Novel compounds |
| EP1541563A4 (en) | 2002-07-10 | 2007-11-07 | Ono Pharmaceutical Co | ANTAGONIST OF CCR4 AND CORRESPONDING MEDICINAL USE |
| SE0301650D0 (sv) | 2003-06-04 | 2003-06-04 | Astrazeneca Ab | Novel compounds |
| SE0301653D0 (sv) * | 2003-06-05 | 2003-06-05 | Astrazeneca Ab | Novel compounds |
| SE0301654D0 (sv) | 2003-06-05 | 2003-06-05 | Astrazeneca Ab | Novel compounds |
| SE0302304D0 (sv) | 2003-08-27 | 2003-08-27 | Astrazeneca Ab | Novel compounds |
| TW200800921A (en) | 2005-09-19 | 2008-01-01 | Astrazeneca Ab | Novel compounds |
| TW200730512A (en) | 2005-12-12 | 2007-08-16 | Astrazeneca Ab | Novel compounds |
-
2003
- 2003-01-07 TW TW092100237A patent/TWI328007B/zh active
- 2003-01-14 MX MXPA04006806A patent/MXPA04006806A/es active IP Right Grant
- 2003-01-14 IL IL16267803A patent/IL162678A0/xx unknown
- 2003-01-14 EP EP03700655A patent/EP1467976B1/en not_active Expired - Lifetime
- 2003-01-14 US US10/501,510 patent/US7662825B2/en not_active Expired - Fee Related
- 2003-01-14 CN CNB038044811A patent/CN100357275C/zh not_active Expired - Fee Related
- 2003-01-14 PL PL03371432A patent/PL371432A1/xx not_active Application Discontinuation
- 2003-01-14 AT AT03700655T patent/ATE534635T1/de active
- 2003-01-14 KR KR10-2004-7010982A patent/KR20040073566A/ko not_active Ceased
- 2003-01-14 WO PCT/SE2003/000041 patent/WO2003059893A1/en not_active Ceased
- 2003-01-14 AU AU2003201802A patent/AU2003201802A1/en not_active Abandoned
- 2003-01-14 JP JP2003559997A patent/JP4504021B2/ja not_active Expired - Fee Related
- 2003-01-14 CA CA002472204A patent/CA2472204A1/en not_active Abandoned
- 2003-01-14 RU RU2004119966/04A patent/RU2312105C9/ru not_active IP Right Cessation
- 2003-01-14 BR BR0306922-2A patent/BR0306922A/pt not_active IP Right Cessation
- 2003-01-14 NZ NZ533750A patent/NZ533750A/xx unknown
- 2003-01-14 ES ES03700655T patent/ES2375107T3/es not_active Expired - Lifetime
- 2003-01-16 AR ARP030100126A patent/AR038179A1/es unknown
-
2004
- 2004-07-08 IS IS7348A patent/IS7348A/is unknown
- 2004-07-15 CO CO04067437A patent/CO5640137A2/es not_active Application Discontinuation
- 2004-08-13 NO NO20043370A patent/NO20043370L/no not_active Application Discontinuation
-
2009
- 2009-05-05 US US12/435,864 patent/US20100081670A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US7662825B2 (en) | 2010-02-16 |
| IS7348A (is) | 2004-07-08 |
| BR0306922A (pt) | 2004-11-09 |
| ATE534635T1 (de) | 2011-12-15 |
| AU2003201802A1 (en) | 2003-07-30 |
| JP2005521650A (ja) | 2005-07-21 |
| WO2003059893A1 (en) | 2003-07-24 |
| HK1068885A1 (en) | 2005-05-06 |
| NZ533750A (en) | 2006-03-31 |
| RU2312105C2 (ru) | 2007-12-10 |
| CN100357275C (zh) | 2007-12-26 |
| US20100081670A1 (en) | 2010-04-01 |
| KR20040073566A (ko) | 2004-08-19 |
| IL162678A0 (en) | 2005-11-20 |
| MXPA04006806A (es) | 2004-12-06 |
| CN1639132A (zh) | 2005-07-13 |
| RU2312105C9 (ru) | 2008-06-10 |
| TWI328007B (en) | 2010-08-01 |
| US20060025423A1 (en) | 2006-02-02 |
| TW200303308A (en) | 2003-09-01 |
| JP4504021B2 (ja) | 2010-07-14 |
| RU2004119966A (ru) | 2005-06-10 |
| AR038179A1 (es) | 2005-01-05 |
| EP1467976A1 (en) | 2004-10-20 |
| NO20043370L (no) | 2004-09-28 |
| EP1467976B1 (en) | 2011-11-23 |
| CA2472204A1 (en) | 2003-07-24 |
| PL371432A1 (en) | 2005-06-13 |
| ES2375107T3 (es) | 2012-02-24 |
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