EA200900605A1 - Новые производные фенилсульфамоил бензамидов в качестве антагонистов брадикининовых рецепторов - Google Patents
Новые производные фенилсульфамоил бензамидов в качестве антагонистов брадикининовых рецепторовInfo
- Publication number
- EA200900605A1 EA200900605A1 EA200900605A EA200900605A EA200900605A1 EA 200900605 A1 EA200900605 A1 EA 200900605A1 EA 200900605 A EA200900605 A EA 200900605A EA 200900605 A EA200900605 A EA 200900605A EA 200900605 A1 EA200900605 A1 EA 200900605A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- antagonists
- new derivatives
- phenylsulfamoil
- bradikinine
- benzamides
- Prior art date
Links
- 239000005557 antagonist Substances 0.000 title abstract 2
- 229940054066 benzamide antipsychotics Drugs 0.000 title 1
- 150000003936 benzamides Chemical class 0.000 title 1
- 101800004538 Bradykinin Proteins 0.000 abstract 1
- QXZGBUJJYSLZLT-UHFFFAOYSA-N H-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg-OH Natural products NC(N)=NCCCC(N)C(=O)N1CCCC1C(=O)N1C(C(=O)NCC(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CO)C(=O)N2C(CCC2)C(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CCCN=C(N)N)C(O)=O)CCC1 QXZGBUJJYSLZLT-UHFFFAOYSA-N 0.000 abstract 1
- 102100035792 Kininogen-1 Human genes 0.000 abstract 1
- QXZGBUJJYSLZLT-FDISYFBBSA-N bradykinin Chemical compound NC(=N)NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(=O)NCC(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CO)C(=O)N2[C@@H](CCC2)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)CCC1 QXZGBUJJYSLZLT-FDISYFBBSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 230000004968 inflammatory condition Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- BVFMYNNAEUPDCO-UHFFFAOYSA-N n-(phenylsulfamoyl)benzamide Chemical class C=1C=CC=CC=1C(=O)NS(=O)(=O)NC1=CC=CC=C1 BVFMYNNAEUPDCO-UHFFFAOYSA-N 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 239000008196 pharmacological composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
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- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- 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
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- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
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- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
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- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/135—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/18—Systems containing only non-condensed rings with a ring being at least seven-membered
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Abstract
Настоящее изобретение относится к новым производным фенилсульфамоил бензамида формулы (I), где R-Rи Z соответствуют тому, как указано в формуле изобретения, и их оптическим антиподам, или рацематам, и/или солям, и/или гидратам, и/или сольватам, которые являются селективными антагонистами брадикинина В1, к способу получения таких соединений, к фармакологическим композициям, их содержащим, и к их применению в лечении и профилактике болевых и воспалительных состояний.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU0600809A HUP0600809A3 (en) | 2006-10-27 | 2006-10-27 | New phenylsulfamoyl-benzamide derivatives as bradykinin antagonists, process and intermediates for their preparation and pharmaceutical compositions containing them |
| PCT/HU2007/000103 WO2008050167A1 (en) | 2006-10-27 | 2007-10-27 | New phenylsulfamoyl benzamide derivatives as bradykinin antagonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA200900605A1 true EA200900605A1 (ru) | 2009-08-28 |
| EA018032B1 EA018032B1 (ru) | 2013-05-30 |
Family
ID=89987106
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA200900605A EA018032B1 (ru) | 2006-10-27 | 2007-10-27 | Производные фенилсульфамоилбензамидов в качестве антагонистов брадикининовых рецепторов, способ их получения и фармацевтическая композиция, их содержащая |
Country Status (19)
| Country | Link |
|---|---|
| US (3) | US20100105686A1 (ru) |
| EP (1) | EP2057116B1 (ru) |
| JP (1) | JP2010507643A (ru) |
| KR (1) | KR20090076926A (ru) |
| CN (1) | CN101528680A (ru) |
| AU (1) | AU2007310587A1 (ru) |
| BR (1) | BRPI0718494A2 (ru) |
| CA (1) | CA2667481C (ru) |
| EA (1) | EA018032B1 (ru) |
| GE (1) | GEP20125393B (ru) |
| HU (1) | HUP0600809A3 (ru) |
| IL (1) | IL197586A0 (ru) |
| MA (1) | MA30912B1 (ru) |
| MX (1) | MX2009004528A (ru) |
| MY (1) | MY155039A (ru) |
| NO (1) | NO20092049L (ru) |
| NZ (1) | NZ575765A (ru) |
| TN (1) | TN2009000108A1 (ru) |
| WO (1) | WO2008050167A1 (ru) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HUP0600810A3 (en) * | 2006-10-27 | 2008-09-29 | Richter Gedeon Nyrt | New sulfonamide derivatives as bradykinin antagonists, process and intermediates for their preparation and pharmaceutical compositions containing them |
| HUP0600808A3 (en) * | 2006-10-27 | 2008-09-29 | Richter Gedeon Nyrt | New benzamide derivatives as bradykinin antagonists, process for their preparation and pharmaceutical compositions containing them |
| WO2009027450A1 (de) | 2007-08-29 | 2009-03-05 | Boehringer Ingelheim International Gmbh | Neue bradykinin b1-antagonisten |
| KR20100081349A (ko) * | 2007-10-27 | 2010-07-14 | 리히터 게데온 닐트. | 브라디키닌 b1 길항제인 신규 비펩티드 유도체 |
| WO2010022304A1 (en) * | 2008-08-21 | 2010-02-25 | Forest Laboratories Holdings Limited | Methods for treating cns disorders |
| US20110190347A1 (en) * | 2008-08-21 | 2011-08-04 | Richter Gedeon Nyrt. | Methods for treating neuropathic pain |
| HU230067B1 (hu) * | 2008-12-17 | 2015-06-29 | Richter Gedeon Nyrt | Új piperazin só és eljárás előállítására |
| AP2011005808A0 (en) * | 2009-02-26 | 2011-08-31 | Boehringer Ingelheim Int | Compounds as bradykinin B1 antagonists. |
| AU2011219885C1 (en) * | 2010-02-23 | 2017-06-29 | Boehringer Ingelheim International Gmbh | Compounds as bradykinin B1 antagonists |
| US8937073B2 (en) | 2010-08-20 | 2015-01-20 | Boehringer Ingelheim International Gmbh | Disubstituted tetrahydrofuranyl compounds and their use as B1-receptor antagonists |
| CN104151248B (zh) * | 2014-07-17 | 2016-02-17 | 陕西师范大学 | 双咪唑丹磺酰衍生物阳离子型荧光探针及其合成方法和应用 |
| CN104693075B (zh) * | 2015-02-13 | 2016-05-11 | 程涛 | p18小分子抑制剂及在人造血干细胞体外扩增中的用途 |
| CN106601606B (zh) * | 2015-10-19 | 2019-09-20 | 中芯国际集成电路制造(上海)有限公司 | Nmos器件、半导体装置及其制造方法 |
| CA3117916A1 (en) | 2018-11-23 | 2020-05-28 | Martin Quibell | Compounds |
| PE20221836A1 (es) | 2020-03-26 | 2022-11-29 | Richter Gedeon Nyrt | Derivados de naftiridina y pirido[3,4-c]piridazina como moduladores del receptor gabaa 5 |
| KR20210150011A (ko) * | 2020-06-03 | 2021-12-10 | 주식회사 삼오파마켐 | 프로베네시드 및 아르기닌의 아미드 유도체, 이를 포함하는 약제학적 조성물 및 이의 제조 방법 |
| HU231691B1 (hu) | 2021-09-29 | 2025-10-28 | Richter Gedeon Nyrt | GABAA ALFA5 receptor modulátor hatású biciklusos aminszármazékok |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5272158A (en) * | 1991-10-29 | 1993-12-21 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| US5714497A (en) * | 1993-02-15 | 1998-02-03 | Sanofi | Compounds bearing sulphamoyl and amidino radicals, their preparation process and pharmaceutical compositions containing them |
| DE19624668A1 (de) * | 1996-06-20 | 1998-02-19 | Klinge Co Chem Pharm Fab | Verwendung von Pyridylalkan-, Pyridylalken- bzw. Pyridylalkinsäureamiden |
| US6451816B1 (en) * | 1997-06-20 | 2002-09-17 | Klinge Pharma Gmbh | Use of pyridyl alkane, pyridyl alkene and/or pyridyl alkine acid amides in the treatment of tumors or for immunosuppression |
| CN100418951C (zh) * | 1997-11-18 | 2008-09-17 | 帝人医药株式会社 | 环胺衍生物及其作为药物的用途 |
| GB9804885D0 (en) * | 1998-03-06 | 1998-04-29 | Merck Sharp & Dohme | Therapeutic combination |
| US6017961A (en) * | 1999-07-08 | 2000-01-25 | Flores; John Anthony | Ketamine and n-butyl-p-aminobezoate in PLO |
| US6638950B2 (en) * | 2000-06-21 | 2003-10-28 | Bristol-Myers Squibb Pharma Company | Piperidine amides as modulators of chemokine receptor activity |
| FR2822827B1 (fr) * | 2001-03-28 | 2003-05-16 | Sanofi Synthelabo | Nouveaux derives de n-(arylsulfonyl) beta-aminoacides comportant un groupe aminomethyle substitue, leur procede de preparation et les compositions pharmaceutiques en contenant |
| KR100890676B1 (ko) * | 2001-07-24 | 2009-03-26 | 리히데 게데온 베기에스제티 기아르 알티 | 신규한 카르복시산 아미드 화합물 |
| EP1643960A2 (en) * | 2003-07-02 | 2006-04-12 | Merck & Co., Inc. | Arylsulfonamide derivatives |
| US20070105902A1 (en) * | 2003-11-12 | 2007-05-10 | Lindsley Craig W | 4-Phenyl piperdine sulfonyl glycine transporter inhibitors |
| HU230518B1 (hu) * | 2005-12-20 | 2016-10-28 | Richter Gedeon Nyrt. | Bradykinin B1 receptor szelektív antagonista hatással rendelkező új fenatridin származékok, eljárás előállításukra, és az ezeket tartalmazó gyógyszerkészítmények |
| HUP0600810A3 (en) * | 2006-10-27 | 2008-09-29 | Richter Gedeon Nyrt | New sulfonamide derivatives as bradykinin antagonists, process and intermediates for their preparation and pharmaceutical compositions containing them |
| HUP0600808A3 (en) * | 2006-10-27 | 2008-09-29 | Richter Gedeon Nyrt | New benzamide derivatives as bradykinin antagonists, process for their preparation and pharmaceutical compositions containing them |
| KR20100081349A (ko) * | 2007-10-27 | 2010-07-14 | 리히터 게데온 닐트. | 브라디키닌 b1 길항제인 신규 비펩티드 유도체 |
| WO2010022304A1 (en) * | 2008-08-21 | 2010-02-25 | Forest Laboratories Holdings Limited | Methods for treating cns disorders |
| US20110190347A1 (en) * | 2008-08-21 | 2011-08-04 | Richter Gedeon Nyrt. | Methods for treating neuropathic pain |
-
2006
- 2006-10-27 HU HU0600809A patent/HUP0600809A3/hu unknown
-
2007
- 2007-10-27 BR BRPI0718494-8A2A patent/BRPI0718494A2/pt not_active IP Right Cessation
- 2007-10-27 EA EA200900605A patent/EA018032B1/ru not_active IP Right Cessation
- 2007-10-27 AU AU2007310587A patent/AU2007310587A1/en not_active Abandoned
- 2007-10-27 JP JP2009533965A patent/JP2010507643A/ja active Pending
- 2007-10-27 CA CA2667481A patent/CA2667481C/en not_active Expired - Fee Related
- 2007-10-27 WO PCT/HU2007/000103 patent/WO2008050167A1/en not_active Ceased
- 2007-10-27 KR KR1020097008093A patent/KR20090076926A/ko not_active Ceased
- 2007-10-27 MX MX2009004528A patent/MX2009004528A/es active IP Right Grant
- 2007-10-27 GE GEAP200711269A patent/GEP20125393B/en unknown
- 2007-10-27 MY MYPI20091575A patent/MY155039A/en unknown
- 2007-10-27 US US12/447,151 patent/US20100105686A1/en not_active Abandoned
- 2007-10-27 NZ NZ575765A patent/NZ575765A/en not_active IP Right Cessation
- 2007-10-27 CN CNA2007800399518A patent/CN101528680A/zh active Pending
- 2007-10-27 EP EP07824995A patent/EP2057116B1/en active Active
-
2009
- 2009-03-12 IL IL197586A patent/IL197586A0/en unknown
- 2009-03-30 TN TN2009000108A patent/TN2009000108A1/fr unknown
- 2009-05-21 MA MA31907A patent/MA30912B1/fr unknown
- 2009-05-26 NO NO20092049A patent/NO20092049L/no not_active Application Discontinuation
-
2012
- 2012-08-01 US US13/564,429 patent/US20130029991A1/en not_active Abandoned
- 2012-08-01 US US13/564,360 patent/US20120295910A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0718494A2 (pt) | 2014-01-21 |
| US20130029991A1 (en) | 2013-01-31 |
| CA2667481C (en) | 2012-09-25 |
| HU0600809D0 (en) | 2006-12-28 |
| EP2057116B1 (en) | 2013-02-13 |
| MY155039A (en) | 2015-08-28 |
| NZ575765A (en) | 2011-12-22 |
| MA30912B1 (fr) | 2009-11-02 |
| US20100105686A1 (en) | 2010-04-29 |
| TN2009000108A1 (en) | 2010-08-19 |
| AU2007310587A1 (en) | 2008-05-02 |
| JP2010507643A (ja) | 2010-03-11 |
| WO2008050167A1 (en) | 2008-05-02 |
| CN101528680A (zh) | 2009-09-09 |
| HUP0600809A3 (en) | 2008-09-29 |
| CA2667481A1 (en) | 2008-05-02 |
| NO20092049L (no) | 2009-07-17 |
| IL197586A0 (en) | 2009-12-24 |
| US20120295910A1 (en) | 2012-11-22 |
| EP2057116A1 (en) | 2009-05-13 |
| GEP20125393B (en) | 2012-02-10 |
| KR20090076926A (ko) | 2009-07-13 |
| HUP0600809A2 (en) | 2008-08-28 |
| EA018032B1 (ru) | 2013-05-30 |
| MX2009004528A (es) | 2009-07-02 |
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