EA200401054A1 - Производные n-бифенилметиламиноциклоалканкарбоксамида с заместителем на метиле, в качестве антагонистов брадикинина - Google Patents
Производные n-бифенилметиламиноциклоалканкарбоксамида с заместителем на метиле, в качестве антагонистов брадикининаInfo
- Publication number
- EA200401054A1 EA200401054A1 EA200401054A EA200401054A EA200401054A1 EA 200401054 A1 EA200401054 A1 EA 200401054A1 EA 200401054 A EA200401054 A EA 200401054A EA 200401054 A EA200401054 A EA 200401054A EA 200401054 A1 EA200401054 A1 EA 200401054A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- antagonists
- derivatives
- methyl
- biphenylmethylaminocyclo
- alkankarboxamide
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/24—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring of the carbon skeleton
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- 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
- A61K31/455—Nicotinic acids, e.g. niacin; Derivatives thereof, e.g. esters, amides
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- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
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- C07—ORGANIC CHEMISTRY
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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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- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
- C07D413/12—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 linked by a chain containing hetero atoms as chain links
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
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- Pulmonology (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
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- Pain & Pain Management (AREA)
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- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
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Abstract
Производные N-бифенил(замещенный метил)аминоциклоалканкарбоксамида являются антагонистами или обратными агонистами брадикинина B1, применимыми в лечении или предупреждении таких симптомов, как боль и воспаление, связанных с путем брадикинина B1.Международная заявка была опубликована вместе с отчетом о международном поиске.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US35506202P | 2002-02-08 | 2002-02-08 | |
US41017202P | 2002-09-12 | 2002-09-12 | |
PCT/US2003/003338 WO2003066577A1 (en) | 2002-02-08 | 2003-02-04 | N-biphenylmethyl aminocycloalkanecarboxamide derivatives with a substiituent on the methyl useful as bradykinin antagonists |
Publications (2)
Publication Number | Publication Date |
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EA200401054A1 true EA200401054A1 (ru) | 2005-02-24 |
EA007297B1 EA007297B1 (ru) | 2006-08-25 |
Family
ID=27737481
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200401054A EA007297B1 (ru) | 2002-02-08 | 2003-02-04 | Производные n-бифенилметиламиноциклоалканкарбоксамида с заместителем на метиле в качестве антагонистов брадикинина |
Country Status (27)
Country | Link |
---|---|
US (2) | US6919343B2 (ru) |
EP (1) | EP1501787B1 (ru) |
JP (1) | JP4098249B2 (ru) |
KR (1) | KR20040083440A (ru) |
CN (1) | CN1328247C (ru) |
AR (1) | AR038377A1 (ru) |
AT (1) | ATE309202T1 (ru) |
AU (1) | AU2003216169B2 (ru) |
BR (1) | BR0307508A (ru) |
CA (1) | CA2474373C (ru) |
DE (1) | DE60302240T2 (ru) |
DK (1) | DK1501787T3 (ru) |
EA (1) | EA007297B1 (ru) |
EC (1) | ECSP045217A (ru) |
ES (1) | ES2250899T3 (ru) |
HR (1) | HRP20040677A2 (ru) |
IS (1) | IS7372A (ru) |
JO (1) | JO2356B1 (ru) |
MA (1) | MA27108A1 (ru) |
MX (1) | MXPA04007660A (ru) |
NO (1) | NO20043739L (ru) |
NZ (1) | NZ534062A (ru) |
PE (1) | PE20030986A1 (ru) |
PL (1) | PL371664A1 (ru) |
RS (1) | RS65404A (ru) |
TW (1) | TWI259079B (ru) |
WO (1) | WO2003066577A1 (ru) |
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WO2003057671A1 (fr) * | 2001-12-28 | 2003-07-17 | Takeda Chemical Industries, Ltd. | Compose biaryle et son utilisation |
ATE316954T1 (de) * | 2002-02-08 | 2006-02-15 | Merck & Co Inc | N-biphenylmethylaminocycloalkancarboxamid- derivative |
RU2005108667A (ru) * | 2002-08-29 | 2005-08-27 | Мерк энд Ко., Инк. (US) | Производные n-биарилметиламиноциклоалканкарбоксамида |
CA2509881A1 (en) * | 2002-12-19 | 2004-07-08 | Elan Pharmaceuticals, Inc. | Substituted n-phenyl sulfonamide bradykinin antagonists |
JP2007501790A (ja) * | 2003-08-07 | 2007-02-01 | メルク エンド カムパニー インコーポレーテッド | スルホニル置換n−(ビアリールメチル)アミノシクロプロパンカルボキサミド |
CA2550372C (en) * | 2003-12-22 | 2009-09-29 | Merck & Co., Inc. | Alpha-hydroxy amides as bradykinin antagonists or inverse agonists |
CA2557858A1 (en) * | 2004-03-02 | 2005-09-15 | Merck & Co., Inc. | Amino cyclopropane carboxamide derivatives as bradykinin antagonists |
US20050245543A1 (en) * | 2004-04-30 | 2005-11-03 | Pfizer Inc | Histamine-3 receptor antagonists |
MX2007001348A (es) * | 2004-08-02 | 2008-03-11 | Bebaas Inc | Composiciones de vitamina b12. |
DE102004060542A1 (de) * | 2004-12-16 | 2006-07-06 | Sanofi-Aventis Deutschland Gmbh | Hydroxybiphenyl-Carbonsäuren und Derivate, Verfahren zu deren Herstellung und deren Verwendung |
SI1830869T1 (sl) * | 2004-12-24 | 2013-12-31 | Spinifex Pharmaceuticals Pty Ltd | Postopek zdravljenja ali profilakse |
US20070178141A1 (en) * | 2005-09-07 | 2007-08-02 | Bebaas, Inc. | Vitamin B12 compositions |
US20130131007A1 (en) | 2005-09-07 | 2013-05-23 | Bebaas, Inc. | Vitamin b12 compositions |
CA2866540A1 (en) * | 2006-03-20 | 2007-09-27 | Spinifex Pharmaceuticals Pty Ltd. | Method of treatment or prophylaxis of inflammatory pain |
US8945505B2 (en) * | 2007-02-02 | 2015-02-03 | Panaphix, Inc. | Use of arsenic compounds for treatment of pain and inflammation |
EP2155643B1 (en) | 2007-06-08 | 2016-08-10 | MannKind Corporation | Ire-1a inhibitors |
CL2008002545A1 (es) * | 2007-08-29 | 2009-10-23 | Boehringer Ingelheim Int | Compuestos derivados de fenoxi-bencil-carbamoilo; composicion farmaceutica; procedimiento para preparar la composicion farmaceutica; y su uso en el tratamiento del dolor. |
WO2009132453A1 (en) * | 2008-04-28 | 2009-11-05 | Neuromed Pharmaceuticals Ltd. | Cyclylamine derivatives as calcium channel blockers |
GEP20135933B (en) * | 2009-02-26 | 2013-10-10 | Boehringer Ingelheim Int | Compounds as bradykinin b1 antagonists |
WO2010097373A1 (de) * | 2009-02-26 | 2010-09-02 | Boehringer Ingelheim International Gmbh | Verbindungen als bradykinin b1 antagonisten |
WO2010097374A1 (de) * | 2009-02-26 | 2010-09-02 | Boehringer Ingelheim International Gmbh | Verbindungen als bradykinin-b1-antagonisten |
WO2011133571A2 (en) | 2010-04-19 | 2011-10-27 | Board Of Trustees Of Michigan State University | Digestible lignocellulosic biomass and extractives and methods for producing same |
US10457810B2 (en) | 2009-08-24 | 2019-10-29 | Board Of Trustees Of Michigan State University | Densified biomass products containing pretreated biomass fibers |
PT2539323E (pt) | 2010-02-23 | 2015-02-16 | Boehringer Ingelheim Int | Compostos como antagonistas da bradicinina b1 |
US8937073B2 (en) * | 2010-08-20 | 2015-01-20 | Boehringer Ingelheim International Gmbh | Disubstituted tetrahydrofuranyl compounds and their use as B1-receptor antagonists |
HUP1000598A2 (en) * | 2010-11-05 | 2012-09-28 | Richter Gedeon Nyrt | Indole derivatives |
US8912221B2 (en) * | 2010-12-27 | 2014-12-16 | Hoffmann-La Roche Inc. | Biaryl amide derivatives |
US8592426B2 (en) * | 2011-01-24 | 2013-11-26 | Hoffmann—La Roche Inc. | Aryl-benzocycloalkyl amide derivatives |
MX2020004557A (es) | 2017-11-02 | 2020-10-05 | Calico Life Sciences Llc | Moduladores de la vía de estrés integrada. |
TWI771621B (zh) | 2018-10-11 | 2022-07-21 | 美商嘉來克生命科學有限責任公司 | 整合應激路徑之前藥調節劑 |
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US5270317A (en) * | 1990-03-20 | 1993-12-14 | Elf Sanofi | N-substituted heterocyclic derivatives, their preparation and the pharmaceutical compositions in which they are present |
IL99372A0 (en) | 1990-09-10 | 1992-08-18 | Ciba Geigy Ag | Azacyclic compounds |
US5208236A (en) * | 1992-09-23 | 1993-05-04 | Schering Corporation | N-(acylaminomethyl)glutaryl amino acids and use |
DE69424846T2 (de) | 1993-11-16 | 2000-11-16 | Novartis Ag | Zyklische Aminosäure-Derivate mit ACE und NEP inhibierender Aktivität |
WO1997011717A1 (en) | 1995-09-27 | 1997-04-03 | Novartis Ag | Treatment of chronic progressive renal failure |
FR2743562B1 (fr) * | 1996-01-11 | 1998-04-03 | Sanofi Sa | Derives de n-(arylsulfonyl) aminoacides, leur preparation, les compositions pharmaceutiques en contenant |
US6433185B1 (en) * | 1996-01-11 | 2002-08-13 | Sanofi-Synthelabo | N-(arylsulphonyl) amino acid derivatives, process for their preparation and pharmaceutical compositions containing them |
BR9909805A (pt) | 1998-04-23 | 2000-12-26 | Novartis Ag | Certos inibidores de tiol de enzima de conversão de endotelina |
ES2237917T3 (es) | 1998-04-23 | 2005-08-01 | Novartis Ag | Ciertos inhibidores tiolicos substituidos con heteroarilo de enzima conversora de endotelina. |
US20020052370A1 (en) | 2000-07-06 | 2002-05-02 | Barber Christopher Gordon | Cyclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase |
DE10036121A1 (de) | 2000-07-25 | 2002-02-07 | Merck Patent Gmbh | N-Substituierte-1-amino-1,1-dialkyl-carbonsäurederivate |
ATE316954T1 (de) | 2002-02-08 | 2006-02-15 | Merck & Co Inc | N-biphenylmethylaminocycloalkancarboxamid- derivative |
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2003
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- 2003-02-04 DE DE60302240T patent/DE60302240T2/de not_active Expired - Lifetime
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- 2003-02-04 US US10/503,501 patent/US20050084463A1/en not_active Abandoned
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