BR0011049A - Fenilciclohexanocarboxamidas substituìdas e seu uso como inibidores de absorção de adenosina - Google Patents
Fenilciclohexanocarboxamidas substituìdas e seu uso como inibidores de absorção de adenosinaInfo
- Publication number
- BR0011049A BR0011049A BR0011049-3A BR0011049A BR0011049A BR 0011049 A BR0011049 A BR 0011049A BR 0011049 A BR0011049 A BR 0011049A BR 0011049 A BR0011049 A BR 0011049A
- Authority
- BR
- Brazil
- Prior art keywords
- substituted
- phenylcyclohexanocarboxamides
- absorption inhibitors
- adenosine absorption
- adenosine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/08—Radicals containing only hydrogen and carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/12—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/14—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Saccharide Compounds (AREA)
Abstract
Patente de Invenção: "FENILCICLOHEXANOCARBOXAMIDAS SUBSTITUìDAS E SEU USO COMO INIBIDORES DE ABSORçãO DE ADENOSINA". A presente invenção refere-se a fenilciclohexanocarboxamidas substituídas de fórmula (I), a processos para sua preparação e ao seu uso em medicamentos, particularmente para o tratamento de distúrbios cardiovasculares.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19924819A DE19924819A1 (de) | 1999-05-29 | 1999-05-29 | Substituierte Phenylcyclohexancarbonsäurebenzylamid (Adenosinaufnahmeinhibitoren) |
PCT/EP2000/004431 WO2000073274A2 (de) | 1999-05-29 | 2000-05-16 | Substituierte phenylcyclohexancarbonsäureamide und ihre verwendung als adenosinaufnahme-inhibitoren |
Publications (1)
Publication Number | Publication Date |
---|---|
BR0011049A true BR0011049A (pt) | 2002-03-19 |
Family
ID=7909713
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR0011049-3A BR0011049A (pt) | 1999-05-29 | 2000-05-16 | Fenilciclohexanocarboxamidas substituìdas e seu uso como inibidores de absorção de adenosina |
Country Status (25)
Country | Link |
---|---|
US (1) | US6984642B1 (pt) |
EP (1) | EP1187812B1 (pt) |
JP (1) | JP2003500474A (pt) |
KR (1) | KR20020000814A (pt) |
CN (1) | CN1165526C (pt) |
AR (1) | AR029639A1 (pt) |
AT (1) | ATE303995T1 (pt) |
AU (1) | AU766140B2 (pt) |
BR (1) | BR0011049A (pt) |
CA (1) | CA2375188A1 (pt) |
CO (1) | CO5170503A1 (pt) |
DE (2) | DE19924819A1 (pt) |
DK (1) | DK1187812T3 (pt) |
ES (1) | ES2248071T3 (pt) |
GT (1) | GT200000085A (pt) |
HK (1) | HK1047107B (pt) |
HN (1) | HN2000000078A (pt) |
IL (1) | IL146231A0 (pt) |
MX (1) | MXPA01012240A (pt) |
PE (1) | PE20010132A1 (pt) |
PL (1) | PL365960A1 (pt) |
TR (1) | TR200103398T2 (pt) |
UY (1) | UY26179A1 (pt) |
WO (1) | WO2000073274A2 (pt) |
ZA (1) | ZA200108894B (pt) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10150310A1 (de) * | 2001-10-11 | 2003-04-24 | Bayer Ag | Substituierte Piperazincyclohexancarbonsäureamide und ihre Verwendung |
KR100762858B1 (ko) * | 2005-03-07 | 2007-10-02 | 김기완 | Pe시트를 이용한 저수조의 방수 공법 |
KR100762857B1 (ko) * | 2005-03-07 | 2007-10-02 | 김기완 | Pe시트를 이용한 저수조의 방수 공법 |
KR100745024B1 (ko) * | 2005-05-09 | 2007-08-01 | 김준 | 거푸집 수평조절장치 |
EP2318352B1 (en) * | 2008-07-16 | 2012-12-19 | Bristol-Myers Squibb Company | Cyclohexenyl compounds as modulators of chemokine receptor activity |
EP2380595A1 (en) | 2010-04-19 | 2011-10-26 | Nlife Therapeutics S.L. | Compositions and methods for selective delivery of oligonucleotide molecules to specific neuron types |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE174913T1 (de) * | 1992-07-31 | 1999-01-15 | Bristol Myers Squibb Co | Diphenyl oxazole-, thiazole- und imidazole- derivate als inhibitoren der wiederaufnahme des adenosins |
DE4304455A1 (de) * | 1993-02-15 | 1994-08-18 | Bayer Ag | Heterocyclisch substituierte Phenyl-cyclohexan-carbonsäurederivate |
DE19503160A1 (de) * | 1995-02-01 | 1996-08-08 | Bayer Ag | Verwendung von Phenylcyclohexylcarbonsäureamiden |
CZ65398A3 (cs) * | 1995-09-22 | 1998-07-15 | Sumitomo Chemical Company, Limited | Derivát pyrazinu-2-on, způsob kontroly nechtěných plevelů a použití derivátu |
US5723313A (en) * | 1995-09-27 | 1998-03-03 | St. Jude Children's Research Hospital | ARF-p19, a novel regulator of the mammalian cell cycle |
-
1999
- 1999-05-29 DE DE19924819A patent/DE19924819A1/de not_active Withdrawn
-
2000
- 2000-05-16 CA CA002375188A patent/CA2375188A1/en not_active Abandoned
- 2000-05-16 PL PL00365960A patent/PL365960A1/xx not_active Application Discontinuation
- 2000-05-16 EP EP00925290A patent/EP1187812B1/de not_active Expired - Lifetime
- 2000-05-16 JP JP2000621340A patent/JP2003500474A/ja active Pending
- 2000-05-16 CN CNB008082170A patent/CN1165526C/zh not_active Expired - Fee Related
- 2000-05-16 KR KR1020017015253A patent/KR20020000814A/ko not_active Application Discontinuation
- 2000-05-16 IL IL14623100A patent/IL146231A0/xx unknown
- 2000-05-16 DK DK00925290T patent/DK1187812T3/da active
- 2000-05-16 BR BR0011049-3A patent/BR0011049A/pt not_active IP Right Cessation
- 2000-05-16 ES ES00925290T patent/ES2248071T3/es not_active Expired - Lifetime
- 2000-05-16 AU AU44057/00A patent/AU766140B2/en not_active Ceased
- 2000-05-16 MX MXPA01012240A patent/MXPA01012240A/es active IP Right Grant
- 2000-05-16 TR TR2001/03398T patent/TR200103398T2/xx unknown
- 2000-05-16 WO PCT/EP2000/004431 patent/WO2000073274A2/de not_active Application Discontinuation
- 2000-05-16 US US09/980,242 patent/US6984642B1/en not_active Expired - Fee Related
- 2000-05-16 DE DE50011122T patent/DE50011122D1/de not_active Expired - Fee Related
- 2000-05-16 AT AT00925290T patent/ATE303995T1/de not_active IP Right Cessation
- 2000-05-17 HN HN2000000078A patent/HN2000000078A/es unknown
- 2000-05-24 CO CO00038312A patent/CO5170503A1/es not_active Application Discontinuation
- 2000-05-26 GT GT200000085A patent/GT200000085A/es unknown
- 2000-05-26 PE PE2000000505A patent/PE20010132A1/es not_active Application Discontinuation
- 2000-05-29 UY UY26179A patent/UY26179A1/es not_active Application Discontinuation
- 2000-05-29 AR ARP000102649A patent/AR029639A1/es not_active Application Discontinuation
-
2001
- 2001-10-29 ZA ZA200108894A patent/ZA200108894B/xx unknown
-
2002
- 2002-12-04 HK HK02108818.1A patent/HK1047107B/zh not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CN1353693A (zh) | 2002-06-12 |
AU766140B2 (en) | 2003-10-09 |
ATE303995T1 (de) | 2005-09-15 |
DK1187812T3 (da) | 2005-12-12 |
UY26179A1 (es) | 2000-12-29 |
KR20020000814A (ko) | 2002-01-05 |
AR029639A1 (es) | 2003-07-10 |
CA2375188A1 (en) | 2000-12-07 |
ES2248071T3 (es) | 2006-03-16 |
HK1047107B (zh) | 2005-05-20 |
US6984642B1 (en) | 2006-01-10 |
PE20010132A1 (es) | 2001-04-12 |
TR200103398T2 (tr) | 2002-03-21 |
MXPA01012240A (es) | 2002-08-12 |
WO2000073274A2 (de) | 2000-12-07 |
CN1165526C (zh) | 2004-09-08 |
ZA200108894B (en) | 2003-01-29 |
CO5170503A1 (es) | 2002-06-27 |
EP1187812B1 (de) | 2005-09-07 |
WO2000073274A3 (de) | 2001-04-19 |
DE19924819A1 (de) | 2000-11-30 |
PL365960A1 (en) | 2005-01-24 |
DE50011122D1 (de) | 2005-10-13 |
HK1047107A1 (en) | 2003-02-07 |
AU4405700A (en) | 2000-12-18 |
GT200000085A (es) | 2001-11-17 |
HN2000000078A (es) | 2001-02-02 |
EP1187812A2 (de) | 2002-03-20 |
JP2003500474A (ja) | 2003-01-07 |
IL146231A0 (en) | 2002-07-25 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 8O E 9O ANUIDADES. |
|
B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: REFERENTE AO DESPACHO 8.6 DA RPI 2008 DE 30/06/2009. |