RU93004577A - Derivatives of imidazole with a side chain of biphenylsulfonylurea - Google Patents
Derivatives of imidazole with a side chain of biphenylsulfonylureaInfo
- Publication number
- RU93004577A RU93004577A RU93004577/04A RU93004577A RU93004577A RU 93004577 A RU93004577 A RU 93004577A RU 93004577/04 A RU93004577/04 A RU 93004577/04A RU 93004577 A RU93004577 A RU 93004577A RU 93004577 A RU93004577 A RU 93004577A
- Authority
- RU
- Russia
- Prior art keywords
- biphenylsulfonylurea
- side chain
- imidazole
- derivatives
- biphenylsulfonylurethane
- Prior art date
Links
- GYWDYDOMTVIFPI-UHFFFAOYSA-N (2-phenylphenyl)sulfonylurea Chemical compound NC(=O)NS(=O)(=O)C1=CC=CC=C1C1=CC=CC=C1 GYWDYDOMTVIFPI-UHFFFAOYSA-N 0.000 title claims 2
- 150000002460 imidazoles Chemical class 0.000 title claims 2
- -1 R 2 - for example Chemical group 0.000 claims 1
- 229940041158 antibacterial for systemic use Imidazole derivatives Drugs 0.000 claims 1
- 229940042051 antimycotic for systemic use Imidazole derivatives Drugs 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- NEESMEYXOMGEIC-UHFFFAOYSA-N ethyl N-(2-phenylphenyl)sulfonylcarbamate Chemical compound CCOC(=O)NS(=O)(=O)C1=CC=CC=C1C1=CC=CC=C1 NEESMEYXOMGEIC-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 229940093910 gyncological antiinfectives Imidazole derivatives Drugs 0.000 claims 1
- 229940079865 intestinal antiinfectives Imidazole derivatives Drugs 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- 239000002464 receptor antagonist Substances 0.000 claims 1
Claims (1)
где R1 - например, этил, R2 - например, метил, n - например, O, R3 - например, COOH и R4 - например, SO2NHCONHCH3, представляют высокоактивные антагонисты ангиотензин-11-рецепторов.The proposed imidazole derivatives with a side chain of biphenylsulfonylurea or biphenylsulfonylurethane, a method for their preparation and their use. Compounds of formula
where R 1 - for example, ethyl, R 2 - for example, methyl, n - for example, O, R 3 - for example, COOH and R 4 - for example, SO 2 NHCONHCH 3 , are highly active angiotensin-11 receptor antagonists.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4207241 | 1992-03-07 | ||
DEP4207241.7 | 1992-03-07 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU93004577A true RU93004577A (en) | 1996-02-27 |
RU2116300C1 RU2116300C1 (en) | 1998-07-27 |
Family
ID=6453463
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU93004577A RU2116300C1 (en) | 1992-03-07 | 1993-03-05 | Imidazole derivatives or their physiologically acceptable salts, method of their synthesis, agent for blood hypertension decrease and pharmaceutical composition for blood pressure decrease |
Country Status (25)
Country | Link |
---|---|
US (1) | US5604251A (en) |
EP (1) | EP0560177B1 (en) |
JP (1) | JP3542813B2 (en) |
KR (1) | KR930019637A (en) |
CN (1) | CN1036341C (en) |
AT (1) | ATE230732T1 (en) |
AU (1) | AU663565B2 (en) |
BR (1) | BR9300761A (en) |
CA (1) | CA2091135A1 (en) |
CZ (1) | CZ281983B6 (en) |
DE (1) | DE59310323D1 (en) |
DK (1) | DK0560177T3 (en) |
ES (1) | ES2187501T3 (en) |
FI (1) | FI930970A (en) |
HU (1) | HUT64041A (en) |
IL (1) | IL104971A0 (en) |
MA (1) | MA22814A1 (en) |
NO (1) | NO303632B1 (en) |
NZ (1) | NZ247059A (en) |
PH (1) | PH31466A (en) |
PL (1) | PL173023B1 (en) |
RU (1) | RU2116300C1 (en) |
SK (1) | SK381192A3 (en) |
TW (1) | TW215434B (en) |
ZA (1) | ZA931585B (en) |
Families Citing this family (43)
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DE4010797A1 (en) * | 1990-04-04 | 1991-10-10 | Hoechst Ag | SUBSTITUTED AZOLES, METHOD FOR THE PRODUCTION THEREOF, MEANS CONTAINING THEM AND THE USE THEREOF |
US5514696A (en) * | 1992-05-06 | 1996-05-07 | Bristol-Myers Squibb Co. | Phenyl sulfonamide endothelin antagonists |
CA2111662C (en) * | 1992-12-17 | 2004-11-23 | Hiroaki Yanagisawa | Biphenyl derivatives, their preparation and their use for the treatment of hypertension and cardiac disease |
FR2716882B1 (en) * | 1994-03-04 | 1996-04-05 | Roussel Uclaf | Use of imidazole derivatives for the treatment of conditions involving the AT1 and AT2 receptors of Angiotensin, some of these products, their preparation, pharmaceutical compositions. |
FR2716883B1 (en) * | 1994-03-04 | 1996-04-26 | Roussel Uclaf | New tetrasubstituted derivatives of imidazole, their preparation, new intermediates obtained, their application as medicaments, pharmaceutical compositions containing them. |
US5612359A (en) * | 1994-08-26 | 1997-03-18 | Bristol-Myers Squibb Company | Substituted biphenyl isoxazole sulfonamides |
US5780473A (en) * | 1995-02-06 | 1998-07-14 | Bristol-Myers Squibb Company | Substituted biphenyl sulfonamide endothelin antagonists |
US5760038A (en) * | 1995-02-06 | 1998-06-02 | Bristol-Myers Squibb Company | Substituted biphenyl sulfonamide endothelin antagonists |
US5846990A (en) * | 1995-07-24 | 1998-12-08 | Bristol-Myers Squibb Co. | Substituted biphenyl isoxazole sulfonamides |
JPH09124620A (en) * | 1995-10-11 | 1997-05-13 | Bristol Myers Squibb Co | Substituted biphenylsulfonamide endothelin antagonist |
CN1211183A (en) | 1996-02-20 | 1999-03-17 | 布里斯托尔-迈尔斯斯奎布公司 | Methods for preparation of biphenyl isoxazole sulfonamides |
US5856507A (en) * | 1997-01-21 | 1999-01-05 | Bristol-Myers Squibb Co. | Methods for the preparation of biphenyl isoxazole sulfonamides |
US5939446A (en) * | 1996-04-09 | 1999-08-17 | Bristol-Myers Squibb Co. | Heteroaryl substituted phenyl isoxazole sulfonamide endothelin antagonists |
CA2274789A1 (en) * | 1996-12-13 | 1998-06-18 | Zymogenetics, Inc. | Compositions and methods for stimulating bone growth |
EP0855392A3 (en) | 1997-01-22 | 2000-01-05 | Hoechst Aktiengesellschaft | Five-membered heterocycles having biphenylsulphonyl substituents, processes for the preparation thereof, their use as medicaments or diagnostic agent and medicaments containing them |
AU6187898A (en) * | 1997-01-30 | 1998-08-25 | Bristol-Myers Squibb Company | Method for preventing or treating low renin hypertension by administering an endothelin antagonist |
TW536540B (en) * | 1997-01-30 | 2003-06-11 | Bristol Myers Squibb Co | Endothelin antagonists: N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide and N-(4,5-dimethyl-3-isoxazolyl)-2'-[(3,3-dimethyl-2-oxo-1-pyrrolidinyl)methyl]-4'-(2-oxazolyl)[1,1'-biphe |
US6657104B1 (en) | 1997-10-16 | 2003-12-02 | Texas Systems, University Of The Board Of The Regents | Transgenic mouse model for cardiac hypertrophy and methods of use thereof |
DE19802969A1 (en) | 1998-01-27 | 1999-07-29 | Hoechst Marion Roussel De Gmbh | Preparation of imidazole derivatives, useful as intermediates for angiotensin II receptor antagonists, by cyclization of aminoacrylate esters |
DE19820064A1 (en) * | 1998-05-06 | 1999-11-11 | Hoechst Marion Roussel De Gmbh | Substituted sulfonylcyanamides, process for their preparation and their use as a medicament |
DE19832429A1 (en) * | 1998-07-18 | 2000-01-20 | Hoechst Marion Roussel De Gmbh | New imidazolylmethyl-biphenyl-sulfonylcyanamides, are sodium-dependent bicarbonate/chloride exchanger inhibitors used e.g. for treating cardiovascular disorders such as cardiac infarction |
DE19832428A1 (en) * | 1998-07-18 | 2000-01-20 | Hoechst Marion Roussel De Gmbh | New imidazolylmethyl-biphenyl-sulfonylcyanamides, are sodium-dependent bicarbonate/chloride exchanger inhibitors used e.g. for treating cardiovascular disorders such as cardiac infarction |
EP1165472A4 (en) | 1999-03-19 | 2002-11-20 | Bristol Myers Squibb Co | Methods for the preparation of biphenyl isoxazole sulfonamides |
AU2003280090A1 (en) * | 2002-06-28 | 2004-01-19 | Baylor College Of Medicine | Modulators of cdk9 as a therapeutic target in cardiac hypertrophy |
US20040106647A1 (en) * | 2002-06-28 | 2004-06-03 | Schneider Michael D. | Modulators of Cdk9 as a therapeutic target in cardiac hypertrophy |
US20050112128A1 (en) * | 2003-05-21 | 2005-05-26 | Myogen, Inc. And Board Of Regents, The University Of Texas System | Inhibition of protein kinase c-mu (PKD) as a treatment for cardiac hypertrophy and heart failure |
US8309562B2 (en) * | 2003-07-03 | 2012-11-13 | Myrexis, Inc. | Compounds and therapeutical use thereof |
EP1660092A2 (en) * | 2003-07-03 | 2006-05-31 | Myriad Genetics, Inc. | 4-arylamino-quinazolines as activators of caspases and inducers of apoptosis |
EP1685107B1 (en) * | 2003-11-03 | 2008-09-10 | Myogen, Inc. | 1,4-dihydropyridine compounds, pharmaceutical compositions, and methods for the treatment of cardiovascular disease |
US20050124634A1 (en) * | 2003-11-03 | 2005-06-09 | Myogen, Inc. | 1,4-dihydropyridine compounds, pharmaceutical compositions, and methods for the treatment of cardiovascular disease |
JP2007514665A (en) * | 2003-12-12 | 2007-06-07 | ミオゲン インコーポレイティッド | Enoximone preparations and methods for their use in the treatment of cardiac hypertrophy and heart failure |
US20060030611A1 (en) * | 2004-03-22 | 2006-02-09 | Myogen, Inc. | Enoximone sulfoxide enantiomers and their use in the treatment of PDE-III mediated diseases |
EP1737448A1 (en) * | 2004-03-22 | 2007-01-03 | Myogen, Inc. | (s) - enoximone sulfoxide and its use in the treatment of pde-iii mediated diseases |
EP1776108A1 (en) * | 2004-06-23 | 2007-04-25 | Myogen, Inc. | Enoximone formulations and their use in the treatment of pde-iii mediated diseases |
US8258145B2 (en) * | 2005-01-03 | 2012-09-04 | Myrexis, Inc. | Method of treating brain cancer |
EP1833482A4 (en) | 2005-01-03 | 2011-02-16 | Myriad Genetics Inc | Compounds and therapeutical use thereof |
WO2007014033A2 (en) * | 2005-07-22 | 2007-02-01 | The Regents Of The University Of Colorado, A Body Corporate | Inhibition of extracellular signal-regulated kinase 1/2 as a treatment for cardiac hypertrophy and heart failure |
JP2009520833A (en) * | 2005-12-20 | 2009-05-28 | ギリード・コロラド・インコーポレーテッド | 4,7-Dihydrothieno [2,3-b] pyridine compound and pharmaceutical composition |
PL2056882T3 (en) | 2006-08-01 | 2013-03-29 | Univ Texas | Identification of a micro-rna that activates expression of beta-myosin heavy chain |
US8440636B2 (en) | 2007-07-31 | 2013-05-14 | The Board Of Regents, The University Of Texas System | Micro-RNA family that modulates fibrosis and uses thereof |
WO2009117418A2 (en) | 2008-03-17 | 2009-09-24 | The Board Of Regents Of The University Of Texas System | Identification of micro-rnas involved in neuromuscular synapse maintenance and regeneration |
WO2012064743A2 (en) | 2010-11-08 | 2012-05-18 | The Johns Hopkins University | Methods for improving heart function |
GB2605148A (en) * | 2021-03-23 | 2022-09-28 | Vicore Pharma Ab | New compounds |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS5671074A (en) * | 1979-11-12 | 1981-06-13 | Takeda Chem Ind Ltd | 1,2-disubstituted-4-halogenoimidazole-5-acetic acid derivative |
US4355044A (en) * | 1980-12-19 | 1982-10-19 | Bernardo Heller | D-Phenylalanine treatment |
CA1334092C (en) * | 1986-07-11 | 1995-01-24 | David John Carini | Angiotensin ii receptor blocking imidazoles |
US5138069A (en) * | 1986-07-11 | 1992-08-11 | E. I. Du Pont De Nemours And Company | Angiotensin II receptor blocking imidazoles |
US5015651A (en) * | 1988-01-07 | 1991-05-14 | E. I. Du Pont De Nemours And Company | Treatment of hypertension with 1,2,4-angiotensin II antagonists |
CA1338238C (en) * | 1988-01-07 | 1996-04-09 | David John Carini | Angiotensin ii receptor blocking imidazoles and combinations thereof with diuretics and nsaids |
US5064825A (en) * | 1989-06-01 | 1991-11-12 | Merck & Co., Inc. | Angiotensin ii antagonists |
DE4010797A1 (en) * | 1990-04-04 | 1991-10-10 | Hoechst Ag | SUBSTITUTED AZOLES, METHOD FOR THE PRODUCTION THEREOF, MEANS CONTAINING THEM AND THE USE THEREOF |
US5135197A (en) * | 1990-08-30 | 1992-08-04 | Qualtec Data Products, Inc. | Equipment security method and apparatus |
US5126342A (en) * | 1990-10-01 | 1992-06-30 | Merck & Co., Inc. | Imidazole angiotensin ii antagonists incorporating acidic functional groups |
US5087634A (en) * | 1990-10-31 | 1992-02-11 | G. D. Searle & Co. | N-substituted imidazol-2-one compounds for treatment of circulatory disorders |
CA2058198A1 (en) * | 1991-01-04 | 1992-07-05 | Adalbert Wagner | Azole derivatives, process for their preparation, and their use |
US5236928A (en) * | 1991-03-19 | 1993-08-17 | Merck & Co., Inc. | Imidazole derivatives bearing acidic functional groups at the 5-position, their compositions and methods of use as angiotensin II antagonists |
JPH06510762A (en) * | 1991-08-19 | 1994-12-01 | イー・アイ・デュポン・ドゥ・ヌムール・アンド・カンパニー | Angiotensin 2 receptor blocking imidazolinone derivative |
DE4221009A1 (en) * | 1992-06-26 | 1994-01-05 | Bayer Ag | Imidazolyl-substituted cyclohexane derivatives |
CA2111662C (en) * | 1992-12-17 | 2004-11-23 | Hiroaki Yanagisawa | Biphenyl derivatives, their preparation and their use for the treatment of hypertension and cardiac disease |
-
1992
- 1992-08-21 TW TW081106607A patent/TW215434B/zh active
- 1992-12-21 CZ CS923811A patent/CZ281983B6/en not_active IP Right Cessation
- 1992-12-21 SK SK3811-92A patent/SK381192A3/en unknown
-
1993
- 1993-03-02 AT AT93103301T patent/ATE230732T1/en active
- 1993-03-02 EP EP93103301A patent/EP0560177B1/en not_active Expired - Lifetime
- 1993-03-02 ES ES93103301T patent/ES2187501T3/en not_active Expired - Lifetime
- 1993-03-02 DE DE59310323T patent/DE59310323D1/en not_active Expired - Lifetime
- 1993-03-02 DK DK93103301T patent/DK0560177T3/en active
- 1993-03-04 FI FI930970A patent/FI930970A/en unknown
- 1993-03-04 NZ NZ247059A patent/NZ247059A/en unknown
- 1993-03-05 BR BR9300761A patent/BR9300761A/en not_active Application Discontinuation
- 1993-03-05 PH PH45819A patent/PH31466A/en unknown
- 1993-03-05 NO NO930817A patent/NO303632B1/en unknown
- 1993-03-05 MA MA23107A patent/MA22814A1/en unknown
- 1993-03-05 CN CN93102412A patent/CN1036341C/en not_active Expired - Fee Related
- 1993-03-05 HU HU9300618A patent/HUT64041A/en unknown
- 1993-03-05 PL PL93297955A patent/PL173023B1/en unknown
- 1993-03-05 KR KR1019930003270A patent/KR930019637A/en not_active Application Discontinuation
- 1993-03-05 AU AU34011/93A patent/AU663565B2/en not_active Ceased
- 1993-03-05 CA CA002091135A patent/CA2091135A1/en not_active Abandoned
- 1993-03-05 JP JP04476993A patent/JP3542813B2/en not_active Expired - Lifetime
- 1993-03-05 RU RU93004577A patent/RU2116300C1/en active
- 1993-03-05 ZA ZA931585A patent/ZA931585B/en unknown
- 1993-03-07 IL IL104971A patent/IL104971A0/en unknown
-
1995
- 1995-06-07 US US08/479,561 patent/US5604251A/en not_active Expired - Lifetime
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