UA40578C2 - Сульфоніламінопіримідини і фармацевтичний препарат на їх основі - Google Patents

Сульфоніламінопіримідини і фармацевтичний препарат на їх основі

Info

Publication number
UA40578C2
UA40578C2 UA94005281A UA94005281A UA40578C2 UA 40578 C2 UA40578 C2 UA 40578C2 UA 94005281 A UA94005281 A UA 94005281A UA 94005281 A UA94005281 A UA 94005281A UA 40578 C2 UA40578 C2 UA 40578C2
Authority
UA
Ukraine
Prior art keywords
sulfonylaminopyrimidines
compounds
formula
diseases
salts
Prior art date
Application number
UA94005281A
Other languages
English (en)
Russian (ru)
Inventor
Волкер БРОЙ
Каспар Буррі
Каспар Бурри
Жан-Марі Кассал
Жан-Мари Кассал
Мартіне Клозел
Мартине КЛОЗЕЛ
Джорж Хірт
Джорж ХИРТ
Бернд-Міхайл Леффлер
Бернд-Михайл ЛЕФФЛЕР
Марсел МЮЛЛЕР
Вернер НАЙДХАРТ
Енрі Рамуз
Энри Рамуз
Original Assignee
Ф.Хоффманн-Ля Рош Аг
Ф. Хоффманн Ля Рош Аг
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ф.Хоффманн-Ля Рош Аг, Ф. Хоффманн Ля Рош Аг filed Critical Ф.Хоффманн-Ля Рош Аг
Publication of UA40578C2 publication Critical patent/UA40578C2/uk

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/69Benzenesulfonamido-pyrimidines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic 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
    • C07D413/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Abstract

Цей винахід належить до нових сульфоніламінопіримідинів і їх застосування як лікарських препаратів. Сполуки наведеної формули є інгібіторами ендотеліальних рецепторів. Тому вони можуть використовуватись для лікування захворювань, пов’язаних з активністю ендотелія, насамперед серцевосудинних захворювань, як гіпертонія, ішемія, спазми судин і стенокардія. Винахід стосується застосування сполук формули I і їх солей для лікування вищенаведених захворювань, їх застосування як біологічно активних речовин для одержання лікарських засобів, призначених для зазначених цілей, а також фармацевтичних препаратів, що містять сполуки формули I або їх солі.
UA94005281A 1993-06-28 1994-06-27 Сульфоніламінопіримідини і фармацевтичний препарат на їх основі UA40578C2 (uk)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH192493 1993-06-28

Publications (1)

Publication Number Publication Date
UA40578C2 true UA40578C2 (uk) 2001-08-15

Family

ID=4221780

Family Applications (1)

Application Number Title Priority Date Filing Date
UA94005281A UA40578C2 (uk) 1993-06-28 1994-06-27 Сульфоніламінопіримідини і фармацевтичний препарат на їх основі

Country Status (41)

Country Link
US (1) US5541186A (uk)
EP (1) EP0633259B1 (uk)
JP (1) JP2545200B2 (uk)
KR (1) KR100338905B1 (uk)
CN (1) CN1050839C (uk)
AT (1) ATE175669T1 (uk)
AU (1) AU678467B2 (uk)
BG (1) BG61691B1 (uk)
BR (2) BR9402558A (uk)
CA (1) CA2125730C (uk)
CO (1) CO4230230A1 (uk)
CZ (1) CZ287184B6 (uk)
DE (1) DE59407626D1 (uk)
DK (1) DK0633259T3 (uk)
EC (1) ECSP941111A (uk)
ES (1) ES2127850T3 (uk)
FI (1) FI112944B (uk)
GR (1) GR3029874T3 (uk)
HR (1) HRP940370B1 (uk)
HU (2) HUT67636A (uk)
IL (1) IL110089A (uk)
IS (1) IS4185A (uk)
LT (1) LT3723B (uk)
LV (1) LV11175B (uk)
MY (1) MY110871A (uk)
NO (1) NO306403B1 (uk)
NZ (1) NZ260842A (uk)
PE (1) PE56794A1 (uk)
PH (1) PH30688A (uk)
PL (2) PL175771B1 (uk)
RO (1) RO114325B1 (uk)
RU (1) RU2142457C1 (uk)
SG (1) SG43888A1 (uk)
SI (1) SI0633259T1 (uk)
SK (1) SK280736B6 (uk)
SV (1) SV1994000028A (uk)
TW (1) TW394761B (uk)
UA (1) UA40578C2 (uk)
UY (1) UY23797A1 (uk)
YU (1) YU40794A (uk)
ZA (1) ZA944434B (uk)

Families Citing this family (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5514696A (en) * 1992-05-06 1996-05-07 Bristol-Myers Squibb Co. Phenyl sulfonamide endothelin antagonists
US6063911A (en) * 1993-12-01 2000-05-16 Marine Polymer Technologies, Inc. Methods and compositions for treatment of cell proliferative disorders
US6743783B1 (en) * 1993-12-01 2004-06-01 Marine Polymer Technologies, Inc. Pharmaceutical compositions comprising poly-β-1→4-N-acetylglucosamine
US5612359A (en) * 1994-08-26 1997-03-18 Bristol-Myers Squibb Company Substituted biphenyl isoxazole sulfonamides
AU714640B2 (en) 1994-11-16 2000-01-06 H. Lundbeck A/S Dihydropyrimidines and uses thereof
US6268369B1 (en) 1994-11-16 2001-07-31 Synaptic Pharmaceutical Corporation 5-(heterocyclic alkyl)-6-aryl-dihydropyrimidines
CA2162630C (en) * 1994-11-25 2007-05-01 Volker Breu Sulfonamides
TW313568B (uk) * 1994-12-20 1997-08-21 Hoffmann La Roche
ES2196090T3 (es) 1994-12-28 2003-12-16 Kowa Co Derivados pirimidinicos.
US5760038A (en) * 1995-02-06 1998-06-02 Bristol-Myers Squibb Company Substituted biphenyl sulfonamide endothelin antagonists
US5780473A (en) * 1995-02-06 1998-07-14 Bristol-Myers Squibb Company Substituted biphenyl sulfonamide endothelin antagonists
US5573762A (en) * 1995-04-24 1996-11-12 Genentech, Inc. Use of leukemia inhibitory factor specific antibodies and endothelin antagonists for treatment of cardiac hypertrophy
US5739333A (en) * 1995-05-16 1998-04-14 Tanabe Seiyaku Co., Ltd. Sulfonamide derivative and process for preparing the same
US5846990A (en) * 1995-07-24 1998-12-08 Bristol-Myers Squibb Co. Substituted biphenyl isoxazole sulfonamides
CN1105711C (zh) * 1995-09-06 2003-04-16 兴和株式会社 嘧啶衍生物
JPH09124620A (ja) 1995-10-11 1997-05-13 Bristol Myers Squibb Co 置換ビフェニルスルホンアミドエンドセリン拮抗剤
CZ260596A3 (en) * 1995-10-12 1997-12-17 Hoffmann La Roche Sulfonamide derivative, process of its preparation and pharmaceutical composition containing thereof
US6228861B1 (en) 1995-11-16 2001-05-08 Synaptic Pharmaceutical Corporation Dihydropyrimidines and uses thereof
ES2156305T3 (es) * 1995-12-20 2001-06-16 Yamanouchi Pharma Co Ltd Derivados de ariletenosulfonamida y composiciones de farmacos que los contienen.
SG87053A1 (en) 1996-02-20 2002-03-19 Bristol Myers Squibb Co High melt polymorth of the compound n-(3,4-dimethyl-5-isoxazolyl)-4'- (2-oxazolyl) [1,1'-biphenyl]-2-sulfonamide
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
US6172066B1 (en) 1996-05-16 2001-01-09 Synaptic Pharmaceutical Corporation Dihydropyrimidines and uses thereof
US6245773B1 (en) 1996-05-16 2001-06-12 Synaptic Pharmaceutical Corporation 5-(heterocyclic alkyl)-6-aryl-dihydropyrimidines
EP0956041A1 (en) * 1996-09-16 1999-11-17 Dalhousie University Use of igf-i for the treatment of polycystic kidney disease and related indications
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
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
US6680323B2 (en) 1998-12-23 2004-01-20 Synaptic Pharmaceutical Corporation Dihydropyrimidines and uses thereof
US6274585B1 (en) 1998-12-23 2001-08-14 Synaptic Pharmaceutical Corporation Dihydropyrimidines and uses thereof
US7566452B1 (en) 1999-05-04 2009-07-28 New York University Cancer treatment with endothelin receptor antagonists
CA2315614C (en) * 1999-07-29 2004-11-02 Pfizer Inc. Pyrazoles
AU2001265871A1 (en) * 2000-04-25 2001-11-07 Actelion Pharmaceuticals Ltd Substituted sulfonylaminopyrimidines
US6720324B2 (en) 2000-07-05 2004-04-13 Synaptic Pharmaceutical Corporation Selective melanin concentrating hormone-1 (MCH1) receptor antagonists and uses thereof
MY140724A (en) 2000-07-21 2010-01-15 Actelion Pharmaceuticals Ltd Novel arylethene-sulfonamides
US6670362B2 (en) 2000-09-20 2003-12-30 Pfizer Inc. Pyridazine endothelin antagonists
US7091201B2 (en) 2000-09-25 2006-08-15 Actelion Pharmaceuticals Ltd. Arylalkane-sulfonamides having endothelin-antagonist activity
US6639082B2 (en) 2000-10-17 2003-10-28 Bristol-Myers Squibb Company Methods for the preparation of biphenyl isoxazole sulfonamides
KR100374326B1 (ko) * 2000-11-29 2003-03-03 한국과학기술연구원 6-히드록시-1, 3-디옥신-4-온 고리를 가진인간면역결핍바이러스 프로테아제 억제 화합물 및 그의제조방법
CN100432070C (zh) 2000-12-18 2008-11-12 埃科特莱茵药品有限公司 新颖的磺酰胺类化合物及其作为内皮素受体拮抗剂的应用
WO2002083650A1 (en) * 2001-04-11 2002-10-24 Actelion Pharmaceuticals Ltd Novel sulfonylamino-pyrimidines
AU2011218661B2 (en) * 2002-05-24 2012-07-05 Millennium Pharmaceuticals, Inc. CCR9 inhibitors and methods of use thereof
AU2003248549B2 (en) 2002-05-24 2010-04-08 Millennium Pharmaceuticals, Inc. CCR9 inhibitors and methods of use thereof
US7741519B2 (en) * 2007-04-23 2010-06-22 Chemocentryx, Inc. Bis-aryl sulfonamides
US7420055B2 (en) * 2002-11-18 2008-09-02 Chemocentryx, Inc. Aryl sulfonamides
CN100360526C (zh) * 2002-11-18 2008-01-09 坎莫森特里克斯公司 芳基磺酰胺
US7227035B2 (en) * 2002-11-18 2007-06-05 Chemocentryx Bis-aryl sulfonamides
ATE423103T1 (de) 2002-12-02 2009-03-15 Actelion Pharmaceuticals Ltd Pyrimidin-sulfonamide und ihre verwendung als endothelin-rezeptor-antagonisten
DE102004027119A1 (de) 2003-06-06 2004-12-30 Schott Ag UV-Strahlung absorbierendes Glas mit geringer Absorption im sichtbaren Bereich, ein Verfahren zu seiner Herstellung sowie dessen Verwendung
JP4717876B2 (ja) * 2004-03-05 2011-07-06 エフ.ホフマン−ラ ロシュ アーゲー P2x3およびp2x2/3アンタゴニストとしてのジアミノピリミジン
TWI380816B (zh) * 2004-04-13 2013-01-01 Synta Pharmaceuticals Corp 抑制介白素-12(il-12)生成之二鹽抑制劑
KR100847203B1 (ko) * 2004-06-28 2008-07-17 에프. 호프만-라 로슈 아게 피리미딘 유도체
ATE509011T1 (de) * 2004-06-28 2011-05-15 Hoffmann La Roche Pyrimidinderivate als 11beta-hsd1-inhibitoren
TW200628467A (en) 2004-11-11 2006-08-16 Actelion Pharmaceuticals Ltd Novel sulfamides
EP1924564B1 (en) * 2005-09-01 2016-11-09 F.Hoffmann-La Roche Ag Diaminopyrimidines as p2x3 and p2x2/3 modulators
CN101300235B (zh) 2005-09-01 2011-12-07 弗·哈夫曼-拉罗切有限公司 作为p2x3和p2x2/3调节剂的二氨基嘧啶类化合物
JP4850912B2 (ja) * 2005-09-01 2012-01-11 エフ.ホフマン−ラ ロシュ アーゲー P2x3およびp3x2/3モジュレーターとしてのジアミノピリミジン
JP2009530284A (ja) * 2006-03-13 2009-08-27 エンサイシブ・ファーマシューティカルズ・インコーポレイテッド 拡張期心不全を治療するための方法と組成物
AU2007225207A1 (en) * 2006-03-13 2007-09-20 Encysive Pharmaceuticals, Inc. Formulations of sitaxsentan sodium
US20080026061A1 (en) * 2006-06-22 2008-01-31 Reichwein John F Crystalline N-(4-chloro-3-methyl-5-isoxazolyl)-2-[2-methyl-4.5-(methylenedioxy)phenylacetyl]-thiophene-3-sulfonamide
AR062501A1 (es) 2006-08-29 2008-11-12 Actelion Pharmaceuticals Ltd Composiciones terapeuticas
US8871247B2 (en) * 2007-02-19 2014-10-28 Marine Polymer Technologies, Inc. Hemostatic compositions and therapeutic regimens
MX2010001837A (es) 2007-08-17 2010-03-10 Actelion Pharmaceuticals Ltd Derivados de 4-pirimidinasulfamida.
WO2011130646A1 (en) 2010-04-15 2011-10-20 Marine Polymer Technologies, Inc. Anti-bacterial applications of poly -n-acetylglucosamine nanofibers
AU2012242479B2 (en) 2011-04-15 2015-04-16 Marine Polymer Technologies, Inc. Treatment of disease with poly-n-acetylglucosamine nanofibers
RU2604060C1 (ru) * 2015-10-06 2016-12-10 федеральное государственное бюджетное образовательное учреждение высшего образования "Санкт-Петербургская государственная химико-фармацевтическая академия" Министерства здравоохранения Российской Федерации (ФГБОУ ВО СПХФА Минздрава России) Способ получения 2,5-дизамещенных 6-гидроксипиримидин-4(3н)-онов
UA120571C2 (uk) 2016-03-22 2019-12-26 Мерк Шарп Енд Дохме Корп. Алостеричні модулятори нікотинових ацетилхолінових рецепторів
RU2643356C2 (ru) * 2016-06-22 2018-02-01 федеральное государственное бюджетное образовательное учреждение высшего образования "Волгоградский государственный медицинский университет" Министерства здравоохранения Российской Федерации Новое n-арилсульфамидное производное о-бензоиламинобензойной кислоты, обладающее анксиолитической, актопротекторной и антидепрессивной активностью

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3663598D1 (en) 1985-07-24 1989-06-29 Siemens Ag Nuclear-fuel assembly
TW270116B (uk) 1991-04-25 1996-02-11 Hoffmann La Roche
RU2086544C1 (ru) 1991-06-13 1997-08-10 Хоффманн-Ля Рош АГ Бензолсульфонамидные производные пиримидина или их соли, фармацевтическая композиция для лечения заболеваний, связанных с активностью эндотелина
TW287160B (uk) * 1992-12-10 1996-10-01 Hoffmann La Roche

Also Published As

Publication number Publication date
SK77994A3 (en) 1995-03-08
AU6594894A (en) 1995-01-05
FI112944B (fi) 2004-02-13
US5541186A (en) 1996-07-30
PL175771B1 (pl) 1999-02-26
DE59407626D1 (de) 1999-02-25
FI943084A (fi) 1994-12-29
BR1100089A (pt) 2000-03-14
YU40794A (sh) 1997-07-31
CN1050839C (zh) 2000-03-29
PL304007A1 (en) 1995-01-09
IL110089A0 (en) 1994-10-07
JP2545200B2 (ja) 1996-10-16
HU211533A9 (en) 1995-12-28
HRP940370A2 (en) 1996-12-31
TW394761B (en) 2000-06-21
BG61691B1 (bg) 1998-03-31
CA2125730A1 (en) 1994-12-29
AU678467B2 (en) 1997-05-29
NZ260842A (en) 1996-05-28
SI0633259T1 (en) 1999-06-30
ES2127850T3 (es) 1999-05-01
IL110089A (en) 2000-08-31
ZA944434B (en) 1995-01-03
NO942428D0 (no) 1994-06-27
SG43888A1 (en) 1997-11-14
KR100338905B1 (ko) 2002-11-13
BR9402558A (pt) 1995-03-28
ECSP941111A (es) 1994-11-16
SK280736B6 (sk) 2000-07-11
HU9401907D0 (en) 1994-09-28
LTIP1979A (en) 1995-01-31
DK0633259T3 (da) 1999-09-06
PE56794A1 (es) 1995-02-07
HRP940370B1 (en) 1999-12-31
BG98880A (bg) 1995-05-31
LV11175A (lv) 1996-04-20
KR950000676A (ko) 1995-01-03
ATE175669T1 (de) 1999-01-15
LT3723B (en) 1996-02-26
CZ287184B6 (en) 2000-10-11
CO4230230A1 (es) 1995-10-19
IS4185A (is) 1994-12-29
EP0633259B1 (de) 1999-01-13
GR3029874T3 (en) 1999-07-30
LV11175B (en) 1996-06-20
CN1106007A (zh) 1995-08-02
JPH0717972A (ja) 1995-01-20
MY110871A (en) 1999-05-31
UY23797A1 (es) 1994-12-16
RU2142457C1 (ru) 1999-12-10
FI943084A0 (fi) 1994-06-27
CA2125730C (en) 2005-10-18
PH30688A (en) 1997-09-16
NO306403B1 (no) 1999-11-01
SV1994000028A (es) 1995-04-19
RO114325B1 (ro) 1999-03-30
EP0633259A1 (de) 1995-01-11
NO942428L (no) 1994-12-29
CZ157394A3 (en) 1995-01-18
RU94022258A (ru) 1996-04-20
PL177031B1 (pl) 1999-09-30
HUT67636A (en) 1995-04-28

Similar Documents

Publication Publication Date Title
UA40578C2 (uk) Сульфоніламінопіримідини і фармацевтичний препарат на їх основі
TR200103178T2 (tr) İntegrinlerin reseptörlere bağlanmasını engelleyen karboksilik asit türevleri.
TW376319B (en) Pharmaceutical composition containing risperidone pamoate and having a long acting activity for treating psychoses induced by the release of dopamine
ES2145913T3 (es) Inhibidores de metaloproteasas.
MX9801716A (es) Derivados de meta-guanidina, urea, tiourea o acido aminobenzoico azaciclico, como antagonistas de integrina.
ATE556705T1 (de) Darreichungsform enthaltend taxol in kristalliner form
MY120064A (en) Indole derivatives as inhibitors or factor xa
NO20005161D0 (no) N,N-disubstituerte amider som inhiberer bindingen av integriner til deres reseptorer
GEP20063885B (en) Indazole compounds and pharmaceutical compositions for inhibiting protein kinases, and methods for their use
ATE278397T1 (de) Verwendung von cytoskelettinhibitoren zur vorbeugung der restenose
ATE264692T1 (de) Verwendung von no synthase hemmern und fängern von reaktiven sauerstoffsformen zur behandlung von ischämie
MY138860A (en) Hiv protease inhibitors.
KR960013371A (ko) 약학적 혼합물
IL146312A (en) 3-(2-oxo-pyridinyl)-acylamino-propanoic acid derivatives that inhibit the binding of integrins to their receptors and pharmaceutical compositions comprising the same
YU63699A (sh) Preparati za tretiranje i prevenciju arterijske tromboze i korišćenje inhibitora faktora xa samog ili u kombinaciji sa plateletnim antiagregacionim agensom
GEP20033118B (en) Meta-Azacyclic Amino Benzoic Acid Compounds and Derivatives Thereof Being Integrin Inhibitors, Pharmaceutical Composition and Use Thereof
GR3035014T3 (en) N-(3-amino-2-hydroxybutyl)sulphonamide derivatives as hiv protease inhibitors
ES2088128T3 (es) Aminosulfonilureas inhibidoras de acat.
EP1019047A4 (en) ANTITHROMBOTIC AGENTS
AU5879798A (en) Agents inhibiting progress of pterygium and postoperative recurrence of the same
EP1027051A4 (en) ANTITHROMBOTIC AGENTS
BR9916733A (pt) Derivados de arilalcanoìla, processos para sua preparação, seu uso e composições farmacêuticas que os contêm
BR9810314A (pt) Derivados de 5-substituìdo-1,2,4-tiadiazolila que inibem de angiogênese
DE59406568D1 (de) Cephalostatin-analoga und ihre verwendung als antitumormittel
RU97122020A (ru) Производные 1,2,5-оксадиазоло[3,4-d]пиридазин-5,6-диоксида в качестве активаторов растворимой формы гуанилатциклазы и средств для лечения заболеваний сердечно-сосудистой системы и фармацевтические композиции на их основе