RU2080321C1 - Азотсодержащие гетероциклические соединения в виде рацемата или отдельных энантиомеров, являющиеся ингибиторами биосинтеза лейкотриена - Google Patents

Азотсодержащие гетероциклические соединения в виде рацемата или отдельных энантиомеров, являющиеся ингибиторами биосинтеза лейкотриена Download PDF

Info

Publication number
RU2080321C1
RU2080321C1 SU925052823A SU5052823A RU2080321C1 RU 2080321 C1 RU2080321 C1 RU 2080321C1 SU 925052823 A SU925052823 A SU 925052823A SU 5052823 A SU5052823 A SU 5052823A RU 2080321 C1 RU2080321 C1 RU 2080321C1
Authority
RU
Russia
Prior art keywords
alkyl
hydrogen
formula
carbon atoms
group
Prior art date
Application number
SU925052823A
Other languages
English (en)
Russian (ru)
Inventor
Лейзер Эдвард
Эдамс Джулиен
Майо Клара
Ферина Питер
Original Assignee
Берингер Ингельгейм Фармасьютикалз Инк.
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 Берингер Ингельгейм Фармасьютикалз Инк. filed Critical Берингер Ингельгейм Фармасьютикалз Инк.
Application granted granted Critical
Publication of RU2080321C1 publication Critical patent/RU2080321C1/ru

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D277/28—Radicals substituted by nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
    • C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
    • C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles 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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/16—Otologicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62—Benzothiazoles
    • C07D277/68—Benzothiazoles 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
    • C07D277/82—Nitrogen atoms
    • 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
    • C07D413/10—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 carbon chain containing aromatic rings
    • 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
    • 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
    • C07D413/14—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
SU925052823A 1991-09-24 1992-09-23 Азотсодержащие гетероциклические соединения в виде рацемата или отдельных энантиомеров, являющиеся ингибиторами биосинтеза лейкотриена RU2080321C1 (ru)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US76459191A 1991-09-24 1991-09-24
US764591 1991-09-24
US07/937,315 US5296486A (en) 1991-09-24 1992-09-04 Leukotriene biosynthesis inhibitors
US937315 1992-09-04

Publications (1)

Publication Number Publication Date
RU2080321C1 true RU2080321C1 (ru) 1997-05-27

Family

ID=27117489

Family Applications (1)

Application Number Title Priority Date Filing Date
SU925052823A RU2080321C1 (ru) 1991-09-24 1992-09-23 Азотсодержащие гетероциклические соединения в виде рацемата или отдельных энантиомеров, являющиеся ингибиторами биосинтеза лейкотриена

Country Status (19)

Country Link
US (2) US5296486A (Direct)
EP (1) EP0535521A3 (Direct)
JP (1) JPH05213911A (Direct)
KR (1) KR930005992A (Direct)
AU (1) AU661034B2 (Direct)
CA (1) CA2078810A1 (Direct)
CZ (1) CZ293392A3 (Direct)
FI (1) FI924277A7 (Direct)
HU (2) HU213113B (Direct)
IL (1) IL103251A (Direct)
LV (1) LV11181B (Direct)
MX (1) MX9205432A (Direct)
NO (1) NO923695L (Direct)
NZ (1) NZ244429A (Direct)
PL (1) PL296038A1 (Direct)
RU (1) RU2080321C1 (Direct)
SG (1) SG46381A1 (Direct)
SK (1) SK293392A3 (Direct)
TW (1) TW218877B (Direct)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2212407C2 (ru) * 1997-11-10 2003-09-20 Бристол-Маерс Сквибб Компани Бензотиазольные ингибиторы протеинтирозинкиназ
RU2334742C2 (ru) * 2003-01-13 2008-09-27 Ф.Хоффманн-Ля Рош Аг Производные бензоксазола и фармацевтическая композиция, обладающая свойствами лигандов рецептора аденозина
RU2434003C2 (ru) * 2006-05-11 2011-11-20 Санофи-Авентис Фениламинобензоксазолзамещенные карбоновые кислоты, способ их получения и их применение в качестве лекарственных средств

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5698550A (en) * 1993-06-14 1997-12-16 Pfizer Inc. Tetralin and chroman derivatives useful in the treatment of asthma, arthritis and related diseases
CO4520280A1 (es) * 1993-10-26 1997-10-15 Boehringer Ingelheim Pharma Derivados de pirrolidina, inhibidores de la bioscientesis de leucotrienos
DE4428531A1 (de) 1994-08-12 1996-02-15 Boehringer Ingelheim Kg Neue enantiomerenreine Pyridylcycloalkylethylamine und deren Salze sowie Verfahren zu ihrer Herstellung
US5616717A (en) * 1995-04-20 1997-04-01 Boehringer Ingelheim Pharmaceuticals, Inc. Process for the preparation of pure enantiomers of 1-(2-pyridyl)-2-cyclohexylethylamine
US5856497A (en) * 1995-12-11 1999-01-05 Boehringer Ingelheim Pharmaceuticals, Inc. Asymmetric synthesis of α-cycloalkylalkyl substituted methanamines
US5952326A (en) * 1997-12-10 1999-09-14 Pfizer Inc. Tetralin and chroman derivatives useful in the treatment of asthma, arthritis and related diseases
US6329372B1 (en) 1998-01-27 2001-12-11 Celltech Therapeutics Limited Phenylalanine derivatives
ATE273273T1 (de) * 1998-02-26 2004-08-15 Celltech Therapeutics Ltd Phenylalaninderivate als inhibitoren von alpha4 integrinen
GB9805655D0 (en) 1998-03-16 1998-05-13 Celltech Therapeutics Ltd Chemical compounds
US6521626B1 (en) 1998-03-24 2003-02-18 Celltech R&D Limited Thiocarboxamide derivatives
GB9811159D0 (en) 1998-05-22 1998-07-22 Celltech Therapeutics Ltd Chemical compounds
GB9811969D0 (en) * 1998-06-03 1998-07-29 Celltech Therapeutics Ltd Chemical compounds
GB9812088D0 (en) 1998-06-05 1998-08-05 Celltech Therapeutics Ltd Chemical compounds
GB9814414D0 (en) 1998-07-03 1998-09-02 Celltech Therapeutics Ltd Chemical compounds
GB9821061D0 (en) * 1998-09-28 1998-11-18 Celltech Therapeutics Ltd Chemical compounds
GB9821222D0 (en) 1998-09-30 1998-11-25 Celltech Therapeutics Ltd Chemical compounds
GB9825652D0 (en) 1998-11-23 1999-01-13 Celltech Therapeutics Ltd Chemical compounds
GB9826174D0 (en) 1998-11-30 1999-01-20 Celltech Therapeutics Ltd Chemical compounds
US6800486B1 (en) 1998-12-07 2004-10-05 Smithkline Beecham Corporation Method for quantitative determination of amino acids
WO2000034251A1 (en) * 1998-12-07 2000-06-15 Smithkline Beecham Corporation A method for quantitative determination of amino acids
PL350050A1 (en) 1999-01-22 2002-10-21 Elan Pharm Inc Acyl derivatives which treat vla-4 related disorders
EP1147091A2 (en) 1999-01-22 2001-10-24 Elan Pharmaceuticals, Inc. Fused ring heteroaryl and heterocyclic compounds which inhibit leukocyte adhesion mediated by vla-4
US6436904B1 (en) 1999-01-25 2002-08-20 Elan Pharmaceuticals, Inc. Compounds which inhibit leukocyte adhesion mediated by VLA-4
WO2000045635A1 (en) * 1999-02-08 2000-08-10 Lion Bioscience Ag Thiazole derivatives and combinatorial libraries thereof
US6518283B1 (en) * 1999-05-28 2003-02-11 Celltech R&D Limited Squaric acid derivatives
US6534513B1 (en) 1999-09-29 2003-03-18 Celltech R&D Limited Phenylalkanoic acid derivatives
US6436977B1 (en) 1999-09-29 2002-08-20 Pfizer Inc. Dosing regimens for lasofoxifene
US6455539B2 (en) 1999-12-23 2002-09-24 Celltech R&D Limited Squaric acid derivates
ES2295150T3 (es) 2000-04-17 2008-04-16 Ucb Pharma, S.A. Derivados de enamina como moleculas de adhesion celular.
FR2808798A1 (fr) * 2000-05-09 2001-11-16 Hoechst Marion Roussel Inc Nouveaux derives antagonistes du recepteur de la vitronectine
US6403608B1 (en) 2000-05-30 2002-06-11 Celltech R&D, Ltd. 3-Substituted isoquinolin-1-yl derivatives
US6545013B2 (en) 2000-05-30 2003-04-08 Celltech R&D Limited 2,7-naphthyridine derivatives
EP1301488A1 (en) 2000-07-07 2003-04-16 Celltech R&D Limited Squaric acid derivatives containing a bicyclic heteroaromatic ring as integrin antagonists
AU2001275724A1 (en) 2000-08-02 2002-02-13 Celltech R&D Limited 3-substituted isoquinolin-1-yl derivatives
DE60139964D1 (de) 2000-12-15 2009-10-29 Vertex Pharma Bakterielle Gyrase-Hemmer sowie deren Verwendung
TWI281470B (en) 2002-05-24 2007-05-21 Elan Pharm Inc Heterocyclic compounds which inhibit leukocyte adhesion mediated by alpha4 integrins
TW200307671A (en) 2002-05-24 2003-12-16 Elan Pharm Inc Heteroaryl compounds which inhibit leukocyte adhesion mediated by α 4 integrins
SE0202429D0 (sv) * 2002-08-14 2002-08-14 Astrazeneca Ab Novel Compounds
PL371841A1 (pl) * 2004-12-20 2006-06-26 ADAMED Sp.z o.o. Nowe związki pochodne kwasu 3-fenylopropionowego
PL372332A1 (pl) * 2005-01-19 2006-07-24 ADAMED Sp.z o.o. Nowe związki, pochodne kwasu 3-fenylopropionowego
PL372356A1 (pl) * 2005-01-20 2006-07-24 ADAMED Sp.z o.o. Nowe związki, pochodne kwasu 3-fenylopropionowego
KR20080059268A (ko) 2005-09-29 2008-06-26 엘란 파마슈티칼스, 인크. Ｖｌａ-4에 의해 매개되는 백혈구 부착을 억제하는피리미디닐 아미드 화합물
ATE502031T1 (de) 2005-09-29 2011-04-15 Elan Pharm Inc Carbamatverbindungen, die die durch vla-4 vermittelte leukozytenadhäsion inhibieren
TWI389904B (zh) 2006-02-27 2013-03-21 Elan Pharm Inc 抑制由ｖｌａ-４所調節的白血球黏附之嘧啶磺醯胺化合物
CL2007001927A1 (es) * 2006-06-30 2008-05-16 Basf Ag Compuestos derivados de 1-(azolin-2-il)-amino-2-aril-1-heteroaril-etano; composicion agricola; composicion veterinaria; metodo para combatir plagas animales; metodo para proteger plantas; metodo para la proteccion de semillas; semilla; uso de dicho c
WO2009126635A1 (en) * 2008-04-09 2009-10-15 Abbott Laboratories 2-amino-benzothiazole derivates useful as inhibitors of rock kinases
SI2336125T1 (sl) * 2008-04-11 2013-04-30 Janssen Pharmaceutica N.V. Tiazolopiridin-2-iloksi-fenil in tiazolopirazin-2-iloksi-fenil amini kot modulatorji levkotrien a4 hidrolaze
WO2010057922A1 (en) 2008-11-24 2010-05-27 Basf Se Curable composition comprising a thermolatent base
EP2424841A1 (en) 2009-04-27 2012-03-07 Elan Pharmaceuticals Inc. Pyridinone antagonists of alpha-4 integrins
UY35592A (es) 2013-06-03 2014-12-31 Bayer Pharma AG Benzoxazoles sustituidos
US20160108027A1 (en) 2013-06-03 2016-04-21 Bayer Pharma Aktiengesellschaft Substituted benzoxazoles

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3419994A1 (de) * 1984-05-29 1985-12-05 Hoechst Ag, 6230 Frankfurt Benzoxazolyl- und benzthiazolyl-aminosaeuren, ihre herstellung und verwendung im pflanzenschutz
DE3533331A1 (de) * 1985-09-18 1987-03-26 Heumann Ludwig & Co Gmbh Pyridothiazolderivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel
US4873346A (en) * 1985-09-20 1989-10-10 The Upjohn Company Substituted benzothiazoles, benzimidazoles, and benzoxazoles
FI91859C (fi) * 1987-06-17 1994-08-25 Eisai Co Ltd Analogiamenetelmä antiallergisena aineena aktiivisen bentsotiatsolijohdannaisen valmistamiseksi
AU653349B2 (en) * 1990-07-24 1994-09-29 Agilent Technologies Australia (M) Pty Ltd Inductively coupled plasma spectroscopy
IE920921A1 (en) * 1991-04-04 1992-10-07 Eisai Co Ltd Benzothiazole derivative

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Патент ФРГ N 3419994, кл. С 07 D 277/82, 1985. S. Advani, J. Sam. J. Pharm. Sci., 1968, v. 57, p. 1965. Патент ЕПВ N 0163236, кл. С 07 D 263/58, 1985. *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2212407C2 (ru) * 1997-11-10 2003-09-20 Бристол-Маерс Сквибб Компани Бензотиазольные ингибиторы протеинтирозинкиназ
RU2334742C2 (ru) * 2003-01-13 2008-09-27 Ф.Хоффманн-Ля Рош Аг Производные бензоксазола и фармацевтическая композиция, обладающая свойствами лигандов рецептора аденозина
RU2434003C2 (ru) * 2006-05-11 2011-11-20 Санофи-Авентис Фениламинобензоксазолзамещенные карбоновые кислоты, способ их получения и их применение в качестве лекарственных средств

Also Published As

Publication number Publication date
NO923695L (no) 1993-03-25
CA2078810A1 (en) 1993-03-25
SG46381A1 (en) 1998-02-20
AU661034B2 (en) 1995-07-13
FI924277L (fi) 1993-03-25
CZ293392A3 (en) 1993-12-15
EP0535521A2 (en) 1993-04-07
HU213113B (en) 1997-02-28
FI924277A7 (fi) 1993-03-25
HU9203033D0 (en) 1992-12-28
HUT64951A (en) 1994-03-28
SK293392A3 (en) 1995-09-13
NZ244429A (en) 1995-07-26
EP0535521A3 (en) 1993-06-16
TW218877B (Direct) 1994-01-11
NO923695D0 (no) 1992-09-23
LV11181A (lv) 1996-04-20
LV11181B (en) 1996-08-20
FI924277A0 (fi) 1992-09-24
MX9205432A (es) 1993-03-31
IL103251A (en) 1996-09-12
US5552421A (en) 1996-09-03
PL296038A1 (en) 1993-10-18
US5296486A (en) 1994-03-22
JPH05213911A (ja) 1993-08-24
HU210881A9 (en) 1995-09-28
AU2527492A (en) 1993-03-25
KR930005992A (ko) 1993-04-20

Similar Documents

Publication Publication Date Title
RU2080321C1 (ru) Азотсодержащие гетероциклические соединения в виде рацемата или отдельных энантиомеров, являющиеся ингибиторами биосинтеза лейкотриена
AU728812B2 (en) Thiazole benzenesulfonamides as beta3 agonists for the treatment of diabetes and obesity
US11396504B2 (en) Alkoxybenzo-five-membered (six-membered) heterocyclic amine compound and pharmaceutical use thereof
BRPI0212775B1 (pt) composto de 1,2,4-triazol e medicamento
PL191118B1 (pl) Kwas 2(S)-(2-benzoilo-fenyloamino)-3-{4-[2-(5-metylo-2-fenylo-oksazol-4-ilo)-etoksy]-fenylo}-propionowy, kompozycja farmaceutyczna zawierająca ten związek oraz jego zastosowanie
BR112013022536B1 (pt) Derivados flúor-piridinona, suas composições farmacêuticas e usos como agentes antibacterianos
AU7451298A (en) Novel cyclic diamine compounds and medicine containing the same
JP2001278886A (ja) ベンゾオキサジン誘導体及びこれを含有する医薬
JP2003525931A6 (ja) 置換された３−フェニル−５−アルコキシ−１，３，４−オキサジアゾール−２−オンおよびホルモン感受性リパーゼを阻害するためのその使用
CA2631652A1 (en) Oxadiazole derivatives with crth2 receptor activity
BRPI0713784A2 (pt) compostos orgánicos
JP6858252B2 (ja) ラパマイシンシグナル伝達経路阻害剤のメカニズム標的、及びその治療応用
FI63573C (fi) Foerfarande foer framstaellning av oxibensotiazin-dioxiders kaboxamider
ES2252765T3 (es) Compuestos de anilida como inhibidores de acat.
RU2265600C2 (ru) Замещенные 3-фенил-5-алкокси-1,3,4-оксадиазол-2-оны и их применение в качестве ингибиторов липазы
BRPI0616150A2 (pt) derivados de amino-alquil-amida como lìquidos receptores de ccr3
FI63937C (fi) Foerfarande foer framstaellning av terapeutiskt anvaendbara feylpiperaziner
US4447439A (en) 2-Cyclic amino-2-(1,2-benzisoxazol-3-yl)acetic acid ester derivatives, process for the preparation thereof and composition containing the same
EP0654028B1 (en) 3- and 5-substituted 1,2,3,4-oxatriazole-5-imine compounds, a process for the preparation thereof, a pharmaceutical preparation containing said compounds and the use of said compounds for the preparation of medicaments
CN115109011B (zh) 一种苯并噻唑类化合物、制备方法和用途
Malešíč et al. Transformations of methyl L‐(—)‐thiazolidine‐4‐carboxylate, 2‐amino‐2‐thiazoline and 2‐aminothiazole into thiazoloazines and azolothiazoles
BRPI0619282A2 (pt) sal de p-toluenossulfonato, sal, composição farmacêutica, método de modular ppar e uso de um sal
JPS625978A (ja) １，４−ジヒドロピリジン誘導体またはその塩の製造法
WO1994003439A1 (en) Antiproliferative tricyclic compounds
KR100670974B1 (ko) 티아졸 유도체의 조합화학적 방법에 의한 분자다양성구축기술