KR890006593A - 아르마타제 억제4(5)- 이미다졸 - Google Patents
아르마타제 억제4(5)- 이미다졸 Download PDFInfo
- Publication number
- KR890006593A KR890006593A KR1019880013196A KR880013196A KR890006593A KR 890006593 A KR890006593 A KR 890006593A KR 1019880013196 A KR1019880013196 A KR 1019880013196A KR 880013196 A KR880013196 A KR 880013196A KR 890006593 A KR890006593 A KR 890006593A
- Authority
- KR
- South Korea
- Prior art keywords
- imidazole
- bis
- benzyl
- propyl
- propen
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (12)
- 하기 일반식(Ⅰ)의 치환된 이미다졸 또는 제약악적으로 허용가능한 이들의 무-독성 산 부가염:상기식에서 R1, R2, R1' 및 R2'는 같거나 다를 수 있는 것을 H, CH3, C2H5, OCH3, OH, CH2OH, NH2, 또는 할로겐이며; R'는 H 또는(여기에서 R3은 H, CH3또는 할로겐임)이며; R4는 H이며 R5는 H 또는 OH이며 R6는 H 또는 OH이거나 R5와 R6중 하나는 H이며 다른 하나는 R4와 함께 결합을 형성하며 X와 Y는 같거나 다를 수 있는 것을 결합, 직쇄 C1-2-알킬 또는 상응하는 알케닐이다.
- 하기 일반구조식의 치환된 이미다졸 또는 제약학적으로 허용 가능한 이들의 무-독성 산 부가염.상기식에서 R1, R2, 와 R1' 및 R2'는 같거나 다를 수 있는 것으로 H, CH3, C2H5, OCH3, OH, CH2OH, NH2, 또는 할로겐이며; R'는 H 또는(여기에서 R3은 H, CH3또는 할로겐임)이며; R4는 H이며 R5는 H이거나 R4와 R5는 함께 결합을 형성한다.
- 제2항에 있어서, R4와 R4가 모두 H인 치환된 이미다졸.
- 제2항에 있어서, R4와 R4가 함께 결합을 형성하는 치환된 이미다졸.
- 제2항 내지 제4항 중 어느한 항에 있어서, R1, R2, R1', R2' 및 중 적어도 한개의 H가 아니며 치환체 R1, R2, R1' 및 R2'중 한개 이상의 페닐기의 3,5,3' 또는 5'위치에 있는 치환된 이미다졸.
- 제5항에 있어서, R2및 R2'는 H 이며 R1및 R1'은 둘다 수소가 아니며 둘다 페닐기의 메타 위치에 있는 치환된 이미다졸.
- 제2항 내지 제6항중 어느 한항에 있어서, R'가 H인 치환된 이미다.
- 제2항 내지 제6항중 어느 한항에 있어서, R'가(여기에서 R3은 H,CH3또는 할로겐임)인 치환된 이미다졸.
- 제8항에 있어서, R3이 H인 치환된 이미다졸.
- 제1항에 있어서, 4-[5-(2,6-디메틸페닐)-3-히드록시-3-(2,6-디메틸페닐-에틸)펜틸]-1H-이미다졸, 4-[3,3-비스(4-클로로페닐)-3-히드록시프로필)-1H-이미다졸, 4-[3,3-디페닐-3-히드록시프로필)-1H-이미다졸, 4-(3,3-디페닐프로펜-2-일)-1H-이미다졸, 4-(3,3-디페닐프로필)-1H-이미다졸, 4-[3,3-비스(2-메틸페닐)-3-히드록시프로필]-1H-이미다졸, 4-[3,3-비스(4-클로로페닐)프로펜-2-일]1H-이미다졸, 4-[3,3-비스-(2-메틸페닐)프로펜-2-일]-1H-이미다졸, 4-[3,3-비스(2-메틸페닐)프로필]-1H-이미다졸, 1-벤질-4-(3,3-디메닐프로필)-1H-이미다졸, 1-벤질-5-(3,3-디페닐 프로필)-1H-이미다졸, 4-[3,3-비스((3-메틸페닐)프로필]-1H-이미다졸, 4-[3,3-비스-(3-메틸페닐)프로펜-2-일]-1H-이미다졸, 1-(4-클로로벤질)-4-(3,3-디페닐프로필)-1H-이미다졸, 1-(4-클로로벤질)-5-(3.3-디페닐프로필)-1H-이미다졸, 4-[5-(2,6-디메틸페닐)-3-(2,6-디메틸페닐에틸)-펜틸]-1H-이미다졸, 4-[3,3-비스(3,5-디메틸페닐)프로필]-1H-이미다졸, 4-[3,3-비스(3-메톡시페닐)프로필]-1H-이미다졸, 4-[3,3-비스(2,3-디메틸페닐)프로필]-1H-이미다졸, 1-벤질-5-[3,3-비스(3-메톡시페닐)프로필]-1H-이미다졸, 1-벤질-5-[3,3-비스(3-메턱시페닐 프로펜-2-일]-1H-이미다졸, 4-[3,3-비스(3,5-디메틸페닐)프로필]-1H-이미다졸, 4-[3,3-비스(4-메톡시페닐)프로필-1H-이미다졸, 4-[3,3-비스(3-플루오로페닐)프로필]-1H-이미다졸,1-벤질 -5[3,3-비스(4-클로로페닐)3-히드록시프로필]-1H-이미다졸, 1-벤질-5-[3,3-1ㅣ스(4-클로로페닐)프로펜-2-일]-1H-이미다졸, 4-[3-(4-클로로페닐)-3-히드록시-3-페닐프로필]-1H-이미다졸, 4-[3,3[-비스(3-메틸페닐)-3-히드록시프로필-1H-이미다졸, 4-[3,3-비스(3-플루오로페닐)ㅡ프로펜-2-일]-1H-이미다졸, 1-벤질-5-[5-(2,6-디메틸페닐)-3-히드록시-3-(2,6-디메틸페닐에틸)-펜틸]-1H-이미다졸, 1-벤질-5-[3,3-비스(3,5-디메틸페닐)-3-히이록시프로필]-1H-이미다졸, 1-벤질-5-[3,3-비스(3,5-디메틸페닐)프로펜-2-일]-1H-이미다졸, 1-벤질-5-[3,3-비스(2-메톡시페닐)프로펜-2-일]-1H-이미다졸, 1-벤질-5[3,3-비스(4-메톡시페닐)프로펜-2-일]-1H-이미다졸, 1-벤질-5-[3,3-비스(2,3-디메틸페닐)프로펜-2-일]-1H-이미다졸, 1-벤질-5-[3,3-비스(2-메틸페닐)프로펜-2-일]-1H-이미다졸, 1-벤질-5-[3,3-비스)(3-메틸페닐)프로펜-2-일]-1H-이미다졸, 4-[3,3-비스(2-메톡시페닐)프로필]-1H-이미다졸, 4-[3,3-비스(4-메톡시페닐)프로필]-1H-이미다졸, 1-벤질-5-[3,3-비스(4-메틸페닐)프로펜-2-일]-1H-이미다졸 또는 1-벤질-5-(3,3-디페닐프로펜-2-일]-1H-이미다졸 또는 제약적으로 허용가능한 이들의 무독성 산부가염인 화합물.
- 제1항 내지 제10항중 어느 한항에 청구된 치환된 이미다졸 및 제약적으로 허용가능한 담체를 포함하는 제약적인 조성물.
- 아로마타지제 억제 제로서 사용하기 위한 제1항 내지 11항중 어느 한항에 따르는 이미다졸 유도체 또는 무독성 산부가염.※참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8723715 | 1987-10-09 | ||
GB8723715A GB2210875B (en) | 1987-10-09 | 1987-10-09 | Aromatase inhibiting 4(5)-imidazoles |
Publications (1)
Publication Number | Publication Date |
---|---|
KR890006593A true KR890006593A (ko) | 1989-06-14 |
Family
ID=10625036
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019880013196A KR890006593A (ko) | 1987-10-09 | 1988-10-08 | 아르마타제 억제4(5)- 이미다졸 |
Country Status (24)
Country | Link |
---|---|
US (1) | US5098923A (ko) |
EP (1) | EP0311447B1 (ko) |
JP (1) | JPH01132568A (ko) |
KR (1) | KR890006593A (ko) |
CN (1) | CN1036993C (ko) |
AU (1) | AU615482B2 (ko) |
CA (1) | CA1329616C (ko) |
DD (1) | DD282912A5 (ko) |
DE (1) | DE3874073T2 (ko) |
DK (1) | DK550988A (ko) |
ES (1) | ES2043839T3 (ko) |
FI (1) | FI93105C (ko) |
GB (1) | GB2210875B (ko) |
GR (1) | GR3006343T3 (ko) |
HU (1) | HU201024B (ko) |
IE (1) | IE61180B1 (ko) |
IL (1) | IL87969A (ko) |
LT (1) | LT3658B (ko) |
NO (1) | NO172048C (ko) |
NZ (1) | NZ226483A (ko) |
PT (1) | PT88717B (ko) |
RU (2) | RU1819263C (ko) |
UA (1) | UA13218A (ko) |
ZA (1) | ZA887545B (ko) |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2210875B (en) | 1987-10-09 | 1991-05-29 | Farmos Oy | Aromatase inhibiting 4(5)-imidazoles |
GB8818561D0 (en) * | 1988-08-04 | 1988-09-07 | Ici Plc | Diphenylethane derivatives |
GB2229719B (en) * | 1989-03-30 | 1992-04-29 | Farmos Oy | Novel aromatase inhibiting 4(5)-imidazoles |
US5439928A (en) * | 1989-03-30 | 1995-08-08 | Orion-Yhtyma Oy | Aromatase inhibiting 4(5)-imidazoles |
AU627559B2 (en) * | 1989-03-30 | 1992-08-27 | Farmos-Yhtyma Oy | Novel aromatase inhibiting 4(5)-imidazoles |
GB2248058B (en) * | 1990-09-21 | 1994-09-14 | Orion Yhtymae Oy | Aromatase inhibiting 4(5)-imidazoles |
GB9125924D0 (en) * | 1991-06-18 | 1992-02-05 | Orion Yhtymae Oy | Stereoisomers of an imidazole derivative |
US6262093B1 (en) | 1995-04-12 | 2001-07-17 | The Proctor & Gamble Company | Methods of treating cancer with benzimidazoles |
ZA962879B (en) * | 1995-04-12 | 1997-03-17 | Procter & Gamble | A pharmaceutical composition for inhibiting the growth of viruses and cancers |
US6479526B1 (en) | 1995-04-12 | 2002-11-12 | The Procter & Gamble Company | Pharmaceutical composition for inhibiting the growth of viruses and cancers |
US6265427B1 (en) | 1995-06-07 | 2001-07-24 | The Proctor & Gamble Company | Pharmaceutical composition for the method of treating leukemia |
US6008372A (en) * | 1996-01-16 | 1999-12-28 | Warner-Lambert Company | Substituted dinaphthylmethyl and diheteroarylmethylacetyl histidine inhibitors of protein farnesyltransferase |
US5900429A (en) | 1997-01-28 | 1999-05-04 | The Procter & Gamble Company | Method for inhibiting the growth of cancers |
US6506783B1 (en) | 1997-05-16 | 2003-01-14 | The Procter & Gamble Company | Cancer treatments and pharmaceutical compositions therefor |
US6245789B1 (en) | 1998-05-19 | 2001-06-12 | The Procter & Gamble Company | HIV and viral treatment |
US6423734B1 (en) | 1999-08-13 | 2002-07-23 | The Procter & Gamble Company | Method of preventing cancer |
US6407105B1 (en) | 2000-09-26 | 2002-06-18 | The Procter & Gamble Company | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6608096B1 (en) * | 2000-09-26 | 2003-08-19 | University Of Arizona Foundation | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6380232B1 (en) | 2000-09-26 | 2002-04-30 | The Procter & Gamble Company | Benzimidazole urea derivatives, and pharmaceutical compositions and unit dosages thereof |
US6462062B1 (en) | 2000-09-26 | 2002-10-08 | The Procter & Gamble Company | Compounds and methods for use thereof in the treatment of cancer or viral infections |
US6515074B2 (en) * | 2001-01-22 | 2003-02-04 | Delphi Technologies, Inc. | Thermoplastic polymer alloy compositions and process for manufacture thereof |
US6903215B2 (en) | 2002-03-26 | 2005-06-07 | Boehringer Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
AU2003230700A1 (en) * | 2002-03-26 | 2003-10-13 | Boehringer Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
US7074806B2 (en) | 2002-06-06 | 2006-07-11 | Boehringer Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
CA2512257A1 (en) | 2003-01-03 | 2004-07-29 | Boehringer Ingelheim Pharmaceuticals, Inc. | 1-propanol and 1-propylamine derivatives and their use as glucocorticoid ligands |
UY28526A1 (es) | 2003-09-24 | 2005-04-29 | Boehringer Ingelheim Pharma | Miméticos de glucocorticoides, métodos de preparación composiciones farmacéuticas y usos de los mismos |
US7795272B2 (en) | 2004-03-13 | 2010-09-14 | Boehringer Ingelheim Pharmaceutical, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions and uses thereof |
US7635711B2 (en) | 2004-12-27 | 2009-12-22 | Boehringer-Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
JP2010512331A (ja) | 2006-12-06 | 2010-04-22 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | グルココルチコイド模倣薬、それらの製造方法、医薬組成物、及びこれらの使用 |
EP2095819A1 (en) * | 2008-02-28 | 2009-09-02 | Maastricht University | N-benzyl imidazole derivatives and their use as aldosterone synthase inhibitors |
MX2010013095A (es) | 2008-06-06 | 2010-12-21 | Boehringer Ingelheim Int | Mimeticos de glucocorticoides, metodos para su fabricacion, composiciones farmaceuticas y usos de los mismos. |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2069481B (en) * | 1980-02-13 | 1983-07-27 | Farmos Oy | Substituted imidazole derivatives |
GB2092569B (en) * | 1981-02-05 | 1984-09-19 | Farmos Oy | Substituted imidazole derivatives and their preparation and use |
GB2096987B (en) * | 1981-04-22 | 1984-04-04 | Farmos Oy | Substituted imidazole and imidazole derivatives and their preparation and use |
GB2101114B (en) * | 1981-07-10 | 1985-05-22 | Farmos Group Ltd | Substituted imidazole derivatives and their preparation and use |
US4605661A (en) * | 1984-06-18 | 1986-08-12 | Eli Lilly And Company | Aromastase inhibiting α,α-diarylimidazole-4(5)-propionitriles, α,α-diarylimidazole-4(5)-propionamides, and 4(5)-(2,2-diarylethyl)imidazoles |
LU85747A1 (fr) * | 1985-01-28 | 1986-08-04 | Continental Pharma | Derives d'imidazole leur preparation et utilisation ainsi que les compositions pharmaceutiques contenant des derives |
GB2210875B (en) | 1987-10-09 | 1991-05-29 | Farmos Oy | Aromatase inhibiting 4(5)-imidazoles |
AU627559B2 (en) | 1989-03-30 | 1992-08-27 | Farmos-Yhtyma Oy | Novel aromatase inhibiting 4(5)-imidazoles |
-
1987
- 1987-10-09 GB GB8723715A patent/GB2210875B/en not_active Revoked
-
1988
- 1988-09-22 CA CA000578192A patent/CA1329616C/en not_active Expired - Fee Related
- 1988-09-30 FI FI884497A patent/FI93105C/fi not_active IP Right Cessation
- 1988-10-03 DK DK550988A patent/DK550988A/da not_active Application Discontinuation
- 1988-10-06 DD DD88320542A patent/DD282912A5/de not_active IP Right Cessation
- 1988-10-06 AU AU23490/88A patent/AU615482B2/en not_active Ceased
- 1988-10-06 NZ NZ226483A patent/NZ226483A/xx unknown
- 1988-10-07 HU HU885213A patent/HU201024B/hu not_active IP Right Cessation
- 1988-10-07 RU SU884356681A patent/RU1819263C/ru active
- 1988-10-07 UA UA4356681A patent/UA13218A/uk unknown
- 1988-10-07 IL IL87969A patent/IL87969A/xx not_active IP Right Cessation
- 1988-10-07 NO NO884473A patent/NO172048C/no unknown
- 1988-10-07 EP EP88309413A patent/EP0311447B1/en not_active Expired - Lifetime
- 1988-10-07 IE IE305588A patent/IE61180B1/en not_active IP Right Cessation
- 1988-10-07 DE DE8888309413T patent/DE3874073T2/de not_active Expired - Fee Related
- 1988-10-07 ES ES88309413T patent/ES2043839T3/es not_active Expired - Lifetime
- 1988-10-07 ZA ZA887545A patent/ZA887545B/xx unknown
- 1988-10-07 PT PT88717A patent/PT88717B/pt not_active IP Right Cessation
- 1988-10-08 CN CN88108425A patent/CN1036993C/zh not_active Expired - Fee Related
- 1988-10-08 JP JP63254665A patent/JPH01132568A/ja active Pending
- 1988-10-08 KR KR1019880013196A patent/KR890006593A/ko not_active Application Discontinuation
-
1990
- 1990-09-27 US US07/588,873 patent/US5098923A/en not_active Expired - Fee Related
-
1992
- 1992-01-23 RU SU925010700A patent/RU2045519C1/ru active
- 1992-11-26 GR GR920402701T patent/GR3006343T3/el unknown
-
1993
- 1993-08-31 LT LTIP916A patent/LT3658B/lt not_active IP Right Cessation
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