KR970021076A - 약제학적 활성 성분으로서 치환된 2,4-이미다졸리딘디온 화합물 - Google Patents
약제학적 활성 성분으로서 치환된 2,4-이미다졸리딘디온 화합물 Download PDFInfo
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- KR970021076A KR970021076A KR1019960048441A KR19960048441A KR970021076A KR 970021076 A KR970021076 A KR 970021076A KR 1019960048441 A KR1019960048441 A KR 1019960048441A KR 19960048441 A KR19960048441 A KR 19960048441A KR 970021076 A KR970021076 A KR 970021076A
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
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- 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
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- 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
- A61P37/02—Immunomodulators
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- 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
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- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
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- 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
- C07D413/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
Abstract
본 발명은 2,4-이미다졸리딘디온 화합물, 이의 제조방법 및 약제학적 제제에서의 이들 화합물의 용도에 관한 것이다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (12)
- 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.상기 화학식에서, R1은 C1-6알킬 또는 C3-6사이클로알킬이고, R2는 C1-6알킬, 페닐, -(CH2)1-3-페닐 또는 -(CH2)1-4-COOR5이거나 R1및 R2가 함께는 -(CH2)4-6-, -(CH2)2-0-(CH2)2- 또는 화학식이거나, R3이 H, C1-5알킬 또는 -(CH2)1-4-COOR5이며, R4가 화학식의 그룹으로부터 선택된 헤테로방향족 그룹이며, R5는 C1-3알킬이고, R6는 H, C1-4알킬, 페닐 또는 벤질이며, R7은 H, C1-4알킬 또는 트리플루오로메틸이다.
- 제1항에 있어서, R1이 C1-4알킬 또는 C3-4사이클로알킬이고, R2가 C3-6알킬, 페닐, -(CH2)1-2-페닐 또는 -(CH2)1-2-COOR5이거나, R1및 R2가 함께는 -(CH2)5- 또는 화학식이고, R3이 H, C1-4알킬 또는 -(CH2)1-2-COOR5이며, R4가 화학식의 그룹으로부터 선택된 헤테로방향족 그룹이며, R5가 C1-3알킬이고, R6이 H 또는 페닐이며, R7이 H, 메틸, 3급 부틸 또는 트리플루오로메틸임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
- 제1항 또는 제2항에 있어서, R1이 에틸 또는 사이클로부틸이고, R2가 페닐이거나, R1및 R2가 함께는 -(CH2)5-임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
- 제1항 내지 제3항중 어느 한 항에 있어서, R1및 R2가 함께 -(CH2)5-임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
- 제1항 내지 제4항중 어느 한 항에 있어서, R3이 H, C1-3알킬 또는 -CH2-COOR5이고, R5가 에틸임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
- 제5항에 있어서, R3이 H임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
- 제1항 내지 제6항중 어느 한 항에 있어서, R4가 피리딘-4-일, 피리딘-3일, 티아졸-2-일, 3-메틸이속사졸-5-일 또는 5-메틸이속사졸-3-일임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
- 제7항에 있어서, R4가 티아졸-2-일임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
- 화학식 (2)의 아민이 1,1′-카보닐디이미다졸 또는 디페닐 카보네이트를 가한 후 화학식 (3)의 화합물과 반응시켜 R3이 H인 화학식 (1)의 화합물을 수득하고, 경우에 따라, 이 화합물을 탈양자화한 후 화학식 (4)의 화합물 또는 화학식 (5)의 화합물과 반응시켜 R3이 C1-5알킬 또는 -(CH2)1-4-COOR5인 화학식 (1)의 화합물을 수득함을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물의 제조 방법.상기 화학식에서, R1은 C1-6알킬 또는 C3-6사이클로알킬이고, R2는 C1-6알킬, 페닐, -(CH2)1-3-페닐 또는 -(CH2)1-4-COOR5이거나 R1및 R2가 함께는 -(CH2)4-6-, -(CH2)2-0-(CH2)2- 또는 화학식이거나, R3은 H, C1-5알킬 또는 -(CH2)1-4-COOR5이고, R4는 화학식의 그룹으로부터 선택된 헤테로방향족 그룹이며, R5는 C1-3알킬이고, R6는 H, C1-4알킬, 페닐 또는 벤질이며, R7은 H, C1-4알킬 또는 트리플루오로메틸이고, R8은 H 또는 C1-3알킬이며, X는 Cl, Br 또는 I이다.
- 약제학적 제제중 활성 성분으로서의, 제1항에 다른 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물의 용도.
- 제10항에 있어서, 약제학적 제제가 면역조절제임을 특징으로 하는 용도.
- 제10항에 있어서, 약제학적 제제가 항맥관염 작용을 갖는 것을 특징으로 하는 용도.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19540027.5 | 1995-10-27 | ||
DE19540027A DE19540027A1 (de) | 1995-10-27 | 1995-10-27 | Substituierte Imidazolidin-2,4-dion-Verbindungen als pharmazeutische Wirkstoffe |
JP7-283270 | 1995-10-31 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR970021076A true KR970021076A (ko) | 1997-05-28 |
KR100445539B1 KR100445539B1 (ko) | 2004-12-30 |
Family
ID=7775931
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019960048441A KR100445539B1 (ko) | 1995-10-27 | 1996-10-25 | 치환된2,4-이미다졸리딘디온화합물및이를함유하는약제학적조성물 |
Country Status (23)
Country | Link |
---|---|
US (1) | US6004963A (ko) |
EP (1) | EP0770613B1 (ko) |
JP (1) | JPH09188677A (ko) |
KR (1) | KR100445539B1 (ko) |
CN (1) | CN1097050C (ko) |
AR (1) | AR004517A1 (ko) |
AT (1) | ATE181072T1 (ko) |
AU (1) | AU707751B2 (ko) |
CA (1) | CA2188908A1 (ko) |
CO (1) | CO4750655A1 (ko) |
DE (2) | DE19540027A1 (ko) |
DK (1) | DK0770613T3 (ko) |
ES (1) | ES2135148T3 (ko) |
GR (1) | GR3030558T3 (ko) |
HK (1) | HK1010367A1 (ko) |
HU (1) | HU222120B1 (ko) |
IL (1) | IL119488A (ko) |
MX (1) | MX9605023A (ko) |
PE (1) | PE20011055A1 (ko) |
PL (1) | PL184446B1 (ko) |
RU (1) | RU2163603C2 (ko) |
SI (1) | SI0770613T1 (ko) |
ZA (1) | ZA968956B (ko) |
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DE19732928C2 (de) * | 1997-07-31 | 2000-05-18 | Gruenenthal Gmbh | Verwendung substituierter Imidazolidin-2,4-dion-Verbindungen als Schmerzmittel |
DE19917961A1 (de) | 1999-04-21 | 2000-10-26 | Degussa | Verfahren zur Herstellung von Aminosäurederivaten |
WO2001007048A1 (en) * | 1999-07-21 | 2001-02-01 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammatory disease |
ES2284641T3 (es) | 2000-05-31 | 2007-11-16 | Tanabe Seiyaku Co., Ltd. | Inhibidores de la adhesion celular mediada por alfa-l-beta-2. |
US7354933B2 (en) | 2003-01-31 | 2008-04-08 | Aventis Pharma Sa | Cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors |
FR2850652B1 (fr) * | 2003-01-31 | 2008-05-30 | Aventis Pharma Sa | Nouveaux derives d'uree cyclique, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases |
WO2005090316A1 (en) * | 2004-03-12 | 2005-09-29 | Wyeth | HYDANTOINS HAVING RNase MODULATORY ACTIVITY |
EP1621536A1 (en) * | 2004-07-27 | 2006-02-01 | Aventis Pharma S.A. | Amino cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors |
EP1621539A1 (en) * | 2004-07-27 | 2006-02-01 | Aventis Pharma S.A. | Heterocycle -substituted cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors |
EP1621535A1 (en) * | 2004-07-27 | 2006-02-01 | Aventis Pharma S.A. | Substituted cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors |
US7709517B2 (en) | 2005-05-13 | 2010-05-04 | The Regents Of The University Of California | Diarylhydantoin compounds |
FR2896504B1 (fr) * | 2006-01-23 | 2012-07-13 | Aventis Pharma Sa | Nouveaux derives d'uree cyclique, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases |
FR2896503B1 (fr) * | 2006-01-23 | 2012-07-13 | Aventis Pharma Sa | Nouveaux derives soufres d'uree cyclique, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases |
AU2012241184B2 (en) * | 2006-03-27 | 2016-01-07 | The Regents Of The University Of California | Androgen receptor modulator for the treatment of prostate cancer and androgen receptor-associated diseases |
AU2016201061B2 (en) * | 2006-03-27 | 2017-03-02 | The Regents Of The University Of California | Androgen receptor modulator for the treatment of prostate cancer and androgen receptor-associated diseases |
AU2013205325B2 (en) * | 2006-03-27 | 2016-03-24 | The Regents Of The University Of California | Androgen receptor modulator for the treatment of prostate cancer and androgen receptor-associated diseases |
EP3412290B1 (en) * | 2006-03-27 | 2021-03-03 | The Regents of The University of California | Androgen receptor modulator for the treatment of prostate cancer and androgen receptor-associated diseases |
CN101460467B (zh) * | 2006-03-29 | 2012-09-19 | 加利福尼亚大学董事会 | 二芳基硫代乙内酰脲化合物 |
WO2008021309A1 (en) * | 2006-08-15 | 2008-02-21 | Wyeth | Imidazolidin-2-one derivatives useful as pr modulators |
US7649007B2 (en) * | 2006-08-15 | 2010-01-19 | Wyeth Llc | Oxazolidine derivatives as PR modulators |
WO2008021337A1 (en) | 2006-08-15 | 2008-02-21 | Wyeth | Oxazinan-2-one derivatives useful as pr modulators |
TW200815428A (en) | 2006-08-15 | 2008-04-01 | Wyeth Corp | Oxazolidone derivatives as PR modulators |
CA2661315C (en) * | 2006-09-08 | 2015-11-24 | Actelion Pharmaceuticals Ltd | Pyridin-3-yl derivatives as immunomodulating agents |
JP5535925B2 (ja) | 2007-10-26 | 2014-07-02 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | アンドロゲン受容体調節物質としてのジアリールヒダントイン化合物 |
SG192439A1 (en) * | 2008-06-27 | 2013-08-30 | Novartis Ag | Organic compounds |
RS53075B (en) | 2009-05-12 | 2014-04-30 | Janssen Pharmaceuticals Inc. | 1,2,4-TRIAZOLO [4,3-A] PYRIDINE DERIVATIVES AND THEIR USE IN THE TREATMENT OR PREVENTION OF NEUROLOGICAL AND PSYCHIATRIC DISORDERS |
SI3124481T1 (en) | 2010-02-16 | 2018-06-29 | Aragon Pharmaceuticals, Inc. | Androgen receptor modulators and their use |
MY180834A (en) | 2012-09-26 | 2020-12-10 | Aragon Pharmaceuticals Inc | Anti-androgens for the treatment of non-metastatic castrate-resistant prostate cancer |
JOP20200097A1 (ar) | 2013-01-15 | 2017-06-16 | Aragon Pharmaceuticals Inc | معدل مستقبل أندروجين واستخداماته |
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AU2018351714A1 (en) | 2017-10-16 | 2020-04-30 | Aragon Pharmaceuticals, Inc. | Anti-androgens for the treatment of non-metastatic castration-resistant prostate cancer |
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EP0091596B1 (de) * | 1982-04-08 | 1991-09-11 | Shell Internationale Researchmaatschappij B.V. | Neue Hydantoine, ihre Herstellung und Verwendung |
US4746669A (en) * | 1985-12-23 | 1988-05-24 | Merck & Co., Inc. | Substituted thiazoles as immunoregulants |
JPH02101065A (ja) * | 1988-10-06 | 1990-04-12 | Tanabe Seiyaku Co Ltd | イミダゾリン誘導体及びその製法 |
EP0557408A4 (en) * | 1990-11-06 | 1993-10-27 | Smith-Kline Beecham Corporation | Imidazolidinone compounds |
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US7466669B2 (en) * | 2003-11-14 | 2008-12-16 | Telefonaktiebolaget Lm Ericsson (Publ) | Reverse link scheduler for CDMA networks |
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1995
- 1995-10-27 DE DE19540027A patent/DE19540027A1/de not_active Withdrawn
-
1996
- 1996-09-26 PE PE1996000688A patent/PE20011055A1/es not_active Application Discontinuation
- 1996-10-04 CO CO96052910A patent/CO4750655A1/es unknown
- 1996-10-08 DK DK96116069T patent/DK0770613T3/da active
- 1996-10-08 ES ES96116069T patent/ES2135148T3/es not_active Expired - Lifetime
- 1996-10-08 DE DE59602155T patent/DE59602155D1/de not_active Expired - Fee Related
- 1996-10-08 AT AT96116069T patent/ATE181072T1/de not_active IP Right Cessation
- 1996-10-08 EP EP96116069A patent/EP0770613B1/de not_active Expired - Lifetime
- 1996-10-08 SI SI9630066T patent/SI0770613T1/xx not_active IP Right Cessation
- 1996-10-14 AU AU68181/96A patent/AU707751B2/en not_active Ceased
- 1996-10-16 AR ARP960104778A patent/AR004517A1/es unknown
- 1996-10-22 MX MX9605023A patent/MX9605023A/es unknown
- 1996-10-24 ZA ZA968956A patent/ZA968956B/xx unknown
- 1996-10-24 HU HU9602932A patent/HU222120B1/hu not_active IP Right Cessation
- 1996-10-24 JP JP8282701A patent/JPH09188677A/ja active Pending
- 1996-10-25 CA CA002188908A patent/CA2188908A1/en not_active Abandoned
- 1996-10-25 US US08/738,232 patent/US6004963A/en not_active Expired - Fee Related
- 1996-10-25 RU RU96121181/04A patent/RU2163603C2/ru not_active IP Right Cessation
- 1996-10-25 IL IL11948896A patent/IL119488A/xx not_active IP Right Cessation
- 1996-10-25 KR KR1019960048441A patent/KR100445539B1/ko not_active IP Right Cessation
- 1996-10-25 PL PL96316706A patent/PL184446B1/pl not_active IP Right Cessation
- 1996-10-26 CN CN96121960A patent/CN1097050C/zh not_active Expired - Fee Related
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1998
- 1998-09-25 HK HK98110963A patent/HK1010367A1/xx not_active IP Right Cessation
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1999
- 1999-06-17 GR GR990401639T patent/GR3030558T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
CO4750655A1 (es) | 1999-03-31 |
HU222120B1 (hu) | 2003-04-28 |
KR100445539B1 (ko) | 2004-12-30 |
EP0770613A1 (de) | 1997-05-02 |
ZA968956B (en) | 1997-05-29 |
IL119488A0 (en) | 1997-01-10 |
IL119488A (en) | 2001-01-11 |
HK1010367A1 (en) | 1999-06-17 |
DE19540027A1 (de) | 1997-04-30 |
SI0770613T1 (en) | 1999-10-31 |
MX9605023A (es) | 1997-06-28 |
HUP9602932A3 (en) | 1998-08-28 |
CN1152573A (zh) | 1997-06-25 |
ATE181072T1 (de) | 1999-06-15 |
AR004517A1 (es) | 1998-12-16 |
AU707751B2 (en) | 1999-07-22 |
EP0770613B1 (de) | 1999-06-09 |
RU2163603C2 (ru) | 2001-02-27 |
CN1097050C (zh) | 2002-12-25 |
AU6818196A (en) | 1997-05-01 |
GR3030558T3 (en) | 1999-10-29 |
DE59602155D1 (de) | 1999-07-15 |
PL316706A1 (en) | 1997-04-28 |
ES2135148T3 (es) | 1999-10-16 |
PL184446B1 (pl) | 2002-10-31 |
HU9602932D0 (en) | 1996-12-30 |
DK0770613T3 (da) | 1999-12-13 |
CA2188908A1 (en) | 1997-04-28 |
HUP9602932A2 (hu) | 1998-07-28 |
PE20011055A1 (es) | 2001-12-29 |
JPH09188677A (ja) | 1997-07-22 |
US6004963A (en) | 1999-12-21 |
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