KR970703301A - 신규 디아미노메틸리덴 유도체(novel diamincmethylidene derivative) - Google Patents
신규 디아미노메틸리덴 유도체(novel diamincmethylidene derivative) Download PDFInfo
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- KR970703301A KR970703301A KR1019960706566A KR19960706566A KR970703301A KR 970703301 A KR970703301 A KR 970703301A KR 1019960706566 A KR1019960706566 A KR 1019960706566A KR 19960706566 A KR19960706566 A KR 19960706566A KR 970703301 A KR970703301 A KR 970703301A
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- -1 Diaminomethylidene Chemical class 0.000 title claims abstract description 9
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract 27
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract 10
- 150000001875 compounds Chemical class 0.000 claims abstract 8
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 7
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 6
- 150000003839 salts Chemical class 0.000 claims abstract 5
- 229910052799 carbon Inorganic materials 0.000 claims abstract 4
- 230000002496 gastric effect Effects 0.000 claims abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 24
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 19
- 125000003118 aryl group Chemical group 0.000 claims 13
- 125000005843 halogen group Chemical group 0.000 claims 10
- 125000001624 naphthyl group Chemical group 0.000 claims 8
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 239000012190 activator Substances 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 208000007882 Gastritis Diseases 0.000 claims 1
- 208000018522 Gastrointestinal disease Diseases 0.000 claims 1
- 208000025865 Ulcer Diseases 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 208000023652 chronic gastritis Diseases 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 230000001079 digestive effect Effects 0.000 claims 1
- 238000013110 gastrectomy Methods 0.000 claims 1
- 208000021302 gastroesophageal reflux disease Diseases 0.000 claims 1
- 208000002551 irritable bowel syndrome Diseases 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 208000000689 peptic esophagitis Diseases 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 231100000397 ulcer Toxicity 0.000 claims 1
- 210000002249 digestive system Anatomy 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/20—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic unsaturated carbon skeleton
- C07C211/24—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic unsaturated carbon skeleton the carbon skeleton being further substituted by halogen atoms or by nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/04—Nitro compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/30—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same unsaturated acyclic carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/34—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D295/145—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
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- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
본 발명은 화학식 (1)로 표시되는 신규한 디아미노메틸리덴 유도체 및 그의 약제학적으로 허용가능한 염에 관한 것이다:
[식중, R1은 수소, C1-C6알킬기, C3-C6시클로알킬기 등이고; R2는, 하기식 등의 기등이고;
R3는 수소원자, C1-C6알킬기 등이고; X는 O, S, CHNO2, C(COOR4)CN, C(CN)2등이다].
상기 화합물은 소화계 질병치료용으로 사용되는 위장 활성 촉진제로서 유용하다.
Description
신규 디아미노메틸리덴 유도체(NOVEL DIAMINCMETHYLIDENE DERIVATIVE)
[도면의 간단한 설명]
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (5)
- 하기 화학식 (1)로 표시된 디아미노메틸리덴 유도체 또는 그의 약리학적으로 허용가능한 염:[식중, R1은 수소원자, C1-C6알킬기, C3-C6시클로알킬기, C3-C6시클로알킬, C1-C4알킬기, 아릴기 또는 아릴 C1-C4알킬기이고, 이중, 아릴기 또는 아릴 C1-C4알킬기중 아릴부가 할로겐원자, C1-C6알킬기, 할로 C1-C6알킬기, C1-C6알콕시기, C1-C6알콕시카르보닐기, 페닐기 또는 아미노기로 임의치환될 수 있으며; X는 O, S, CHNO2, C(COOR4)2, C(COOR4)CN 또는 C(CN)2이고, 이중, R4는 C1-C6알킬기, C3-C6시클로알킬기, 아릴기 또는 아릴 C1-C4알킬기이며; R3는 하기 일반식 II 내지 IX의 기이고:일반식 II 내지 IX(식중, R5는 C1-C6알킬기, 아릴 C1-C4알킬기, 혜테로아릴 C1-C4알킬기, 아릴옥시 C2-C6알킬기 또는 피롤리디닐카르보닐 C1-C4알킬기이고, 이중, 상기 기의 아릴부는 할로겐원자, C1-C6알킬기, 할로 C1-C6알킬기, C1-C6알콕시기, C1-C6알콕시카르보닐기, 페닐기 또는 아미노기로 임의치환될 수 있으며; R6은 수소원자 C1-C6알킬기, 아릴기 또는 아릴 C1-C4알킬기이며; Z1및 Z2는 O, S, N(C1-C4알킬) 또는 CH2이고, Z3는 N 또는 CH이고; 1은 0-2이고, m이 0일때 n은 4이고, m이 1일때 n은 1 또는 3이고, m이 2일때 n은 2이고, P는 1-2이고, j는 0-3이고, k는 0-3이고, j와 k의 합은 1-6이고, h는 1-6이며; Q는 O, NR8, CHOR9또는 OCH2CH2O이며; R7및 R8은 동일하거나 상이할 수 있고, 각각은 수소원자, C1-C6알킬기 또는 C1-C4알콕시 C2-C4알킬기이며; R9은 수소원자 또는 C1-C6알킬기이다); R3는 수소원자, C1-C6알킬기 또는 C1-C6알콕시 C2-C6알킬기이고; 또는 R2및 R3는, 부착되어 있는 질소 원자와 함께, 하기 일반식 X의 N-치환된 피페라진 고리를 나타낼 수 있다:(식중, R5는 상기 정의되어진 기를 나타낸다); 단, R1이 아릴기이고, X가 0이며, R2는, R5가 C1-C2알킬기인 일반식 II의 기인 화합물은 제외한다.].
- 제1항에 있어서, R1은 수소원자, C1-C6알킬기, C3-C6시클로알킬기, 페닐기, 나프틸기, C3-C6시클로알킬 C1-C4알킬기, 또는 페닐 C1-C4알킬기이며, 이중, 페닐기, 나프틸기 또는 페닐 C1-C4알킬기의 페닐 고리는 할로겐원자, C1-C6알킬기, 할로 C1-C6알킬기, C1-C6알콕시기, C1-C6알콕시카르보닐기 또는 페닐기와 임의로 모노-내지 트리-치환될 수 있으며; X는 O, S. CHNO2, C(COOR4)2. C(COOR4)CN 또는 C(CN)2으로, 이중, R4는 C1-C6알킬기, C3-C6시클로알킬기, 페닐기 또는 페닐 C1-C4알킬기이고; R3가 수소원자, C1-C6알킬기 또는 C1-C6알콕시 C2-C6알킬기일 때, R2는 일반식 II 내지 IX의 기이며(R5가 C1-C6알킬기, 페닐 C1-C4알킬기, 나프틸 C1-C4알킬기, 피리닐 C1-C4알킬기, 페녹시 C2-C6알킬기 또는 피롤리디닐카르보닐 C1-C4알킬기이며, 이중, 패닐, 페녹시 또는 나프틸부가 할로겐원자, C1-C6알킬기, 할로 C1-C6알킬기, C1-C6알콕시기, C1-C6알콕시카르보닐기 또는 페닐기와 임의로 모노- 내지 트리-치환될 수 있고 R6는 수소원자, C1-C6알킬기, 페닐기, 나프틸기 또는 페닐 C1-C4알킬기이며, Z1은 O, S, N(C1-C6알킬) 또는 CH2이고, Z2는 O, N(C1-C6알킬) 또는 CH2이고, Z3는 N 또는 CH이며; 1은 0-2이고, m이 0일때 n은 4이고, m이 1일때 n은 1 또는 3이고, m이 2일때 n은 2이고, p는 1-2이고, j는 0-3이고, k는 0-3이고, j와 k의 합은 1-6이고, h는 1-6이며; Q는 O, NR8, CHOR9또는 OCH2CH2O이며; R7및 R8은 동일하거나 상이할 수 있고, 각각은 수소원자, C1-C6알킬기 또는 C1-C4알콕시 C2-C4알킬기이며; R9은 수소원자 또는 C1-C6알킬기이다); 단, R1이 페닐기 또는 나프틸기이고, X가 0이며, R2는, R5가 C1-C2알킬기인 일반식 II의 기인 화합물은 제외하는 것을 특징으로 하는, 화학식 (1)로 표시되는 화합물 또는 그의 약리학적으로 허용가능한 염.
- 제1항에 있어서, R1은 수소원자, C1-C6알킬기, C3-C6시클로알킬기, 페닐기, 나프틸기, C3-C6시클로알킬 C1-C4알킬기, 또는 페닐 C1-C4알킬기이며, 이중, 페닐기, 나프틸기 또는 페닐 C1-C4알킬기의 페닐 고리는 선택적으로 할로겐원자, C1-C6알킬기, 할로 C1-C6알킬기, C1-C6알콕시기, C1-C6알콕시카르보닐기 또는 페닐기로 임의로 모노-내지 트리-치환될 수 있으며; X는 O, S, CHNO2, C(COOR4)2, C(COOR4)CN 또는 C(CN)2으로, 이중, R4는 C1-C6알킬기, C3-C6시클로알킬기, 페닐기 또는 페닐 C1-C4알킬기이고; R2및 R3는, 부착되어 있는 질소와 함께, R5가 상기 정의된 기를 나타내는 상기 일반식 X의 N-치환된 피페라진 고리인 것을 특징으로 하는, 화학식 (1)로 표시되는 화합물 또는 그의 약리학적으로 허용가능한 염.
- 활성 성분으로 청구항 1에 정의된 화학식 (1)로 표시되는 화합물, 그의 약리학적으로 허용가능한 염 또는, 필요에 따라, 약학적으로 허용가능한 첨가제와의 혼합물의 형태로 함유하는 위장 활성촉진제.
- 제4항에 있어서, 만성 위염, 당뇨병, 후-위절제증 및 소화성 궤양으로부터 유래된 소화관 장애 및 역류성 식도염, 과민성 장중후군 밋 가성 장폐색증을 포함하는 소화관 질병의 치료에 사용되는 위장 활성촉진제.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP94-103570 | 1994-05-18 | ||
| JP10357094 | 1994-05-18 | ||
| PCT/JP1995/000938 WO1995031431A1 (en) | 1994-05-18 | 1995-05-17 | Novel diaminomethylidene derivative |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR970703301A true KR970703301A (ko) | 1997-07-03 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019960706566A Withdrawn KR970703301A (ko) | 1994-05-18 | 1995-05-17 | 신규 디아미노메틸리덴 유도체(novel diamincmethylidene derivative) |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0760362B1 (ko) |
| KR (1) | KR970703301A (ko) |
| BR (1) | BR9507892A (ko) |
| CA (1) | CA2189964A1 (ko) |
| DE (1) | DE69527786T2 (ko) |
| WO (1) | WO1995031431A1 (ko) |
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| US6152966A (en) * | 1998-05-13 | 2000-11-28 | Novo Nordisk A/S | Treatment of cork with a phenol oxidizing enzyme |
| WO2000027805A1 (en) * | 1998-11-05 | 2000-05-18 | Novo Nordisk A/S | Substituted 3,3-diamino-2-propenenitriles, their preparation and use |
| US6362205B2 (en) | 1998-11-05 | 2002-03-26 | Novo Nordisk A/S | Substituted 3,3-diamino-2-propenenitriles, their preparation and use |
| NZ525056A (en) | 2000-09-29 | 2004-11-26 | Glaxo Group Ltd | Morpholin-acetamide derivatives for the treatment of inflammatory diseases |
| DE60124576T2 (de) * | 2000-09-29 | 2007-06-21 | Glaxo Group Ltd., Greenford | Verbindungen verwendbar für die behandlung von entzündungskrankheiten |
| GB0207447D0 (en) * | 2002-03-28 | 2002-05-08 | Glaxo Group Ltd | Novel compounds |
| GB0207432D0 (en) | 2002-03-28 | 2002-05-08 | Glaxo Group Ltd | Novel compounds |
| GB0207436D0 (en) * | 2002-03-28 | 2002-05-08 | Glaxo Group Ltd | Novel compounds |
| GB0211759D0 (en) * | 2002-05-22 | 2002-07-03 | Glaxo Group Ltd | Novel compounds |
| GB0212357D0 (en) * | 2002-05-29 | 2002-07-10 | Glaxo Group Ltd | Novel compounds |
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| US3585142A (en) * | 1968-09-30 | 1971-06-15 | Richardson Co | Method of removing copper-containing incrustations from ferrous metal surfaces using an aqueous acid solution of aminoalkyl thiourea |
| JPS50117790A (en) * | 1974-03-06 | 1975-09-16 | Sankyo Co | Shukugofukusokankagobutsu no seiho |
| US4071524A (en) * | 1976-11-08 | 1978-01-31 | Riker Laboratories, Inc. | Derivatives of urea |
| US4416669A (en) * | 1982-02-22 | 1983-11-22 | Shell Oil Company | Fuel and lubricant compositions for octane requirement reduction |
| IT1190793B (it) * | 1982-04-27 | 1988-02-24 | Magis Farmaceutici | Composti attivi nel trattamento dell'ulcera e sintomi allergici della pelle |
| NZ223654A (en) * | 1987-03-09 | 1990-03-27 | Janssen Pharmaceutica Nv | 1-alkyl-substituted-benzimidazole-4-piperidinamines and pharmaceutical compositions |
| GB8829079D0 (en) * | 1988-12-13 | 1989-01-25 | Beecham Group Plc | Novel compounds |
| JPH0477464A (ja) * | 1990-07-19 | 1992-03-11 | Res Assoc Util Of Light Oil | 水溶性カルボジイミドの合成法 |
| FR2679555B1 (fr) * | 1991-07-25 | 1993-11-19 | Fabre Medicament Pierre | Nouveaux derives de l'uree, leur preparation et leur application en therapeutique. |
-
1995
- 1995-05-17 CA CA002189964A patent/CA2189964A1/en not_active Abandoned
- 1995-05-17 DE DE69527786T patent/DE69527786T2/de not_active Expired - Fee Related
- 1995-05-17 BR BR9507892A patent/BR9507892A/pt not_active Application Discontinuation
- 1995-05-17 EP EP95918729A patent/EP0760362B1/en not_active Expired - Lifetime
- 1995-05-17 KR KR1019960706566A patent/KR970703301A/ko not_active Withdrawn
- 1995-05-17 WO PCT/JP1995/000938 patent/WO1995031431A1/ja not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| EP0760362B1 (en) | 2002-08-14 |
| DE69527786D1 (de) | 2002-09-19 |
| DE69527786T2 (de) | 2003-04-10 |
| EP0760362A1 (en) | 1997-03-05 |
| CA2189964A1 (en) | 1995-11-23 |
| WO1995031431A1 (en) | 1995-11-23 |
| BR9507892A (pt) | 1997-11-18 |
| EP0760362A4 (en) | 1999-09-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 19961118 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |