KR930016413A - 벤조푸라닐- 및 티오페닐메틸티오-알칸카르복실산 유도체 - Google Patents
벤조푸라닐- 및 티오페닐메틸티오-알칸카르복실산 유도체 Download PDFInfo
- Publication number
- KR930016413A KR930016413A KR1019930000297A KR930000297A KR930016413A KR 930016413 A KR930016413 A KR 930016413A KR 1019930000297 A KR1019930000297 A KR 1019930000297A KR 930000297 A KR930000297 A KR 930000297A KR 930016413 A KR930016413 A KR 930016413A
- Authority
- KR
- South Korea
- Prior art keywords
- carbon atoms
- straight
- branched alkyl
- phenyl
- hydrogen
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 239000002253 acid Substances 0.000 title claims abstract 12
- 150000001875 compounds Chemical class 0.000 claims abstract 7
- 239000003814 drug Substances 0.000 claims abstract 4
- 208000037976 chronic inflammation Diseases 0.000 claims abstract 2
- 230000006020 chronic inflammation Effects 0.000 claims abstract 2
- -1 methyl compound Chemical class 0.000 claims abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 23
- 125000000217 alkyl group Chemical group 0.000 claims 18
- 229910052739 hydrogen Inorganic materials 0.000 claims 13
- 239000001257 hydrogen Substances 0.000 claims 13
- 150000002431 hydrogen Chemical class 0.000 claims 9
- 229910052760 oxygen Inorganic materials 0.000 claims 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 9
- 125000001424 substituent group Chemical group 0.000 claims 9
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 8
- 125000000623 heterocyclic group Chemical group 0.000 claims 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- 229910052717 sulfur Inorganic materials 0.000 claims 8
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 125000003118 aryl group Chemical group 0.000 claims 5
- 150000001721 carbon Chemical group 0.000 claims 5
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 239000001301 oxygen Substances 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 239000011737 fluorine Chemical group 0.000 claims 4
- 125000005842 heteroatom Chemical group 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 125000004434 sulfur atom Chemical group 0.000 claims 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical group [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 3
- 229910052794 bromium Inorganic materials 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 239000000460 chlorine Chemical group 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- 229920006395 saturated elastomer Polymers 0.000 claims 3
- 125000003831 tetrazolyl group Chemical group 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 2
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 claims 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 239000012442 inert solvent Substances 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 2
- YMHOBZXQZVXHBM-UHFFFAOYSA-N 2,5-dimethoxy-4-bromophenethylamine Chemical compound COC1=CC(CCN)=C(OC)C=C1Br YMHOBZXQZVXHBM-UHFFFAOYSA-N 0.000 claims 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 206010061216 Infarction Diseases 0.000 claims 1
- 241000534944 Thia Species 0.000 claims 1
- 241000545067 Venus Species 0.000 claims 1
- 229960000583 acetic acid Drugs 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 230000002862 amidating effect Effects 0.000 claims 1
- 230000009435 amidation Effects 0.000 claims 1
- 238000007112 amidation reaction Methods 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 238000007796 conventional method Methods 0.000 claims 1
- QPJDMGCKMHUXFD-UHFFFAOYSA-N cyanogen chloride Chemical group ClC#N QPJDMGCKMHUXFD-UHFFFAOYSA-N 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 239000002552 dosage form Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 239000007789 gas Substances 0.000 claims 1
- 239000012362 glacial acetic acid Substances 0.000 claims 1
- 230000007574 infarction Effects 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 230000001681 protective effect Effects 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 229940124530 sulfonamide Drugs 0.000 claims 1
- 150000003456 sulfonamides Chemical class 0.000 claims 1
- 230000001629 suppression Effects 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 abstract 2
- 102000004722 NADPH Oxidases Human genes 0.000 abstract 1
- 108010002998 NADPH Oxidases Proteins 0.000 abstract 1
- 208000038016 acute inflammation Diseases 0.000 abstract 1
- 230000006022 acute inflammation Effects 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 229940102396 methyl bromide Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D307/80—Radicals substituted by oxygen atoms
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/54—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D333/56—Radicals substituted by oxygen atoms
Landscapes
- 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)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP9200623.8 | 1992-01-13 | ||
| GB929200623A GB9200623D0 (en) | 1992-01-13 | 1992-01-13 | Benzofuranyl and thiophenyl-methylthio-alkanecarboxylic acid derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR930016413A true KR930016413A (ko) | 1993-08-26 |
Family
ID=10708497
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019930000297A Withdrawn KR930016413A (ko) | 1992-01-13 | 1993-01-12 | 벤조푸라닐- 및 티오페닐메틸티오-알칸카르복실산 유도체 |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP0551662A1 (https=) |
| JP (1) | JPH05271214A (https=) |
| KR (1) | KR930016413A (https=) |
| CN (1) | CN1074904A (https=) |
| AU (1) | AU3108293A (https=) |
| CA (1) | CA2086987A1 (https=) |
| GB (1) | GB9200623D0 (https=) |
| HU (1) | HUT64952A (https=) |
| IL (1) | IL104356A0 (https=) |
| MX (1) | MX9207557A (https=) |
| PL (1) | PL297337A1 (https=) |
| TW (1) | TW212796B (https=) |
| ZA (1) | ZA93190B (https=) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HRP950288A2 (en) * | 1994-05-31 | 1997-08-31 | Bayer Ag | Oxalylamino-benzofuran- and benzothienyl-derivatives |
| ATE175667T1 (de) * | 1994-05-31 | 1999-01-15 | Bayer Ag | Aminobenzofuryl- und -thienylderivate |
| GB9410877D0 (en) * | 1994-05-31 | 1994-07-20 | Bayer Ag | Heterocyclycarbonyl substituted benzoduranyl-and-thiophenyl-alkanecarboxyclic acid derivatives |
| GB9504460D0 (en) * | 1995-03-06 | 1995-04-26 | Bayer Ag | N-(3-Benzofuranyl)urea-derivatives |
| US5763496A (en) * | 1995-11-27 | 1998-06-09 | The Research Foundation Of State University Of New York | Prevention of atherosclerosis using NADPH oxidase inhibitors |
| GB9614718D0 (en) | 1996-07-12 | 1996-09-04 | Bayer Ag | 3-ureido-pyridofurans and -pyridothiophenes |
| US5908859A (en) * | 1997-08-11 | 1999-06-01 | Eli Lilly And Company | Benzothiophenes for inhibiting hyperlipidemia |
| WO1999012539A1 (en) * | 1997-09-10 | 1999-03-18 | The Johns Hopkins University School Of Medicine | The use of an nadph-oxidase inhibitor in the treatment of reperfusion injury |
| US6242473B1 (en) * | 1999-01-08 | 2001-06-05 | Maxim Pharmaceuticals, Inc. | Treatment and prevention of reactive oxygen metabolite-mediated cellular damage |
| CN1639146A (zh) | 2002-02-22 | 2005-07-13 | 拜尔药品公司 | 用于治疗过度增生疾病的稠合三环杂环 |
| US7144885B2 (en) | 2002-02-22 | 2006-12-05 | Bayer Pharmaceuticals Corporation | Fused tricyclic heterocycles useful for treating hyper-proliferative disorders |
| EP1499742B1 (en) | 2002-04-17 | 2010-11-03 | Glucox Biotech AB | Nad(p)h oxidase inhibitors for increased glucose uptake and treatment of type ii diabetes |
| AU2003252140A1 (en) * | 2002-07-24 | 2004-02-09 | Janssen Pharmaceutica N.V. | Acetylenic compounds useful in treating inflammatory disorders |
| US7022703B2 (en) | 2003-07-24 | 2006-04-04 | Janssen Pharmaceutica, N.V. | Acetylenic compound useful in treating inflammatory disorders |
| US7119214B2 (en) * | 2004-04-13 | 2006-10-10 | Cephalon France | Thio-substituted tricyclic and bicyclic aromatic methanesulfinyl derivatives |
| CN102267990B (zh) * | 2011-06-03 | 2013-11-13 | 浙江工业大学 | 一种2,3-二氢苯并呋喃类衍生物及其制备与应用 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0146243A1 (en) * | 1983-10-31 | 1985-06-26 | Merck Frosst Canada Inc. | Lipoxygenase inhibitors |
| JP2855341B2 (ja) * | 1988-06-10 | 1999-02-10 | 武田薬品工業株式会社 | 新規２―置換クマラン誘導体 |
-
1992
- 1992-01-13 GB GB929200623A patent/GB9200623D0/en active Pending
- 1992-12-12 TW TW081109961A patent/TW212796B/zh active
- 1992-12-24 MX MX9207557A patent/MX9207557A/es unknown
- 1992-12-31 EP EP92122178A patent/EP0551662A1/en not_active Withdrawn
-
1993
- 1993-01-07 AU AU31082/93A patent/AU3108293A/en not_active Abandoned
- 1993-01-07 JP JP5017110A patent/JPH05271214A/ja active Pending
- 1993-01-08 CA CA002086987A patent/CA2086987A1/en not_active Abandoned
- 1993-01-08 PL PL29733793A patent/PL297337A1/xx unknown
- 1993-01-11 IL IL104356A patent/IL104356A0/xx unknown
- 1993-01-12 KR KR1019930000297A patent/KR930016413A/ko not_active Withdrawn
- 1993-01-12 ZA ZA93190A patent/ZA93190B/xx unknown
- 1993-01-13 CN CN93100403A patent/CN1074904A/zh active Pending
- 1993-01-13 HU HU9300078A patent/HUT64952A/hu unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUT64952A (en) | 1994-03-28 |
| EP0551662A1 (en) | 1993-07-21 |
| ZA93190B (en) | 1993-08-13 |
| AU3108293A (en) | 1993-07-15 |
| MX9207557A (es) | 1993-07-01 |
| PL297337A1 (en) | 1994-01-24 |
| HU9300078D0 (en) | 1993-04-28 |
| TW212796B (https=) | 1993-09-11 |
| JPH05271214A (ja) | 1993-10-19 |
| GB9200623D0 (en) | 1992-03-11 |
| CN1074904A (zh) | 1993-08-04 |
| IL104356A0 (en) | 1993-05-13 |
| CA2086987A1 (en) | 1993-07-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR930016413A (ko) | 벤조푸라닐- 및 티오페닐메틸티오-알칸카르복실산 유도체 | |
| KR930017898A (ko) | 술포닐벤질 치환 피리돈 | |
| KR950002755A (ko) | 워트마닌 및 그의 유사체에 의한 포스파티딜이노시톨 3-키나제의 억제 | |
| KR900006318A (ko) | 피페리디닐 벤즈이미다졸 | |
| ES8103751A1 (es) | Procedimiento para la preparacion de acidos 3-cefem-4-carbo-xilicos sustituidos en la posicion 7 | |
| ES8600263A1 (es) | Un compuesto. | |
| KR930007937A (ko) | 치환 이미다졸릴- 프로펜산 유도체 | |
| KR890014486A (ko) | N-시클로프로필아닐, 및 1-시클로프로필-퀴놀론카르복실산 및 그의 유도체의 제조에 있어서 n-시클로프로필아닐린의 용도 | |
| KR920000730A (ko) | 신규 벤즈이미다졸 유도체, 그의 제조방법, 그의 신규 중간체, 그의 약물 용도 및 그를 함유하는 제약 조성물 | |
| KR910004569A (ko) | 고리형 치환체를 갖는 (퀴놀린-2-일-메톡시)페닐아세트산 유도체 | |
| KR930007936A (ko) | 이미다졸릴- 프로펜산 유도체 | |
| KR960031442A (ko) | 페닐시클로헥실카르복스아미드의 용도 | |
| ES449096A1 (es) | Un procedimiento para la preparacion de 11-desoxi-16-ariloxi-omega-tetranorprostaglandinas. | |
| KR930021642A (ko) | 9-플루오로-7-옥소-7h-피리도[1,2,3-데][1,4]벤족사진-6-카르복실산 및 에스테르 | |
| KR930019634A (ko) | 이미다졸릴 치환 페닐아세트아미드 | |
| KR900011709A (ko) | 신규한 테트랄린 유도체 | |
| KR930021641A (ko) | 7-옥소-7H-피리도[1,2,3-d,e][1,4]벤족사진-6-카르복실산 및 에스테르 | |
| KR930000520A (ko) | 아미노메틸 치환 2,3-디히드로피라노[2,3-b]피리딘, 그의 제조 방법 및 약제로서의 그의 용도 | |
| KR930021621A (ko) | 프로페노일-이미다졸 유도체 | |
| FR2351113A1 (fr) | Derives de prostaglandines et medicaments contenant ces derives | |
| KR880007490A (ko) | 치환된 아미노프로피온아미드, 이의 제조방법, 이를 함유하는 약제, 이의 용도 및 이의 제조시에 생성된 중간체 | |
| KR940021532A (ko) | 헤테로시클릭 치환된 페닐아세트산 유도체의 페닐글리산아미드 | |
| ES2062860T3 (es) | Composicion farmaceutica para la mejoria de la disuria. | |
| KR930017896A (ko) | 술포닐벤질 치환 이미다졸릴프로펜산 유도체 | |
| ATE66920T1 (de) | Neue carbonsaeurederivate, verfahren zu ihrer herstellung sowie arzneimittel, die diese verbindungen enthalten. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19930112 |
|
| 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 |