KR920021516A - 기관지 확장제 및 소염제로서의 페닐 피라졸리디논 - Google Patents
기관지 확장제 및 소염제로서의 페닐 피라졸리디논 Download PDFInfo
- Publication number
- KR920021516A KR920021516A KR1019920007212A KR920007212A KR920021516A KR 920021516 A KR920021516 A KR 920021516A KR 1019920007212 A KR1019920007212 A KR 1019920007212A KR 920007212 A KR920007212 A KR 920007212A KR 920021516 A KR920021516 A KR 920021516A
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- methoxyphenyl
- cyclopentyloxy
- methyl
- oxo
- Prior art date
Links
- 229940121363 anti-inflammatory agent Drugs 0.000 title 1
- 239000002260 anti-inflammatory agent Substances 0.000 title 1
- 229940124630 bronchodilator Drugs 0.000 title 1
- 239000000168 bronchodilator agent Substances 0.000 title 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 38
- -1 5- [3- (cyclopentyloxy) -4-methoxyphenyl] -1,2-dimethyl-3-pyrazolidinone hydroiodide Chemical compound 0.000 claims 17
- 125000000217 alkyl group Chemical group 0.000 claims 11
- 125000001887 cyclopentyloxy group Chemical group C1(CCCC1)O* 0.000 claims 9
- 229910052739 hydrogen Inorganic materials 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 4
- BTTLYSINHUOEJD-UHFFFAOYSA-N 5-(3-cyclopentyloxy-4-methoxyphenyl)-3-oxopyrazolidine-1-carboxamide Chemical compound COC1=CC=C(C2N(NC(=O)C2)C(N)=O)C=C1OC1CCCC1 BTTLYSINHUOEJD-UHFFFAOYSA-N 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- LGXHBKLMBYNKRN-BIAFCPFJSA-N (3s)-3-(3-cyclopentyloxy-4-methoxyphenyl)-2-methyl-n-(1-naphthalen-1-ylethyl)-5-oxopyrazolidine-1-carboxamide Chemical compound COC1=CC=C([C@H]2N(N(C(=O)C2)C(=O)NC(C)C=2C3=CC=CC=C3C=CC=2)C)C=C1OC1CCCC1 LGXHBKLMBYNKRN-BIAFCPFJSA-N 0.000 claims 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 claims 1
- RYNACNWTGQURAQ-AATRIKPKSA-N 2-[(e)-3-(5-bromopyridin-3-yl)prop-2-enyl]-5-(3-cyclopentyloxy-4-methoxyphenyl)-1-methylpyrazolidin-3-one Chemical compound COC1=CC=C(C2N(N(C\C=C\C=3C=C(Br)C=NC=3)C(=O)C2)C)C=C1OC1CCCC1 RYNACNWTGQURAQ-AATRIKPKSA-N 0.000 claims 1
- BFZGPZLQAPCRRT-UHFFFAOYSA-N 2-acetyl-5-(3-cyclopentyloxy-4-methoxyphenyl)-1-methylpyrazolidin-3-one;hydrochloride Chemical compound Cl.COC1=CC=C(C2N(N(C(=O)C2)C(C)=O)C)C=C1OC1CCCC1 BFZGPZLQAPCRRT-UHFFFAOYSA-N 0.000 claims 1
- KCBSXNNILRBIPT-UHFFFAOYSA-N 3-(3-cyclopentyloxy-4-methoxyphenyl)-2-methyl-1h-pyrazol-5-one Chemical compound COC1=CC=C(C=2N(NC(=O)C=2)C)C=C1OC1CCCC1 KCBSXNNILRBIPT-UHFFFAOYSA-N 0.000 claims 1
- VLKWTOGGEGZGCP-UHFFFAOYSA-N 3-(3-cyclopentyloxy-4-methoxyphenyl)-2-methyl-5-oxo-n-phenylpyrazolidine-1-carboxamide;hydrochloride Chemical compound Cl.COC1=CC=C(C2N(N(C(=O)C2)C(=O)NC=2C=CC=CC=2)C)C=C1OC1CCCC1 VLKWTOGGEGZGCP-UHFFFAOYSA-N 0.000 claims 1
- YOELPLLVKQWBMD-UHFFFAOYSA-N 5-(3-cyclopentyloxy-4-methoxyphenyl)-1-ethylpyrazolidin-3-one Chemical compound CCN1NC(=O)CC1C1=CC=C(OC)C(OC2CCCC2)=C1 YOELPLLVKQWBMD-UHFFFAOYSA-N 0.000 claims 1
- WQLAFOTVJACOSH-UHFFFAOYSA-N 5-(3-cyclopentyloxy-4-methoxyphenyl)-1-methyl-2-(3-pyridin-3-ylpropyl)pyrazolidin-3-one Chemical compound COC1=CC=C(C2N(N(CCCC=3C=NC=CC=3)C(=O)C2)C)C=C1OC1CCCC1 WQLAFOTVJACOSH-UHFFFAOYSA-N 0.000 claims 1
- TYTQNPFLWZBHGG-UHFFFAOYSA-N 5-(3-cyclopentyloxy-4-methoxyphenyl)-1-methyl-2-(pyridine-3-carbonyl)pyrazolidin-3-one Chemical compound COC1=CC=C(C2N(N(C(=O)C2)C(=O)C=2C=NC=CC=2)C)C=C1OC1CCCC1 TYTQNPFLWZBHGG-UHFFFAOYSA-N 0.000 claims 1
- YZVPWLDZKDUWQK-UHFFFAOYSA-N 5-(3-cyclopentyloxy-4-methoxyphenyl)-3-oxopyrazolidine-1-carboxylic acid Chemical compound COC1=CC=C(C2N(NC(=O)C2)C(O)=O)C=C1OC1CCCC1 YZVPWLDZKDUWQK-UHFFFAOYSA-N 0.000 claims 1
- WZROEATXAXBHDC-UHFFFAOYSA-N 5-(3-cyclopentyloxy-4-methoxyphenyl)pyrazolidin-3-one Chemical compound COC1=CC=C(C2NNC(=O)C2)C=C1OC1CCCC1 WZROEATXAXBHDC-UHFFFAOYSA-N 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 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
- 150000003840 hydrochlorides Chemical class 0.000 claims 1
- RBROWVSVHFQZFH-UHFFFAOYSA-N methyl 2-[5-(3-cyclopentyloxy-4-methoxyphenyl)-3-oxopyrazolidin-1-yl]acetate Chemical compound COC(=O)CN1NC(=O)CC1C1=CC=C(OC)C(OC2CCCC2)=C1 RBROWVSVHFQZFH-UHFFFAOYSA-N 0.000 claims 1
- 150000004702 methyl esters Chemical class 0.000 claims 1
- YOBRAYQWJMFDMW-UHFFFAOYSA-N n-benzyl-3-(3-cyclopentyloxy-4-methoxyphenyl)-2-methyl-5-oxopyrazolidine-1-carboxamide;hydrochloride Chemical compound Cl.COC1=CC=C(C2N(N(C(=O)C2)C(=O)NCC=2C=CC=CC=2)C)C=C1OC1CCCC1 YOBRAYQWJMFDMW-UHFFFAOYSA-N 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- OHCJOXLKRQZMQE-UHFFFAOYSA-N n-butyl-3-(3-cyclopentyloxy-4-methoxyphenyl)-2-methyl-5-oxopyrazolidine-1-carboxamide;hydrochloride Chemical compound Cl.C1C(=O)N(C(=O)NCCCC)N(C)C1C1=CC=C(OC)C(OC2CCCC2)=C1 OHCJOXLKRQZMQE-UHFFFAOYSA-N 0.000 claims 1
- WEIKGRGABDTLPZ-UHFFFAOYSA-N n-cyclohexyl-3-(3-cyclopentyloxy-4-methoxyphenyl)-2-methyl-5-oxopyrazolidine-1-carboxamide;hydrochloride Chemical compound Cl.COC1=CC=C(C2N(N(C(=O)C2)C(=O)NC2CCCCC2)C)C=C1OC1CCCC1 WEIKGRGABDTLPZ-UHFFFAOYSA-N 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- 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]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D231/08—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with oxygen or sulfur atoms directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
- C07D231/26—1-Phenyl-3-methyl-5- pyrazolones, unsubstituted or substituted on the phenyl ring
-
- 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
- C07D401/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical 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)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Peptides Or Proteins (AREA)
- Hydrogenated Pyridines (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (38)
- 일반식(Ⅰ)의 화합물 및 약리학적으로 허용되는 이의 염.상기식에서, R1은 수소 또는 저급 알킬이고, R2는 C3-7알킬 또는 C3-7사이클로알킬이고, R3은 수소, 저급알킬, 카복시 저급 알킬, 저급 알콕시카보닐, 저급 알콕시카보닐 저급 알킬, 아릴, 아르알킬 또는 CONH2이고, R4는 수소, C1-8알킬,이고, B는 결합, NH 또는 O이고, Y는 O 또는 S이고, A는 결합 또는 -C=C- 이고, n은 0 내지 5이고, R5는 저급 알킬, C3-8사이클로알킬, 아릴, 치환된 아릴, 아르알킬, 치환된 아르알킬, 아르알케닐, 아르알케닐알킬 또는이고, B가 NH일때 R5는 또한 수소를 나타낼 수 있으며, R6은 수소 또는 할로깅고, 점선은 임의의 이중결합을 나타낸다.
- 제1항에 있어서, R1는 C1-3알킬이고, R2는 C4-6알킬 또는 C5-6사이클로알킬이고, R3은 C1-3알킬 또는 아르알킬이고,이고, B는 결합 또는 NH이고, R5는 B가 NH인 경우 수소이거나 아르알킬 또는이고, A는 결합 모는 -C=C-이고, n은 0내지 2이고, R6는 수소 또는 할로인 일반식(Ⅰ)의 화합물.
- 제1항에 있어서, R1는 저급 알킬이고, R2는 n-부틸 또는 사이클로펜틸이고 R3는 메틸이고 R4는이고, R5는 수소, 아르알킬 또는이고, R6는 수소 또는 할로인 일반식(Ⅰ)의 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-3-피라졸리디논인 화합물.
- 제1항에 있어서, 5-[3-사이클로펜틸옥시)-4-메톡시페닐]-1-메틸-3-피라졸리디논인 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1,2-디메틸-3-피라졸리디논 하이드로요오다이드인 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-3-옥소-1-피라졸리딘아세트산메틸 에스테르인 화합물.
- 제l항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-3-옥소-1-피라졸리딘카복스아미드인 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-3-옥소-1-피라졸리딘카복스아미드인 메틸 에스테르인 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-3-옥소-피라졸리딘카복실산인 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2-메틸-5-옥소-피라졸리딘카복스아미드 하이드로클로라이드인 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2-메틸-N-옥소-1H-피라졸라딘카복스아미드 1/2수화물인 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1,2-디하이드로-1-메틸-3H-피라졸-3-온인 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2,5-디하이드로-2-메틸-5-옥소-1H-피라졸-1-카복스아미드인 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2,5-디하이드로-2-메틸-5-옥소-N-(2-피리디닐메틸)-1H-피라졸-1-카복스아미드인 화합물.
- 제1항에 있어서, (S)-3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2-메틸-N-[1-(1-나프탈레닐)에틸]-5-옥소-1-피라졸리딘카복스아미드인 화합물.
- 제1항에 있어서, N-부틸-3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2-메틸-5-옥소-1-피라졸리딘카복스아미드 하이드로클로라이드인 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2-메틸-5-옥소-1-피라졸리딘카복스아미드 하이드로클로라이드 수화물인 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2-메틸-5-옥소-N-페닐-1-피라졸리딘카복스아미드 하이드로클로라이드인 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2-메틸-5-옥소-N-(페닐메틸)-1-피라졸리딘카복스아미드 하이드로클로라이드인 화합물.
- 제1항에 있어서, N-사이클로헥실-3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2-메틸-5-옥소-1-피라졸리딘카복스아미드 하이드로클로라이드인 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-N-(4-메톡시페닐)-2-메틸-5-옥소-1-피라졸리딘카복스아미드 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-N[(4-플루오로페닐)메틸]-2-메틸-5-옥소-1-피라졸리딘카복스아미드 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-N[(4-플루오로페닐)메틸]-2-메틸-5-옥소-1-피라졸리딘카복스아미드 화합물.
- 제l항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-N[(4-플루오로페닐)메틸]-2-메틸-5-옥소-1-피라졸리딘카복스아미드 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-5-옥소-2-(페닐메틸)-1-피라졸리딘카복스아미드 화합물.
- 제1항에 있어서, 3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2-메틸-5-옥소-N-(3-피리디닐메틸)-1-피라졸리딘카복스아미드 화합물.
- 제1항에 있어서, 5,3-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1-메틸-2-(3-피리디닐메틸)-3-피라졸디논 하이드로클로라이드 2수화물인 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-2-헵틸-1-3-피라졸디논 하이드로클로라이드 화합물.
- 제1항에 있어서, 2-[(5-브로모-3-피리디닐)메틸]-5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1-메틸-3-피라졸디논 하이드로클로라이드 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1-메틸-2-(5-브로모-3-필디닐카보닐)-3-피라졸리디논인 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1-메틸-2-[3-(3-피리디닐)프로필]-3-피라졸리디논 1/4디클로로메탄인 와합물.
- 제1항에 있어서, 2-[(E)-3-(5-브로모-3-피리디닐)-2-프로페닐]-5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1-메틸-3-피라졸리디논 1/2(디클로로메탄)인 화합물.
- 제1항에 있어서, 2-아세틸-5-[3-(사이클로펜틸옥시)-4-메토시페닐]-1-메틸-3-피라졸리디논 하이드로클로라이드인 화합물.
- 제1항에있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1-메틸-2-(3-피리디닐카보닐)-3-피라졸리디논 1/2수화물인 화합물.
- 제1항에 있어서, 2-[(E)-3-(5-브로모-3-피리디닐)-1-옥소-2-프로페닐]-5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1-메틸-3-피라졸리디논 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1-(메틸페닐)-3-피라졸리디논인 화합물.
- 제1항에 있어서, 5-[3-(사이클로펜틸옥시)-4-메톡시페닐]-1-에틸-3-피라졸리디논인 화합물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/694,197 US5191084A (en) | 1991-05-01 | 1991-05-01 | Phenyl pyrazolidinones as bronchodilators and anti-inflammatory agents |
US07/694,197 | 1991-05-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR920021516A true KR920021516A (ko) | 1992-12-18 |
Family
ID=24787818
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019920007212A KR920021516A (ko) | 1991-05-01 | 1992-04-29 | 기관지 확장제 및 소염제로서의 페닐 피라졸리디논 |
Country Status (20)
Country | Link |
---|---|
US (1) | US5191084A (ko) |
EP (1) | EP0511865B1 (ko) |
JP (1) | JPH05117239A (ko) |
KR (1) | KR920021516A (ko) |
AT (1) | ATE148460T1 (ko) |
AU (1) | AU653806B2 (ko) |
CA (1) | CA2067298A1 (ko) |
DE (1) | DE69217112T2 (ko) |
DK (1) | DK0511865T3 (ko) |
ES (1) | ES2097872T3 (ko) |
FI (1) | FI921920A (ko) |
GR (1) | GR3023240T3 (ko) |
HK (1) | HK1000104A1 (ko) |
HU (1) | HUT61001A (ko) |
IL (1) | IL101663A (ko) |
MX (1) | MX9202032A (ko) |
PH (1) | PH30772A (ko) |
SG (1) | SG49713A1 (ko) |
TW (1) | TW200467B (ko) |
ZA (1) | ZA923126B (ko) |
Families Citing this family (82)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ238912A (en) * | 1990-07-17 | 1992-12-23 | Lilly Co Eli | Pyrazole derivatives and medicaments |
KR0133550B1 (ko) * | 1991-01-21 | 1998-04-23 | 요시또시 가즈오 | 3-벤질리덴-1-카르바모일-2-피롤리돈 유사체 |
GB9212673D0 (en) * | 1992-06-15 | 1992-07-29 | Celltech Ltd | Chemical compounds |
GB9222253D0 (en) * | 1992-10-23 | 1992-12-09 | Celltech Ltd | Chemical compounds |
ATE234270T1 (de) * | 1992-12-02 | 2003-03-15 | Pfizer | Cathecoldiether als selektive pde iv hemmungsmittel |
US5814651A (en) * | 1992-12-02 | 1998-09-29 | Pfizer Inc. | Catechol diethers as selective PDEIV inhibitors |
US5622977A (en) * | 1992-12-23 | 1997-04-22 | Celltech Therapeutics Limited | Tri-substituted (aryl or heteroaryl) derivatives and pharmaceutical compositions containing the same |
GB9226830D0 (en) * | 1992-12-23 | 1993-02-17 | Celltech Ltd | Chemical compounds |
GB9304920D0 (en) * | 1993-03-10 | 1993-04-28 | Celltech Ltd | Chemical compounds |
GB9304919D0 (en) * | 1993-03-10 | 1993-04-28 | Celltech Ltd | Chemical compounds |
US5459151A (en) * | 1993-04-30 | 1995-10-17 | American Home Products Corporation | N-acyl substituted phenyl piperidines as bronchodilators and antiinflammatory agents |
GB9312853D0 (en) * | 1993-06-22 | 1993-08-04 | Euro Celtique Sa | Chemical compounds |
US5665754A (en) * | 1993-09-20 | 1997-09-09 | Glaxo Wellcome Inc. | Substituted pyrrolidines |
US5728705A (en) * | 1993-10-04 | 1998-03-17 | The Trustees Of Columbia University In The City Of New York | Method of inducing vasorelaxation to treat pulmonary hypertension |
US5502072A (en) * | 1993-11-26 | 1996-03-26 | Pfizer Inc. | Substituted oxindoles |
GB9326173D0 (en) * | 1993-12-22 | 1994-02-23 | Celltech Ltd | Chemical compounds and process |
JP3806144B2 (ja) * | 1993-12-22 | 2006-08-09 | セルテック セラピューティックス リミテッド | 三置換フェニル誘導体、その調製方法とホスホジエステラーゼ(iv型)阻害剤としてのその使用 |
CA2143143A1 (en) * | 1994-03-08 | 1995-09-09 | Toshihiko Tanaka | 3-phenylpyrrolidine derivatives |
US5786354A (en) * | 1994-06-21 | 1998-07-28 | Celltech Therapeutics, Limited | Tri-substituted phenyl derivatives and processes for their preparation |
US6245774B1 (en) | 1994-06-21 | 2001-06-12 | Celltech Therapeutics Limited | Tri-substituted phenyl or pyridine derivatives |
GB9412573D0 (en) | 1994-06-22 | 1994-08-10 | Celltech Ltd | Chemical compounds |
GB9412571D0 (en) * | 1994-06-22 | 1994-08-10 | Celltech Ltd | Chemical compounds |
GB9412672D0 (en) * | 1994-06-23 | 1994-08-10 | Celltech Ltd | Chemical compounds |
AU735590B2 (en) * | 1994-06-24 | 2001-07-12 | Euro-Celtique S.A. | Compounds for and method of inhibiting phosphodiesterase IV |
US5591776A (en) * | 1994-06-24 | 1997-01-07 | Euro-Celtique, S.A. | Pheynl or benzyl-substituted rolipram-based compounds for and method of inhibiting phosphodiesterase IV |
DE69526790T2 (de) * | 1994-06-24 | 2003-03-06 | Euro Celtique Sa | Verbindungen zur hemmung von phosphodiesrerase iv |
US5922751A (en) * | 1994-06-24 | 1999-07-13 | Euro-Celtique, S.A. | Aryl pyrazole compound for inhibiting phosphodiesterase IV and methods of using same |
US5665737B1 (en) * | 1994-10-12 | 1999-02-16 | Euro Celtique Sa | Substituted benzoxazoles |
DE69531506T2 (de) * | 1994-12-13 | 2004-06-24 | Euroceltique S.A. | Arylthioxanthine |
ATE247655T1 (de) * | 1994-12-13 | 2003-09-15 | Euro Celtique Sa | Dreifachsubstituierte thioxanthine |
US6025361A (en) * | 1994-12-13 | 2000-02-15 | Euro-Celtique, S.A. | Trisubstituted thioxanthines |
US6268373B1 (en) | 1995-06-07 | 2001-07-31 | Euro-Celtique S.A. | Trisubstituted thioxanthines |
US6166041A (en) * | 1995-10-11 | 2000-12-26 | Euro-Celtique, S.A. | 2-heteroaryl and 2-heterocyclic benzoxazoles as PDE IV inhibitors for the treatment of asthma |
GB9523675D0 (en) | 1995-11-20 | 1996-01-24 | Celltech Therapeutics Ltd | Chemical compounds |
GB9526245D0 (en) * | 1995-12-21 | 1996-02-21 | Celltech Therapeutics Ltd | Chemical compounds |
GB9526246D0 (en) * | 1995-12-21 | 1996-02-21 | Celltech Therapeutics Ltd | Chemical compounds |
US6075016A (en) * | 1996-04-10 | 2000-06-13 | Euro-Celtique S.A. | 6,5-fused aromatic ring systems having enhanced phosphodiesterase IV inhibitory activity |
GB9608435D0 (en) * | 1996-04-24 | 1996-06-26 | Celltech Therapeutics Ltd | Chemical compounds |
US6011052A (en) * | 1996-04-30 | 2000-01-04 | Warner-Lambert Company | Pyrazolone derivatives as MCP-1 antagonists |
US5864037A (en) * | 1996-06-06 | 1999-01-26 | Euro-Celtique, S.A. | Methods for the synthesis of chemical compounds having PDE-IV inhibitory activity |
JP4017214B2 (ja) | 1996-06-11 | 2007-12-05 | 興和創薬株式会社 | 5−フェニル−3−ピリダジノン誘導体 |
WO1997048697A1 (en) | 1996-06-19 | 1997-12-24 | Rhone-Poulenc Rorer Limited | Substituted azabicylic compounds and their use as inhibitors of the production of tnf and cyclic amp phosphodiesterase |
DE69730980T2 (de) | 1996-07-31 | 2006-02-23 | Nikken Chemicals Co., Ltd. | 6-phenyltetrahydro-1,3-oxazin-2-on derivate und medizinische zusammensetzungen, die sie enthalten |
EP0924204A4 (en) | 1996-08-27 | 2002-10-23 | Nikken Chemicals Co Ltd | 2-PHENYLMORPHOLIN-5-ONE DERIVATIVES AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME |
US5744473A (en) * | 1996-09-16 | 1998-04-28 | Euro-Celtique, S.A. | PDE IV inhibitors: "bis-compounds" |
GB9619284D0 (en) * | 1996-09-16 | 1996-10-30 | Celltech Therapeutics Ltd | Chemical compounds |
GB9622363D0 (en) | 1996-10-28 | 1997-01-08 | Celltech Therapeutics Ltd | Chemical compounds |
GB9625184D0 (en) * | 1996-12-04 | 1997-01-22 | Celltech Therapeutics Ltd | Chemical compounds |
US6057329A (en) * | 1996-12-23 | 2000-05-02 | Celltech Therapeutics Limited | Fused polycyclic 2-aminopyrimidine derivatives |
GB9705361D0 (en) | 1997-03-14 | 1997-04-30 | Celltech Therapeutics Ltd | Chemical compounds |
GB9713087D0 (en) * | 1997-06-20 | 1997-08-27 | Celltech Therapeutics Ltd | Chemical compounds |
US6235736B1 (en) | 1997-06-24 | 2001-05-22 | Nikken Chemicals Co., Ltd. | 3-anilino-2-cycloalkenone derivatives |
FR2773153A1 (fr) * | 1997-12-29 | 1999-07-02 | Rhone Poulenc Agrochimie | Nouveaux composes fongicides |
GB9914258D0 (en) | 1999-06-18 | 1999-08-18 | Celltech Therapeutics Ltd | Chemical compounds |
EP2193808A1 (en) | 1999-08-21 | 2010-06-09 | Nycomed GmbH | Synergistic combination |
GB9924862D0 (en) | 1999-10-20 | 1999-12-22 | Celltech Therapeutics Ltd | Chemical compounds |
TW200400821A (en) * | 1999-11-02 | 2004-01-16 | Pfizer | Pharmaceutical composition (II) useful for treating or preventing pulmonary hypertension in a patient |
IT1317049B1 (it) | 2000-06-23 | 2003-05-26 | Sigma Tau Ind Farmaceuti | Composti utili per la preparazione di medicamenti ad attivita'inibitrice della fosfodiesterasi iv. |
ATE445838T1 (de) | 2001-07-25 | 2009-10-15 | Raptor Pharmaceutical Inc | Zusammensetzungen und verfahren zur modulation des transports durch die blut-hirn-schranke |
PL379544A1 (pl) * | 2002-09-09 | 2006-10-02 | Amgen Inc. | 1,4,5-podstawione pochodne 1,2-dihydro-pirazol-3-onu i 3-alkoksy 1H-pirazolu jako środki obniżające poziom TNF-alfa oraz interleukin do leczenia stanów zapalnych |
US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
EA200501548A1 (ru) | 2003-04-01 | 2006-02-24 | Апплайд Резеч Системз Арс Холдинг Н.В. | Ингибиторы фосфодиэстераз при бесплодии |
DK1889198T3 (da) | 2005-04-28 | 2015-02-09 | Proteus Digital Health Inc | Farma-informatiksystem |
WO2007061172A1 (en) | 2005-11-28 | 2007-05-31 | Atlab Inc. | Time to digital converting circuit and pressure sensing device using the same |
WO2008036682A2 (en) | 2006-09-18 | 2008-03-27 | Raptor Pharmaceutical Inc. | Treatment of liver disorders by administration of receptor-associated protein (rap)-conjugates |
KR100820246B1 (ko) * | 2006-10-10 | 2008-04-07 | 한국화학연구원 | 1-(3,4-디알콕시벤질)-1h-피라졸 화합물, 이의 제조방법및 이를 포함하는 천식 및 만성폐쇄성 폐질환을 포함한염증관련 질환, 관절염, 아토피 피부염, 암 및 뇌질환의치료 및 예방을 위한 약제학적 조성물 |
US8969514B2 (en) | 2007-06-04 | 2015-03-03 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases |
EA020466B1 (ru) | 2007-06-04 | 2014-11-28 | Синерджи Фармасьютикалз Инк. | Агонисты гуанилатциклазы, пригодные для лечения желудочно-кишечных нарушений, воспаления, рака и других заболеваний |
CA2726917C (en) | 2008-06-04 | 2018-06-26 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
CA2730603C (en) | 2008-07-16 | 2019-09-24 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
ES2728225T3 (es) | 2009-02-20 | 2019-10-23 | 2 Bbb Medicines B V | Sistema de administración de fármacos a base de glutatión |
US8445002B2 (en) | 2009-05-06 | 2013-05-21 | Laboratory Skin Care, Inc. | Dermal delivery compositions comprising active agent-calcium phosphate particle complexes and methods of using the same |
NZ603268A (en) | 2010-05-04 | 2015-02-27 | Alkermes Pharma Ireland Ltd | Process for synthesizing oxidized lactam compounds |
US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
US20120077778A1 (en) | 2010-09-29 | 2012-03-29 | Andrea Bourdelais | Ladder-Frame Polyether Conjugates |
WO2012118972A2 (en) | 2011-03-01 | 2012-09-07 | Synegy Pharmaceuticals Inc. | Process of preparing guanylate cyclase c agonists |
WO2014131024A2 (en) | 2013-02-25 | 2014-08-28 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase and their uses |
EP2970384A1 (en) | 2013-03-15 | 2016-01-20 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase and their uses |
CA2905435A1 (en) | 2013-03-15 | 2014-09-25 | Synergy Pharmaceuticals Inc. | Compositions useful for the treatment of gastrointestinal disorders |
CN113388007A (zh) | 2013-06-05 | 2021-09-14 | 博士医疗爱尔兰有限公司 | 鸟苷酸环化酶c的超纯激动剂、制备和使用所述激动剂的方法 |
MX2016001714A (es) | 2013-08-09 | 2016-10-03 | Ardelyx Inc | Compuestos y metodos para inhibir el transporte de fosfato. |
US20200368223A1 (en) | 2019-05-21 | 2020-11-26 | Ardelyx, Inc. | Methods for inhibiting phosphate transport |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR82186E (fr) * | 1959-04-10 | 1964-01-04 | Kodak Pathe | Nouveau produit photographique et procédé pour le traitement de ce produit |
FR2529786A1 (fr) * | 1982-07-12 | 1984-01-13 | Nativelle Sa Ets | Compositions pharmaceutiques a base de derives de la pyrazolone-5, nouveaux produits et procede de preparation |
US5089622A (en) * | 1988-12-12 | 1992-02-18 | Mitsui Toatsu Chemicals Incorporated | (-)-2-pyrazoline compounds and therapeutic agent for cerebrovascular disorders containing the same as effective ingredient |
NZ238912A (en) * | 1990-07-17 | 1992-12-23 | Lilly Co Eli | Pyrazole derivatives and medicaments |
-
1991
- 1991-05-01 US US07/694,197 patent/US5191084A/en not_active Expired - Lifetime
-
1992
- 1992-04-21 IL IL10166392A patent/IL101663A/en not_active IP Right Cessation
- 1992-04-27 JP JP4107326A patent/JPH05117239A/ja active Pending
- 1992-04-27 CA CA002067298A patent/CA2067298A1/en not_active Abandoned
- 1992-04-27 TW TW081103280A patent/TW200467B/zh active
- 1992-04-29 FI FI921920A patent/FI921920A/fi unknown
- 1992-04-29 AU AU15244/92A patent/AU653806B2/en not_active Ceased
- 1992-04-29 KR KR1019920007212A patent/KR920021516A/ko not_active Application Discontinuation
- 1992-04-29 ZA ZA923126A patent/ZA923126B/xx unknown
- 1992-04-30 DK DK92303917.6T patent/DK0511865T3/da active
- 1992-04-30 SG SG1996004304A patent/SG49713A1/en unknown
- 1992-04-30 HU HU9201454A patent/HUT61001A/hu unknown
- 1992-04-30 DE DE69217112T patent/DE69217112T2/de not_active Expired - Fee Related
- 1992-04-30 PH PH44300A patent/PH30772A/en unknown
- 1992-04-30 AT AT92303917T patent/ATE148460T1/de not_active IP Right Cessation
- 1992-04-30 EP EP92303917A patent/EP0511865B1/en not_active Expired - Lifetime
- 1992-04-30 MX MX9202032A patent/MX9202032A/es unknown
- 1992-04-30 ES ES92303917T patent/ES2097872T3/es not_active Expired - Lifetime
-
1997
- 1997-04-22 GR GR970400905T patent/GR3023240T3/el unknown
- 1997-07-16 HK HK97101561A patent/HK1000104A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP0511865B1 (en) | 1997-01-29 |
DE69217112D1 (de) | 1997-03-13 |
PH30772A (en) | 1997-10-17 |
IL101663A0 (en) | 1992-12-30 |
AU653806B2 (en) | 1994-10-13 |
HU9201454D0 (en) | 1992-07-28 |
HUT61001A (en) | 1992-11-30 |
GR3023240T3 (en) | 1997-07-30 |
DK0511865T3 (ko) | 1997-02-17 |
SG49713A1 (en) | 1998-06-15 |
CA2067298A1 (en) | 1992-11-02 |
TW200467B (ko) | 1993-02-21 |
ZA923126B (en) | 1993-10-29 |
IL101663A (en) | 1995-12-31 |
MX9202032A (es) | 1992-11-01 |
HK1000104A1 (en) | 1997-11-28 |
FI921920A (fi) | 1992-11-02 |
US5191084A (en) | 1993-03-02 |
ATE148460T1 (de) | 1997-02-15 |
DE69217112T2 (de) | 1997-05-28 |
FI921920A0 (fi) | 1992-04-29 |
JPH05117239A (ja) | 1993-05-14 |
AU1524492A (en) | 1992-11-05 |
EP0511865A1 (en) | 1992-11-04 |
ES2097872T3 (es) | 1997-04-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR920021516A (ko) | 기관지 확장제 및 소염제로서의 페닐 피라졸리디논 | |
JP2004532209A5 (ko) | ||
PL318327A1 (en) | Heterocyclic antagonists of tachykinin receptors | |
BR9408343A (pt) | Derivados 5-(2-imidazolinil amino) benzimidazol sua preparação e seu uso como agonistas alfa-2 adrenoceptor | |
ATE230732T1 (de) | Imidazol-derivate mit biphenylsulfonylharnstoff- oder biphenylsulfonylurethan-seitenkette, verfahren zu ihrer herstellung und ihre verwendung | |
KR940007019A (ko) | 카르복스아닐리드, 그의 제조방법 및 그를 함유하는 유해 진균류를 방제하기 위한 조성물 | |
NO20021875L (no) | Fremgangsmåte for stabilisering av benzimidazolforbindelser | |
DK1031569T3 (da) | Salt af et 7-isoindolinquinoloncarboxylsyre-derivat, monohydrat deraf og sammensætning, der indeholder dette som aktiv bestanddel | |
JP2005507880A5 (ko) | ||
ATA20991A (de) | Neue imidazolderivate, verfahren zu ihrer herstellung und ihre verwendung | |
BR9914736A (pt) | Compostos de 3-(fenil substituìdo)-5-tienil-1,2,4-triazol com atividade contra mosca branca | |
FI940030A0 (fi) | Uusi menetelmä imidatsolin rikkijohdannaisten valmistamiseksi ja uusiavälituotteita | |
RU2002119405A (ru) | Ингибиторы фарнезилтрансферазы | |
FI95243B (fi) | Typpiheterosyklien substituoidut 2-propenyylijohdannaiset | |
EP1193548A3 (en) | Silver halide color photographic light-sensitive material, pyrrolotriazole compound, and dye-forming compound | |
ID25446A (id) | Bentuk stabil secara termodinamika dari asam (r)-3-((4-fluora)sulfonil) amino-1,2,3,4-tetrahidro-9h-karbazol-9-propanoat (ramatroban) | |
US4115649A (en) | Phenyl pyrazole morpholine amides | |
ATE218124T1 (de) | Ein 1/2-sulfat des ((s)-1-((s)-2-((trans-4- aminocyclohexylmethyl)carbamoyl)-pyrrolidine-1- carbonyl)-2-iso-propylthio-2-methylpropyl)- carbamidsäurepropylesters | |
BR9506763A (pt) | Derivados de carbamoil metil uréia | |
KR880013932A (ko) | 4-[(α, α-디아릴)-하이드록시메틸]-l-피페리디닐알킬-사이클릭카바메이트 유도체 | |
KR900014360A (ko) | 피리딘카복실산 아미드 유도체 및 이를 함유하는 약학 조성물 | |
KR850000456A (ko) | 세팔로스포린 에스테르의 제조방법 | |
KR840000509A (ko) | 1-페닐-1,2,3-트리아졸의 제조방법 | |
KR850003721A (ko) | 2-아릴-치환된 이미다졸린온의 제조방법 | |
KR940018386A (ko) | 티오펜 화합물 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |