UA6158A1 - ЛІВООБЕРТАЮЧИЙ ЕНАНТІОМЕР (S)-alРha-ЕТІЛ-2-ОКСО-1-ПІРРОЛІДІНАЦЕТАМІД,ЩО ВИЯВЛЯЄ АНТИГІПОКСИЧНУ І АНТИІШЕМІЧНУ АКТИВНІСТЬ - Google Patents
ЛІВООБЕРТАЮЧИЙ ЕНАНТІОМЕР (S)-alРha-ЕТІЛ-2-ОКСО-1-ПІРРОЛІДІНАЦЕТАМІД,ЩО ВИЯВЛЯЄ АНТИГІПОКСИЧНУ І АНТИІШЕМІЧНУ АКТИВНІСТЬInfo
- Publication number
- UA6158A1 UA6158A1 UA3968802A UA3968802A UA6158A1 UA 6158 A1 UA6158 A1 UA 6158A1 UA 3968802 A UA3968802 A UA 3968802A UA 3968802 A UA3968802 A UA 3968802A UA 6158 A1 UA6158 A1 UA 6158A1
- Authority
- UA
- Ukraine
- Prior art keywords
- oxo
- ethyl
- pad
- active
- antihypoxic
- Prior art date
Links
- 230000000141 anti-hypoxic effect Effects 0.000 title abstract 2
- 230000002253 anti-ischaemic effect Effects 0.000 title abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- IODGAONBTQRGGG-UHFFFAOYSA-N 2-(2-oxopyrrolidin-1-yl)butanoic acid Chemical compound CCC(C(O)=O)N1CCCC1=O IODGAONBTQRGGG-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- RQEUFEKYXDPUSK-SSDOTTSWSA-N (1R)-1-phenylethanamine Chemical compound C[C@@H](N)C1=CC=CC=C1 RQEUFEKYXDPUSK-SSDOTTSWSA-N 0.000 abstract 1
- ZLKXLRFDTRFXJV-CYVRTLFJSA-N (2s)-2-(2-oxopyrrolidin-1-yl)butanoic acid;(1r)-1-phenylethanamine Chemical compound C[C@@H](N)C1=CC=CC=C1.CC[C@@H](C(O)=O)N1CCCC1=O ZLKXLRFDTRFXJV-CYVRTLFJSA-N 0.000 abstract 1
- 239000008346 aqueous phase Substances 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000004090 dissolution Methods 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- 230000008020 evaporation Effects 0.000 abstract 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 239000000706 filtrate Substances 0.000 abstract 1
- HPHUVLMMVZITSG-LURJTMIESA-N levetiracetam Chemical compound CC[C@@H](C(N)=O)N1CCCC1=O HPHUVLMMVZITSG-LURJTMIESA-N 0.000 abstract 1
- 239000002244 precipitate Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 238000010992 reflux Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 150000001420 substituted heterocyclic compounds Chemical class 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 230000001988 toxicity Effects 0.000 abstract 1
- 231100000419 toxicity Toxicity 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/273—2-Pyrrolidones 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 other ring carbon atoms
- C07D207/277—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- 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
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Detergent Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Seasonings (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB848412357A GB8412357D0 (en) | 1984-05-15 | 1984-05-15 | Pharmaceutical composition |
Publications (1)
Publication Number | Publication Date |
---|---|
UA6158A1 true UA6158A1 (uk) | 1994-12-29 |
Family
ID=10560974
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA3968802A UA6158A1 (uk) | 1984-05-15 | 1985-05-14 | ЛІВООБЕРТАЮЧИЙ ЕНАНТІОМЕР (S)-alРha-ЕТІЛ-2-ОКСО-1-ПІРРОЛІДІНАЦЕТАМІД,ЩО ВИЯВЛЯЄ АНТИГІПОКСИЧНУ І АНТИІШЕМІЧНУ АКТИВНІСТЬ |
Country Status (33)
Country | Link |
---|---|
US (3) | US4696943A (uk) |
EP (1) | EP0162036B1 (uk) |
JP (1) | JPH0629186B2 (uk) |
KR (1) | KR920003819B1 (uk) |
CN (1) | CN1015541B (uk) |
AT (1) | ATE45567T1 (uk) |
AU (1) | AU574465B2 (uk) |
BG (2) | BG50156A3 (uk) |
CA (1) | CA1235129A (uk) |
CY (2) | CY1567A (uk) |
DE (3) | DE10199005I2 (uk) |
DK (1) | DK163501C (uk) |
ES (2) | ES8608485A1 (uk) |
FI (1) | FI80673C (uk) |
GB (1) | GB8412357D0 (uk) |
GE (1) | GEP20002001B (uk) |
GR (1) | GR851155B (uk) |
HK (1) | HK52391A (uk) |
IE (1) | IE59950B1 (uk) |
IL (1) | IL75179A (uk) |
LT (1) | LT2584B (uk) |
LU (2) | LU90615I2 (uk) |
LV (1) | LV5233A3 (uk) |
MY (2) | MY101725A (uk) |
NL (1) | NL300028I2 (uk) |
NO (2) | NO164534C (uk) |
PL (2) | PL147386B1 (uk) |
PT (1) | PT80460B (uk) |
SA (1) | SA01210656A (uk) |
SG (1) | SG80090G (uk) |
SU (3) | SU1402260A3 (uk) |
UA (1) | UA6158A1 (uk) |
ZA (1) | ZA853635B (uk) |
Families Citing this family (95)
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GB8827389D0 (en) * | 1988-11-23 | 1988-12-29 | Ucb Sa | Process for preparation of(s)alpha-ethyl-2-oxo-1-pyrrolidineacetamide |
IT1231477B (it) * | 1989-07-12 | 1991-12-07 | Sigma Tau Ind Farmaceuti | (pirrolidin-2-one-1-il) acetammidi quali attivatori dei processi di apprendimento e della memoria e composizioni farmaceutiche comprendenti tali composti |
GB9319732D0 (en) | 1993-09-24 | 1993-11-10 | Ucb Sa | Use of (s)-alpha-ethyl-2-oxo-l-pyrrolidineacetamide for the treatment of anxiety |
US6124473A (en) * | 1998-05-08 | 2000-09-26 | Ucb, S.A. | Process for preparing (s)- and (R)-α-ethyl-2-oxo-1-pyrrolidineacetamide |
US6107492A (en) * | 1998-05-08 | 2000-08-22 | Ucb, S.A. | Process for the preparation of levetiracetam |
EA002379B1 (ru) * | 1999-07-21 | 2002-04-25 | Российский Государственный Педагогический Университет Им. А.И.Герцена | Средство, обладающее антиишемической, гипотензивной и антигипоксической активностью |
EA002380B1 (ru) * | 1999-07-21 | 2002-04-25 | Российский Государственный Педагогический Университет Им. А.И.Герцена | Антиишемическое средство |
AR026610A1 (es) * | 1999-12-01 | 2003-02-19 | Ucb Sa | Un derivado pirrolidinacetamida solo o en combinacion para tratamiento de desordenes del sistema nervioso central |
GB0004297D0 (en) | 2000-02-23 | 2000-04-12 | Ucb Sa | 2-oxo-1 pyrrolidine derivatives process for preparing them and their uses |
US6686477B2 (en) * | 2000-09-29 | 2004-02-03 | Eastman Chemical Company | Highly enantiomerically pure lactam-substituted propanoic acid derivatives and methods of making and using same |
AU2002224847A1 (en) * | 2000-11-21 | 2002-06-03 | U C B, S.A. | N-alkylated gaba compounds, processes for their preparation and their use as medicaments |
WO2002053153A1 (fr) | 2000-12-28 | 2002-07-11 | Daiichi Pharmaceutical Co., Ltd. | Medicaments permettant de traiter et de prevenir une douleur neurologique |
US20040116505A1 (en) * | 2001-02-23 | 2004-06-17 | Gregory Krauss | Treatment of tics, tremors and related disorders |
AU2002329233B2 (en) * | 2001-08-10 | 2007-08-16 | Ucb Pharma | Oxopyrrolidine compounds, preparation of said compounds and their use in the manufacturing of levetiracetam and analogues |
MXPA04002714A (es) * | 2001-10-08 | 2004-07-05 | Ucb Sa | Uso de derivados de 2-oxo-1-pirrolidina para el tratamiento de trastornos del movimiento y de la discinesia. |
AU2003242538A1 (en) * | 2002-05-14 | 2003-11-11 | Ucb, S.A. | Use of 2-oxo-1-pyrrolidone derivatives for the preparation of a drug |
CN1802352A (zh) * | 2003-02-03 | 2006-07-12 | 特瓦制药工业有限公司 | 制备左乙拉西坦的方法 |
ES2214147B1 (es) | 2003-02-28 | 2005-10-01 | Farma-Lepori S.A. | Procedimiento de obtencion de un agente antiepileptico. |
AU2003217438A1 (en) * | 2003-03-18 | 2004-10-11 | Hetero Drugs Limited | Novel crystalline forms of levetiracetam |
EP1663968A1 (en) * | 2003-09-05 | 2006-06-07 | Ranbaxy Laboratories Limited | Process for the preparation of pure levetiracetam |
ES2390455T3 (es) * | 2003-09-24 | 2012-11-13 | Ucb Pharma, S.A. | Procedimiento para la preparación de derivados de 2-oxo-1-pirrolidina |
AU2004295083B2 (en) | 2003-12-02 | 2010-08-19 | Ucb Pharma | Imidazole derivatives, processes for preparing them and their uses |
US7531673B2 (en) | 2004-02-18 | 2009-05-12 | Dr. Reddy's Laboratories Limited | Preparation of amino acid amides |
CA2488325C (en) * | 2004-11-22 | 2010-08-24 | Apotex Pharmachem Inc. | Improved process for the preparation of (s)-alpha-ethyl-2-oxo-1-pyrrolidineacetamide and (r)-alpha-ethyl-2-oxo-1-pyrrolidineacetamide |
EP1843761B1 (en) * | 2005-01-27 | 2018-01-31 | Alembic Limited | Extended release formulation of levetiracetam |
US20070298098A1 (en) * | 2005-02-16 | 2007-12-27 | Elan Pharma International Limited | Controlled Release Compositions Comprising Levetiracetam |
WO2006088864A1 (en) * | 2005-02-16 | 2006-08-24 | Elan Pharma International Limited | Controlled release compositions comprising levetiracetam |
WO2006090265A2 (en) * | 2005-02-28 | 2006-08-31 | Ranbaxy Laboratories Limited | Processes for the preparation of levetiracetam, its intermediate and the use of levetiracetam in pharmaceutical compositions |
EP1863761A1 (en) * | 2005-03-10 | 2007-12-12 | Rubamin Limited | Process for preparing levetiracetam |
AU2006228947A1 (en) * | 2005-03-30 | 2006-10-05 | Mylan Pharmaceuticals Ulc | Combined-step process for pharmaceutical compositions |
EP1879861A2 (en) * | 2005-04-01 | 2008-01-23 | Rubamin Laboratories Limited | Process for preparing levetiracetam and racemization of (r)- and (s)-2-amino butynamide and the corresponding acid derivatives |
WO2006128692A2 (en) | 2005-06-01 | 2006-12-07 | Ucb Pharma, S.A. | 2-oxo-1-pyrrolidine derivatives and their therapeutic use on the central nervous system |
TW200738280A (en) * | 2005-07-26 | 2007-10-16 | Ucb Sa | Novel pharmaceutical compositions comprising levetiracetam and process for their preparation |
US8338621B2 (en) | 2005-12-21 | 2012-12-25 | Ucb S.A. | Process for the preparation of 2-oxo-1-pyrrolidine derivatives |
PT1810676E (pt) * | 2006-01-24 | 2009-01-02 | Teva Pharma | Formulações de levetiracetam e métodos para a sua preparação |
US20080014264A1 (en) * | 2006-07-13 | 2008-01-17 | Ucb, S.A. | Novel pharmaceutical compositions comprising levetiracetam |
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CN101130504B (zh) * | 2006-08-25 | 2010-07-28 | 苏州雅本化学股份有限公司 | 经合成、拆分与消旋化制备手性药物左乙拉西坦中间体(s)-(+)-2-氨基丁酰胺盐酸盐的方法 |
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CN101333180B (zh) * | 2007-06-29 | 2011-05-18 | 浙江华海药业股份有限公司 | 一种制备左乙拉西坦中间体的方法 |
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US20090263481A1 (en) * | 2008-04-17 | 2009-10-22 | Atul Vishvanath Patil | Levetiracetam formulations |
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EA033130B1 (ru) * | 2008-10-16 | 2019-08-30 | Дзе Джонс Хопкинс Юниверсити | Способы и композиции для улучшения когнитивной функции |
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JP5969003B2 (ja) | 2011-04-18 | 2016-08-10 | ユセベ ファルマ ソシエテ アノニム | 2−オキソ−1−イミダゾリジニルイミダゾチアジアゾール誘導体 |
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CN102633675A (zh) * | 2012-04-10 | 2012-08-15 | 南京大学 | 一种dl-2-氨基丁酰胺制备方法 |
CN102675181B (zh) * | 2012-06-07 | 2013-11-20 | 北京师宏药物研制中心 | 一种左乙拉西坦的制备方法 |
CN102702063B (zh) * | 2012-06-15 | 2013-09-04 | 孙威 | 一种左乙拉西坦制备方法 |
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EP2919788A4 (en) | 2012-11-14 | 2016-05-25 | Univ Johns Hopkins | METHODS AND COMPOSITIONS FOR THE TREATMENT OF SCHIZOPHRENIA |
CN103012190B (zh) * | 2012-12-05 | 2015-03-18 | 江苏拜克新材料有限公司 | 一种s-2-氨基丁酰胺盐酸盐的合成方法 |
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US10806717B2 (en) | 2013-03-15 | 2020-10-20 | The Johns Hopkins University | Methods and compositions for improving cognitive function |
ES2881081T3 (es) | 2013-03-15 | 2021-11-26 | Agenebio Inc | Procedimientos y composiciones para mejorar la función cognitiva |
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JP6629740B2 (ja) | 2014-01-21 | 2020-01-15 | ヤンセン ファーマシューティカ エヌ.ベー. | 代謝型グルタミン酸作動性受容体サブタイプ2の正のアロステリック調節因子またはオルトステリックアゴニストを含む組み合わせ、およびそれらの使用 |
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CN104860863B (zh) * | 2015-04-10 | 2017-06-20 | 惠州信立泰药业有限公司 | 左乙拉西坦和含其的药物组合物 |
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CN106432032B (zh) * | 2016-09-14 | 2019-07-12 | 苏州天马药业有限公司 | 一种左乙拉西坦的制备方法 |
CN106591179B (zh) * | 2016-12-05 | 2018-07-03 | 长兴制药股份有限公司 | 甲基包囊菌及其在选择性拆分制备(S)-α-乙基-2-氧-1-吡咯烷乙酸盐上的应用 |
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BR112023017222A2 (pt) | 2021-02-26 | 2023-11-21 | Syndesi Therapeutics Sa | Composto que é um triazol de 2-oxo-1-pirrolidinila substituído de fórmula (i), e, composição farmacêutica compreendendo um composto que é um triazol de 2-oxo-1-pirrolidinila substituído de fórmula (i) |
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Publication number | Priority date | Publication date | Assignee | Title |
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GB1309692A (en) * | 1970-02-13 | 1973-03-14 | Ucb Sa | N-substituted lactams |
GB1583871A (en) * | 1976-10-19 | 1981-02-04 | Ucb Sa | Anti-aggregants |
FR2418790A1 (fr) * | 1978-03-02 | 1979-09-28 | Philagro Sa | Nouveaux derives de pyrrolidinone-2 et compositions herbicides les contenant |
GB8412358D0 (en) * | 1984-05-15 | 1984-06-20 | Ucb Sa | Pharmaceutical composition |
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1984
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1985
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1986
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