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DERIVATI DIHIDRO-OKSAZOLBENZODIAZEPINONA, POSTUPAK NJIHOVE PRIPRAVE TE FARMACEUTSKI PRIPRAVCI KOJI SADRŽE OVE SPOJEVE
专利权人:
LES LABORATOIRES SERVIER;EGIS GYOGYSZERGYAR NYRT
发明人:
LING, ISTVAN,BARKOCZY, JOZSEF,ANTONI, FERENC,GACSALYI, ISTVAN,LEVAY, GYOERGY,SPEDDING, MICHAEL,HARSING, LASZLO
申请号:
HRP20140050
公开号:
HRP20140050T1
申请日:
2014.01.16
申请国别(地区):
HR
年份:
2014
代理人:
摘要:
Dihydro-oxazolobenzodiazepinone derivatives (I) are new. Dihydro-oxazolobenzodiazepinone derivatives of formula (I) and their positional isomers, enantiomers, diastereoisomers or addition salts with acids, solvates, complexes or adducts, are new. R1 : H or 1-4C alkyl; R2 : 1-4C alkyl; and R3 : (hetero)aryl. An independent claim is included for the preparation of (I). [Image] ACTIVITY : Neuroleptic; Antidepressant; Neuroprotective; Nootropic; Antiparkinsonian; Anticonvulsant; Tranquilizer; Vulnerary; Cerebroprotective. MECHANISM OF ACTION : gamma -Aminobutyric acid (GABA) receptor agonist. The GABA receptor agonistic activity of (I) was tested in human embryonic kidney (HEK-293) cells. The result showed that 5-(6-fluoro-1-benzothien-2-yl)-8-methyl-1,9-dihydro-2H-[1,3]oxazolo[4,5-h][2,3]benzodiazepin-2-one exhibited an IC 5 0value of 100 nM.
来源网站:
中国工程科技知识中心
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http://www.ckcest.cn/home/

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