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Yao Xue Xue Bao ; 37(3): 181-5, 2002 Mar.
Article in Chinese | MEDLINE | ID: mdl-12579757

ABSTRACT

AIM: To study the synthesis and anti alpha-adrenoceptor activity of 1,2-dihydro-quinoline-2-one compounds. METHODS: Acylation, bromination and cyclization, and substitute reactions were used in the synthesis of the title compounds IV. A proposed mechanism was showed to explain the unusual compounds 5 and 6 in the route C. The inhibition activity of the six target compounds were tested. RESULTS: Twelve new compounds were synthesized (II1-6 and IV1-6). Among them, six new compounds (IV1-6) are the title compounds. Structure of the title compounds were determined by IR, 1HNMR, MS and HRMS. CONCLUSION: Compounds IV3, IV4 and IV6 showed inhibitiion activity, and were worth further studying.


Subject(s)
Adrenergic alpha-Antagonists/chemical synthesis , Phenethylamines/chemical synthesis , Quinolones/chemical synthesis , Adrenergic alpha-Antagonists/pharmacology , Animals , Aorta/drug effects , In Vitro Techniques , Molecular Structure , Phenethylamines/pharmacology , Quinolones/pharmacology , Rabbits , Receptors, Adrenergic, alpha/drug effects , Receptors, Adrenergic, alpha/metabolism , Technology, Pharmaceutical
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