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Volumn 40, Issue 5, 2006, Pages 261-267
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Synthesis and biological activity of N-acylmethyl derivatives of 9H-2,3-dihydroimidazo- and 10H-2,3,4,10-tetrahydropyrimido[1,2-a]benzimidazoles and their reduction products
a
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Author keywords
[No Author keywords available]
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Indexed keywords
10 (4 METHOXYPHENACYL) 2,3,4,10 TETRAHYDROPYRIMIDO[1,2 A]BENZIMIDAZOLE HYDROBROMIDE;
10 ACETONYL 2,3,4,10 TETRAHYDROPYRIMIDO[1,2 A]BENZIMIDAZOLE;
10 ACETONYL 2,3,4,10 TETRAHYDROPYRIMIDO[1,2 A]BENZIMIDAZOLE HYDROBROMIDE;
10 PHENACYL 2,3,4,10 TETRAHYDROPYRIMIDO[1,2 A]BENZIMIDAZOLE;
10 PIVALOYLMETHYL 2,3,4,10 TETRAHYDROPYRIMIDO[1,2 A]BENZIMIDAZOLE HYDROBROMIDE;
9 (4 METHOXYPHENACYL) 2,3 DIHYDROIMIDAZO[1,2 A]BENZIMIDAZOLE HYDROBROMIDE;
9 ACETONYL 2,3 DIHYDROIMIDAZO[1,2 A]BENZIMIDAZOLE;
9 ACETONYL 2,3 DIHYDROIMIDAZO[1,2 A]BENZIMIDAZOLE HYDROBROMIDE;
9 PHENACYL 2,3 DIHYDROIMIDAZO[1,2 A]BENZIMIDAZOLE HYDROBROMIDE;
9 PIVALOYLMETHYL 2,3 DIHYDROIMIDAZO[1,2 A]BENZIMIDAZOLE;
9 PIVALOYLMETHYL 2,3 DIHYDROIMIDAZO[1,2 A]BENZIMIDAZOLE HYDROBROMIDE;
BENZIMIDAZOLE DERIVATIVE;
GLUCOSE;
SPASMOLYTIC AGENT;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
ANTIOXIDANT ACTIVITY;
ARTICLE;
BIOLOGICAL ACTIVITY;
BLOOD RHEOLOGY;
CONTROLLED STUDY;
DRUG SYNTHESIS;
GLUCOSE BLOOD LEVEL;
MOUSE;
NONHUMAN;
SPASMOLYSIS;
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EID: 33750910031
PISSN: 0091150X
EISSN: 15739031
Source Type: Journal
DOI: 10.1007/s11094-006-0105-8 Document Type: Article |
Times cited : (9)
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References (25)
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