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Synthesis and Hiv-1 activity of some novel 2,2 - diphenylamine derivatives
Bulletin of Faculty of Pharmacy-Cairo University. 1998; 36 (3): 99-105
in En | IMEMR | ID: emr-47805
Responsible library: EMRO
ABSTRACT
A number of new 2,2'-diphenylamine derivatives have been synthesized through reacting the dihydrazide 3 with acid anhydrides, carbonyl compounds, isothiocyanates, and CS2/KOH/hydrazine hydrate to give 4, 5, 7, and 10, respectively. Furthermore, cyclization of 5 and 7 have been achieved. 4b, 5g, 7a, and 9 have been shown to possess moderate anti-HIV activities. Compound 5a was pleaded active in the in vitro anticancer screening program. The intermediate 3 had been shown to fulfill the requirements of good synthones to design and synthesize new molecules
Subject(s)
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Index: IMEMR Main subject: HIV-1 / Diphenylamine Language: En Journal: Bull. Fac. Pharm.-Cairo Univ. Year: 1998
Search on Google
Index: IMEMR Main subject: HIV-1 / Diphenylamine Language: En Journal: Bull. Fac. Pharm.-Cairo Univ. Year: 1998