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  • Antimicrobial and hypoglycemic activities of novel N-Mannich bases derived from 5-(1-adamantyl)-4-substituted-1,2,4-triazoline-3-thiones.

Antimicrobial and hypoglycemic activities of novel N-Mannich bases derived from 5-(1-adamantyl)-4-substituted-1,2,4-triazoline-3-thiones.

International journal of molecular sciences (2014-12-17)
Ebtehal S Al-Abdullah, Hanaa M Al-Tuwaijri, Hanan M Hassan, Mogedda E Haiba, Elsayed E Habib, Ali A El-Emam
ABSTRACT

The reaction of 5-(1-adamantyl)-4-ethyl or allyl-1,2,4-triazoline-3-thione with formaldehyde solution and various 1-substituted piperazines yielded the corresponding N-Mannich bases. The newly synthesized N-Mannich bases were tested for in vitro inhibitory activities against a panel of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Six compounds showed potent antibacterial activity against one or more of the tested microorganisms, while two compounds exhibited moderate activity against the tested Gram-positive bacteria. None of the newly synthesized compounds were proved to possess marked activity against Candida albicans. The oral hypoglycemic activity of six compounds was determined in streptozotocin (STZ)-induced diabetic rats. Four compounds produced significant strong dose-dependent reduction of serum glucose levels, compared to gliclazide at 10 mg/kg dose level (potency ratio > 75%).

MATERIALS
Product Number
Brand
Product Description

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Ampicillin trihydrate, VETRANAL®, analytical standard
USP
Ampicillin trihydrate, United States Pharmacopeia (USP) Reference Standard
Ampicillin trihydrate, European Pharmacopoeia (EP) Reference Standard
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Supelco
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USP
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Clotrimazole, European Pharmacopoeia (EP) Reference Standard
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