Synthesis and structure-activity relationships for anticipated molluscicidal activity of some 2-amino-5-substituted pyridine derivatives
β Scribed by El-Zemity, Saad R; Radwan, Mohamed A
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 111 KB
- Volume
- 55
- Category
- Article
- ISSN
- 1526-498X
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β¦ Synopsis
A series of 2-amino-5-substituted pyridine derivatives was synthesized and their molluscicidal activity against white garden, Theba pisana (Mu Γ ller), and brown garden, Helix aspersa (Mu Γ ller), snails was investigated by two methods of application. Some of these compounds showed strong activity under laboratory conditions against the two types of snail. T pisana was more sensitive to the tested compounds than H aspersa. The most effective compounds were 2-amino-5-(benzotriazole-1-ylmethyl)-3-methylpyridine, 2-amino-5-[1-(benzotriazole-1-yl)nonyl]-3-methylpyridine and 2-[(1,2,4-triazole-1-ylmethyl)amino]-3-methylpyridine which exhibited high molluscicidal activity. The toxicity results are discussed in relation to the chemical structures.
π SIMILAR VOLUMES
Novel analogs of the P2 receptor antagonist pyridoxal-5β²-phosphate-6-phenylazo-2β²,4β²disulfonate (PPADS) were synthesized. Modifications were made through functional group substitution on the sulfophenyl ring and at the phosphate moiety through the inclusion of phosphonates, demonstrating that a phos