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Antiradiation Compounds XV: Condensations of Carbon Disulfide with Amino, Chloro, Cyanomethyl, and Sulfonamido Heterocycles

Journal Article · · J. Pharm. Sci., v. 64, no. 8, pp. 1371-1374
Condensations of carbon disulfide were carried out with amino, chloro, and diamino heterocycles to give condensed ring thiazoline-2-thiones and imidazoline-2-thiones, with cyanomethyl heterocycles to give dithio acid derivatives, and with heterocyclic sulfonamides to give sulfonyldithiocarbamates. Of several examples tested, pyrido[3,2-d]thiazoline-2-thione, disodium 2-(5-chloro-2-thienyl)-3,3-dimercaptoacrylonitrile, triethylammonium 4-sulfamoylphenyldithiocarbamate, ammonium β-phenethyldithiocarbamate, and methyl N-(thiophene-2-sulfonyl)dithiocarbamate, only the last-named compound showed any radiation protection for mice. Several compounds gave negative tests for antimalarial activity.
Research Organization:
Massachusetts Coll. of Pharmacy, Boston
NSA Number:
NSA-33-029709
OSTI ID:
4044341
Journal Information:
J. Pharm. Sci., v. 64, no. 8, pp. 1371-1374, Journal Name: J. Pharm. Sci., v. 64, no. 8, pp. 1371-1374; ISSN JPMSA
Country of Publication:
United States
Language:
English

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