Mazzone, G. published the artcileReactivity of 3-aryl-4-amino-5-mercapto-4H-1,2,4-triazoles: synthesis and biological evaluation of 3,6-diaryl derivatives of 7H-1,2,4-triazolo[3,4-b][1,3,4]thiadiazine, 3-aryl-4-amino-5-carboxymethylthio-4H-1,2,4-triazoles and some 3-aryl-4H-1,2,4-triazoles, Recommanded Product: 4H-1,2,4-Triazole, the publication is Farmaco, Edizione Scientifica (1987), 42(7), 525-39, database is CAplus and MEDLINE.
Thirty-eight compounds belonging to the various title groups were synthesized and were tested for antimicrobial activity in vitro and for various pharmacol. properties in vivo. The carboxymethylthiotriazoles had weak anti-inflammatory activity and a more consistent superoxide-scavenging effect. The triazolothiadiazine and triazole derivatives had moderate antifungal properties. Some structure-activity relations are discussed.
Farmaco, Edizione Scientifica published new progress about 63598-71-0. 63598-71-0 belongs to triazoles, auxiliary class Triazole, name is 4H-1,2,4-Triazole, and the molecular formula is C2H3N3, Recommanded Product: 4H-1,2,4-Triazole.
Referemce:
https://en.wikipedia.org/wiki/1,2,3-Triazole,
Triazoles – an overview | ScienceDirect Topics