
As a model of metabolic transformations of antiviral drug “Triazaverin” and its analogues‑2-alkylthio‑6-nitro‑1,2,4-triazolo[5,1-c][1,2,4]triazine‑7-ones 1a-d examined the oxidation of alkylthio groups to the corresponding sulfoxides 2a-d and sulfones 3a-d, as well as the process of nucleophilic substitution sulfonyloxy group of cysteine and cysteamine with the formation of compounds 5 and 6.
биологически активные соединения, ANTIVIRAL DRUG, гетероциклы, TRIAZINE, БИОЛОГИЧЕСКИ АКТИВНЫЕ СОЕДИНЕНИЯ, антивирусные препараты, BIOLOGICAL ACTIVE COMPOUNDS, ТРИАЗИ, TRIAZAVERIN, biological active compounds; heterocycles; triazine; Triazaverin; antiviral drug, Chemistry, ГЕТЕРОЦИКЛЫ, триазаверин, ТРИАЗАВЕРИН, QD1-999, HETEROCYCLES, биологически активные соединения; гетероциклы; триазаверин; антивирусные препараты, АНТИВИРУСНЫЕ ПРЕПАРАТЫ
биологически активные соединения, ANTIVIRAL DRUG, гетероциклы, TRIAZINE, БИОЛОГИЧЕСКИ АКТИВНЫЕ СОЕДИНЕНИЯ, антивирусные препараты, BIOLOGICAL ACTIVE COMPOUNDS, ТРИАЗИ, TRIAZAVERIN, biological active compounds; heterocycles; triazine; Triazaverin; antiviral drug, Chemistry, ГЕТЕРОЦИКЛЫ, триазаверин, ТРИАЗАВЕРИН, QD1-999, HETEROCYCLES, биологически активные соединения; гетероциклы; триазаверин; антивирусные препараты, АНТИВИРУСНЫЕ ПРЕПАРАТЫ
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