Cas No.: | 1072-93-1 |
Chemical Name: | Epigoitrin |
Synonyms: | Epigoitrin;D-Goitrin;(R)-5-Ethenyl-2-oxazolidinethione;Goitrine;5-vinyl-2-oxazolidinethione;5-VINYL-2-THIOOXAZOLIDONE;5-vinyloxazolidine-2-thione;Goitrine Epigoitrin;R-GOITRIN;BA-51-090278;Goitrine Epigoitrin;(-)5-VINYL-2-OXAZOLIDINETHIONE;(R)-5-Vinyl-2-oxazolidinethione;Table in the spring;(R,S)-goitrin;Epigoitrin/(R,S)-goitrin;(R)-Goitrin;C5H7NOS;R-5-Vinyl-2-oxazolidinethione;2-Oxazolidinethione, 5-vinyl-, (R)-;Goitrin;(r)-5-vinyloxazolidine-2-thione;(5R)-5-vinyloxazolidine-2-thione;2N815D740R;2-Oxazolidinethione, 5-ethenyl-, (5R)-;Epigotrin;(5R)-5-ethenyl-1,3-oxazolidine-2-thione;goitrin, (R)-isomer;2-Oxazolidinethione, 5-ethenyl-, (R)-;2-O;Ethyl-p-methoxycinnamate;2-Oxazolidinethione, 5-ethenyl-, (R)- (9CI);s9078;FCH844233 |
SMILES: | S=C1O[C@H](C=C)CN1 |
Formula: | C5H7NOs |
M.Wt: | 129.1802 |
Purity: | >98%, Standard References Grade |
Sotrage: | 4°C for 1 year, -20°C for more than 2 years |
Description: | Epigoitrin is a natural alkaloid from Isatis indigotica, with antiviral activities. Epigoitrin reduces susceptibility to influenza virus via mitochondrial antiviral signaling[1][2]. |
References: | [1]. Luo Z, et al. Epigoitrin, an Alkaloid From Isatis indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model in vivo and in vitro. Front Pharmacol. 2019 Feb 7;10:78. [2]. Xiao P, et al. Antiviral activities against influenza virus (FM1) of bioactive fractions and representative compounds extracted from Banlangen (Radix Isatidis). J Tradit Chin Med. 2016 Jun;36(3):369-76. |