Cas No.: | 149488-17-5 |
Synonyms: | LY300046; LY-300046; LY 300046 |
SMILES: | C1=CC=NC(=C1)CCNC(=S)NC2=NC=C(C=C2)Br |
Formula: | C13H13BrN4S |
M.Wt: | 337.24 |
Purity: | >98% |
Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: | Trovirdine inhibits HIV-1 RT with an IC50 of 7 nM when employing heteropolymeric primer/template (oligo-DNA/ribosomal RNA)and dGTP as substrate.Trovirdine is currently in phase I clinical trials for potential use in thetreatment of AIDS. |
Target: | IC50 value: 7 nM Target: HIV-1 |
References: | [1]. Zhang, H. et al. Inhibition of human immunodeficiency virus type 1 wild-type and mutant reverse transcriptases by the phenyl ethylthiazolyl thiourea derivatives trovirdine and MSC-127. [2]. Cantrell, A.S. et al. Phenethylthiazolylthiourea (PETT) compounds as a newclass of HIV-1 reverse transcriptase inhibitors. 2. Synthesis and further structure-activity relationship studies of PETT analogs. |