| Literature DB >> 1646687 |
K Hirabayashi1, S Iwata, H Matsumoto, T Mori, S Shibata, M Baba, M Ito, S Shigeta, H Nakashima, N Yamamoto.
Abstract
Chemically modified compounds of glycyrrhizin have been synthesized and evaluated for their inhibitory effect on the replication of human immunodeficiency virus type 1 (HIV-1) and herpes simplex virus type 1 (HSV-1). Among them, the 11-deoxo compound having a heteroannular diene structure at the C and D rings proved as active against HIV-1 as glycyrrhizin in MT-4 and MOLT-4 cells. It completely inhibited HIV-1-induced cytopathogenicity in both cell lines at a concentration of 0.16 mM. The compound was also effective against HSV-1 with a 50% inhibitory concentration of 0.5 mM [corrected].Entities:
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Year: 1991 PMID: 1646687 DOI: 10.1248/cpb.39.112
Source DB: PubMed Journal: Chem Pharm Bull (Tokyo) ISSN: 0009-2363 Impact factor: 1.645