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Acta Pharmaceutica Sinica ; (12): 683-687, 2011.
Article in Chinese | WPRIM | ID: wpr-348900

ABSTRACT

In order to find antiviral compounds with novel structures, geldanamycin and lamivudine with different antiviral mechanisms were conjunctively synthesized to acquire a new compound TC-GM, and the antiviral activity of TC-GM was measured. The antiviral activity against HIV-1 was examined by p24 antigen ELISA kit. The activity against HBV was examined by dotblot. The activity against HSV and CoxB virus was examined by CPE. TC-GM exhibited broad-spectrum antiviral activities similarly like geldanamycin. TC-GM inhibited the replication of different viruses, including HIV-1, HBV, HSV 1 and 2, CoxB6. TC-GM showed more potent inhibitory activity against HIV-1 and HBV than other detected virus.


Subject(s)
Animals , Humans , Anti-HIV Agents , Chemistry , Pharmacology , Antiviral Agents , Chemistry , Pharmacology , Benzoquinones , Chemistry , Pharmacology , Cell Line, Tumor , Chlorocebus aethiops , Enterovirus B, Human , Physiology , HIV-1 , Physiology , Hep G2 Cells , Hepatitis B virus , Physiology , Herpesvirus 1, Human , Physiology , Herpesvirus 2, Human , Physiology , Lactams, Macrocyclic , Chemistry , Pharmacology , Lamivudine , Chemistry , Pharmacology , Madin Darby Canine Kidney Cells , Precursor Cell Lymphoblastic Leukemia-Lymphoma , Pathology , Virology , Vero Cells , Virus Replication
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