Journal of Medicinal Chemistry p. 1144 - 1148 (1980)
Update date:2022-08-02
Topics:
Bialer, Meir
Yagen, Boris
Mechoulam, Raphael
Becker, Yechiel
Representatives of three types of congocidine (1) analogues were synthesized.These were tested for cytotoxicity, inhibition of herpes simplex virus (HSV) replication in cultured cells, and effects on the synthesis of HSV DNA in isolation nuclei in vitro, as well as on DNA synthesis by purified HSV-DNA polymerase.All synthesized tripyrrole derivatives of congocidine were less cytotoxic and more active than the parent drug in all the three antiviral tests.
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