The compound named Histidine-pyridine-histidine (HPH) is an oxygen-activating ligand derived from the structure of bleomycin. We synthesized HPH derivatives, namely HPH-1 to -8, and investigated their antiviral activities against herpes simplex virus type 1. HPH-8 showed potent antiviral activity with an EC50 of 15 microM, and relatively high cytotoxicity with a CC50 of 37 microM. In contrast, HPH-4 indicated a weaker antiviral activity with an EC50 of 79 microM, but exhibited a far more less cytotoxicity (CC50 500 microM). Other HPH derivatives showed no effects against antiviral activities and cytotoxicities.
Antiviral activities against herpes simplex virus type 1 by HPH derivatives and their structure-activity relationships. Publishing Authors By Initials
Antiviral activities against herpes simplex virus type 1 by HPH derivatives and their structure-activity relationships. Journal Published:
PUBLICATION TYPE: Journal Article
Journal: Bioorganic & medicinal chemistry letters
VOLUME: 18
Page Numbers: 371-4
Journal Abbreviation: Bioorg. Med. Chem. Lett.
ISSN: 1464-3405
DAY: 24
MONTH: 10
YEAR: 2007
Antiviral activities against herpes simplex virus type 1 by HPH derivatives and their structure-activity relationships. Information
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LANGUAGE: eng
NlmUniqueID: 9107377
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Grant and Affiliation Information for Antiviral activities against herpes simplex virus type 1 by HPH derivatives and their structure-activity relationships.
AFFILIATION: Laboratory of Medicinal Microbiology, Yokohama College of Pharmacy, Kanagawa 245-0066, Japan. t.hosono@hamayaku.ac.jp
Country: England
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MEDLINETA: Bioorg Med Chem Lett
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