| Literature DB >> 31170642 |
Christophe Guillon1, Yi-Hua Jan2, Diane E Heck3, Thomas M Mariano2, Robert D Rapp4, Michele Jetter4, Keith Kardos4, Marilyn Whittemore5, Eric Akyea4, Ivan Jabin6, Jeffrey D Laskin2, Ned D Heindel4.
Abstract
Seventy-one 7-oxycoumarins, 66 synthesized and 5 commercially sourced, were tested for their ability to inhibit growth in murine PAM212 keratinocytes. Forty-nine compounds from the library demonstrated light-induced lethality. None was toxic in the absence of UVA light. Structure-activity correlations indicate that the ability of the compounds to inhibit cell growth was dependent not only on their physiochemical characteristics, but also on their ability to absorb UVA light. Relative lipophilicity was an important factor as was electron density in the pyrone ring. Coumarins with electron withdrawing moieties - cyano and fluoro at C3 - were considerably less active while those with bromines or iodine at that location displayed enhanced activity. Coumarins that were found to inhibit keratinocyte growth were also tested for photo-induced DNA plasmid nicking. A concentration-dependent alteration in migration on neutral gels caused by nicking was observed.Entities:
Keywords: 7-hydroxycoumarins; 7-oxycoumarins; 8-MOP; DNA photo-damage; Furocoumarins; Methoxsalen; PAM212 keratinocytes; Phototoxicity; Psoralens
Year: 2019 PMID: 31170642 PMCID: PMC6656587 DOI: 10.1016/j.bioorg.2019.103014
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275