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Life Science : Hoiamide D, a marine cyanobacteria-derived inhibitor of p53/MDM2 interaction
( Karla L Malloy ) , ( Hyuk Jae Choi ) , ( Catherine Fiorilla ) , ( Fred A Valeriote ) , ( Teatulohi Matainaho )
UCI I410-ECN-0102-2015-500-002238471
This article is 4 pages or less.
* This article is not available.

Bioassay-guided fractionation of two cyanobacterial extracts from Papua New Guinea has yieldedhoiamide D in both its carboxylic acid and conjugate base forms. Hoiamide D is a polyketide synthase (PKS)/non-ribosomal peptide synthetase (NRPS)-derived natural product that features two consecutive thiazolines and a thiazole, as well as a modified isoleucine residue. Hoiamide D displayed inhibitory activity against p53/MDM2 interaction (EC(50)=4.5 μM), an attractive target for anticancer drug development.

[자료제공 : 네이버학술정보]
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