Literature DB >> 22104152

Hoiamide D, a marine cyanobacteria-derived inhibitor of p53/MDM2 interaction.

Karla L Malloy1, Hyukjae Choi, Catherine Fiorilla, Fred A Valeriote, Teatulohi Matainaho, William H Gerwick.   

Abstract

Bioassay-guided fractionation of two cyanobacterial extracts from Papua New Guinea has yielded hoiamide 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.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22104152      PMCID: PMC3248991          DOI: 10.1016/j.bmcl.2011.10.054

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  15 in total

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7.  Phormidepistatin from the Cyanobacterium UIC 10484: Assessing the Phylogenetic Distribution of the Statine Pharmacophore.

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Review 8.  Marine low molecular weight natural products as potential cancer preventive compounds.

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10.  Stereoselective access to tubuphenylalanine and tubuvaline: improved Mn-mediated radical additions and assembly of a tubulysin tetrapeptide analog.

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