4.7 Article

Synthesis of Sansalvamide A derivatives and their cytotoxicity in the MSS colon cancer cell line HT-29

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 14, Issue 16, Pages 5625-5631

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2006.04.031

Keywords

macrocycles; peptides; macrocyclic peptides; cytotoxicity; colon cancer; MSS; Sansalvamide A

Funding

  1. NIAID NIH HHS [AI058241-01] Funding Source: Medline
  2. NIGMS NIH HHS [5T34GM08303, 5R25GM58906] Funding Source: Medline

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We report the synthesis of thirty-six Sansalvamide A derivatives, and their biological activity against colon cancer HT-29 cell line, a microsatellite stable (MSS) colon cancer cell-line. The thirty-six compounds can be divided into three subsets, where the first subset of compounds contains L-amino acids, the second subset contains D-amino acids, and the third subset contains both D- and L-amino acids. Five compounds exhibited excellent inhibitory activity (> 75% inhibition). The structure-activity relationship (SAR) of the compounds established that a single D-amino acid in position 2 or 3 gave up to a 10-fold improved cytotoxicity over Sansalvamide A peptide. This work highlights the importance of residues 2 and 3 and the role Of D-amino acids in the extraordinary SAR for this compound class. (c) 2006 Elsevier Ltd. All rights reserved.

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