4.7 Article

Halogenated Fatty Acid Amides and Cyclic Depsipeptides from an Eastern Caribbean Collection of the Cyanobacterium Lyngbya majuscula

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 72, Issue 9, Pages 1573-1578

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/np900173d

Keywords

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Funding

  1. NIH [P20 RR-16467]
  2. HPU Trustees' Scholarly Endeavors Fund
  3. CRIF program of the National Science Foundation [CH E9974921]
  4. Elsa U. Pardee Foundation
  5. Department of Defense [W911NF-04-1-0344]

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A lipophilic extract of an eastern Caribbean collection of Lyngbya majuscula yielded two new halogenated fatty acid amides, grenadamides B (1) and C (2), and two new depsipeptides, itralamides A (3) and B (4), along with the known compounds hectochlorin and deacetylhectochlorin. The recently reported depsipeptide carriebowmide (5) was also present in the extract and isolated as its sulfone artifact (6). Compounds 1-4 were identified by spectroscopic methods. The configurations of the amino acid residues of 3, 4, and 6 were determined by LC-MS analyses of diastereomeric derivatives of the acid hydrolysates (advanced Marfey's method). Based on the configurational analysis of 6, in direct comparison with authentic carriebowmide (5), a minor structural revision of 5 is proposed. Compounds I and 2 displayed marginal activity against the beet armyworm (Spodoptera exigua). Compounds 1-4 and 6 were assessed for general cell toxicity in human embryonic kidney (HEK293) cells. Only itralamide B (4) displayed significant cytotoxicity, showing an IC50 value of 6 +/- 1 mu M.

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