Salternamides A-D from a Halophilic Streptomyces sp. Actinobacterium

J Nat Prod. 2015 Apr 24;78(4):836-43. doi: 10.1021/acs.jnatprod.5b00002. Epub 2015 Feb 20.

Abstract

Salternamides A-D (1-4), the first secondary metabolites discovered from saltern-derived actinomycetes, were isolated from a halophilic Streptomyces strain isolated from a saltern on Shinui Island in the Republic of Korea. The planar structures of the salternamides, which are new members of the manumycin family, were elucidated by a combination of spectroscopic analyses. The absolute configurations of the salternamides were determined by chemical and spectroscopic methods, including the modified Mosher's method, J-based configuration analysis, and circular dichroism spectroscopy. Salternamide A (1), which is the first chlorinated compound in the manumycin family, exhibited potent cytotoxicity against a human colon cancer cell line (HCT116) and a gastric cancer cell line (SNU638) with submicromolar IC50 values. Salternamides A and D were also determined to be weak Na(+)/K(+) ATPase inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actinobacteria
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / isolation & purification*
  • Antineoplastic Agents / pharmacology*
  • Circular Dichroism
  • Colonic Neoplasms
  • Drug Screening Assays, Antitumor
  • Humans
  • Inhibitory Concentration 50
  • Molecular Structure
  • Polyenes / chemistry
  • Polyenes / isolation & purification*
  • Polyenes / pharmacology*
  • Polyunsaturated Alkamides / chemistry
  • Polyunsaturated Alkamides / isolation & purification*
  • Polyunsaturated Alkamides / pharmacology*
  • Republic of Korea
  • Salt-Tolerant Plants / chemistry*
  • Sodium-Potassium-Exchanging ATPase / antagonists & inhibitors*
  • Streptomyces / chemistry*

Substances

  • Antineoplastic Agents
  • Polyenes
  • Polyunsaturated Alkamides
  • salternamide A
  • Sodium-Potassium-Exchanging ATPase
  • manumycin