4.7 Article

Nine New and Five Known Polyketides Derived from a Deep Sea-Sourced Aspergillus sp 16-02-1

Journal

MARINE DRUGS
Volume 12, Issue 6, Pages 3116-3137

Publisher

MDPI
DOI: 10.3390/md12063116

Keywords

Aspergillus sp 16-02-1; fungal strain from deep sea sediment; aspiketolactonol; aspilactonol; aspyronol; lactone; epiaspinonediol; polyketide; structure; cytotoxicity

Funding

  1. NHTRDP [2013AA092901, 2007AA09Z411]
  2. NSFC [81172976]
  3. NSTMP [2012ZX09301-003, 2009ZX09103-019, 2009ZX09301-002]
  4. CAS [KSCX2-EW-G-6]
  5. COMRA, China [DYXM-115-02-2-09]

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Nine new C-9 polyketides, named aspiketolactonol (1), aspilactonols A-F (2-7), aspyronol (9) and epiaspinonediol (11), were isolated together with five known polyketides, (S)-2-(2'-hydroxyethyl)-4-methyl-gamma-butyrolactone (8), dihydroaspyrone (10), aspinotriol A (12), aspinotriol B (13) and chaetoquadrin F (14), from the secondary metabolites of an Aspergillus sp. 16-02-1 that was isolated from a deep-sea sediment sample. Structures of the new compounds, including their absolute configurations, were determined by spectroscopic methods, especially the 2D NMR, circular dichroism (CD), Mo-2-induced CD and Mosher's H-1 NMR analyses. Compound 8 was isolated from natural sources for the first time, and the possible biosynthetic pathways for 1-14 were also proposed and discussed. Compounds 1-14 inhibited human cancer cell lines, K562, HL-60, HeLa and BGC-823, to varying extents.

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