A natural product found in Endophytic fungi.

Identification

Molecular Formula
C15H24O5
Mass
284.34810
Monoisotopic Mass
284.16237
Charge
0
InChI
InChI=1S/C15H24O5/c1-12(2)5-4-10(17)13(3)15(12)7-6-14(18,9-16)11(8-15)19-20-13/h11,16,18H,4-9H2,1-3H3/t11-,13+,14+,15-/m0/s1
InChIKey
HYSZRAXVRXDIDT-MYPMTAMASA-N
SMILES
CC1(C)CCC(=O)[C@@]2(C)OO[C@H]3C[C@@]12CC[C@@]3(O)CO

Species

endophytic fungi

NCBI:txid475121954864

Europe PubMed Central results


Antiangiogenic effect of chamigrane endoperoxides from a Thai mangrove-derived fungus.

Author: Chokpaiboon S, Sommit D, Bunyapaiboonsri T, Matsubara K, Pudhom K.

Abstract: As part of our ongoing efforts to investigate natural products with potential for use as cancer treatments, we have recently disclosed the cytotoxicity of unique nor-chamigrane (1) and chamigrane (2, 3) endoperoxides from a Thai mangrove-derived fungus. Reinvestigation of this fungus in a large-scale fermentation led to the isolation of an additional new chamigrane endoperoxide (4) and one known analogue (5). Among these isolated metabolites, compound 3 (merulin C) exhibited potent antiangiogenic activity mainly by suppression of endothelial cell proliferation and migration in a dose-dependent manner, and its effect is mediated by reduction in the phosphorylation of Erk1/2. Merulin C also displayed promising activity in a rat aortic ring sprouting (ex vivo) and a mouse Matrigel (in vivo) assay.