PubMed 24992702
Referenced in: none
Automatically associated channels: TRP , TRPM , TRPM7
Title: Spongiapyridine and related spongians isolated from an Indonesian Spongia sp.
Authors: Stephen M Parrish, Wesley Y Yoshida, Tamara P Kondratyuk, Eun-Jung Park, John M Pezzuto, Michelle Kelly, Philip G Williams
Journal, date & volume: J. Nat. Prod., 2014 Jul 25 , 77, 1644-9
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/24992702
Abstract
New compounds 18-nor-3,17-dihydroxyspongia-3,13(16),14-trien-2-one (1), 18-nor-3,5,17-trihydroxyspongia-3,13(16),14-trien-2-one (2), and spongiapyridine (3) and the known compound 17-hydroxy-4-epi-spongialactone A (4) were isolated from an Indonesian sponge of the genus Spongia. The structures of 1-3 were deduced by analyses of physical and spectroscopic data. Diterpene 3 is unusual, as the D-ring is a pyridyl ring system rather than the standard δ-lactone. The structure elucidation of this compound was complicated by facile exchange of the axial proton at the C-11 methylene with deuterium from methanol-d4. The isolated compounds were tested for biological activity in a battery of in vitro assays (TNF-α-induced NFκB, LPS-induced iNOS, RXR stimulation, quinone reductase 1 induction, aromatase inhibition, TRPM7 ion channels, and aspartic protease BACE1 inhibition). Norditerpene 2 modestly inhibited aromatase with an IC50 of 34 μM and induced quinone reductase 1 activity with a CD (the concentration needed to double the enzymatic response) of 11.2 μM. The remaining isolates were inactive.