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Accession:CHEBI:66527 term browser browse the term
Definition:A diterpenoid that is 15,17-epoxypodocarpan-15-one substituted by a hydroxy group at position 13, methyl groups at positions 8 and 13 and a (5-methoxy-3,6-dioxocyclohexa-1,4-dien-1-yl)methyl group at position 14 (the 13alpha,14beta stereoisomer). Isolated from the marine sponge Petrosia corticata, it exhibits antineoplastic activity.
Synonyms:exact_synonym: 2-{[(13alpha,14beta)-13-hydroxy-8,13-dimethyl-15-oxo-15,17-epoxypodocarpan-14-yl]methyl}-6-methoxycyclohexa-2,5-diene-1,4-dione
 related_synonym: Formula=C27H36O6;   InChI=1S/C27H36O6/c1-24-10-6-20-25(2)8-5-9-27(20,15-33-23(25)30)19(24)7-11-26(3,31)21(24)13-16-12-17(28)14-18(32-4)22(16)29/h12,14,19-21,31H,5-11,13,15H2,1-4H3/t19-,20-,21-,24+,25-,26-,27-/m0/s1;   InChIKey=AMOGVPDDGBDGJG-FOMYWIRZSA-N;   SMILES=[H][C@]12CC[C@](C)(O)[C@@H](CC3=CC(=O)C=C(OC)C3=O)[C@]1(C)CC[C@@]1([H])[C@]3(C)CCC[C@]21COC3=O
 xref: PMID:15332859 "Europe PMC";   PMID:15897241 "Europe PMC";   PMID:17407351 "Europe PMC";   Reaxys:10738211 "Reaxys"

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                            organic group 18299
                              organic divalent group 18289
                                organodiyl group 18289
                                  carbonyl group 18176
                                    carbonyl compound 18176
                                      ketone 15646
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.