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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
06. Name of Biological Source of Chemical
06. Name of Biological Source of Chemical
Fomitopsis pinicola (3)
08. Chemical Category
08. Chemical Category
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
fomitoside E [CHEBI:65903] (1)
ChEBI Compound Accession Identifier :
[CHEBI:65903]
ChEBI Compound Description :
A triterpene glycoside that consists of lanost-8,23-dien-21-oic acid substituted at by a alpha-acetyloxy group at position 3, a hydroxy group at position 25 and a beta-D-xylopyranosyl moiety at position 21 via a glycosidic linkage. Isolated from the fruit body of Fomitopsis pinicola, it exhibits inhibitory activity against COX-1 and COX-2.
ChEBI Compound Identification Number :
65903
ChEBI InChI Value :
InChI=1S/C37H58O9/c1-21(38)45-28-15-17-35(6)24-14-19-36(7)23(13-18-37(36,8)25(24)11-12-27(35)34(28,4)5)22(10-9-16-33(2,3)43)31(42)46-32-30(41)29(40)26(39)20-44-32/h9,16,22-23,26-30,32,39-41,43H,10-15,17-20H2,1-8H3/b16-9+/t22-,23-,26-,27+,28-,29+,30-,32+,35-,36-,37+/m1/s1
ChEBI InChIKey Value :
SZJHDEBBAHZWAS-JYUDEBFNSA-N
ChEBI Compound Name :
fomitoside E
ChEBI SMILES Value :
[H][C@@]1(CC[C@@]2(C)C3=C(CC[C@]12C)[C@@]1(C)CC[C@@H](OC(C)=O)C(C)(C)[C@]1([H])CC3)[C@@H](C\C=C\C(C)(C)O)C(=O)O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O
ChEBI Substance ID :
160709600
ChEBI URL :
ChEBI:65903
ChemSpider ID :
9333133
Ontomatica Chemical Accession Key (OnChAKey) :
SZJHDEBBAHZWAS_JYUDEBFNSA_N_000_000000
PubChem Compound ID :
11158025