CHEBI:66213 - 1,3,5,6-tetrahydroxy-4,7,8-tri(3-methyl-2-butenyl)xanthone

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ChEBI Name 1,3,5,6-tetrahydroxy-4,7,8-tri(3-methyl-2-butenyl)xanthone
ChEBI ID CHEBI:66213
Definition A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 3, 4, 6 and 8 and prenyl groups at positions 1, 2 and 5. Isolated from Garcinia xanthochymus, it exhibits enhancement of nerve growth factor-mediated neurite outgrowth in PC12D cells.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C28H32O6
Net Charge 0
Average Mass 464.55010
Monoisotopic Mass 464.21989
InChI InChI=1S/C28H32O6/c1-14(2)7-10-17-18(11-8-15(3)4)24(31)26(33)28-22(17)25(32)23-21(30)13-20(29)19(27(23)34-28)12-9-16(5)6/h7-9,13,29-31,33H,10-12H2,1-6H3
InChIKey HAHRYXGQWSJKPI-UHFFFAOYSA-N
SMILES CC(C)=CCc1c(O)c(O)c2oc3c(CC=C(C)C)c(O)cc(O)c3c(=O)c2c1CC=C(C)C
Metabolite of Species Details
Garcinia xanthochymus (NCBI:txid198766) Found in xylem (BTO:0001468). Previous component: wood; See: PubMed
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
nerve growth factor stimulator
Any molecule shown to have the potentiality in stimulating the effect of nerve growth factor.
Application(s): nerve growth factor stimulator
Any molecule shown to have the potentiality in stimulating the effect of nerve growth factor.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1,3,5,6-tetrahydroxy-4,7,8-tri(3-methyl-2-butenyl)xanthone (CHEBI:66213) has role metabolite (CHEBI:25212)
1,3,5,6-tetrahydroxy-4,7,8-tri(3-methyl-2-butenyl)xanthone (CHEBI:66213) has role nerve growth factor stimulator (CHEBI:72294)
1,3,5,6-tetrahydroxy-4,7,8-tri(3-methyl-2-butenyl)xanthone (CHEBI:66213) is a phenols (CHEBI:33853)
1,3,5,6-tetrahydroxy-4,7,8-tri(3-methyl-2-butenyl)xanthone (CHEBI:66213) is a xanthones (CHEBI:51149)
IUPAC Name
3,4,6,8-tetrahydroxy-1,2,5-tris(3-methylbut-2-en-1-yl)-9H-xanthen-9-one
Registry Number Type Source
9599599 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
14600386 PubMed citation Europe PMC
Last Modified
11 July 2013