Summary

IMPPAT Phytochemical identifier: IMPHY010051

Phytochemical name: 1-Hydroxy-3,6,7-trimethoxy-2-(3-methyl-2-butenyl)-8-(2-hydroxy-3-methyl-3-butenyl)-xanthone

Synonymous chemical names:
1-hydroxy-8-(2-hydroxy-3-methyl-but-3-enyl)-3,6,7-trimethoxy-2-(3-methylbut-2-enyl)-xanthone

External chemical identifiers:
CID:20978310, ChEBI:175625

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Chemical structure information

SMILES:
COc1cc2oc3cc(OC)c(c(c3c(=O)c2c(c1CC=C(C)C)O)CC(C(=C)C)O)OC

InChI:
InChI=1S/C26H30O7/c1-13(2)8-9-15-18(30-5)11-20-23(24(15)28)25(29)22-16(10-17(27)14(3)4)26(32-7)21(31-6)12-19(22)33-20/h8,11-12,17,27-28H,3,9-10H2,1-2,4-7H3

InChIKey:
IUZNOAOULJFDJI-UHFFFAOYSA-N

DeepSMILES:
COcccocccOC))ccc6c=O)c%10cc%14CC=CC)C)))))O)))))CCC=C)C))O))))OC

Functional groups:
C=C(C)C, CC=C(C)C, CO, c=O, cO, cOC, coc

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=c1c2ccccc2oc2ccccc12

Scaffold Graph/Node level:
OC1C2CCCCC2OC2CCCCC21

Scaffold Graph level:
CC1C2CCCCC2CC2CCCCC21

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Organoheterocyclic compounds

ClassyFire Class: Benzopyrans

ClassyFire Subclass: 1-benzopyrans

NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids

NP Classifier Superclass: Xanthones

NP Classifier Class: Plant xanthones

NP-Likeness score: 2.204

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Chemical structure download