Summary
IMPPAT Phytochemical identifier: IMPHY003736
Phytochemical name: Scandoside
Synonymous chemical names:scandoside, scandoside (iridoid glycoside), scandosides
External chemical identifiers:CID:21602023, ChEMBL:CHEMBL459415, ZINC:ZINC000038321680, SureChEMBL:SCHEMBL307654, MolPort-039-338-648
Chemical structure information
SMILES:
OCC1=C[C@H]([C@H]2[C@@H]1[C@@H](OC=C2C(=O)O)O[C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O)OInChI:
InChI=1S/C16H22O11/c17-2-5-1-7(19)10-6(14(23)24)4-25-15(9(5)10)27-16-13(22)12(21)11(20)8(3-18)26-16/h1,4,7-13,15-22H,2-3H2,(H,23,24)/t7-,8-,9-,10+,11-,12+,13-,15+,16+/m1/s1InChIKey:
ZVXWFPTVHBWJOU-AWQYILTISA-NDeepSMILES:
OCC=C[C@H][C@H][C@@H]5[C@@H]OC=C6C=O)O)))))O[C@@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O)))))))))OFunctional groups:
CC(C)=CC, CO, CO[C@H](C)O[C@H]1CCC(C(=O)O)=CO1
Molecular scaffolds
Scaffold Graph/Node/Bond level:
C1=CC2C(C=COC2OC2CCCCO2)C1Scaffold Graph/Node level:
C1CCC(OC2OCCC3CCCC32)OC1Scaffold Graph level:
C1CCC(CC2CCCC3CCCC32)CC1
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Prenol lipids
ClassyFire Subclass: Terpene glycosides
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Monoterpenoids
NP Classifier Class: Iridoids monoterpenoids
NP-Likeness score: 2.85
Chemical structure download