Summary
IMPPAT Phytochemical identifier: IMPHY001526
Phytochemical name: Sonchuside H
Synonymous chemical names:sonchuside h
External chemical identifiers:CID:15628130, ZINC:ZINC000255208723
Chemical structure information
SMILES:
OC[C@@H]1CC[C@H]([C@]2([C@H]1[C@H]1OC(=O)[C@H]([C@@H]1CC2)C)C)O[C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)OInChI:
InChI=1S/C21H34O9/c1-9-11-5-6-21(2)13(4-3-10(7-22)14(21)18(11)30-19(9)27)29-20-17(26)16(25)15(24)12(8-23)28-20/h9-18,20,22-26H,3-8H2,1-2H3/t9-,10-,11-,12+,13+,14+,15+,16-,17+,18-,20-,21-/m0/s1InChIKey:
FALKIRIZGCTQBY-PNTLOSRKSA-NDeepSMILES:
OC[C@@H]CC[C@H][C@][C@H]6[C@H]OC=O)[C@H][C@@H]5CC9)))C))))))C))O[C@@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))OFunctional groups:
CO, COC(C)=O, CO[C@@H](C)OC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1CC2CCC3C(OC4CCCCO4)CCCC3C2O1Scaffold Graph/Node level:
OC1CC2CCC3C(OC4CCCCO4)CCCC3C2O1Scaffold Graph level:
CC1CC2CCC3C(CC4CCCCC4)CCCC3C2C1
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Prenol lipids
ClassyFire Subclass: Terpene lactones
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Sesquiterpenoids
NP Classifier Class: Eudesmane sesquiterpenoids
NP-Likeness score: 2.75
Chemical structure download