Summary
SMILES: OC[C@H]1O[C@@H](Oc2ccc(cc2)/C=C/C(=O)OC[C@@H]2CCN3[C@@H]2CCC3)[C@@H]([C@H]([C@@H]1O)O)OInChI: InChI=1S/C23H31NO8/c25-12-18-20(27)21(28)22(29)23(32-18)31-16-6-3-14(4-7-16)5-8-19(26)30-13-15-9-11-24-10-1-2-17(15)24/h3-8,15,17-18,20-23,25,27-29H,1-2,9-13H2/b8-5+/t15-,17+,18+,20+,21-,22+,23+/m0/s1InChIKey: VRWXOVDCMDXQDO-VDEBYVOPSA-N
DeepSMILES: OC[C@H]O[C@@H]Occcccc6))/C=C/C=O)OC[C@@H]CCN[C@@H]5CCC5))))))))))))))))))[C@@H][C@H][C@@H]6O))O))O
Scaffold Graph/Node/Bond level: O=C(C=Cc1ccc(OC2CCCCO2)cc1)OCC1CCN2CCCC12
Scaffold Graph/Node level: OC(CCC1CCC(OC2CCCCO2)CC1)OCC1CCN2CCCC12
Scaffold Graph level: CC(CCC1CCC(CC2CCCCC2)CC1)CCC1CCC2CCCC21
Functional groups: CN(C)C; CO; c/C=C/C(=O)OC; cO[C@@H](C)OC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organic oxygen compoundsClassyFire Class: Organooxygen compounds
ClassyFire Subclass: Carbohydrates and carbohydrate conjugates
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Lysine alkaloids
NP Classifier Class: Quinolizidine alkaloids
Synonymous chemical names:thesinine-4'-o-beta-d-glucoside, thesinine-4-o-beta-d-glucoside
External chemical identifiers:CID:90478759; FDASRS:DPG1D4BJHB
Chemical structure download