IMPPAT Phytochemical information: 
Rebaudioside A
Rebaudioside A
Summary

SMILES: OC[C@H]1O[C@@H](O[C@@]23CC[C@@H]4[C@@](C2)(CC3=C)CC[C@H]2[C@@]4(C)CCC[C@@]2(C)C(=O)O[C@@H]2O[C@H](CO)[C@H]([C@@H]([C@H]2O)O)O)[C@@H]([C@H]([C@@H]1O)O[C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O)O[C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O
InChI: InChI=1S/C44H70O23/c1-17-11-43-9-5-22-41(2,7-4-8-42(22,3)40(59)66-38-33(58)30(55)26(51)20(14-47)62-38)23(43)6-10-44(17,16-43)67-39-35(65-37-32(57)29(54)25(50)19(13-46)61-37)34(27(52)21(15-48)63-39)64-36-31(56)28(53)24(49)18(12-45)60-36/h18-39,45-58H,1,4-16H2,2-3H3/t18-,19-,20-,21-,22+,23+,24-,25-,26-,27-,28+,29+,30+,31-,32-,33-,34+,35-,36+,37+,38+,39+,41-,42-,43-,44+/m1/s1
InChIKey: HELXLJCILKEWJH-NCGAPWICSA-N
DeepSMILES: OC[C@H]O[C@@H]O[C@@]CC[C@@H][C@@]C6)CC7=C)))CC[C@H][C@@]6C)CCC[C@@]6C)C=O)O[C@@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O)))))))))))))))))))))[C@@H][C@H][C@@H]6O))O[C@@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O)))))))O[C@@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O
Scaffold Graph/Node/Bond level: C=C1CC23CCC4C(C(=O)OC5CCCCO5)CCCC4C2CCC1(OC1OCCC(OC2CCCCO2)C1OC1CCCCO1)C3
Scaffold Graph/Node level: CC1CC23CCC4C(C(O)OC5CCCCO5)CCCC4C2CCC1(OC1OCCC(OC2CCCCO2)C1OC1CCCCO1)C3
Scaffold Graph level: CC(CC1CCCCC1)C1CCCC2C1CCC13CC(C)C(CC4CCCC(CC5CCCCC5)C4CC4CCCCC4)(CCC21)C3
Functional groups: CO; CO[C@@H](C)OC; C=C(C)C; CO[C@@H](OC(C)=O)C
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like molecules
ClassyFire Class: Prenol lipids
ClassyFire Subclass: Terpene glycosides
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Diterpenoids
NP Classifier Class: Kaurane and Phyllocladane diterpenoids|Tetracyclic diterpenoids
Synonymous chemical names:
rebaudioside a
External chemical identifiers:
CID:CID_6918840; ChEBI:CHEBI:145012; ZINC:ZINC000242498440; FDASRS:B3FUD0528F; SureChEMBL:SCHEMBL19769999; MolPort-023-220-755
Chemical structure download
2D:2D MOL2D MOL22D SDF
3D:3D MOL3D MOL23D SDF3D PDB3D PDBQT
Rebaudioside A
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 967.02
Log P RDKit -5.11
Topological polar surface area (Å2) RDKit 374.13
Number of hydrogen bond acceptors RDKit 23
Number of hydrogen bond donors RDKit 14
Number of carbon atoms RDKit 44
Number of heavy atoms RDKit 67
Number of heteroatoms RDKit 23
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 26
Stereochemical complexity RDKit 0.59
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 3
Number of sp3 hybridized carbon atoms RDKit 41
Shape complexity RDKit 0.93
Number of rotatable bonds RDKit 13
Number of aliphatic carbocycles RDKit 4
Number of aliphatic heterocycles RDKit 4
Number of aliphatic rings RDKit 8
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 0
Total number of rings RDKit 8
Number of saturated carbocycles RDKit 4
Number of saturated heterocycles RDKit 4
Number of saturated rings RDKit 8
Number of Smallest Set of Smallest Rings (SSSR) RDKit 8
Rebaudioside A
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 3
Lipinski’s rule of 5 RDKit Failed
Number of Ghose rule violations RDKit 4
Ghose rule RDKit Failed
Veber rule RDKit Bad
Egan rule RDKit Bad
GSK 4/400 rule RDKit Bad
Pfizer 3/75 rule RDKit Good
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.05
Rebaudioside A
Human target proteins
Protein identifierHGNC symbolCombined score from STITCH database
ENSP00000387662GCG817
The human target proteins were predicted using STITCH, a database of Chemical-Protein interaction networks.