IMPPAT Phytochemical information: 
beta-D-Glucopyranoside, (3R,5S,5aS,6R,7S,8R,8aS)-hexahydro-8,8a-dihydroxy-7-((4-hydroxy-3-methoxybenzoyl)oxy)-3,6-methano-1H-cyclopenta(e)(1,3)dioxepin-5-yl

beta-D-Glucopyranoside, (3R,5S,5aS,6R,7S,8R,8aS)-hexahydro-8,8a-dihydroxy-7-((4-hydroxy-3-methoxybenzoyl)oxy)-3,6-methano-1H-cyclopenta(e)(1,3)dioxepin-5-yl
Summary

SMILES: OC[C@@H]1O[C@H](O[C@@H]2O[C@H]3OC[C@]4([C@@H]2[C@@H](C3)[C@@H]([C@H]4O)OC(=O)c2ccc(c(c2)OC)O)O)[C@H]([C@@H]([C@H]1O)O)O
InChI: InChI=1S/C23H30O14/c1-32-11-4-8(2-3-10(11)25)20(30)36-18-9-5-13-33-7-23(31,19(18)29)14(9)21(35-13)37-22-17(28)16(27)15(26)12(6-24)34-22/h2-4,9,12-19,21-22,24-29,31H,5-7H2,1H3/t9-,12+,13-,14-,15+,16-,17+,18+,19-,21+,22-,23-/m1/s1
InChIKey: DTNNYXMHYVWWHO-RYLNZNLUSA-N
DeepSMILES: OC[C@@H]O[C@H]O[C@@H]O[C@H]OC[C@][C@@H]7[C@@H]C7)[C@@H][C@H]5O))OC=O)cccccc6)OC)))O))))))))))O))))))))[C@H][C@@H][C@H]6O))O))O
Scaffold Graph/Node/Bond level: O=C(OC1CC2COC3CC1C2C(OC1CCCCO1)O3)c1ccccc1
Scaffold Graph/Node level: OC(OC1CC2COC3CC1C2C(OC1CCCCO1)O3)C1CCCCC1
Scaffold Graph level: CC(CC1CC2CCC3CC(CC4CCCCC4)C2C1C3)C1CCCCC1
Functional groups: CO; CO[C@@H](C)O[C@@H](O[C@H](C)OC)C; cC(=O)OC; cOC; cO
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketides
ClassyFire Class: Tannins
ClassyFire Subclass: Hydrolyzable tannins
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Monoterpenoids
NP Classifier Class: Iridoids monoterpenoids
Synonymous chemical names:
pikuroside
External chemical identifiers:
CID:CID_132472101
Chemical structure download


beta-D-Glucopyranoside, (3R,5S,5aS,6R,7S,8R,8aS)-hexahydro-8,8a-dihydroxy-7-((4-hydroxy-3-methoxybenzoyl)oxy)-3,6-methano-1H-cyclopenta(e)(1,3)dioxepin-5-yl
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 530.48
Log P RDKit -2.82
Topological polar surface area (Å2) RDKit 214.06
Number of hydrogen bond acceptors RDKit 14
Number of hydrogen bond donors RDKit 7
Number of carbon atoms RDKit 23
Number of heavy atoms RDKit 37
Number of heteroatoms RDKit 14
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 12
Stereochemical complexity RDKit 0.52
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 7
Number of sp3 hybridized carbon atoms RDKit 16
Shape complexity RDKit 0.7
Number of rotatable bonds RDKit 7
Number of aliphatic carbocycles RDKit 1
Number of aliphatic heterocycles RDKit 4
Number of aliphatic rings RDKit 5
Number of aromatic carbocycles RDKit 1
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 1
Total number of rings RDKit 6
Number of saturated carbocycles RDKit 1
Number of saturated heterocycles RDKit 4
Number of saturated rings RDKit 5
Number of Smallest Set of Smallest Rings (SSSR) RDKit 6


beta-D-Glucopyranoside, (3R,5S,5aS,6R,7S,8R,8aS)-hexahydro-8,8a-dihydroxy-7-((4-hydroxy-3-methoxybenzoyl)oxy)-3,6-methano-1H-cyclopenta(e)(1,3)dioxepin-5-yl
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 3
Lipinski’s rule of 5 filter RDKit Failed
Number of Ghose filter violations RDKit 2
Ghose filter RDKit Failed
Veber filter RDKit Bad
Pfizer 3/75 filter RDKit Good
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.184918


beta-D-Glucopyranoside, (3R,5S,5aS,6R,7S,8R,8aS)-hexahydro-8,8a-dihydroxy-7-((4-hydroxy-3-methoxybenzoyl)oxy)-3,6-methano-1H-cyclopenta(e)(1,3)dioxepin-5-yl
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.17
Solubility class [ESOL] SwissADME Very soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME Low
Log Kp (Skin permeation, cm/s) SwissADME -10.96
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 0
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME No
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME No