IMPPAT Phytochemical information: 
D-Galactose

D-Galactose
Summary

SMILES: OC[C@H]1OC(O)[C@@H]([C@H]([C@H]1O)O)O
InChI: InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6?/m1/s1
InChIKey: WQZGKKKJIJFFOK-SVZMEOIVSA-N
DeepSMILES: OC[C@H]OCO)[C@@H][C@H][C@H]6O))O))O
Scaffold Graph/Node/Bond level: C1CCOCC1
Scaffold Graph/Node level: C1CCOCC1
Scaffold Graph level: C1CCCCC1
Functional groups: CO; COC(O)C
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organic oxygen compounds
ClassyFire Class: Organooxygen compounds
ClassyFire Subclass: Carbohydrates and carbohydrate conjugates
NP Classifier Biosynthetic pathway: Carbohydrates|Shikimates and Phenylpropanoids
NP Classifier Superclass: Saccharides|Flavonoids
NP Classifier Class: Disaccharides|Flavones|Monosaccharides|Polysaccharides
Synonymous chemical names:
sugar galactose, d-galactose, d-galactopyranose, galactose
External chemical identifiers:
CID:CID_6036; ChEMBL:CHEMBL195923; ChEBI:CHEBI:4139; SureChEMBL:SCHEMBL38935; MolPort-003-934-464
Chemical structure download


D-Galactose
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 180.16
Log P RDKit -3.22
Topological polar surface area (Å2) RDKit 110.38
Number of hydrogen bond acceptors RDKit 6
Number of hydrogen bond donors RDKit 5
Number of carbon atoms RDKit 6
Number of heavy atoms RDKit 12
Number of heteroatoms RDKit 6
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 5
Stereochemical complexity RDKit 0.83
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 0
Number of sp3 hybridized carbon atoms RDKit 6
Shape complexity RDKit 1
Number of rotatable bonds RDKit 1
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 1
Number of aliphatic rings RDKit 1
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 0
Total number of rings RDKit 1
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 1
Number of saturated rings RDKit 1
Number of Smallest Set of Smallest Rings (SSSR) RDKit 1


D-Galactose
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 0
Lipinski’s rule of 5 filter RDKit Passed
Number of Ghose filter violations RDKit 2
Ghose filter RDKit Failed
Veber filter RDKit Good
Pfizer 3/75 filter RDKit Good
GSK 4/400 filter RDKit Good
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.290153


D-Galactose
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Highly soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME Low
Log Kp (Skin permeation, cm/s) SwissADME -9.70
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 Yes


D-Galactose
Human target proteins
Protein identifierHGNC symbolCombined score from STITCH database
ENSP00000352584AKR1B10900
ENSP00000272252GALM908
ENSP00000264162LCT910
ENSP00000261304GALC800
ENSP00000218516GLA909
ENSP00000306920GLB1915
ENSP00000285930AKR1B1900
The human target proteins were predicted using STITCH, a database of Chemical-Protein interaction networks.