IMPPAT Phytochemical information: 
2,3-Butanediol

2,3-Butanediol
Summary

SMILES: CC(C(O)C)O
InChI: InChI=1S/C4H10O2/c1-3(5)4(2)6/h3-6H,1-2H3
InChIKey: OWBTYPJTUOEWEK-UHFFFAOYSA-N
DeepSMILES: CCCO)C))O
Functional groups: CO
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organic oxygen compounds
ClassyFire Class: Organooxygen compounds
ClassyFire Subclass: Alcohols and polyols
NP Classifier Biosynthetic pathway: Fatty acids
NP Classifier Superclass: Fatty acyls
NP Classifier Class: Fatty alcohols
Synonymous chemical names:
2, 3-butanediol, 2,3-butanediol, butane-2,3-diol
External chemical identifiers:
CID:262; ChEMBL:CHEMBL2312529; ChEBI:62064; SureChEMBL:SCHEMBL22162; MolPort-003-927-421
Chemical structure download


2,3-Butanediol
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 90.12
Log P RDKit -0.25
Topological polar surface area (Å2) RDKit 40.46
Number of hydrogen bond acceptors RDKit 2
Number of hydrogen bond donors RDKit 2
Number of carbon atoms RDKit 4
Number of heavy atoms RDKit 6
Number of heteroatoms RDKit 2
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 2
Stereochemical complexity RDKit 0.5
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 0
Number of sp3 hybridized carbon atoms RDKit 4
Shape complexity RDKit 1
Number of rotatable bonds RDKit 1
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 0
Number of aliphatic rings RDKit 0
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 0
Total number of rings RDKit 0
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 0
Number of saturated rings RDKit 0
Number of Smallest Set of Smallest Rings (SSSR) RDKit 0


2,3-Butanediol
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 3
Ghose filter RDKit Failed
Veber filter RDKit Good
Pfizer 3/75 filter RDKit Bad
GSK 4/400 filter RDKit Good
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.4657


2,3-Butanediol
ADMET 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 High
Log Kp (Skin permeation, cm/s) SwissADME -7.5
Number of PAINS structural alerts SwissADME 0.0
Number of Brenk structural alerts SwissADME 0.0
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


2,3-Butanediol
Predicted human target proteins
Protein identifierHGNC symbolCombined score from STITCH database
ENSP00000218032TLR8800
ENSP00000228740LTA4H705
ENSP00000261733ALDH2732
ENSP00000270357RNPEPL1705
ENSP00000295640RNPEP705
ENSP00000309591PRKACA854
ENSP00000343577TPSAB1800
ENSP00000354511COMT795
ENSP00000355924SMYD2800
ENSP00000381717UBE2D2932
ENSP00000431254IGLL5800
ENSP00000433511GRK6800
The human target proteins were predicted using STITCH, a database of Chemical-Protein interaction networks.