(2R,3R,4S,5S)-2,3,4,5-Tetrahydroxyhexanal

Odors

No information available

Receptor Interaction

No receptors available

General Information

Common Name: (2R,3R,4S,5S)-2,3,4,5-Tetrahydroxyhexanal
IUPAC Name: (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal
Molecular Formula: C6H12O5
SMILES: C[C@@H]([C@@H]([C@H]([C@H](C=O)O)O)O)O
Inchi: 1S/C6H12O5/c1-3(8)5(10)6(11)4(9)2-7/h2-6,8-11H,1H3/t3-,4-,5-,6-/m0/s1
Inchi Key: PNNNRSAQSRJVSB-BXKVDMCESA-N
Cas No: 3615-41-6

Functional Group

Drug Likeness

Name Value
Lipinski Violations 0
Ghose Violations 2
Veber Violations 0
Egan Violations 0
Muegge Violations 2

Cross References

PubChem: 19233
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 164.16
Mass (g/mol) 164.069
Molar Refractivity 35.80
Net Charge
HBD 4
HBA 5
Rt Bonds 4
Rings
TPSA 97.99
Hetero Atoms
Heavy Atoms 11
Aromatic Heavy Atoms 0
Melting Point (°C) 122
Boiling Point (°C@760.00mm Hg) 398.00 to 399.00
Vapor Pressure (mmHg@25.00 °C)
Vapor Density (Air =1)
Fraction Csp3 0.83
LogP
iLOGP 0.47
XLOGP3 -2.38
WLOGP -2.35
MLOGP -2.10
ESOL Log S 0.91
ESOL Solubility (mg/ml) 1320
ESOL Solubility (mol/l) 8.05
ESOL Class: esol_class Highly soluble
Ali Log S 0.86
Ali Solubility (mg/ml) 1190
Ali Solubility (mol/l) 7.26
Ali Class Highly soluble
Silicos-IT LogSw 1.90
Silicos-IT Solubility (mg/ml) 13000
Silicos-IT Solubility (mol/l) 79.3
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption Low
BBB Permeable 0
PgP Substrate 0
Log Kp (cm/s) -8.99
Bioavailability Score 0.55
Caco2 0
Human Intestinal Absorption 1
Plasm Protein Binding 0.789
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 0.259
Carcinogenicity (Binary) 0
Carcinogenicity (Trinary) Non-required
Eye Irritation 0
Hepatotoxicity 0
Androgen Receptor Binding 0
Aromatase Binding 0
Estrogen Receptor Binding 0
Glucocorticoid Receptor Binding 0
Thyroid Receptor Binding 0
BRCP inhibitor 0
BSEP inhibitor 0
OATP1B1 inhibitor 1
OATP1B3 inhibitor 1
OATP2B1 inhibitor 0
OCT1 inhibitor 0
OCT2 inhibitor 0