trans-4,5-Epoxy-(E)-oct-2-enal

Odors

Receptor Interaction

No receptors available

General Information

Common Name: trans-4,5-Epoxy-(E)-oct-2-enal
IUPAC Name: (E)-3-[(2R,3R)-3-propyloxiran-2-yl]prop-2-enal
Molecular Formula: C8H12O2
SMILES: CCC[C@@H]1[C@H](O1)/C=C/C=O
Inchi: 1S/C8H12O2/c1-2-4-7-8(10-7)5-3-6-9/h3,5-8H,2,4H2,1H3/b5-3+/t7-,8-/m1/s1
Inchi Key: RBBPXPMPGIPSJY-LFHXBRCSSA-N
Cas No: 134452-45-2

Functional Group

Aldehydes
Alkene
Oxirane

Drug Likeness

Name Value
Lipinski Violations 0
Ghose Violations 2
Veber Violations 0
Egan Violations 0
Muegge Violations 1

Cross References

PubChem: 6429299
Zinc: ZINC39131889
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 140.18
Mass (g/mol) 140.084
Molar Refractivity 39.27
Net Charge
HBD
HBA 2
Rt Bonds 4
Rings 1
TPSA 29.60
Hetero Atoms 2
Heavy Atoms 10
Aromatic Heavy Atoms 0
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 239.00 to 240.00
Vapor Pressure (mmHg@25.00 °C) 0.0393
Vapor Density (Air =1)
Fraction Csp3 0.62
LogP 1.309
iLOGP 1.96
XLOGP3 0.96
WLOGP 1.31
MLOGP 0.65
ESOL Log S -1.05
ESOL Solubility (mg/ml) 12.5
ESOL Solubility (mol/l) 0.089
ESOL Class: esol_class Very soluble
Ali Log S -1.17
Ali Solubility (mg/ml) 9.5
Ali Solubility (mol/l) 0.07
Ali Class Very soluble
Silicos-IT LogSw -0.92
Silicos-IT Solubility (mg/ml) 16.9
Silicos-IT Solubility (mol/l) 0.12
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -6.47
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.751
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.81
Carcinogenicity (Binary) 0
Carcinogenicity (Trinary) Non-required
Eye Irritation 1
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