2,4,4-Trimethyl-1,3-oxathiane

Odors

Receptor Interaction

No receptors available

Odor Profile

Strength: high

General Information

Common Name: 2,4,4-Trimethyl-1,3-oxathiane
IUPAC Name: 2,4,4-trimethyl-1,3-oxathiane
Molecular Formula: C8H16OS
SMILES: CC1OCCC(S1)(C)C
Inchi: 1S/C7H14OS/c1-6-8-5-4-7(2,3)9-6/h6H,4-5H2,1-3H3
Inchi Key: RRVYBZOPLAEEFE-UHFFFAOYSA-N
Cas No: 72472-02-7

Functional Group

Cyclic
S-compounds

Drug Likeness

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

Cross References

PubChem: 18539813
Zinc: ZINC146446290
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 160.28
Mass (g/mol) 146.077
Molar Refractivity 47.17
Net Charge
HBD
HBA 1
Rt Bonds 1
Rings 1
TPSA 34.53
Hetero Atoms 2
Heavy Atoms 10
Aromatic Heavy Atoms 0
Melting Point (°C) 32
Boiling Point (°C@760.00mm Hg) 191.00 to 192.00
Vapor Pressure (mmHg@25.00 °C) 0.708
Vapor Density (Air =1)
Fraction Csp3 1.00
LogP 2.264
iLOGP 2.46
XLOGP3 2.53
WLOGP 2.65
MLOGP 1.83
ESOL Log S -2.36
ESOL Solubility (mg/ml) 0.697
ESOL Solubility (mol/l) 0.004
ESOL Class: esol_class Soluble
Ali Log S -2.90
Ali Solubility (mg/ml) 0.2
Ali Solubility (mol/l) 0
Ali Class Soluble
Silicos-IT LogSw -2.15
Silicos-IT Solubility (mg/ml) 1.13
Silicos-IT Solubility (mol/l) 0.01
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -5.48
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.742
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 2.1
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