5-Chloro-2-hydroxybenzophenone

Odors

No information available

Receptor Interaction

No receptors available

General Information

Common Name: 5-Chloro-2-hydroxybenzophenone
IUPAC Name: (5-chloro-2-hydroxyphenyl)-phenylmethanone
Molecular Formula: C13H9ClO2
SMILES: C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)Cl)O
Inchi: 1S/C13H9ClO2/c14-10-6-7-12(15)11(8-10)13(16)9-4-2-1-3-5-9/h1-8,15H
Inchi Key: OMWSZDODENFLSV-UHFFFAOYSA-N
Cas No: 85-19-8

Functional Group

Drug Likeness

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

Cross References

PubChem: 6799
Zinc: ZINC136128
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 232.66
Mass (g/mol) 232.029
Molar Refractivity 63.35
Net Charge -1
HBD 1
HBA 2
Rt Bonds 2
Rings 2
TPSA 37.30
Hetero Atoms 3
Heavy Atoms 16
Aromatic Heavy Atoms 12
Melting Point (°C) 95.3
Boiling Point (°C@760.00mm Hg) 355.5
Vapor Pressure (mmHg@25.00 °C)
Vapor Density (Air =1)
Fraction Csp3 0.00
LogP 3.277
iLOGP 2.43
XLOGP3 3.95
WLOGP 3.28
MLOGP 2.87
ESOL Log S -4.19
ESOL Solubility (mg/ml) 0.015
ESOL Solubility (mol/l) 0
ESOL Class: esol_class Moderately soluble
Ali Log S -4.43
Ali Solubility (mg/ml) 0.01
Ali Solubility (mol/l) 0
Ali Class Moderately soluble
Silicos-IT LogSw -4.91
Silicos-IT Solubility (mg/ml) 0
Silicos-IT Solubility (mol/l) 0
Silicos-IT Class Moderately soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -4.91
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.996
CYP1A2 Inhibitor 1
CYP2C19 Inhibitor 1
CYP2C9 Inhibitor 1
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 2.324
Carcinogenicity (Binary) 0
Carcinogenicity (Trinary) Non-required
Eye Irritation 1
Hepatotoxicity 1
Androgen Receptor Binding 1
Aromatase Binding 1
Estrogen Receptor Binding 1
Glucocorticoid Receptor Binding 1
Thyroid Receptor Binding 1
BRCP inhibitor 0
BSEP inhibitor 0
OATP1B1 inhibitor 1
OATP1B3 inhibitor 1
OATP2B1 inhibitor 0
OCT1 inhibitor 0
OCT2 inhibitor 0