Molecule Name DB00332
DrugBank Groups Approved
Cluster No 75
Smiles O=C(OC1(CC2(N(C(C)C)(C)C(C1)CC2)))C(C3(=CC=CC=C3))CO
Download mol2, pdbqt
TPSA 49,77
Non-H Atoms 24
Non-C/H Atoms 4
Metal-Atoms 0
Electronegative Atoms 4
Stereo Centers 5
Rotatable Bonds 6
Rings Closures 3
Small Rings 4
Aromatic Rings 1
Aromatic Atoms 6
sp3-Atoms 16
Symmetric atoms 3
cLogS -3,025
MW 332,462
cLogP 1,6186
HBA 4
HBD 1
Ro5 violations 0
Druglikeness 4,2225
DrugScore 0,862810143157316
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Blood-Brain Barrier BBB+
Human Intestinal Absorption HIA-
Caco-2 Permeability Caco2+
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor Non-inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Inhibitor
Aqueous solubility -2,4673
Caco-2 Permeability 2 1,1125
Subcellular localization Mitochondria
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 1A2 Inhibitor Non-inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Non-inhibitor
CYP450 3A4 Inhibitor Non-inhibitor
CYP Inhibitory Promiscuity Low CYP Inhibitory Promiscuity
Human Ether-a-go-go-Related Gene Inhibition Weak inhibitor
Human Ether-a-go-go-Related Gene Inhibition 2 Inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 0,9523
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,8893
Honey Bee Toxicity High HBT
Biodegradation Ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,8149
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.