Molecule Name DB01562
DrugBank Groups Experimental
Cluster No 27
Smiles O=C(OC3(C1(=CC=CC=C1))(CCN(CCC2(=CC=CC=C2))CC3))C
Download mol2, pdbqt
TPSA 262,8
Non-H Atoms 24
Non-C/H Atoms 3
Metal-Atoms 0
Electronegative Atoms 3
Stereo Centers 0
Rotatable Bonds 6
Rings Closures 3
Small Rings 3
Aromatic Rings 2
Aromatic Atoms 12
sp3-Atoms 10
Symmetric atoms 6
cLogS -3,339
MW 323,435
cLogP 4,0622
HBA 3
HBD 0
Ro5 violations 0
Druglikeness 6,48
DrugScore 0,598200754250035
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant low
Blood-Brain Barrier BBB+
Human Intestinal Absorption HIA+
Caco-2 Permeability Caco2+
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor Inhibitor
P-glycoprotein Inhibitor 2 Inhibitor
Renal Organic Cation Transporter Inhibitor
Aqueous solubility -2,459
Caco-2 Permeability 2 0,9417
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 Inhibitor
CYP450 2C19 Inhibitor Non-inhibitor
CYP450 3A4 Inhibitor 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) 1,5426
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,3284
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,7903
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.