Molecule Name DB01529
DrugBank Groups Experimental
Cluster No 43
Smiles O=C(N1(CCCC1))C(C2(=CC=CC=C2))(C3(=CC=CC=C3))C(CN4(CCOCC4))C
Download mol2, pdbqt
TPSA 313,38
Non-H Atoms 29
Non-C/H Atoms 4
Metal-Atoms 0
Electronegative Atoms 4
Stereo Centers 1
Rotatable Bonds 6
Rings Closures 4
Small Rings 4
Aromatic Rings 2
Aromatic Atoms 12
sp3-Atoms 14
Symmetric atoms 12
cLogS -2,3
MW 392,541
cLogP 3,227
HBA 4
HBD 0
Ro5 violations 0
Druglikeness 4,8899
DrugScore 0,798244542893122
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 Inhibitor
P-glycoprotein Inhibitor 2 Non-inhibitor
Renal Organic Cation Transporter Inhibitor
Aqueous solubility -2,474
Caco-2 Permeability 2 1,24
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 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 Non-inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity Low FHMT
Fish Toxicity (pLC50, mg/L) 1,6686
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,2159
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity II
Rat Acute Toxicity (LD50, mol/kg) 3,7072
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.