Molecule Name DB01462
DrugBank Groups Experimental
Cluster No 21
Smiles O=[N+]([O-])C3(=CC=2(N=C(CC1(=CC=C(OCC)C=C1))N(C=2C=C3)CCN(CC)CC))
Download mol2, pdbqt
TPSA 318,89
Non-H Atoms 29
Non-C/H Atoms 7
Metal-Atoms 0
Electronegative Atoms 7
Stereo Centers 0
Rotatable Bonds 10
Rings Closures 3
Small Rings 3
Aromatic Rings 3
Aromatic Atoms 15
sp3-Atoms 12
Symmetric atoms 4
cLogS -2,991
MW 396,489
cLogP 1,59
HBA 7
HBD 0
Ro5 violations 0
Druglikeness -0,44358
DrugScore 0,343034988545649
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant high
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 -3,911
Caco-2 Permeability 2 1,2161
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 Inhibitor
CYP Inhibitory Promiscuity High CYP Inhibitory Promiscuity
Human Ether-a-go-go-Related Gene Inhibition Strong inhibitor
Human Ether-a-go-go-Related Gene Inhibition 2 Inhibitor
AMES Toxicity AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 1,0974
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,7664
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6746
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.