Molecule Name DB01523
DrugBank Groups Experimental
Cluster No 21
Smiles ClC3(=CC=C(CC1(=NC=2(C=C([N+](=O)[O-])C=CC=2(N1CCN(CC)CC))))C=C3)
Download mol2, pdbqt
TPSA 298,29
Non-H Atoms 27
Non-C/H Atoms 7
Metal-Atoms 0
Electronegative Atoms 7
Stereo Centers 0
Rotatable Bonds 8
Rings Closures 3
Small Rings 3
Aromatic Rings 3
Aromatic Atoms 15
sp3-Atoms 9
Symmetric atoms 4
cLogS -3,409
MW 386,882
cLogP 1,8597
HBA 6
HBD 0
Ro5 violations 0
Druglikeness 1,0839
DrugScore 0,421781924717379
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 Non-inhibitor
P-glycoprotein Inhibitor 2 Inhibitor
Renal Organic Cation Transporter Inhibitor
Aqueous solubility -4,0638
Caco-2 Permeability 2 0,928
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 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) 1,02
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 1,0177
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6223
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.