Molecule Name DB04289
DrugBank Groups Experimental
Cluster No 1375
Smiles O=C(N4(CCN(C2(C1(=C(C=CC=C1)C3(=C2C=CC=C3))))CC4))C6(=CC5(=C(NC=C5)C=C6))
Download mol2, pdbqt
TPSA 295,84
Non-H Atoms 30
Non-C/H Atoms 4
Metal-Atoms 0
Electronegative Atoms 4
Stereo Centers 0
Rotatable Bonds 2
Rings Closures 6
Small Rings 6
Aromatic Rings 4
Aromatic Atoms 21
sp3-Atoms 6
Symmetric atoms 8
cLogS -4,936
MW 393,489
cLogP 4,7906
HBA 4
HBD 1
Ro5 violations 0
Druglikeness 7,1102
DrugScore 0,188629260879651
Mutagenic high
Tumorigenic high
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 Inhibitor
Renal Organic Cation Transporter Inhibitor
Aqueous solubility -2,8048
Caco-2 Permeability 2 1,0238
Subcellular localization Mitochondria
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Substrate
CYP450 3A4 Substrate Substrate
CYP450 1A2 Inhibitor Inhibitor
CYP450 2C9 Inhibitor Inhibitor
CYP450 2D6 Inhibitor Inhibitor
CYP450 2C19 Inhibitor Inhibitor
CYP450 3A4 Inhibitor Inhibitor
CYP Inhibitory Promiscuity High 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) 1,3957
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,554
Honey Bee Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6913
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.