Molecule Name DB07513
DrugBank Groups Experimental
Cluster No 2036
Smiles ClC1(=CC(=CC=C1)COC3(=CC=2(OC(=O)C=C(C=2C=C3)CNC)))
Download mol2, pdbqt
TPSA 248,64
Non-H Atoms 23
Non-C/H Atoms 5
Metal-Atoms 0
Electronegative Atoms 5
Stereo Centers 0
Rotatable Bonds 5
Rings Closures 3
Small Rings 3
Aromatic Rings 2
Aromatic Atoms 12
sp3-Atoms 6
Symmetric atoms 0
cLogS -3,661
MW 329,782
cLogP 2,5567
HBA 4
HBD 1
Ro5 violations 0
Druglikeness -0,62317
DrugScore 0,32821168537323
Mutagenic none
Tumorigenic none
Reproductive Effective high
Irritant none
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 Non-inhibitor
Aqueous solubility -3,6826
Caco-2 Permeability 2 1,2076
Subcellular localization Lysosome
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Non-substrate
CYP450 1A2 Inhibitor Inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Inhibitor
CYP450 3A4 Inhibitor Non-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 Non-inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity High FHMT
Fish Toxicity (pLC50, mg/L) 0,5847
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) 0,8976
Honey Bee Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity (LD50, mol/kg) 2,6461
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.