SMILES c1cn(cn1)-c1ccccc1
Download BDB-kin111625.mol2, BDB-kin111625.pdbqt
Total Surface Area 120,98
TPSA 17,82
cLogS -3,72
MW 144,177
cLogP 1,2822
H-Acceptors 2
H-Donors 0
Ro5 violations 0
Druglikeness 1,5972
DrugScore 0,800957829468965
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Human Intestinal Absorption HIA+
Blood-Brain Barrier BBB+
Caco-2 Permeability I Caco2+
Caco-2 Permeability II 1,5131
P-glycoprotein Substrate Non-substrate
P-glycoprotein Inhibitor I Non-inhibitor
P-glycoprotein Inhibitor II Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
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 Inhibitor
CYP450 2C19 Inhibitor Inhibitor
CYP450 3A4 Inhibitor Non-inhibitor
CYP Inhibitory Promiscuity High CYP Inhibitory Promiscuity
AMES Toxicity AMES toxic
Carcinogenicity (Three-class) Warning
Biodegradation Not ready biodegradable
Rat Acute Toxicity 2,642
hERG inhibition (predictor I) Weak inhibitor
hERG inhibition (predictor II) Non-inhibitor
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, mg/L) 0,5255
Fish Toxicity High FHMT
Fish Toxicity (pLC50 mg/L) 0,9652
Acute Oral Toxicity II
Carcinogens Non-carcinogens
Honey Bee Toxicity Low HBT
Subcellular localization Nucleus
These data are only available for scientific research purposes.