SMILES CN(CC1)CC=C1c(c1nc(-c2ccccc2)cc(O)c1c(O)c1)c1O
Download 50451017.mol2, BDB-kin50451017.pdbqt
Total Surface Area 260,48
TPSA 76,82
cLogS -3,088
MW 348,401
cLogP 3,0063
H-Acceptors 5
H-Donors 3
Ro5 violations 0
Druglikeness 5,0222
DrugScore 0,293582429860898
Mutagenic none
Tumorigenic high
Reproductive Effective high
Irritant none
Human Intestinal Absorption HIA+
Blood-Brain Barrier BBB-
Caco-2 Permeability I Caco2+
Caco-2 Permeability II 1,2237
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor I Non-inhibitor
P-glycoprotein Inhibitor II Non-inhibitor
Renal Organic Cation Transporter Inhibitor
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 1A2 Inhibitor Inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Non-inhibitor
CYP450 3A4 Inhibitor Non-inhibitor
CYP Inhibitory Promiscuity Low CYP Inhibitory Promiscuity
AMES Toxicity Non AMES toxic
Carcinogenicity (Three-class) Non-required
Biodegradation Not ready biodegradable
Rat Acute Toxicity 2,7642
hERG inhibition (predictor I) Weak inhibitor
hERG inhibition (predictor II) Non-inhibitor
Tetrahymena Pyriformis Toxicity High TPT
Tetrahymena Pyriformis Toxicity (pIGC50, mg/L) 0,6016
Fish Toxicity High FHMT
Fish Toxicity (pLC50 mg/L) 1,1384
Acute Oral Toxicity III
Carcinogens Non-carcinogens
Honey Bee Toxicity Low HBT
Subcellular localization Mitochondria
These data are only available for scientific research purposes.