BindingDB Link |
7886
|
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
|