BindingDB Link |
3219
|
SMILES |
COc1cc(C(O[C@@H](CCCNC2)[C@H]2NC(c(cc2)ccc2O)=O)=O)cc(OC)c1C(c(c(O)ccc1)c1O)=O
|
Download |
3219.mol2, BDB-kin3219.pdbqt
|
Total Surface Area |
409,06
|
TPSA |
163,65
|
cLogS |
-4,869
|
MW |
550,562
|
cLogP |
2,7178
|
H-Acceptors |
11
|
H-Donors |
5
|
Ro5 violations |
2
|
Druglikeness |
2,4143
|
DrugScore |
0,47406828877027
|
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 |
0,3442
|
P-glycoprotein Substrate |
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 |
Substrate
|
CYP450 1A2 Inhibitor |
Non-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 |
2,4748
|
hERG inhibition (predictor I) |
Weak inhibitor
|
hERG inhibition (predictor II) |
Inhibitor
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, mg/L) |
0,3194
|
Fish Toxicity |
High FHMT
|
Fish Toxicity (pLC50 mg/L) |
1,4621
|
Acute Oral Toxicity |
III
|
Carcinogens |
Non-carcinogens
|
Honey Bee Toxicity |
Low HBT
|
Subcellular localization |
Mitochondria
|