Molecule Name |
PE000677
|
Refractivity |
128
|
SMILES format |
COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)\C(=C\C)[C@@H]1CC(=O)OCCC1=CC(O)=C(O)C=C1
|
Resonant Structures |
21
|
TPSA |
202
|
ASA hydrophobic |
530
|
ASA polar |
277
|
Accessible Surface Area |
807
|
LogS |
-2
|
MW |
541
|
cLogP |
0
|
H-Acceptors |
13
|
H-Donors |
6
|
Ro5 violations |
3
|
DrugScore |
0
|
Druglikeness |
-7
|
Irritant |
none
|
Mutagenic |
none
|
Reproductive Effective |
none
|
Tumorigenic |
none
|
Fish Toxicity |
High FHMT
|
Fish Toxicity 2 |
1.1647
|
Rat Acute Toxicity |
3
|
Acute Oral Toxicity |
III
|
Caco-2 Permeability |
Caco2-
|
Caco-2 Permeability 2 |
0
|
P-glycoprotein Substrate |
Substrate
|
P-glycoprotein Inhibitor |
Non-inhibitor
|
P-glycoprotein Inhibitor 2 |
Non-inhibitor
|
Human Ether-a-go-go-Related Gene Inhibition |
Weak inhibitor
|
Human Ether-a-go-go-Related Gene Inhibition 2 |
Inhibitor
|
CYP450 2C9 Substrate |
Non-substrate
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity 2 |
1
|
AMES Toxicity |
Non AMES toxic
|
CYP450 3A4 Inhibitor |
Non-inhibitor
|
CYP450 3A4 Substrate |
Substrate
|
CYP450 2C19 Inhibitor |
Non-inhibitor
|
CYP450 2C9 Inhibitor |
Non-inhibitor
|
CYP450 2D6 Inhibitor |
Non-inhibitor
|
CYP450 1A2 Inhibitor |
Non-inhibitor
|
CYP450 2D6 Substrate |
Non-substrate
|
Biodegradation |
Ready biodegradable
|
Carcinogens |
Non-carcinogens
|
Blood-Brain Barrier |
BBB-
|
CYP Inhibitory Promiscuity |
Low CYP Inhibitory Promiscuity
|
Honey Bee Toxicity |
High HBT
|
Renal Organic Cation Transporter |
Non-inhibitor
|
Carcinogenicity (Three-class) |
Non-required
|
Human Intestinal Absorption |
HIA-
|