Molecule Name |
DB00170
|
DrugBank Groups |
Approved
|
Cluster No |
44
|
Smiles |
O=C1(C2(=C(C(=O)C=C1C)C=CC=C2))
|
Download |
mol2, pdbqt
|
TPSA |
34,14
|
Non-H Atoms |
13
|
Non-C/H Atoms |
2
|
Metal-Atoms |
0
|
Electronegative Atoms |
2
|
Stereo Centers |
0
|
Rotatable Bonds |
0
|
Rings Closures |
2
|
Small Rings |
2
|
Aromatic Rings |
1
|
Aromatic Atoms |
6
|
sp3-Atoms |
1
|
Symmetric atoms |
0
|
cLogS |
-2,966
|
MW |
172,183
|
cLogP |
1,8796
|
HBA |
2
|
HBD |
0
|
Ro5 violations |
0
|
Druglikeness |
-1,5482
|
DrugScore |
0,115944077019293
|
Mutagenic |
high
|
Tumorigenic |
high
|
Reproductive Effective |
high
|
Irritant |
none
|
Blood-Brain Barrier |
BBB+
|
Human Intestinal Absorption |
HIA+
|
Caco-2 Permeability |
Caco2+
|
P-glycoprotein Substrate |
Non-substrate
|
P-glycoprotein Inhibitor |
Inhibitor
|
P-glycoprotein Inhibitor 2 |
Non-inhibitor
|
Renal Organic Cation Transporter |
Non-inhibitor
|
Aqueous solubility |
-3,5777
|
Caco-2 Permeability 2 |
2,0145
|
Subcellular localization |
Mitochondria
|
CYP450 2C9 Substrate |
Non-substrate
|
CYP450 2D6 Substrate |
Non-substrate
|
CYP450 3A4 Substrate |
Non-substrate
|
CYP450 1A2 Inhibitor |
Inhibitor
|
CYP450 2C9 Inhibitor |
Inhibitor
|
CYP450 2D6 Inhibitor |
Inhibitor
|
CYP450 2C19 Inhibitor |
Inhibitor
|
CYP450 3A4 Inhibitor |
Non-inhibitor
|
CYP Inhibitory Promiscuity |
High CYP Inhibitory Promiscuity
|
Human Ether-a-go-go-Related Gene Inhibition |
Weak inhibitor
|
Human Ether-a-go-go-Related Gene Inhibition 2 |
Non-inhibitor
|
AMES Toxicity |
AMES toxic
|
Carcinogens |
Non-carcinogens
|
Fish Toxicity |
High FHMT
|
Fish Toxicity (pLC50, mg/L) |
-0,834
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
1,2488
|
Honey Bee Toxicity |
High HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
II
|
Rat Acute Toxicity (LD50, mol/kg) |
2,7195
|
Carcinogenicity (Three-class) |
Non-required
|