Molecule Name |
DB09002
|
DrugBank Groups |
Approved
|
Cluster No |
1055
|
Smiles |
ClC3(=CC=C(C(OCCN1(CCCCC1))C2(=CC=CC=C2))C=C3)
|
Download |
mol2, pdbqt
|
TPSA |
12,47
|
Non-H Atoms |
23
|
Non-C/H Atoms |
3
|
Metal-Atoms |
0
|
Electronegative Atoms |
3
|
Stereo Centers |
1
|
Rotatable Bonds |
6
|
Rings Closures |
3
|
Small Rings |
3
|
Aromatic Rings |
2
|
Aromatic Atoms |
12
|
sp3-Atoms |
10
|
Symmetric atoms |
6
|
cLogS |
-4,003
|
MW |
329,87
|
cLogP |
4,6448
|
HBA |
2
|
HBD |
0
|
Ro5 violations |
0
|
Druglikeness |
2,4681
|
DrugScore |
0,622183522667192
|
Mutagenic |
none
|
Tumorigenic |
none
|
Reproductive Effective |
none
|
Irritant |
none
|
Blood-Brain Barrier |
BBB+
|
Human Intestinal Absorption |
HIA+
|
Caco-2 Permeability |
Caco2+
|
P-glycoprotein Substrate |
Substrate
|
P-glycoprotein Inhibitor |
Inhibitor
|
P-glycoprotein Inhibitor 2 |
Inhibitor
|
Renal Organic Cation Transporter |
Inhibitor
|
Aqueous solubility |
-3,1812
|
Caco-2 Permeability 2 |
1,1577
|
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 |
Non-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 |
Strong inhibitor
|
Human Ether-a-go-go-Related Gene Inhibition 2 |
Inhibitor
|
AMES Toxicity |
Non AMES toxic
|
Carcinogens |
Non-carcinogens
|
Fish Toxicity |
High FHMT
|
Fish Toxicity (pLC50, mg/L) |
1,7599
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,8261
|
Honey Bee Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
2,6925
|
Carcinogenicity (Three-class) |
Non-required
|