Molecule Name |
DB00153
|
DrugBank Groups |
Approved
|
Cluster No |
22
|
Smiles |
OC1(CC(C(=C)CC1)=CC=C3(C2(C(C(C(C=CC(C(C)C)C)C)CC2)(CCC3)C)))
|
Download |
mol2, pdbqt
|
TPSA |
20,23
|
Non-H Atoms |
29
|
Non-C/H Atoms |
1
|
Metal-Atoms |
0
|
Electronegative Atoms |
1
|
Stereo Centers |
6
|
Rotatable Bonds |
5
|
Rings Closures |
3
|
Small Rings |
3
|
Aromatic Rings |
0
|
Aromatic Atoms |
0
|
sp3-Atoms |
21
|
Symmetric atoms |
1
|
cLogS |
-5,927
|
MW |
396,656
|
cLogP |
7,6423
|
HBA |
1
|
HBD |
1
|
Ro5 violations |
1
|
Druglikeness |
-5,8133
|
DrugScore |
0,121887015434529
|
Mutagenic |
none
|
Tumorigenic |
none
|
Reproductive Effective |
low
|
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 |
Non-inhibitor
|
Renal Organic Cation Transporter |
Non-inhibitor
|
Aqueous solubility |
-4,5363
|
Caco-2 Permeability 2 |
1,635
|
Subcellular localization |
Lysosome
|
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
|
Human Ether-a-go-go-Related Gene Inhibition |
Weak inhibitor
|
Human Ether-a-go-go-Related Gene Inhibition 2 |
Non-inhibitor
|
AMES Toxicity |
Non AMES toxic
|
Carcinogens |
Non-carcinogens
|
Fish Toxicity |
High FHMT
|
Fish Toxicity (pLC50, mg/L) |
-0,1791
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,9458
|
Honey Bee Toxicity |
High HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
I
|
Rat Acute Toxicity (LD50, mol/kg) |
3,6931
|
Carcinogenicity (Three-class) |
Non-required
|