Molecule Name |
DB08906
|
DrugBank Groups |
Approved
|
Cluster No |
52
|
Smiles |
S(C(=O)C5(OC(=O)C=1(OC=CC=1))(C4(C(C3(C(F)(C2(C(=CC(=O)C=C2)C(C3)F)(C))C(C4)O))CC5C)(C)))CF
|
Download |
mol2, pdbqt
|
TPSA |
119,11
|
Non-H Atoms |
37
|
Non-C/H Atoms |
10
|
Metal-Atoms |
0
|
Electronegative Atoms |
10
|
Stereo Centers |
9
|
Rotatable Bonds |
6
|
Rings Closures |
5
|
Small Rings |
5
|
Aromatic Rings |
1
|
Aromatic Atoms |
5
|
sp3-Atoms |
19
|
Symmetric atoms |
0
|
cLogS |
-5,68
|
MW |
538,581
|
cLogP |
2,9108
|
HBA |
6
|
HBD |
1
|
Ro5 violations |
1
|
Druglikeness |
3,3239
|
DrugScore |
0,429996918161359
|
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 |
Non-inhibitor
|
Aqueous solubility |
-5,1846
|
Caco-2 Permeability 2 |
0,9063
|
Subcellular localization |
Mitochondria
|
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 |
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) |
0,0402
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
1,2407
|
Honey Bee Toxicity |
High HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
2,6232
|
Carcinogenicity (Three-class) |
Non-required
|