Molecule Name |
DB08540
|
DrugBank Groups |
Experimental
|
Cluster No |
2641
|
Smiles |
S1(C4(=C(N=C(C1)N3(CCN(C=2(SC=C(N=2)C(=O)OCC))CC3))C=CC=C4))
|
Download |
mol2, pdbqt
|
TPSA |
284,35
|
Non-H Atoms |
26
|
Non-C/H Atoms |
8
|
Metal-Atoms |
0
|
Electronegative Atoms |
8
|
Stereo Centers |
0
|
Rotatable Bonds |
4
|
Rings Closures |
4
|
Small Rings |
4
|
Aromatic Rings |
2
|
Aromatic Atoms |
11
|
sp3-Atoms |
9
|
Symmetric atoms |
2
|
cLogS |
-3,545
|
MW |
388,515
|
cLogP |
1,9579
|
HBA |
6
|
HBD |
0
|
Ro5 violations |
0
|
Druglikeness |
2,3795
|
DrugScore |
0,759207228234755
|
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 |
-4,1359
|
Caco-2 Permeability 2 |
0,7963
|
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 |
Non-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 |
Inhibitor
|
AMES Toxicity |
Non AMES toxic
|
Carcinogens |
Non-carcinogens
|
Fish Toxicity |
High FHMT
|
Fish Toxicity (pLC50, mg/L) |
1,3412
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,8488
|
Honey Bee Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
2,5237
|
Carcinogenicity (Three-class) |
Non-required
|