Molecule Name |
DB08893
|
DrugBank Groups |
Approved
|
Cluster No |
1009
|
Smiles |
S1(C(=NC(=C1)CC(=O)NC3(=CC=C(CCNCC(O)C2(=CC=CC=C2))C=C3))N)
|
Download |
mol2, pdbqt
|
TPSA |
128,51
|
Non-H Atoms |
28
|
Non-C/H Atoms |
7
|
Metal-Atoms |
0
|
Electronegative Atoms |
7
|
Stereo Centers |
1
|
Rotatable Bonds |
9
|
Rings Closures |
3
|
Small Rings |
3
|
Aromatic Rings |
3
|
Aromatic Atoms |
17
|
sp3-Atoms |
7
|
Symmetric atoms |
4
|
cLogS |
-3,801
|
MW |
396,514
|
cLogP |
2,3718
|
HBA |
6
|
HBD |
4
|
Ro5 violations |
0
|
Druglikeness |
6,0413
|
DrugScore |
0,757757815646674
|
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 |
Non-inhibitor
|
P-glycoprotein Inhibitor 2 |
Non-inhibitor
|
Renal Organic Cation Transporter |
Non-inhibitor
|
Aqueous solubility |
-2,5858
|
Caco-2 Permeability 2 |
0,8344
|
Subcellular localization |
Mitochondria
|
CYP450 2C9 Substrate |
Non-substrate
|
CYP450 2D6 Substrate |
Non-substrate
|
CYP450 3A4 Substrate |
Non-substrate
|
CYP450 1A2 Inhibitor |
Non-inhibitor
|
CYP450 2C9 Inhibitor |
Inhibitor
|
CYP450 2D6 Inhibitor |
Non-inhibitor
|
CYP450 2C19 Inhibitor |
Non-inhibitor
|
CYP450 3A4 Inhibitor |
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) |
1,9153
|
Tetrahymena Pyriformis Toxicity |
Low TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,1716
|
Honey Bee Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
2,4527
|
Carcinogenicity (Three-class) |
Non-required
|