| Molecule Name |
DB04016
|
| DrugBank Groups |
Experimental
|
| Cluster No |
1268
|
| Smiles |
P(=O)(O)(O)C(C=1(C=2(C(C=CC=1)=CC=CC=2)))C(=O)C=6(C(C(=O)N(C5(CCN(C(=O)C4(=CC=3(C(=CC=CC=3)C=C4)))CC5))C)=CC7(=CC=CC=C7(C=6)))
|
| Download |
mol2, pdbqt
|
| TPSA |
485,7
|
| Non-H Atoms |
49
|
| Non-C/H Atoms |
9
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
9
|
| Stereo Centers |
1
|
| Rotatable Bonds |
7
|
| Rings Closures |
7
|
| Small Rings |
7
|
| Aromatic Rings |
6
|
| Aromatic Atoms |
30
|
| sp3-Atoms |
10
|
| Symmetric atoms |
3
|
| cLogS |
-8,371
|
| MW |
670,7
|
| cLogP |
4,8242
|
| HBA |
8
|
| HBD |
2
|
| Ro5 violations |
1
|
| Druglikeness |
-3,1706
|
| DrugScore |
6,93338036548376E-02
|
| Mutagenic |
none
|
| Tumorigenic |
high
|
| 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 |
-2,9427
|
| Caco-2 Permeability 2 |
0,0589
|
| 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 |
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 |
Inhibitor
|
| AMES Toxicity |
Non AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity |
Low FHMT
|
| Fish Toxicity (pLC50, mg/L) |
1,5933
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,5406
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,788
|
| Carcinogenicity (Three-class) |
Non-required
|
