| Molecule Name |
DB03157
|
| DrugBank Groups |
Experimental
|
| Cluster No |
925
|
| Smiles |
S(=O)(=O)(OC3(=CC=C(CC(NS(=O)(=O)C=2(C=1(C(=C(N(C)C)C=CC=1)C=CC=2)))C(=O)O)C=C3))C=5(C=4(C(=C(N(C)C)C=CC=4)C=CC=5))
|
| Download |
mol2, pdbqt
|
| TPSA |
460,6
|
| Non-H Atoms |
45
|
| Non-C/H Atoms |
12
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
12
|
| Stereo Centers |
1
|
| Rotatable Bonds |
10
|
| Rings Closures |
5
|
| Small Rings |
5
|
| Aromatic Rings |
5
|
| Aromatic Atoms |
26
|
| sp3-Atoms |
12
|
| Symmetric atoms |
6
|
| cLogS |
-6,515
|
| MW |
647,771
|
| cLogP |
4,7767
|
| HBA |
10
|
| HBD |
2
|
| Ro5 violations |
1
|
| Druglikeness |
-4,9817
|
| DrugScore |
4,76257669511425E-02
|
| Mutagenic |
high
|
| Tumorigenic |
high
|
| Reproductive Effective |
none
|
| Irritant |
none
|
| Blood-Brain Barrier |
BBB+
|
| Human Intestinal Absorption |
HIA+
|
| Caco-2 Permeability |
Caco2-
|
| P-glycoprotein Substrate |
Non-substrate
|
| P-glycoprotein Inhibitor |
Non-inhibitor
|
| P-glycoprotein Inhibitor 2 |
Non-inhibitor
|
| Renal Organic Cation Transporter |
Non-inhibitor
|
| Aqueous solubility |
-3,6949
|
| Caco-2 Permeability 2 |
-0,0138
|
| Subcellular localization |
Lysosome
|
| CYP450 2C9 Substrate |
Non-substrate
|
| CYP450 2D6 Substrate |
Non-substrate
|
| CYP450 3A4 Substrate |
Non-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 |
Carcinogens
|
| Fish Toxicity |
High FHMT
|
| Fish Toxicity (pLC50, mg/L) |
1,2483
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,159
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,5109
|
| Carcinogenicity (Three-class) |
Non-required
|
