| Molecule Name |
DB04330
|
| DrugBank Groups |
Experimental
|
| Cluster No |
1393
|
| Smiles |
ClC1(=C(Cl)C=CC(=C1)C4(OC2(C(=O)C=3(C=C(C)C=CC=3(C2=O)))(C(C4C(=O)NC6(=CC=C(C=5(N=NSC=5))C=C6))C(=O)O)))
|
| Download |
mol2, pdbqt
|
| TPSA |
408,82
|
| Non-H Atoms |
41
|
| Non-C/H Atoms |
12
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
12
|
| Stereo Centers |
4
|
| Rotatable Bonds |
5
|
| Rings Closures |
6
|
| Small Rings |
6
|
| Aromatic Rings |
4
|
| Aromatic Atoms |
23
|
| sp3-Atoms |
7
|
| Symmetric atoms |
2
|
| cLogS |
-8,118
|
| MW |
608,457
|
| cLogP |
4,6238
|
| HBA |
9
|
| HBD |
2
|
| Ro5 violations |
1
|
| Druglikeness |
-0,88769
|
| DrugScore |
5,85761272332843E-02
|
| Mutagenic |
none
|
| Tumorigenic |
high
|
| Reproductive Effective |
high
|
| 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 |
-4,3386
|
| Caco-2 Permeability 2 |
0,8042
|
| 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 |
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 |
Non-inhibitor
|
| AMES Toxicity |
Non AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity |
High FHMT
|
| Fish Toxicity (pLC50, mg/L) |
1,2274
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,8005
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,4133
|
| Carcinogenicity (Three-class) |
Non-required
|
