| Molecule Name |
DB02702
|
| DrugBank Groups |
Experimental
|
| Cluster No |
376
|
| Smiles |
S1(C(=NC=C1)NC(=O)C2(=CC(=CC=C2)CN4(C(=O)N(C(CC3(=CC=CC=C3))C(C(C4CC5(=CC=CC=C5))O)O)CC7(=CC(C(=O)NC=6(SC=CN=6))=CC=C7))))
|
| Download |
mol2, pdbqt
|
| TPSA |
562,47
|
| Non-H Atoms |
54
|
| Non-C/H Atoms |
13
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
13
|
| Stereo Centers |
4
|
| Rotatable Bonds |
12
|
| Rings Closures |
7
|
| Small Rings |
7
|
| Aromatic Rings |
6
|
| Aromatic Atoms |
34
|
| sp3-Atoms |
10
|
| Symmetric atoms |
28
|
| cLogS |
-7,956
|
| MW |
758,922
|
| cLogP |
6,8511
|
| HBA |
11
|
| HBD |
4
|
| Ro5 violations |
3
|
| Druglikeness |
5,0515
|
| DrugScore |
0,154874048613821
|
| 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 |
-3,2898
|
| Caco-2 Permeability 2 |
0,9138
|
| 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 |
Non-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 |
Inhibitor
|
| AMES Toxicity |
Non AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity |
High FHMT
|
| Fish Toxicity (pLC50, mg/L) |
1,5968
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,343
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,2455
|
| Carcinogenicity (Three-class) |
Non-required
|
