| Molecule Name |
DB01934
|
| DrugBank Groups |
Experimental
|
| Cluster No |
257
|
| Smiles |
O=C(O)C1(N=C(O)C(N=C(O)C(N(C(=O)CN=C(O)C(N=C(O)C(N(C(=O)CCCCCCCCC(C)C)C)CO)C)C)C=3(C=CC(=C(C=2(C=C(C1)C=CC=2O))C=3)O))C)
|
| Download |
mol2, pdbqt
|
| TPSA |
635,97
|
| Non-H Atoms |
59
|
| Non-C/H Atoms |
17
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
17
|
| Stereo Centers |
5
|
| Rotatable Bonds |
18
|
| Rings Closures |
3
|
| Small Rings |
2
|
| Aromatic Rings |
2
|
| Aromatic Atoms |
12
|
| sp3-Atoms |
31
|
| Symmetric atoms |
1
|
| cLogS |
-4,825
|
| MW |
824,969
|
| cLogP |
2,2939
|
| HBA |
17
|
| HBD |
8
|
| Ro5 violations |
3
|
| Druglikeness |
-7,0097
|
| DrugScore |
0,190795745152946
|
| 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 |
Inhibitor
|
| Renal Organic Cation Transporter |
Non-inhibitor
|
| Aqueous solubility |
-3,3959
|
| Caco-2 Permeability 2 |
0,3345
|
| 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 |
Non-inhibitor
|
| AMES Toxicity |
Non AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity |
High FHMT
|
| Fish Toxicity (pLC50, mg/L) |
1,2536
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,5811
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,6334
|
| Carcinogenicity (Three-class) |
Non-required
|
