| Molecule Name |
DB03481
|
| DrugBank Groups |
Experimental
|
| Cluster No |
1060
|
| Smiles |
P(=O)(OC(C(=O)O)CCC(=O)O)(OCC5(OC(OCC(O)C(O)C(O)CC4(=CC=C(N1(C(C2(C(NC3(=C(N2(C1))C(=O)NC(=N3)N))C))C))C=C4))C(C5O)O))O
|
| Download |
mol2, pdbqt
|
| TPSA |
529,59
|
| Non-H Atoms |
54
|
| Non-C/H Atoms |
23
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
23
|
| Stereo Centers |
12
|
| Rotatable Bonds |
17
|
| Rings Closures |
5
|
| Small Rings |
5
|
| Aromatic Rings |
1
|
| Aromatic Atoms |
6
|
| sp3-Atoms |
33
|
| Symmetric atoms |
2
|
| cLogS |
-3,44
|
| MW |
788,698
|
| cLogP |
-6,2299
|
| HBA |
22
|
| HBD |
11
|
| Ro5 violations |
3
|
| Druglikeness |
-34,965
|
| DrugScore |
0,235219741069896
|
| 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 |
-3,4451
|
| Caco-2 Permeability 2 |
-0,5705
|
| 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 |
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 |
High FHMT
|
| Fish Toxicity (pLC50, mg/L) |
1,3413
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,5247
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,7478
|
| Carcinogenicity (Three-class) |
Non-required
|
