| Molecule Name |
DB02137
|
| DrugBank Groups |
Experimental
|
| Cluster No |
63
|
| Smiles |
[Mo]3(SC=4(C2(NC1(=C(O)N=C(N)N=C1NC2OC(C=4(S3))COP(=O)(OP(=O)(OCC6(OC(N5(C(=O)N=C(N)C=C5))C(C6O)O))O)O))))(=O)(O)([O-])
|
| Download |
mol2, pdbqt
|
| TPSA |
463,39
|
| Non-H Atoms |
48
|
| Non-C/H Atoms |
29
|
| Metal-Atoms |
1
|
| Electronegative Atoms |
28
|
| Stereo Centers |
9
|
| Rotatable Bonds |
9
|
| Rings Closures |
6
|
| Small Rings |
6
|
| Aromatic Rings |
1
|
| Aromatic Atoms |
6
|
| sp3-Atoms |
26
|
| Symmetric atoms |
0
|
| cLogS |
0,759
|
| MW |
844,475
|
| cLogP |
-7,1275
|
| HBA |
24
|
| HBD |
10
|
| Ro5 violations |
3
|
| Druglikeness |
-33,31
|
| DrugScore |
0,162267371793329
|
| Mutagenic |
low
|
| Tumorigenic |
low
|
| 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 |
-3,2677
|
| Caco-2 Permeability 2 |
-0,0462
|
| 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 |
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) |
1,3164
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,5465
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,6195
|
| Carcinogenicity (Three-class) |
Non-required
|
