| Molecule Name |
DB02524
|
| DrugBank Groups |
Experimental
|
| Cluster No |
63
|
| Smiles |
P(=O)(OP(=O)(OCC3(OC(N2(C1(=NC=NC(=C1N=C2)N)))C5(C3OC4(C([N+](=O)[O-])=CC(=[N+](O)[OH-])C=C4[N+](=O)[O-])(O5))))O)(OP(=O)(O)O)O
|
| Download |
mol2, pdbqt
|
| TPSA |
424,19
|
| Non-H Atoms |
46
|
| Non-C/H Atoms |
30
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
30
|
| Stereo Centers |
6
|
| Rotatable Bonds |
10
|
| Rings Closures |
5
|
| Small Rings |
5
|
| Aromatic Rings |
2
|
| Aromatic Atoms |
9
|
| sp3-Atoms |
23
|
| Symmetric atoms |
6
|
| cLogS |
-0,289
|
| MW |
719,278
|
| cLogP |
-11,814
|
| HBA |
27
|
| HBD |
7
|
| Ro5 violations |
3
|
| Druglikeness |
-31,052
|
| DrugScore |
0,265597888882022
|
| Mutagenic |
none
|
| Tumorigenic |
none
|
| Reproductive Effective |
none
|
| 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 |
-3,4005
|
| Caco-2 Permeability 2 |
-0,4846
|
| Subcellular localization |
Plasma membrane
|
| 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 |
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 |
AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity |
High FHMT
|
| Fish Toxicity (pLC50, mg/L) |
1,2812
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,6296
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,6379
|
| Carcinogenicity (Three-class) |
Non-required
|
