| Molecule Name |
DB02931
|
| DrugBank Groups |
Experimental
|
| Cluster No |
63
|
| Smiles |
S(CC(O)=NCCC=2(C1(=C(C=CC=C1)NC=2)))CCN=C(O)CCN=C(O)C(O)C(COP(=O)(OP(=O)(OCC5(OC(N4(C3(=NC=NC(=C3N=C4)N)))C(C5OP(=O)(O)O)O))O)O)(C)C
|
| Download |
mol2, pdbqt
|
| TPSA |
658,42
|
| Non-H Atoms |
63
|
| Non-C/H Atoms |
30
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
30
|
| Stereo Centers |
7
|
| Rotatable Bonds |
24
|
| Rings Closures |
5
|
| Small Rings |
5
|
| Aromatic Rings |
4
|
| Aromatic Atoms |
18
|
| sp3-Atoms |
35
|
| Symmetric atoms |
2
|
| cLogS |
-1,452
|
| MW |
967,778
|
| cLogP |
-7,9871
|
| HBA |
26
|
| HBD |
11
|
| Ro5 violations |
3
|
| Druglikeness |
-29,279
|
| DrugScore |
0,24739879115005
|
| 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 |
Inhibitor
|
| P-glycoprotein Inhibitor 2 |
Non-inhibitor
|
| Renal Organic Cation Transporter |
Non-inhibitor
|
| Aqueous solubility |
-3,3214
|
| Caco-2 Permeability 2 |
-0,5304
|
| Subcellular localization |
Lysosome
|
| 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 |
Inhibitor
|
| AMES Toxicity |
Non AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity |
High FHMT
|
| Fish Toxicity (pLC50, mg/L) |
1,3883
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,5216
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,6287
|
| Carcinogenicity (Three-class) |
Non-required
|
