| Molecule Name |
DB01590
|
| DrugBank Groups |
Approved
|
| Cluster No |
154
|
| Smiles |
O=C2(N4(C(C(=O)OC(C(CC1(CC(OC)C(OCCO)CC1))C)CC(=O)C(C=C(C(O)C(OC)C(=O)C(C)CC(C=CC=CC=C(C(CC3(OC(C2=O)(O)C(CC3)C))OC)C)C)C)C)CCCC4))
|
| Download |
mol2, pdbqt
|
| TPSA |
204,66
|
| Non-H Atoms |
68
|
| Non-C/H Atoms |
15
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
15
|
| Stereo Centers |
15
|
| Rotatable Bonds |
9
|
| Rings Closures |
4
|
| Small Rings |
3
|
| Aromatic Rings |
0
|
| Aromatic Atoms |
0
|
| sp3-Atoms |
49
|
| Symmetric atoms |
0
|
| cLogS |
-6,634
|
| MW |
958,235
|
| cLogP |
6,4181
|
| HBA |
15
|
| HBD |
3
|
| Ro5 violations |
3
|
| Druglikeness |
1,9808
|
| DrugScore |
0,163891943448478
|
| 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 |
Inhibitor
|
| Renal Organic Cation Transporter |
Non-inhibitor
|
| Aqueous solubility |
-2,678
|
| Caco-2 Permeability 2 |
0,3973
|
| 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 |
Low FHMT
|
| Fish Toxicity (pLC50, mg/L) |
1,4631
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,4933
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,7442
|
| Carcinogenicity (Three-class) |
Danger
|
