| Molecule Name |
DB01229
|
| DrugBank Groups |
Approved
|
| Cluster No |
722
|
| Smiles |
O=C4(C2(C(C1(OC(=O)C)(C(OC1)CC2O))C(OC(=O)C3(=CC=CC=C3))C5(O)(CC(C(=C(C4OC(=O)C)C5(C)(C))C)OC(=O)C(O)C(NC(=O)C6(=CC=CC=C6))C7(=CC=CC=C7)))(C))
|
| Download |
mol2, pdbqt
|
| TPSA |
221,29
|
| Non-H Atoms |
62
|
| Non-C/H Atoms |
15
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
15
|
| Stereo Centers |
11
|
| Rotatable Bonds |
14
|
| Rings Closures |
7
|
| Small Rings |
6
|
| Aromatic Rings |
3
|
| Aromatic Atoms |
18
|
| sp3-Atoms |
29
|
| Symmetric atoms |
7
|
| cLogS |
-6,289
|
| MW |
853,915
|
| cLogP |
3,188
|
| HBA |
15
|
| HBD |
4
|
| Ro5 violations |
2
|
| Druglikeness |
0,82049
|
| DrugScore |
0,242843031569427
|
| 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 |
-3,8728
|
| Caco-2 Permeability 2 |
0,4145
|
| 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 |
High FHMT
|
| Fish Toxicity (pLC50, mg/L) |
0,6419
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,6557
|
| Honey Bee Toxicity |
High HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,4391
|
| Carcinogenicity (Three-class) |
Non-required
|
