| Molecule Name |
DB00602
|
| DrugBank Groups |
Approved
|
| Cluster No |
52
|
| Smiles |
O=C5(OC2(CC1(OC(C(C)CC1)C(CC)C)(OC(C2)CC=C(C(OC4(OC(C(OC3(OC(C(O)C(C3)OC)C))C(C4)OC)C))C(C=CC=C7(C6(C5C=C(C(O)C6OC7)C)(O)))C)C)))
|
| Download |
mol2, pdbqt
|
| TPSA |
170,06
|
| Non-H Atoms |
62
|
| Non-C/H Atoms |
14
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
14
|
| Stereo Centers |
20
|
| Rotatable Bonds |
8
|
| Rings Closures |
7
|
| Small Rings |
6
|
| Aromatic Rings |
0
|
| Aromatic Atoms |
0
|
| sp3-Atoms |
52
|
| Symmetric atoms |
0
|
| cLogS |
-6,61
|
| MW |
875,102
|
| cLogP |
5,41
|
| HBA |
14
|
| HBD |
3
|
| Ro5 violations |
3
|
| Druglikeness |
5,2314
|
| DrugScore |
0,205684601362493
|
| 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 |
-4,2367
|
| Caco-2 Permeability 2 |
0,5354
|
| 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) |
0,5638
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
1,1327
|
| Honey Bee Toxicity |
High HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
3,513
|
| Carcinogenicity (Three-class) |
Non-required
|
