| Molecule Name |
DB02169
|
| DrugBank Groups |
Experimental
|
| Cluster No |
154
|
| Smiles |
O=C(O)C(O)(CC7(OC6(OC(C(C=CC5(OC4(OC3(C(O)C(=C)C(C(O)CC(C2(OC1(OCCCC1)(CCC2C)))C)OC3CC4))(CC5)))C)CC(=C6)C)(C(O)CC7)))C
|
| Download |
mol2, pdbqt
|
| TPSA |
584,3
|
| Non-H Atoms |
57
|
| Non-C/H Atoms |
13
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
13
|
| Stereo Centers |
17
|
| Rotatable Bonds |
10
|
| Rings Closures |
7
|
| Small Rings |
7
|
| Aromatic Rings |
0
|
| Aromatic Atoms |
0
|
| sp3-Atoms |
49
|
| Symmetric atoms |
0
|
| cLogS |
-6,822
|
| MW |
805,011
|
| cLogP |
3,6988
|
| HBA |
13
|
| HBD |
5
|
| Ro5 violations |
2
|
| Druglikeness |
-4,9408
|
| DrugScore |
0,131280215146179
|
| 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 |
Non-inhibitor
|
| P-glycoprotein Inhibitor 2 |
Non-inhibitor
|
| Renal Organic Cation Transporter |
Non-inhibitor
|
| Aqueous solubility |
-4,5472
|
| Caco-2 Permeability 2 |
0,313
|
| 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) |
0,5143
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,9784
|
| Honey Bee Toxicity |
High HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
I
|
| Rat Acute Toxicity (LD50, mol/kg) |
3,626
|
| Carcinogenicity (Three-class) |
Non-required
|
