| Molecule Name |
DB03021
|
| DrugBank Groups |
Experimental
|
| Cluster No |
861
|
| Smiles |
O=C2(OC(C(C(OC)CC=CC=1(OC=C(N=1)C=4(OC=C(C3(=NC(C(CC(CCCC(C2)O)=O)C)=CO3))N=4)))C)CC(OC)C(CCC(=O)C(C(OC(=O)C)C(C=CN(CO)C)C)C)C)
|
| Download |
mol2, pdbqt
|
| TPSA |
704,57
|
| Non-H Atoms |
63
|
| Non-C/H Atoms |
17
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
17
|
| Stereo Centers |
10
|
| Rotatable Bonds |
16
|
| Rings Closures |
4
|
| Small Rings |
3
|
| Aromatic Rings |
3
|
| Aromatic Atoms |
15
|
| sp3-Atoms |
36
|
| Symmetric atoms |
0
|
| cLogS |
-8,634
|
| MW |
883,045
|
| cLogP |
5,6604
|
| HBA |
17
|
| HBD |
2
|
| Ro5 violations |
3
|
| Druglikeness |
-3,0547
|
| DrugScore |
1,17563255781075E-02
|
| Mutagenic |
high
|
| Tumorigenic |
high
|
| Reproductive Effective |
high
|
| Irritant |
high
|
| 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 |
-2,73
|
| Caco-2 Permeability 2 |
0,5683
|
| 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) |
1,3787
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,5584
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,5326
|
| Carcinogenicity (Three-class) |
Non-required
|
