| Molecule Name |
DB02860
|
| DrugBank Groups |
Experimental
|
| Cluster No |
781
|
| Smiles |
P(=O)(OC3(C(C1(OC(C(C)C(C1)O)CC=CC=2(N=C(C(CCNC(=O)C(O)C(O)C(N(C)C)COC)C)OC=2))(OC3C(OC)CC(O)C(C(O)C(C=C(C(=CC=CC(=CC#N)C)C)C)C)C))(C)C))(O)O
|
| Download |
mol2, pdbqt
|
| TPSA |
779,04
|
| Non-H Atoms |
70
|
| Non-C/H Atoms |
20
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
20
|
| Stereo Centers |
15
|
| Rotatable Bonds |
26
|
| Rings Closures |
3
|
| Small Rings |
3
|
| Aromatic Rings |
1
|
| Aromatic Atoms |
5
|
| sp3-Atoms |
49
|
| Symmetric atoms |
3
|
| cLogS |
-3,689
|
| MW |
1009,18
|
| cLogP |
0,3674
|
| HBA |
19
|
| HBD |
8
|
| Ro5 violations |
3
|
| Druglikeness |
-19,475
|
| DrugScore |
0,13372566288476
|
| Mutagenic |
none
|
| Tumorigenic |
none
|
| Reproductive Effective |
none
|
| 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 |
Non-inhibitor
|
| Renal Organic Cation Transporter |
Non-inhibitor
|
| Aqueous solubility |
-2,6269
|
| Caco-2 Permeability 2 |
-0,6107
|
| 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) |
1,275
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,4609
|
| Honey Bee Toxicity |
High HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,7759
|
| Carcinogenicity (Three-class) |
Non-required
|
