| Molecule Name |
DB00104
|
| DrugBank Groups |
Approved
|
| Cluster No |
3
|
| Smiles |
S1(SCC(NC(=O)C(NC(=O)C(NC(C(NC(C(NC(C(C1)NC(=O)C(N)CC2(=CC=CC=C2))=O)CC3(=CC=CC=C3))=O)CC=5(C4(=C(C=CC=C4)NC=5)))=O)CCCCN)C(O)C)C(=O)NC(C(O)C)CO)
|
| Download |
mol2, pdbqt
|
| TPSA |
382,82
|
| Non-H Atoms |
71
|
| Non-C/H Atoms |
22
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
22
|
| Stereo Centers |
10
|
| Rotatable Bonds |
17
|
| Rings Closures |
5
|
| Small Rings |
4
|
| Aromatic Rings |
4
|
| Aromatic Atoms |
21
|
| sp3-Atoms |
29
|
| Symmetric atoms |
4
|
| cLogS |
-6,34
|
| MW |
1019,26
|
| cLogP |
-1,1103
|
| HBA |
20
|
| HBD |
13
|
| Ro5 violations |
3
|
| Druglikeness |
-2,2022
|
| DrugScore |
0,16610686511802
|
| 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 |
-2,9345
|
| Caco-2 Permeability 2 |
-0,1668
|
| Subcellular localization |
Nucleus
|
| CYP450 2C9 Substrate |
Non-substrate
|
| CYP450 2D6 Substrate |
Non-substrate
|
| CYP450 3A4 Substrate |
Non-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 |
Inhibitor
|
| AMES Toxicity |
Non AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity |
High FHMT
|
| Fish Toxicity (pLC50, mg/L) |
1,5438
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,3483
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,6174
|
| Carcinogenicity (Three-class) |
Non-required
|
