| Molecule Name |
DB09027
|
| DrugBank Groups |
Approved
|
| Cluster No |
1068
|
| Smiles |
FC6(F)(C1(=C(C=CC(=C1)C5(=CC=4(NC(C2(N(C(=O)C(N=C(OC)O)C(C)C)C3(CCC2C3)))=NC=4C=C5)))C%10(=C6C=C(C=9(NC(C7(N(C(=O)C(N=C(OC)O)C(C)C)CC8(C7)(CC8)))=NC=9))C=C%10)))
|
| Download |
mol2, pdbqt
|
| TPSA |
181,62
|
| Non-H Atoms |
65
|
| Non-C/H Atoms |
16
|
| Metal-Atoms |
0
|
| Electronegative Atoms |
16
|
| Stereo Centers |
6
|
| Rotatable Bonds |
12
|
| Rings Closures |
10
|
| Small Rings |
11
|
| Aromatic Rings |
5
|
| Aromatic Atoms |
26
|
| sp3-Atoms |
27
|
| Symmetric atoms |
4
|
| cLogS |
-9,555
|
| MW |
889,014
|
| cLogP |
7,914
|
| HBA |
14
|
| HBD |
4
|
| Ro5 violations |
3
|
| Druglikeness |
0,32198
|
| DrugScore |
0,038115212197712
|
| Mutagenic |
high
|
| Tumorigenic |
high
|
| 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 |
-3,7058
|
| Caco-2 Permeability 2 |
0,259
|
| 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 |
Inhibitor
|
| CYP450 2D6 Inhibitor |
Non-inhibitor
|
| CYP450 2C19 Inhibitor |
Inhibitor
|
| CYP450 3A4 Inhibitor |
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) |
1,2053
|
| Tetrahymena Pyriformis Toxicity |
High TPT
|
| Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,658
|
| Honey Bee Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity (LD50, mol/kg) |
2,7234
|
| Carcinogenicity (Three-class) |
Non-required
|
