Molecule Name |
DB09338
|
DrugBank Groups |
Approved
|
Cluster No |
1176
|
Smiles |
[Hg](O)CC(OC)CNC(=O)C1(=C(OCC(=O)O)C=CC=C1)
|
Download |
mol2, pdbqt
|
TPSA |
105,09
|
Non-H Atoms |
21
|
Non-C/H Atoms |
8
|
Metal-Atoms |
1
|
Electronegative Atoms |
7
|
Stereo Centers |
1
|
Rotatable Bonds |
9
|
Rings Closures |
1
|
Small Rings |
1
|
Aromatic Rings |
1
|
Aromatic Atoms |
6
|
sp3-Atoms |
9
|
Symmetric atoms |
0
|
cLogS |
-2,47
|
MW |
483,869
|
cLogP |
0,3963
|
HBA |
7
|
HBD |
3
|
Ro5 violations |
0
|
Druglikeness |
2,8383
|
DrugScore |
0,295468380411584
|
Mutagenic |
low
|
Tumorigenic |
low
|
Reproductive Effective |
low
|
Irritant |
low
|
Blood-Brain Barrier |
BBB-
|
Human Intestinal Absorption |
HIA+
|
Caco-2 Permeability |
Caco2-
|
P-glycoprotein Substrate |
Non-substrate
|
P-glycoprotein Inhibitor |
Non-inhibitor
|
P-glycoprotein Inhibitor 2 |
Non-inhibitor
|
Renal Organic Cation Transporter |
Non-inhibitor
|
Aqueous solubility |
-1,8838
|
Caco-2 Permeability 2 |
0,0785
|
Subcellular localization |
Mitochondria
|
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 |
Non-inhibitor
|
AMES Toxicity |
Non AMES toxic
|
Carcinogens |
Non-carcinogens
|
Fish Toxicity |
High FHMT
|
Fish Toxicity (pLC50, mg/L) |
1,6256
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
-0,2883
|
Honey Bee Toxicity |
Low HBT
|
Biodegradation |
Ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
2,1682
|
Carcinogenicity (Three-class) |
Non-required
|