Molecule Name |
DB08432
|
DrugBank Groups |
Experimental
|
Cluster No |
48
|
Smiles |
S=P(OCC2(OC(N1(C(=O)NC(=O)C(=C1)C))CC2O))(O)O
|
Download |
mol2, pdbqt
|
TPSA |
223,53
|
Non-H Atoms |
21
|
Non-C/H Atoms |
11
|
Metal-Atoms |
0
|
Electronegative Atoms |
11
|
Stereo Centers |
3
|
Rotatable Bonds |
4
|
Rings Closures |
2
|
Small Rings |
2
|
Aromatic Rings |
0
|
Aromatic Atoms |
0
|
sp3-Atoms |
13
|
Symmetric atoms |
1
|
cLogS |
-1,372
|
MW |
338,276
|
cLogP |
-2,715
|
HBA |
9
|
HBD |
4
|
Ro5 violations |
0
|
Druglikeness |
-6,5331
|
DrugScore |
0,106700841443439
|
Mutagenic |
low
|
Tumorigenic |
high
|
Reproductive Effective |
low
|
Irritant |
high
|
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 |
-3,1808
|
Caco-2 Permeability 2 |
-0,1092
|
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) |
1,591
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,447
|
Honey Bee Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
2,4921
|
Carcinogenicity (Three-class) |
Non-required
|