Molecule Name |
DB09009
|
DrugBank Groups |
Approved
|
Cluster No |
1058
|
Smiles |
S1(C(=C(N=C(O)C(NCCC)C)C(=C1)C)C(=O)OC)
|
Download |
mol2, pdbqt
|
TPSA |
99,16
|
Non-H Atoms |
19
|
Non-C/H Atoms |
6
|
Metal-Atoms |
0
|
Electronegative Atoms |
6
|
Stereo Centers |
1
|
Rotatable Bonds |
7
|
Rings Closures |
1
|
Small Rings |
1
|
Aromatic Rings |
1
|
Aromatic Atoms |
5
|
sp3-Atoms |
10
|
Symmetric atoms |
0
|
cLogS |
-2,605
|
MW |
284,379
|
cLogP |
1,5119
|
HBA |
5
|
HBD |
2
|
Ro5 violations |
0
|
Druglikeness |
3,3707
|
DrugScore |
0,895865114021681
|
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 |
-2,8734
|
Caco-2 Permeability 2 |
0,4794
|
Subcellular localization |
Mitochondria
|
CYP450 2C9 Substrate |
Non-substrate
|
CYP450 2D6 Substrate |
Non-substrate
|
CYP450 3A4 Substrate |
Non-substrate
|
CYP450 1A2 Inhibitor |
Inhibitor
|
CYP450 2C9 Inhibitor |
Non-inhibitor
|
CYP450 2D6 Inhibitor |
Non-inhibitor
|
CYP450 2C19 Inhibitor |
Non-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 |
Non-inhibitor
|
AMES Toxicity |
Non AMES toxic
|
Carcinogens |
Non-carcinogens
|
Fish Toxicity |
High FHMT
|
Fish Toxicity (pLC50, mg/L) |
1,475
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,4265
|
Honey Bee Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
2,5174
|
Carcinogenicity (Three-class) |
Non-required
|