Molecule Name |
DB11256
|
DrugBank Groups |
Approved
|
Cluster No |
6
|
Smiles |
O=C1(N=C(NC2(=C1N(C(CN2)CNC3(=CC=C(C(=O)NC(C(=O)O)CCC(=O)O)C=C3))C))N)
|
Download |
mol2, pdbqt
|
TPSA |
198,48
|
Non-H Atoms |
33
|
Non-C/H Atoms |
13
|
Metal-Atoms |
0
|
Electronegative Atoms |
13
|
Stereo Centers |
2
|
Rotatable Bonds |
9
|
Rings Closures |
3
|
Small Rings |
3
|
Aromatic Rings |
1
|
Aromatic Atoms |
6
|
sp3-Atoms |
10
|
Symmetric atoms |
2
|
cLogS |
-3,625
|
MW |
459,461
|
cLogP |
-2,8245
|
HBA |
13
|
HBD |
7
|
Ro5 violations |
2
|
Druglikeness |
-6,5502
|
DrugScore |
0,364416480865935
|
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 |
-3,0736
|
Caco-2 Permeability 2 |
-1,0407
|
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) |
1,6198
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,3156
|
Honey Bee Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
2,6188
|
Carcinogenicity (Three-class) |
Non-required
|