Molecule Name |
DB00143
|
DrugBank Groups |
Approved
|
Cluster No |
27
|
Smiles |
SCC(NC(=O)CCC(N)C(=O)O)C(=O)NCC(=O)O
|
Download |
mol2, pdbqt
|
TPSA |
197,62
|
Non-H Atoms |
20
|
Non-C/H Atoms |
10
|
Metal-Atoms |
0
|
Electronegative Atoms |
10
|
Stereo Centers |
2
|
Rotatable Bonds |
9
|
Rings Closures |
0
|
Small Rings |
0
|
Aromatic Rings |
0
|
Aromatic Atoms |
0
|
sp3-Atoms |
10
|
Symmetric atoms |
0
|
cLogS |
-0,99
|
MW |
307,326
|
cLogP |
-4,8991
|
HBA |
9
|
HBD |
5
|
Ro5 violations |
0
|
Druglikeness |
-23,224
|
DrugScore |
0,47320446911557
|
Mutagenic |
none
|
Tumorigenic |
none
|
Reproductive Effective |
none
|
Irritant |
none
|
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 |
-1,7442
|
Caco-2 Permeability 2 |
-0,402
|
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 |
AMES toxic
|
Carcinogens |
Non-carcinogens
|
Fish Toxicity |
Low FHMT
|
Fish Toxicity (pLC50, mg/L) |
2,4477
|
Tetrahymena Pyriformis Toxicity |
Low TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
-0,4198
|
Honey Bee Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
1,7842
|
Carcinogenicity (Three-class) |
Non-required
|