Molecule Name |
DB00080
|
DrugBank Groups |
Approved
|
Cluster No |
3
|
Smiles |
O=C3(OC(C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)CCCCCCCCC)CC=2(C1(=C(C=CC=C1)NC=2)))CC(=O)N)CC(=O)O)C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C)C(NC(C(NCC(NC(C(NC(C(NC3CC(=O)C4(=C(N)C=CC=C4))=O)C(CC(=O)O)C)=O)CO)=O)=O)CC(=O)O)=O)CC(=O)O)CCCN)C)
|
Download |
mol2, pdbqt
|
TPSA |
702,02
|
Non-H Atoms |
115
|
Non-C/H Atoms |
43
|
Metal-Atoms |
0
|
Electronegative Atoms |
43
|
Stereo Centers |
13
|
Rotatable Bonds |
35
|
Rings Closures |
4
|
Small Rings |
3
|
Aromatic Rings |
3
|
Aromatic Atoms |
15
|
sp3-Atoms |
45
|
Symmetric atoms |
0
|
cLogS |
-6,255
|
MW |
1620,69
|
cLogP |
-9,499
|
HBA |
43
|
HBD |
22
|
Ro5 violations |
3
|
Druglikeness |
-17,937
|
DrugScore |
0,152729658839434
|
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 |
-3,6856
|
Caco-2 Permeability 2 |
-0,0041
|
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) |
1,2732
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,5111
|
Honey Bee Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
2,9781
|
Carcinogenicity (Three-class) |
Non-required
|