Molecule Name |
DB13170
|
DrugBank Groups |
Approved
|
Cluster No |
1229
|
Smiles |
S1(SCC(N=C(O)CN=C(O)C(N=C(O)C2(N=C(O)C(N=C(C(N=C(C(N=C(C(N=C(C(C1)N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N=C(O)C(N)CC(O)=N)CC(=O)O)CCC(=O)O)CSSC2)CCC(=O)O)CC(C)C)O)C(C)C)O)CC(O)=N)O)C(C)C)O)C))C(O)C)C(O)=NC(C(=O)O)CC(C)C)
|
Download |
mol2, pdbqt
|
TPSA |
873,66
|
Non-H Atoms |
113
|
Non-C/H Atoms |
48
|
Metal-Atoms |
0
|
Electronegative Atoms |
48
|
Stereo Centers |
16
|
Rotatable Bonds |
28
|
Rings Closures |
2
|
Small Rings |
0
|
Aromatic Rings |
0
|
Aromatic Atoms |
0
|
sp3-Atoms |
71
|
Symmetric atoms |
4
|
cLogS |
-4,619
|
MW |
1681,9
|
cLogP |
-9,2126
|
HBA |
44
|
HBD |
25
|
Ro5 violations |
3
|
Druglikeness |
-3,175
|
DrugScore |
0,165806664330512
|
Mutagenic |
none
|
Tumorigenic |
none
|
Reproductive Effective |
low
|
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 |
-2,7998
|
Caco-2 Permeability 2 |
-0,4501
|
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) |
1,7053
|
Tetrahymena Pyriformis Toxicity |
High TPT
|
Tetrahymena Pyriformis Toxicity (pIGC50, ug/L) |
0,261
|
Honey Bee Toxicity |
Low HBT
|
Biodegradation |
Not ready biodegradable
|
Acute Oral Toxicity |
III
|
Rat Acute Toxicity (LD50, mol/kg) |
2,8424
|
Carcinogenicity (Three-class) |
Non-required
|