| PUBCHEM ID |
71587148
|
| UNII |
41G0335UA0
|
| Preferred Term |
VIOMYCIN TRIHYDROCHLORIDE
|
| CAS |
39750-31-7
|
| INCHIKEY |
AVXDCWXBRLUSCG-JJEOMLORSA-N
|
| Download |
mol2, pdbqt
|
| mol2 |
|
| Smiles |
NCCC[C@@H](CC(N[C@@H](CNC([C@H]([C@@H](C1)NC(N)=N[C@H]1O)NC(/C(/NC([C@H](CO)NC([C@H](CO)N1)=O)=O)=C/NC(N)=O)=O)=O)C1=O)=O)N
|
| Total Surface Area |
500,82
|
| Relative PSA |
0,58873
|
| TPSA |
392,86
|
| cLogS |
-1,312
|
| MW |
685,697
|
| cLogP |
-9,1132
|
| H-Acceptors |
23
|
| H-Donors |
15
|
| Ro5 violations |
3
|
| Druglikeness |
5,7625
|
| DrugScore |
0,541070655994916
|
| Mutagenic |
none
|
| Tumorigenic |
none
|
| Reproductive Effective |
none
|
| Irritant |
none
|
| Blood-Brain Barrier |
BBB-
|
| Human Intestinal Absorption |
HIA+
|
| Caco-2 Permeability I |
Caco2-
|
| Caco-2 Permeability II |
-0,3457
|
| P-glycoprotein Substrate |
Substrate
|
| P-glycoprotein Inhibitor I |
Non-inhibitor
|
| P-glycoprotein Inhibitor II |
Non-inhibitor
|
| Renal Organic Cation Transporter |
Non-inhibitor
|
| 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 I |
Weak inhibitor
|
| Human Ether-a-go-go-Related Gene Inhibition II |
Non-inhibitor
|
| AMES Toxicity |
Non AMES toxic
|
| Carcinogens |
Non-carcinogens
|
| Fish Toxicity I |
Low FHMT
|
| Fish Toxicity II |
1,8994
|
| Tetrahymena Pyriformis Toxicity I |
High TPT
|
| Tetrahymena Pyriformis Toxicity II |
0,2554
|
| Tetrahymena Pyriformis Toxicity |
Low HBT
|
| Biodegradation |
Not ready biodegradable
|
| Acute Oral Toxicity |
III
|
| Rat Acute Toxicity |
2,4849
|
| Carcinogenicity (Three-class) |
Non-required
|
