Ziconotideacetate , ≥95% , 107452-89-1
                            Synonym(s):
SNX-111;Ziconotide
                            
                        
                CAS NO.:107452-89-1
Empirical Formula: C102H172N36O32S7
Molecular Weight: 2639.13
MDL number: MFCD00145036
| Pack Size | Price | Stock | Quantity | 
| 5mg | RMB2000.00 | In Stock | 
                                                 | 
                                        
| 25mg | RMB4400.00 | In Stock | 
                                                 | 
                                        
| 50mg | RMB6560.00 | In Stock | 
                                                 | 
                                        
| others | Enquire | 
PRODUCT Properties
| Density | 1.60±0.1 g/cm3(Predicted) | 
                                    
| storage temp. | -20°C | 
                                    
| solubility | DMSO (Slightly, Sonicated), Methanol (Slightly) | 
                                    
| form | Solid | 
                                    
| color | White to Off-White | 
                                    
| InChIKey | BPKIMPVREBSLAJ-QTBYCLKRSA-N | 
                                    
Description and Uses
ω-conotoxin MVIIA, also knwn as Ziconotide acetate, is a peptide consisting of 25 amino acid. It is a disulfide-bridged polypeptide from the venom of the sea snail Conusmagus that binds to neuronal N-type calcium channels. It forms a compact folded structure, presenting a loop between Cys8 and Cys15 that contains a set of residues critical for its binding. Both ω-conotoxins GVIA and MVIIA could bind to neuronal N-type calcium channels. ω-conotoxin GVIA is rich in hydroxyl groups while ω-conotoxin MVIIA contains a large number of positively charged side chains[1-2].
Ziconotide acetate (ω-Conotoxin MVIIA), the peptide toxin of the Conus magus (cone snail) is a selective antagonist of N-type voltage sensitive calcium channels (VSCC). As a most well-known identified conotoxin so far, it has been used as a effective drug to treat intractable chronic pain in cancer and ADIS patients[2]. Blocks neurotransmitter release by preventing depolarization-induced calcium influx. Used as a ligand for binding studies of voltage sensitive calcium channels. Analgesic; neuroprotective.
Safety
| Symbol(GHS) | ![]() GHS06  | 
                                    
| Signal word | Danger | 
| Hazard statements | H301+H331 | 
| Precautionary statements | P261-P304+P340+P312-P403+P233 | 
| RIDADR | 3172 | 
| WGK Germany | 3 | 
| HazardClass | 6.1(b) | 
| PackingGroup | III | 
| Hazardous Substances Data | 107452-89-1(Hazardous Substances Data) | 







