107452-89-1
CHEMICAL AND PHYSICAL PROPERTIES
Solubility | Freely soluble in water and is practically insoluble in methyl tert-butyl ether |
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Stability/Shelf Life | The results /of stability studies/ justify a retest period of 36 months when stored at -20 °C in the proposed packaging. |
Other Experimental Properties | Hydrophilic |
SAFETY INFORMATION
Signal word | Danger |
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Pictogram(s) |
Skull and Crossbones Acute Toxicity GHS06 |
Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P403+P233:Store in a well-ventilated place. Keep container tightly closed. |
COMPUTED DESCRIPTORS
Molecular Weight | 2639.2 g/mol |
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XLogP3 | -14 |
Hydrogen Bond Donor Count | 42 |
Hydrogen Bond Acceptor Count | 46 |
Rotatable Bond Count | 40 |
Exact Mass | 2638.1016905 g/mol |
Monoisotopic Mass | 2637.0983357 g/mol |
Topological Polar Surface Area | 1310 Ų |
Heavy Atom Count | 177 |
Formal Charge | 0 |
Complexity | 5480 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 22 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently-Bonded Unit Count | 1 |
Compound Is Canonicalized | Yes |
PRODUCT INTRODUCTION
description
Ziconotide (also known as SNX-111) is a neurotoxic peptide derived from the cone snail Conus magus comprising 25 amino acids with three disulphide bonds. Other such peptides, collectively termed conotoxins, exist, and some have shown efficacy in binding specific subsets of calcium channels; ziconotide is used in part because it can be synthesized without loss of proper bond formation or structural elements. Ziconotide is used to manage severe chronic pain refractory to other methods, through its ability to inhibit N-type calcium channels involved in nociceptive signalling. Ziconotide was granted FDA approval on December 28, 2004 for marketing by TerSera therapeutics LLC. under the name Prialt. To date, ziconotide is the only calcium channel blocking peptide approved for use by the FDA.