ChemicalBook--->CAS DataBase List--->914454-03-8

914454-03-8

914454-03-8 Structure

914454-03-8 Structure
IdentificationBack Directory
[Name]

Ziconotide Acetate
[CAS]

914454-03-8
[Synonyms]

Prialt Acetate
ω-Conotoxin M VIIA Acetate
ω-Conopeptide MVIIA Acetate
[Molecular Formula]

C104H176N36O34S7
[MOL File]

914454-03-8.mol
[Molecular Weight]

2699.19
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C, protect from light, stored under nitrogen
[solubility ]

DMSO : 25 mg/mL (Need ultrasonic)
[form ]

Solid
[color ]

White to off-white
[Sequence]

Cys-Lys-Gly-Lys-Gly-Ala-Lys-Cys-Ser-Arg-Leu-Met-Tyr-Asp-Cys-Cys-Thr-Gly-Ser-Cys-Arg-Ser-Gly-Lys-Cys-NH2 (Disulfide bridge:Cys1-Cys16;Cys8-Cys20;Cys15-Cys25)
Hazard InformationBack Directory
[Uses]

Ziconotide Acetate is a selective antagonist of N-type voltage sensitive calcium channels (VSCC). Blocks neurotransmitter release by preventing depolarization-induced calcium influx. Used as a ligand for binding studies of voltage sensitive calcium channels. it can be used for analgesic.
[in vivo]

Ziconotide (i.t.; 25-100 pmol/site; 5 μL; on the 4 th, 10 th, 15 th, 20 th, and 24 th days) acetate reduces the levels of IL-1β and IL-23 in the CNS, as well as IL-17 production in the spleen, 25 days after MOG35-55-elicited EAE, in the mouse model of experimental autoimmune encephalomyelitis (EAE)[2].

Animal Model:Female C57BL/6mice (18-22 g, 6-8 weeks old) injected with myelin oligodendrocytes glycoprotein[2]
Dosage:25 pmol/site, 50 pmol/site, 100 pmol/site
Administration:Intrathecal injection; on the 4 th, 10 th, 15 th, 20 th, and 24 th days
Result:Significantly reduced the mechanical hypersensitivity in animals with EAE.
[IC 50]

N-type calcium channel
[storage]

Store at -20°C, protect from light, stored under nitrogen
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