ChemicalBook--->CAS DataBase List--->107452-89-1

107452-89-1

107452-89-1 Structure

107452-89-1 Structure
IdentificationBack Directory
[Name]

Ziconotide acetate
[CAS]

107452-89-1
[Synonyms]

snx111
Ziconotide
OMEGA-CGTX MVII A
ω-conotoxin mviia
o-Conotoxin MVIIA
Zicontide Acetate
ZICONOTIDE ACETATE
SNX-111, Ziconotide
Ziconotide [USAN:INN]
OMEGA-CONOTOXIN MVIIA
omega-conopeptide MVIIA
CONOTOXIN MVII A (Omega-)
Ziconotide acetate USP/EP/BP
omega-Conopeptide MVIIA (Conus)
CKGKGAKCSRLMYDCCTGSCRSGKC-NH2 (DISULFIDE BRIDGE: 1-16,8-20, AND 15-25)
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
H-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
H-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, disulfid bridges 1-16/8-20/15-25
H-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: 1-16, 8-20, AND 15-25)
REF DUPL: H-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, disulfid bridges 1-16/8-20/15-25
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,Cys1-Cys16, Cys8-Cys20,Cys15-Cys25)
L-Cysteinamide, L-cysteinyl-L-lysylglycyl-L-lysylglycyl-L-alanyl-L-lysyl-L-cysteinyl-L-seryl-L-arginyl-L-leucyl-L-methionyl-L-tyrosyl-L-α-aspartyl-L-cysteinyl-L-cysteinyl-L-threonylglycyl-L-seryl-L-cysteinyl-L-arginyl-L-serylglycyl-L-lysyl-, cyclic (1→16),(8→20),(15→25)-tris(disulfide)
[Molecular Formula]

C102H172N36O32S7
[MDL Number]

MFCD00145036
[MOL File]

107452-89-1.mol
[Molecular Weight]

2639.13
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
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
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Dermal
Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
[Hazardous Substances Data]

107452-89-1(Hazardous Substances Data)
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Ziconotide acetate(107452-89-1).msds
Hazard InformationBack Directory
[Description]

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].
[Uses]

Ligand for binding studies of voltage sensitive calcium channels.
[Brand name]

Prialt (Elan).
[General Description]

ω-Conotoxin MVIIA functions as a selective inhibitor of N-type voltage-sensitive calcium channels (VSCCs). It has analgesic and neuroprotective effects. ω-Conotoxin MVIIA is used to treat neuropathic pain.
[Biochem/physiol Actions]

Neuronal N-type Ca2+ channel blocker in mammalian and amphibian brain; blocks release of GABA and glutamate at neuronal synapses.
[storage]

Store at -20°C
[References]

[1] Wang R, et al. Development of an ic-ELISA and immunochromatographic strip based on IgG antibody for detection of ω-conotoxin MVIIA. Journal of Hazardous Materials, 2019; 378: 120510.
[2] Zhou Y, et al. A Chemoenzymatic Approach To Produce a Cyclic Analogue of the Analgesic Drug MVIIA (Ziconotide). Angew. Chem. Int. Ed., 2023; 62: e202302812.
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