Mivacurium chloride, nicotinic acetylcholine antagonist (ab143667)
Key features and details
- Competitive nicotinic acetylcholine antagonist
- CAS Number: 106861-44-3
- Purity: > 98%
- Soluble in water
- Form / State: Solid
- Source: Synthetic
Overview
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Product name
Mivacurium chloride, nicotinic acetylcholine antagonist -
Description
Competitive nicotinic acetylcholine antagonist -
Purity
> 98% -
CAS Number
106861-44-3 -
Chemical structure
Properties
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Chemical name
Bis[3-[(1R)-6,7-dimethoxy-2-methyl-1-[(3,4,5-trimethoxyphenyl)methyl]-3,4-dihydro-1H-isoquinolin-2-ium-2-yl]propyl] (E)-oct-4-enedioate dichloride -
Molecular weight
1100.17 -
Molecular formula
C58H80Cl2N2O14 -
PubChem identifier
5281080 -
Storage instructions
Store at Room Temperature. The product can be stored for up to 12 months. -
Solubility overview
Soluble in water -
Handling
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Toxic, refer to SDS for further information.
Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
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SMILES
C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C(=C3)OC)OC)OC)OC)OC)CCCOC(=O)CCC=CCCC(=O)OCCC[N+]4(CCC5=CC(=C(C=C5C4CC6=CC(=C(C(=C6)OC)OC)OC)OC)OC)C.[Cl-].[Cl-] -
Source
Synthetic
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Research areas
Images
Protocols
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
Datasheets and documents
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SDS download
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Datasheet download
References (1)
ab143667 has been referenced in 1 publication.
- Almeida RG et al. Myelination induces axonal hotspots of synaptic vesicle fusion that promote sheath growth. Curr Biol 31:3743-3754.e5 (2021). PubMed: 34270947