cas: 96946-42-8 — see every product listed under this CAS number, including other names
Cisatracurium Besylate (CAS 96946-42-8) is a chemical reagent available from Chemat. Available pack sizes: 100mg, 25mg, 10mM (in 1ml dmso), 0,25g, 0,1g, 0,5g, 2g, 1g. Offered by: GLPBio, Biosynth.
| brand | GLPBio |
|---|---|
| catalog number | GC12226-100 |
| cas | 96946-42-8 |
| size | 100mg |
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| brand | size | price | |
|---|---|---|---|
| GLPBio | 100mg | 1322.52 Pln | |
| GLPBio | 25mg | 681.29 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 723.41 Pln | |
| Biosynth | 0,25g | price on request | |
| Biosynth | 0,1g | price on request | |
| Biosynth | 0,5g | price on request | |
| Biosynth | 2g | price on request | |
| Biosynth | 1g | price on request |
| purity | No data |
|---|---|
| delivery time | To be confirmed by Chemat |
Cisatracurium besylate is the (1R,1'R,2R,2'R)-diastereoisomer of atracurium besylate. Commercial preparations of atracurium are mixtures of 10 stereoisomers, of which cisatracurium generally constitutes about 15%. Cisatracurium besylate is about 3 times more potent than the mixture of atracurium isomers as a neuromuscular blocking agent, and is used as a muscle relaxant for endotracheal intubation, to aid controlled ventilation, and in general anaesthesia. It has a role as a nicotinic antagonist and a muscle relaxant. It is an atracurium besylate, a quaternary ammonium salt and an organosulfonate salt. It contains a cisatracurium.
Source: ChEBI
| Molecular formula | C65H82N2O18S2 |
|---|---|
| Molecular weight | 1243.5 g/mol |
| IUPAC name | benzenesulfonate;5-[3-[(1R,2R)-1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-2-ium-2-yl]propanoyloxy]pentyl 3-[(1R,2R)-1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-2-ium-2-yl]propanoate |
| InChIKey | XXZSQOVSEBAPGS-DONVQRBFSA-L |
| SMILES | C[N@@+]1(CCC2=CC(=C(C=C2[C@H]1CC3=CC(=C(C=C3)OC)OC)OC)OC)CCC(=O)OCCCCCOC(=O)CC[N@+]4(CCC5=CC(=C(C=C5[C@H]4CC6=CC(=C(C=C6)OC)OC)OC)OC)C.C1=CC=C(C=C1)S(=O)(=O)[O-].C1=CC=C(C=C1)S(=O)(=O)[O-] |
Computed by PubChem (NCBI)