Chemical Property of Sugammadex Sodium
Chemical Property:
- PSA：994.80000
- Density:1.275g/cm3 (calc.)
- LogP:-18.35920
- Storage Temp.:Inert atmosphere,Room Temperature
- Hydrogen Bond Donor Count:16
- Hydrogen Bond Acceptor Count:56
- Rotatable Bond Count:32
- Exact Mass:2176.2644287
- Heavy Atom Count:136
- Complexity:2790
- Purity/Quality:
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98% up *data from raw suppliers
SugammadexSodium *data from reagent suppliers
Safty Information:
- Pictogram(s):
- Hazard Codes:
- MSDS Files:
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SDS file from LookChem
Useful:
- Canonical SMILES:C(CSCC1C2C(C(C(O1)OC3C(OC(C(C3O)O)OC4C(OC(C(C4O)O)OC5C(OC(C(C5O)O)OC6C(OC(C(C6O)O)OC7C(OC(C(C7O)O)OC8C(OC(C(C8O)O)OC9C(OC(O2)C(C9O)O)CSCCC(=O)[O-])CSCCC(=O)[O-])CSCCC(=O)[O-])CSCCC(=O)[O-])CSCCC(=O)[O-])CSCCC(=O)[O-])CSCCC(=O)[O-])O)O)C(=O)[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]
- Isomeric SMILES:C(CSC[C@@H]1[C@@H]2[C@@H]([C@H]([C@H](O1)O[C@@H]3[C@H](O[C@@H]([C@@H]([C@H]3O)O)O[C@@H]4[C@H](O[C@@H]([C@@H]([C@H]4O)O)O[C@@H]5[C@H](O[C@@H]([C@@H]([C@H]5O)O)O[C@@H]6[C@H](O[C@@H]([C@@H]([C@H]6O)O)O[C@@H]7[C@H](O[C@@H]([C@@H]([C@H]7O)O)O[C@@H]8[C@H](O[C@@H]([C@@H]([C@H]8O)O)O[C@@H]9[C@H](O[C@H](O2)[C@@H]([C@H]9O)O)CSCCC(=O)[O-])CSCCC(=O)[O-])CSCCC(=O)[O-])CSCCC(=O)[O-])CSCCC(=O)[O-])CSCCC(=O)[O-])CSCCC(=O)[O-])O)O)C(=O)[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]
- Recent ClinicalTrials:Postoperative Sugammadex After COVID-19
- Recent EU Clinical Trials:Randomized clinical trial to compare the efficacy of opioid-free versus traditional balanced anesthesia in laparoscopic colorectal surgery
- Recent NIPH Clinical Trials:Comparison of reversal with neostigmine vs. sugammadex for postoperative bowel function in patients undergoing colorectal surgery
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Description
To facilitate tracheal intubation, mechanical ventilation, and surgical
access, NMB agents are frequently used as non-anesthetic adjuncts in
surgical procedures.
Sugammadex is able to function as a pharmacologic sink of rocuronium and vecuronium, another non-depolarizing
neuromuscular blocker, without the cardiovascular adverse effects
experienced with reversal agents that directly interact with the
cholinergic system. The γ-cyclodextrin has been designed to enhance
binding of the guest by incorporating acidic side chains to promote an
electrostatic interaction with the positive nitrogen of the blocker. Starting
with γ-cyclodextrin, these side chains are readily installed by first
halogenating with iodine or bromine to provide a handle for nucleophilic
displacement with either 3-mercaptopropionic acid in the presence of
sodium hydride or with 3-mercaptopropionic acid methyl ester
and cesium carbonate. The latter requires hydrolysis with sodium
hydroxide to generate sugammadex sodium.
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Uses
Sugammadex Sodium is the first in a class of drugs called selective relaxant binding agents that offers improved termination of the paralytic effects of neuromuscular blocking agents and may have many potential peri-operative benefits.
