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Cisatracurium Besylate

HCID 62886
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Basic information

CAS
96946-42-8
Standard SMILES
COc1ccc(C[C@@H]2c3cc(OC)c(OC)cc3CC[N@+]2(C)CCC(=O)OCCCCCOC(=O)CC[N@@+]2(C)CCc3cc(OC)c(OC)cc3[C@H]2Cc2ccc(OC)c(OC)c2)cc1OC.O=S(=O)([O-])c1ccccc1.O=S(=O)([O-])c1ccccc1
InChIKey
XXZSQOVSEBAPGS-DONVQRBFSA-L
Molecular formula
C65H82N2O18S2
Average molar mass
1,243.5 g/mol
Monoisotopic mass
1,242.50040612

Overview

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.

Names & identifiers

Preferred name
Cisatracurium Besylate
IUPAC
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
English name
Cisatracurium besylate
Molecular formula
C53H72N2O12.2C6H5O3S
Molecular weight
1243.49

Names & synonyms

Cisatracurium besylate96946-42-8Cisatracurium besilateNimbex51W89NIMBEX PRESERVATIVE FREECisatracurium (as besilate)80YS8O1MBSBesilato de cisatracurioBesilate de cisatracurium51-W8951-W-89
Show more names
Cisatracurium1 kg - 1.5kgCis-AttacuriuMMikhail Zayats(1R,1'R,2R,2'R)-Cisatracurium besyLCisatracurium besylaCisatrcurium Besylate
Cisatracurium Besylate Preservative FreeCHEBI:3721(1R,2R)-2-(2-Carboxyethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-veratrylisoquinolinium benzenesulfonate, pentamethylene esterDTXSID1089504551W-89(1R,2R,1'R,2'R)-2,2'-(PENTANE-1,5-DIYLBIS(OXY(3-OXOPROPANE-3,1-DIYL)))BIS(1-(3,4-DIMETHOXYBENZYL)-6,7-DIMETHOXY-2-METHYL-1,2,3,4-TETRAHYDROISOQUINOLINIUM) BISBENZENESULFONATE(1R,2R,1'R,2'R)-2,2'-{pentane-1,5-diylbis[oxy(3-oxopropane-3,1-diyl)]}bis[1-(3,4-dimethoxybenzyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinolinium] bisbenzenesulfonateCisatracurii besilas

Properties

Computed structural properties

Topological polar surface area
258 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
18
Rotatable bonds
26
Heavy atoms
87
Formal charge
0
Complexity
1,560

Experimental & physicochemical properties

Human Drugs · 3 items

Breast Feeding; Lactation; Milk, Human; Muscle Relaxants; Neuromuscular Nondepolarizing Agents

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

Endocrine DisruptorsPotential endocrine disrupting compound

Physicochemical properties

Melting point
90 · 90-93°C
storage temp.
-20 °C · Sealed in dry,Store in freezer, under -20°C
solubility
2 O: · H2O: soluble1mg/mL
form
Powder
color
white
Major Application
pharmaceutical (small molecule)
InChIKey
XXZSQOVSEBAPGS-UHFFFAOYSA-L
FDA UNII
80 YS8O1MBS · 80YS8O1MBS
NCI Drug Dictionary
cisatracurium besylate
ATC code
3 AC11 · M03AC11

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 4 items

Danger

H301 (94.9%): Toxic if swallowed [Danger Acute toxicity, oral]

P264, P264+P265, P270, P280, P301+P316, P305+P351+P338, P321, P330, P337+P317, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 98 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Hazard Classes and CategoriesAcute Tox. 3 (94.9%)

Toxicology

Drug Induced Liver Injury · 6 items

Drug Induced Liver Injury Rank (DILIrank 2.0)

Cisatracurium besylate

vNo-DILI-concern

0

No match

DOI:10.1016/j.drudis.2016.02.015

Effects During Pregnancy and Lactation◉ Summary of Use during Lactation

Safety data

wgk
3
ridadr
UN 2811 6.1 / PGIII
hs_code
29145090
risk_code
25-36
Signal word
Danger
Symbol(GHS)
GHS06
hazard_code
T
safety_code
45
Storage Class

Chemistry & industry

Pharmacology

FDA Pharmacological Classification · 2 items

CISATRACURIUM BESYLATE

Nondepolarizing Neuromuscular Blocker [EPC]; Neuromuscular Nondepolarizing Blockade [PE]

MeSH Pharmacological Classification · 1 item

Drugs that interrupt transmission of nerve impulses at the skeletal neuromuscular junction. They can be of two types, competitive, stabilizing blockers (NEUROMUSCULAR NONDEPOLARIZING AGENTS) or noncompetitive, depolarizing agents (NEUROMUSCULAR DEPOLARIZING AGENTS). Both prevent acetylcholine from triggering the muscle contraction and they are used as anesthesia adjuvants, as relaxants during electroshock, in convulsive states, etc.

Uses & manufacturing

UsesUse (kg; approx.) in Germany (2009): >10
Applications · 3 items

DescriptionCisatracurium besylate is a new intermediate-duration non-depolarizing muscle relaxant launched in the U.S.A. for intubation and maintenance of muscle relaxation during surgery and intensive care. Cisatracurium besylate is the single 1 R cis-1'R cis isomer of the commercial preparation of atracurium, a mixture of 10 isomers. It is 3 to 5 times more potent than the mixture with similar onset and duration of action. The single isomer was also reported to have reduced propensity to release histamine and have a stable cardiovascular profile. Similar to structurally related mivacurium, cisatracurium has distinct advantages of rapid degradation, enzymatic metabolism that is independent of liver or kidney resulting in short duration of action and fast, complete recovery.

UsesCisatracurium Besylate is a nondepolarizing neuromuscular blocking agent, antagonizing the action of acetylcholine by inhibiting neuromuscular transmission.

UsesAn enantiomer of Atracurium Besylate (A794500). A neuromuscular blocking agent. It could be used in liver transplant patient with safety.

Related reactions

2 records
New reaction record
HRID 1808316 reaction equation
HRID 1808316As productuspto-grants-2013_01
HRID 2067921 reaction equation
HRID 2067921As productuspto-grants-2012_10

Compound notes

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Database identifiers

CAS
96946-42-8
PubChem CID
62886
DTXSID
DTXSID10895045
ChEMBL
CHEMBL1200641
ChEBI
CHEBI:3721
UNII
80YS8O1MBS、Y78PS7MEDE
EC Number
620-579-9
UNSPSC Code
41116107 · 41116107
NACRES
24 · NA.24
Symbol(GHS)
6 · GHS06
Signal word
Danger
Hazard statements
301 · H301
Precautionary statements
264 · P264-P270-P301+P310-P405-P501
Hazard Codes
T
Risk Statements
25 · 25-36
Safety Statements
45 · 45
RIDADR
2811 · UN 2811 6.1 / PGIII
WGK Germany
3 · 3
HS Code
29145090 · 29145090
Storage Class
6.1 C · 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
Hazard Classifications
3 Oral · Acute Tox. 3 Oral
6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
Hazard statements
H301
Hazard Classifications
Acute Tox. 3 Oral
Precautionary statements
P264-P270-P301+P310-P405-P501

Upstream & downstream products

Upstream raw materials

(+/-)-TetrahydropapaverineAcryloyl chloride1,5-Diaminopentane dihydrochloride
Additional notes · 1 item

DefinitionChEBI: 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%. isatracurium 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.