Cisatracurium Besylate
The besylate salt formulation of cisatracurium is the standard preparation used intravenously in intensive care and anesthesia settings. It provides reliable muscle paralysis with an intermediate duration of action. Reversal of blockade with cholinesterase inhibitors or sugammadex is used at the end of its required use.
Khối lượng phân tử
1243,5000 g/mol
TPSA
258,00 Ų
Lĩnh vực điều trị
Cơ chế tác dụng
Inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine in the synaptic cleft. This increases acetylcholine availability at cholinergic synapses, enhancing cholinergic neurotransmission.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine in the synaptic cleft. This increases acetylcholine availability at cholinergic synapses, enhancing cholinergic neurotransmission.
Cấu trúc 2D
Cite this structure
Embed this structure
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
InChI
InChI=1S/C53H72N2O12.2C6H6O3S/c1-54(22-18-38-32-48(62-7)50(64-9)34-40(38)42(54)28-36-14-16-44(58-3)46(30-36)60-5)24-20-52(56)66-26-12-11-13-27-67-53(57)21-25-55(2)23-19-39-33-49(63-8)51(65-10)35-41(39)43(55)29-37-15-17-45(59-4)47(31-37)61-6;2*7-10(8,9)6-4-2-1-3-5-6/h14-17,30-35,42-43H,11-13,18-29H2,1-10H3;2*1-5H,(H,7,8,9)/q+2;;/p-2/t42-,43-,54-,55-;;/m1../s1
Molecular Formula
C65H82N2O18S2
HBD / HBA
- / 18
Liên kết có thể quay
26
Nguyên tử nặng
87
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Câu hỏi thường gặp
The besylate salt formulation of cisatracurium is the standard preparation used intravenously in intensive care and anesthesia settings. It provides reliable muscle paralysis with an intermediate duration of action. Reversal of blockade with cholinesterase inhibitors or sugammadex is used at the end of its required use.
Inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine in the synaptic cleft. This increases acetylcholine availability at cholinergic synapses, enhancing cholinergic neurotransmission.
Yes, Cisatracurium Besylate is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200641. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 62886. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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