Mivacurium chloride
CAS No. 106861-44-3
Mivacurium chloride( —— )
Catalog No. M23275 CAS No. 106861-44-3
Mivacurium chloride is a non-depolarising, rapid neuromuscular blocker of short duration, used therefore as anesthetic, to provide skeletal muscle relaxation in minor surgical operations.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 36 | In Stock |
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| 5MG | 57 | In Stock |
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| 10MG | 82 | In Stock |
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| 25MG | 119 | In Stock |
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| 50MG | 188 | In Stock |
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| 100MG | 286 | In Stock |
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| 200MG | 434 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameMivacurium chloride
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NoteResearch use only, not for human use.
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Brief DescriptionMivacurium chloride is a non-depolarising, rapid neuromuscular blocker of short duration, used therefore as anesthetic, to provide skeletal muscle relaxation in minor surgical operations.
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DescriptionMivacurium chloride is a non-depolarising, rapid neuromuscular blocker of short duration, used therefore as anesthetic, to provide skeletal muscle relaxation in minor surgical operations, in emergency surgical procedures of short to intermediate duration and during intubation of the trachea.(In Vitro):Mivacurium induces LAD2 cell degranulation in a dose-dependent manner. Mivacurium stimulates intracellular Ca2+ influx in MRGPRX2-HEK293 cells but not in NC-HEK293 cells. Mivacurium induces the release of only low levels of mediators in LAD2 cells transfected with MRGPRX2-targeted small interfering siRNA.(In Vivo):Mivacurium causes pseudo-allergic reactions in C57 wild-type mice by inducing mast cells to release histamine and a decrease in body temperature.Mivacurium is rapidly hydrolyzed in the plasma and has a short duration of action (< 10 min). Mivacurium has many advantages, such as a rapid effect, nonneurological toxicity and a lack of heart rate alteration.
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In VitroMivacurium induces LAD2 cell degranulation in a dose-dependent manner. Mivacurium stimulates intracellular Ca2+ influx in MRGPRX2-HEK293 cells but not in NC-HEK293 cells. Mivacurium induces the release of only low levels of mediators in LAD2 cells transfected with MRGPRX2-targeted small interfering siRNA.
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In VivoMivacurium causes pseudo-allergic reactions in C57 wild-type mice by inducing mast cells to release histamine and a decrease in body temperature. Mivacurium is rapidly hydrolyzed in the plasma and has a short duration of action (< 10 min). Mivacurium has many advantages, such as a rapid effect, nonneurological toxicity and a lack of heart rate alteration.
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Synonyms——
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PathwayEndocrinology/Hormones
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TargetAChR
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RecptornAChR
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Research Area——
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Indication——
Chemical Information
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CAS Number106861-44-3
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Formula Weight1100.17
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Molecular FormulaC58H80Cl2N2O14
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Purity>98% (HPLC)
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SolubilityDMSO:100 mg/ml (90.9 mM); Ethanol:100 mg/ml (90.9 mM); Water:100 mg/ml (90.9 mM)
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SMILESC[N+](CCCOC(CC/C=C/CCC(OCCC[N+](C)(CC1)[C@H](Cc(cc2OC)cc(OC)c2OC)c(cc2OC)c1cc2OC)=O)=O)(CC1)[C@H](Cc(cc2OC)cc(OC)c2OC)c(cc2OC)c1cc2OC.[Cl-].[Cl-]
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Delu Che, et al. Mivacurium Induce Mast Cell Activation and Pseudo-Allergic Reactions via MAS-related G Protein Coupled receptor-X2. Cell Immunol. 2018 Oct;332:121-128.
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