Laudanosine

CAS No. 1699-51-0

Laudanosine( DL-LAUDANOSINE )

Catalog No. M21227 CAS No. 1699-51-0

Laudanosine is a recognized metabolite of atracurium and cisatracurium.

Laudanosine is a recognized metabolite of atracurium and cisatracurium.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 38 In Stock
10MG 53 In Stock
25MG 84 In Stock
50MG 122 In Stock
100MG 177 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Laudanosine
  • Note
    Research use only, not for human use.
  • Brief Description
    Laudanosine is a recognized metabolite of atracurium and cisatracurium.
  • Description
    Laudanosine is a recognized metabolite of atracurium and cisatracurium.
  • In Vitro
    ——
  • In Vivo
    DL-Laudanosine (Laudanosine) appears to be unique in its ability to produce cerebral stimulation in lightly anaesthetized animals and it is reported to cause arousal from anaesthesia in subconvulsive doses. Animal Model:Male CFLP mice weighing 18-25 g, and male Wistar rats weighing 120-150 g .Dosage:10-20 mg/kg.Administration:IV.Result:Caused convulsions and hind limb extensions.
  • Synonyms
    DL-LAUDANOSINE
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1699-51-0
  • Formula Weight
    357.4
  • Molecular Formula
    C21H27NO4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (279.77 mM)
  • SMILES
    CN(CCc1c2)C(Cc(cc3)cc(OC)c3OC)c1cc(OC)c2OC
  • Chemical Name
    1-(34-dimethoxybenzyl)-67-dimethoxy-2-methyl-1234-tetrahydroisoquinoline

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Shi W Z Fahey M R Fisher D M et al. Laudanosine (A Metabolite of Atracurium) Increases the Minimum Alveolar Concentration of Halothane in Rabbits[J]. Anesthesiology 1985 63(6):584-588.
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