Alverine citrate

CAS No. 5560-59-8

Alverine citrate( NSC 35459 )

Catalog No. M15021 CAS No. 5560-59-8

Alverine Citrate(NSC35459) is a drug used for functional gastrointestinal disorders.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
500MG 37 In Stock
1G 67 In Stock

Biological Information

  • Product Name
    Alverine citrate
  • Note
    Research use only, not for human use.
  • Brief Description
    Alverine Citrate(NSC35459) is a drug used for functional gastrointestinal disorders.
  • Description
    Alverine Citrate(NSC35459) is a drug used for functional gastrointestinal disorders.(In Vitro):Alverine is a drug used for functional gastrointestinal disorders. Alverine acts directly on the muscle in the gut, causing it to relax. Alverine Citrate (20 mg/kg) suppresses the effect of 5-HTP, but not that of 8-OH-DPAT. However, when injected intracerebroventricularly (75 μg/rat) alverine citrate reduces 8-OH-DPAT-induced enhancement of rectal distension-induced abdominal contractions. In-vitro binding studies reveal that Alverine citrate has a high affinity for 5-HT1A receptors and a weak affinity for 5-HT3 and 5-HT4 subtypes. Alverine may increase Ca influx during action potentials due to inhibition of the inactivation of L-type Ca channels, but may also suppress evoked activity by inhibiting the sensitivity of contractile proteins to Ca2+.
  • In Vitro
    Alverine is a drug used for functional gastrointestinal disorders. Alverine acts directly on the muscle in the gut, causing it to relax. Alverine Citrate (20 mg/kg) suppresses the effect of 5-HTP, but not that of 8-OH-DPAT. However, when injected intracerebroventricularly (75 μg/rat) alverine citrate reduces 8-OH-DPAT-induced enhancement of rectal distension-induced abdominal contractions. In-vitro binding studies reveal that Alverine citrate has a high affinity for 5-HT1A receptors and a weak affinity for 5-HT3 and 5-HT4 subtypes. Alverine may increase Ca influx during action potentials due to inhibition of the inactivation of L-type Ca channels, but may also suppress evoked activity by inhibiting the sensitivity of contractile proteins to Ca2+.
  • In Vivo
    ——
  • Synonyms
    NSC 35459
  • Pathway
    Endocrinology/Hormones
  • Target
    5-HT Receptor
  • Recptor
    5-HT
  • Research Area
    Metabolic Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    5560-59-8
  • Formula Weight
    473.57
  • Molecular Formula
    C26H35NO7
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 95 mg/mL (200.6 mM)
  • SMILES
    OC(=O)CC(O)(CC(O)=O)C(O)=O.CCN(CCCC1=CC=CC=C1)CCCC1=CC=CC=C1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Coelho AM, et al. J Pharm Pharmacol. 2001 Oct; 53(10):1419-26.
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