Pipamperone

CAS No. 1893-33-0

Pipamperone ( Floropipamide; McN-JR 3345; R 3345 )

Catalog No. M26378 CAS No. 1893-33-0

Pipamperone binds 5-HT2A closely as receptor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 69 Get Quote
5MG 110 Get Quote
10MG 160 Get Quote
25MG 267 Get Quote
50MG 408 Get Quote
100MG 590 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Pipamperone
  • Note
    Research use only, not for human use.
  • Brief Description
    Pipamperone binds 5-HT2A closely as receptor.
  • Description
    Pipamperone binds 5-HT2A closely as receptor.
  • Synonyms
    Floropipamide; McN-JR 3345; R 3345
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1893-33-0
  • Formula Weight
    375.5
  • Molecular Formula
    C21H30FN3O2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    NC(=O)C1(CCN(CCCC(=O)c2ccc(F)cc2)CC1)N1CCCCC1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Ono M, Kanemaru Y, Yasuda S, Okawa M, Kinjo J, Miyashita H, Yokomizo K, Yoshimitsu H, Nohara T. A new resin glycoside from Calystegia soldanella and its antiviral activity towards herpes. Nat Prod Res. 2017 Nov;31(22):2660-2664. doi: 10.1080/14786419.2017.1280492. Epub 2017 Jan 20. PubMed PMID: 28105860.
molnova catalog
related products
  • 1-Methyl-hydantoin

    1-Methylhydantoin is a small molecular weight polar substance the product of degradation of creatinine by bacteria. In mammals the metabolism of 1-methylhydantoin occurs via 5-hydroxy-1-methylhydantoin. In a reported human case 1-Methylhydantoin was found as an unexpected metabolite of the intelligence-affecting substance dupracetam.

  • EN106

    EN106 is a potent inhibitor of FEMIB and is a cysteine-reactive covalent ligand. EN106 disrupts recognition of the key reductive stress substrate of FEM1B, FNIP1.

  • OGT-IN-2

    OGT-IN-2 is a potent O-GlcNAc transferase (OGT) inhibitor. OGT-IN-2 inhibits sOGT and ncOGT with IC50 values of 30 μM and 53 μM, respectively. OGT-IN-2 can be used for the research of articular diseases.