Abametapir

CAS No. 1762-34-1

Abametapir ( HA-44; BRN 0123183 )

Catalog No. M20813 CAS No. 1762-34-1

Abametapir a metalloproteinase inhibitor is able to target metalloproteinases critical to egg hatching and louse development.

Purity : >98% (HPLC)

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

Biological Information

  • Product Name
    Abametapir
  • Note
    Research use only not for human use.
  • Brief Description
    Abametapir a metalloproteinase inhibitor is able to target metalloproteinases critical to egg hatching and louse development.
  • Description
    Abametapir a metalloproteinase inhibitor is able to target metalloproteinases critical to egg hatching and louse development.
  • Synonyms
    HA-44; BRN 0123183
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    metalloproteinases
  • Research Area
    Others
  • Indication
    Pediculosis

Chemical Information

  • CAS Number
    1762-34-1
  • Formula Weight
    184.24
  • Molecular Formula
    C12H12N2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:37mg/mL(200.83mM)
  • SMILES
    Cc1ccc(-c2ccc(C)cn2)nc1
  • Chemical Name
    55'-dimethyl-22'-bipyridinyl

Shipping & Storage Information

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

Reference

1.Bowles VM Hanegraaf S Ahveninen T.et al.Effect of a New Head Lice Treatment Abametapir Lotion 0.74% on Louse Eggs: A Randomized Double-Blind Study.Glob Pediatr Health. 2019 Feb 22.
molnova catalog
related products
  • PTZ-343

    PTZ-343 is a potent enhancer of Luminol, acts as an electron transfer mediator, reacting with HRP-II to release HRP and a PTZ-343 radical, which oxidizes luminol anions to induce light emission.

  • Tigloylgomisin P

    Tigloylgomisin P shows moderate to marginal cytotoxicity against A549, PC-3, KB and KBvin human cancer cell lines.

  • UDP-g acid

    UDP-g acid is a sugar used in the production of polysaccharides and is an intermediate in the biosynthesis of ascorbic acid.