I-XW-053

CAS No. 5496-35-5

I-XW-053( I XW 053 | IXW053 | 4-(4,5-Diphenyl-1H-iMidazol-2-yl)benzoic Acid )

Catalog No. M27211 CAS No. 5496-35-5

I-XW-053 is an inhibitor of capsid targeted HIV-1 replication using the hybrid structure based method to block the interface between CA N-terminal domains (NTD-NTD interface) with micromolar affinity.

I-XW-053 is an inhibitor of capsid targeted HIV-1 replication using the hybrid structure based method to block the interface between CA N-terminal domains (NTD-NTD interface) with micromolar affinity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 45 In Stock
10MG 63 In Stock
25MG 103 In Stock
50MG 150 In Stock
100MG 223 In Stock
500MG 482 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    I-XW-053
  • Note
    Research use only, not for human use.
  • Brief Description
    I-XW-053 is an inhibitor of capsid targeted HIV-1 replication using the hybrid structure based method to block the interface between CA N-terminal domains (NTD-NTD interface) with micromolar affinity.
  • Description
    I-XW-053 is an inhibitor of capsid targeted HIV-1 replication using the hybrid structure based method to block the interface between CA N-terminal domains (NTD-NTD interface) with micromolar affinity.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    I XW 053 | IXW053 | 4-(4,5-Diphenyl-1H-iMidazol-2-yl)benzoic Acid
  • Pathway
    Microbiology/Virology
  • Target
    HIV
  • Recptor
    Smoothened
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    5496-35-5
  • Formula Weight
    340.382
  • Molecular Formula
    C22H16N2O2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    OC(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccccc1)-c1ccccc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Manetti F, et al. Design, synthesis and biological characterization of a new class of osteogenic (1H)-quinolone derivatives. Eur J Med Chem. 2016;121:747-757.
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