HIV-1 inhibitor 18A

CAS No. 331261-50-8

HIV-1 inhibitor 18A( Compound 18A )

Catalog No. M14111 CAS No. 331261-50-8

HIV-1 inhibitor 18A is a novel broad HIV-1 inhibitor that blocks envelope glycoprotein transitions critical for entry.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 218 In Stock
5MG 227 In Stock
10MG 313 In Stock
25MG 535 In Stock
50MG 736 In Stock
100MG 1042 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    HIV-1 inhibitor 18A
  • Note
    Research use only, not for human use.
  • Brief Description
    HIV-1 inhibitor 18A is a novel broad HIV-1 inhibitor that blocks envelope glycoprotein transitions critical for entry.
  • Description
    HIV-1 inhibitor 18A is a novel broad HIV-1 inhibitor that blocks envelope glycoprotein transitions critical for entry, specifically inhibits the entry of a wide range of HIV-1 isolates with mean IC50 of 6.4 uM; inhibits the CD4-induced disruption of quaternary structures at the trimer apex and the exposure of the gp41 HR1 coiled coil, does not interfere with CD4 or CCR5 binding.
  • In Vitro
    Cell Viability Assay Cell Line:PBMCs Concentration:0.01-10 μM Incubation Time:40-44 h Result:Inhibited infection of HIV-1JR-FL, with an IC50 value of 0.4 μM.
  • In Vivo
    ——
  • Synonyms
    Compound 18A
  • Pathway
    Microbiology/Virology
  • Target
    HIV
  • Recptor
    HIV
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    331261-50-8
  • Formula Weight
    313.33
  • Molecular Formula
    C14H11N5O2S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(N/N=C/C1=CC=C(O)C=C1)NC2=CC=CC3=NSN=C32
  • Chemical Name
    N-2,1,3-Benzothiadiazol-4-yl-2-[(4-hydroxyphenyl)methylene]-hydrazinecarboxamide

Shipping & Storage Information

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

Reference

1. Herschhorn A, et al. Nat Chem Biol. 2014 Oct;10(10):845-52. 2. Berinyuy E, et al. J Recept Signal Transduct Res. 2016;36(2):119-29.
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