ZL0580

CAS No. 2377151-10-3

ZL0580( —— )

Catalog No. M24093 CAS No. 2377151-10-3

ZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 49 In Stock
5MG 80 In Stock
10MG 140 In Stock
25MG 259 In Stock
50MG 383 In Stock
100MG 565 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    ZL0580
  • Note
    Research use only, not for human use.
  • Brief Description
    ZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
  • Description
    ZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
  • In Vitro
    Cell Viability Assay Cell Line:HIV-infected human CD4+ T cells.Concentration:0-8 μM.Incubation Time:2 days.Result:Suppress HIV in primary CD4+ T cell.Single treatment (8 μM) led to almost completed loss of productive HIV infection in CD4+ T cells.RT-PCR Cell Line:PBMCs of viremic HIV-infected individuals.Concentration:8 μM.Incubation Time:2 days.Result:Suppresses HIV transcription ex vivo in PBMCs of viremic HIV-infected individuals.Cell Cytotoxicity Assay Cell Line:J-Lat cells. Concentration:0-80 μM.Incubation Time:1 and 3 days.Result:Did not cause significant cell death at concentrations below 40 μM.Treatment of J-Lat cells with ZL0580 (10 μM) also did not cause significant cell death on days 2, 7, and 14 compared with NC in both PMA-activated and unstimulated cells.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Chromatin/Epigenetic
  • Target
    Epigenetic Reader Domain
  • Recptor
    BRD4|HIV
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2377151-10-3
  • Formula Weight
    532.53
  • Molecular Formula
    C25H23F3N4O4S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:250 mg/mL (469.46 mM; Need ultrasonic)
  • SMILES
    C1C[C@H](N(C1)S(=O)(=O)C2=CC=C(C=C2)NC(=O)NC3=CC=C(C=C3)C(F)(F)F)C(=O)NC4=CC=CC=C4
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Niu Q, et al. Structure-guided drug design identifies a BRD4-selective small molecule that suppresses HIV. J Clin Invest. 2019 Jul 22;129(8):3361-3373.
molnova catalog
related products
  • C646

    C646 is an inhibitor for histone acetyltransferase, and inhibits p300 with a Ki of 400 nM in a cell-free assay.

  • BRD4-IN-4

    BRD4-IN-4 is a selective BRD4 inhibitor with an IC50 value of 6.83 μM for BRD4.BRD4-IN-4 selectively inhibits the proliferation of the MV4-11 cell line and arrests the cells in G1 phase.BRD4-IN-4 can be used to study MLL leukemias.

  • Pocenbrodib

    Pocenbrodib (FT-7051) is a potent inhibitor of the bromodomain of the CBP/p300 family with potential antitumour activity and is palatable for cancer research.