L82-G17

CAS No. 92285-87-5

L82-G17( —— )

Catalog No. M28986 CAS No. 92285-87-5

L82-G17 is an uncompetitive LigI-selective inhibitor in human cells with utility as a probe of the catalytic activity and cellular functions of LigI.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 69 In Stock
10MG 113 In Stock
25MG 259 In Stock
50MG 375 In Stock
100MG 533 In Stock
200MG 724 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    L82-G17
  • Note
    Research use only, not for human use.
  • Brief Description
    L82-G17 is an uncompetitive LigI-selective inhibitor in human cells with utility as a probe of the catalytic activity and cellular functions of LigI.
  • Description
    L82-G17 is an uncompetitive LigI-selective inhibitor in human cells with utility as a probe of the catalytic activity and cellular functions of LigI.
  • In Vitro
    L82-G17 (200 μM, 30 min) has selective uncompetitive inhibitory effect for LigI. L82-G17 (0-100 μM) increases LigI binding to non-ligatable nicked DNA binding.L82-G17 inhibits step 3 of the ligation reaction, phosphodiester bond formation.L82-G17 (0-100 μM) inhibits DNA synthesis, cell viability and s induces DNA damage. Cell Viability Assay Cell Line:HeLa cells Concentration:0-30 μM Incubation Time:5 days Result:Reduced cell number by about 70% at 20 μM.Cell Proliferation Assay Cell Line:CH12F3 WT and CH12F3Δ/Δ cells Concentration:0-100 μM Incubation Time:72 h Result:Had great effect on the proliferation and survival of the parental CH12F3 cells.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    DNA/RNA Synthesis
  • Recptor
    FGFR2
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    92285-87-5
  • Formula Weight
    264.67
  • Molecular Formula
    C11H9ClN4O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (472.29 mM)
  • SMILES
    OC1=CC=CC(\C=N\NC2=C(Cl)C(=O)NN=C2)=C1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Lescarbeau, Andre, et al. Preparation of substituted pyrrolopyrimidines as FGFR inhibitors and methods of making and using the same. WO2022109577.
molnova catalog
related products
  • T2AA

    T2AA is an inhibitor of proliferating cell nuclear antigen (PCNA) with IC50 of 1 μM for PCNA/PIP-box peptide interaction.

  • Cerevisterol

    Cerevisterol is a cytotoxic steroid, can inhibit the activity of DNA polymerase alpha. It can stimulate NGF-mediated neurite outgrowth on PC12 cells.

  • Blasticidin S HCl

    Blasticidin S HCl is a nucleoside antibiotic isolated from Stretomyces girseochromogenes and acts as a DNA and protein synthesis inhibitor.