FEN1-IN-3

CAS No. 2109805-87-8

FEN1-IN-3( —— )

Catalog No. M37614 CAS No. 2109805-87-8

FEN1-IN-3 is a human flap endonuclease-1 ( hFEN1 ) inhibitor that stabilizes hFEN1 with an EC 50 of 6.8 μM .

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 33 In Stock
5MG 30 In Stock
10MG 51 In Stock
25MG 91 In Stock
50MG 145 In Stock
100MG 243 In Stock
200MG 338 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    FEN1-IN-3
  • Note
    Research use only, not for human use.
  • Brief Description
    FEN1-IN-3 is a human flap endonuclease-1 ( hFEN1 ) inhibitor that stabilizes hFEN1 with an EC 50 of 6.8 μM .
  • Description
    FEN1-IN-3 (Compound 4) is a human flap endonuclease-1 (hFEN1) inhibitor. FEN1-IN-3 stabilizes hFEN1 with an EC50 of 6.8 μM.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2109805-87-8
  • Formula Weight
    284.27
  • Molecular Formula
    C15H12N2O4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 250 mg/mL (879.45 mM; Ultrasonic )
  • SMILES
    COc1ccc(cc1)-n1c2ccccc2c(=O)n(O)c1=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Jack C Exell, et al. Cellularly Active N-hydroxyurea FEN1 Inhibitors Block Substrate Entry to the Active Site. Nat Chem Biol. 2016 Oct;12(10):815-21.?
molnova catalog
related products
  • TAK-448 acetate

    TAK-448 is a KISS1R protein agonist as a oligopeptide analog of kisspeptin,TAK-448 acetate (MVT-602 acetate) is a potent and full KISS1R agonist with an IC50 of 460 pM and an EC50 of 632 pM.

  • Neurokinin A(4-10) T...

    Neurokinin A (4-10) TFA is a tachykinin NK2 receptor agonist.

  • Dimethylaminomicheli...

    Dimethylaminomicheliolide HCl has potential anti-inflammatory and anti-tumor activity and inhibits the proliferation of glioblastoma cells by targeting pyruvate kinase 2 (PKM2) and reconnecting aerobic cell populations.