MK2 inhibitor III

CAS No. 1186648-22-5

MK2 inhibitor III( —— )

Catalog No. M10637 CAS No. 1186648-22-5

A potent, cell-permeable inhibitor of MK2 with IC50 of 8.5 nM; less potently blocks MK3 and MK5 (IC50s=210 and 81 nM, respectively).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 147 Get Quote
10MG 237 Get Quote
25MG 475 Get Quote
50MG 692 Get Quote
100MG 972 Get Quote
500MG 1944 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    MK2 inhibitor III
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, cell-permeable inhibitor of MK2 with IC50 of 8.5 nM; less potently blocks MK3 and MK5 (IC50s=210 and 81 nM, respectively).
  • Description
    A potent, cell-permeable inhibitor of MK2 with IC50 of 8.5 nM; less potently blocks MK3 and MK5 (IC50s=210 and 81 nM, respectively) and is weak or inactive against several other kinases, including P38 MAPKs; prevents LPS-induced synthesis of TNF-α in human monocyte-like U937 cells with IC50 of 4.4 uM.
  • In Vitro
    MK2-IN-3 hydrate suppresses TNFα production in U397 cells with an IC50 of 4.4 μM.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    MAPK/ERK Signaling
  • Target
    MAPKAPK2 (MK2)
  • Recptor
    MAPKAPK2 (MK2)
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1186648-22-5
  • Formula Weight
    358.4
  • Molecular Formula
    C21H16N4O ? H2O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (348.78 mM)
  • SMILES
    C1CNC(=O)C2=C1NC(=C2)C3=CC(=NC=C3)C4=CC5=CC=CC=C5N=C4.O
  • Chemical Name
    2-(2-(quinolin-3-yl)pyridin-4-yl)-1,5,6,7-tetrahydro-4H-pyrrolo[3,2-c]pyridin-4-one hydrate

Shipping & Storage Information

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

Reference

1. Anderson DR, et al. J Med Chem. 2007 May 31;50(11):2647-54. 2. Gurgis F, et al. Cell Death Discov. 2015 Sep 7;1:15028.
molnova catalog
related products
  • MK2-IN-1 hydrochlori...

    MK2-IN-1 is a potent, selecitve, non-ATP competitive MAPKAPK2(MK2) inhibitor with IC50 of 0.11 uM.

  • MK2 inhibitor III

    A potent, cell-permeable inhibitor of MK2 with IC50 of 8.5 nM; less potently blocks MK3 and MK5 (IC50s=210 and 81 nM, respectively).

  • PF-3644022

    PF-3644022 is a potent and selective, freely reversible, ATP-competitive inhibitor of MAPKAP2 (MK2) with Ki of 3 nM.