Necrostatin-34

CAS No. 375835-43-1

Necrostatin-34 ( 2-{[3-cyano-4-(4-methylphenyl)-6-oxo-1,4 )

Catalog No. M24335 CAS No. 375835-43-1

Necrostatin-34 is a RIPK1 kinase inhibitor, stabilizing RIPK1 kinase in an inactive conformation by occupying a distinct binding pocket in the kinase domain.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 130 In Stock
5MG 112 In Stock
10MG 164 In Stock
25MG 306 In Stock
50MG 432 In Stock
100MG 603 In Stock
200MG 814 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Necrostatin-34
  • Note
    Research use only, not for human use.
  • Brief Description
    Necrostatin-34 is a RIPK1 kinase inhibitor, stabilizing RIPK1 kinase in an inactive conformation by occupying a distinct binding pocket in the kinase domain.
  • Description
    Necrostatin-34 is a RIPK1 kinase inhibitor, stabilizing RIPK1 kinase in an inactive conformation by occupying a distinct binding pocket in the kinase domain.(In Vitro):Necrostatin-34 (Nec-34) exhibits IC50 values of 667 nM and 134 nM for TNFα in FADD def-Jurkat cells and L939 cells, respectively.Necrostatin-34 (Nec-34, 10 μM) inhibits the dimerization-induced RIPK1 activation as examined by phosphorylation of Ser166 (p-S166) of RIPK1, a biomarker for RIPK1 activation.Necrostatin-34 (Nec-34) may block TNFα-induced complex II formation by inhibiting the activation of RIPK1 kinase.
  • In Vitro
    Necrostatin-34 (Nec-34) exhibits IC50 values of 667 nM and 134 nM for TNFα in FADD def-Jurkat cells and L939 cells, respectively.Necrostatin-34 (Nec-34, 10?μM) inhibits the dimerization-induced RIPK1 activation as examined by phosphorylation of Ser166 (p-S166) of RIPK1, a biomarker for RIPK1 activation.Necrostatin-34 (Nec-34) may block TNFα-induced complex II formation by inhibiting the activation of RIPK1 kinase. Western Blot Analysis Cell Line:RIPK1 knockout L929 cells transfected with an expressing vector encoding an inducible and dimerizable RIPK1 fused with FKBP at the C-terminus.Concentration:10?μM.Incubation Time:30 min (and then 100?ng/mL TNFα was added for indicated periods of time).Result:Downregulated p-S166 levels.
  • In Vivo
    ——
  • Synonyms
    2-{[3-cyano-4-(4-methylphenyl)-6-oxo-1,4
  • Pathway
    Apoptosis
  • Target
    RIP kinase
  • Recptor
    RIPK1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    375835-43-1
  • Formula Weight
    384.48
  • Molecular Formula
    C18H16N4O2S2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:125 mg/mL (325.11 mM; Need ultrasonic)
  • SMILES
    O=C(NC1=NC=CS1)CSC2=C(C#N)C(C3=CC=C(C)C=C3)CC(N2)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Huyan Meng, et al. Discovery of a cooperative mode of inhibiting RIPK1 kinase. Cell Discov. 2021 Jun 1;7(1):41.
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