NMS-859

CAS No. 1449236-96-7

NMS-859( ZINC169324353 )

Catalog No. M26335 CAS No. 1449236-96-7

NMS-859 is an effective and covalent inhibitor of valosin-containing protein (VCP)/p97 with IC50s of 0.37 μM and 0.36 μM for wild-type VCP in the presence of 60 μM and 1 mM ATP in cells, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 218 In Stock
2MG 129 In Stock
5MG 188 In Stock
10MG 283 In Stock
25MG 451 In Stock
50MG 631 In Stock
100MG 848 In Stock
200MG Get Quote In Stock
500MG 1655 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    NMS-859
  • Note
    Research use only, not for human use.
  • Brief Description
    NMS-859 is an effective and covalent inhibitor of valosin-containing protein (VCP)/p97 with IC50s of 0.37 μM and 0.36 μM for wild-type VCP in the presence of 60 μM and 1 mM ATP in cells, respectively.
  • Description
    NMS-859 is an effective and covalent inhibitor of valosin-containing protein (VCP)/p97 with IC50s of 0.37 μM and 0.36 μM for wild-type VCP in the presence of 60 μM and 1 mM ATP in cells, respectively.(In Vitro):NMS-859 suppresses the cell proliferation with IC50s of 3.0 μM and 3.5 μM in HeLa and HCT116 cell lines, respectively. NMS-859 shows weak inhibitory activity against VCPC522T.
  • In Vitro
    NMS-859 is a potent VCP inhibitor, with IC50s of 0.37 and 0.36 μM for wild-type VCP in the presence of 60 μM and 1 mM ATP in cells, respectively. NMS-859 shows very weak inhibitory activity against VCPC522T. NMS-859 also suppresses the proliferation of cells, with IC50s of 3.5 μM and 3.0 μM in HCT116 and HeLa cell lines, respectively.
  • In Vivo
    ——
  • Synonyms
    ZINC169324353
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ADC Cytotoxin| Microtubule/Tubulin
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1449236-96-7
  • Formula Weight
    349.79
  • Molecular Formula
    C15H12ClN3O3S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (142.94 mM)
  • SMILES
    ClCC(=O)Nc1cccc(NC2=NS(=O)(=O)c3ccccc23)c1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Francisco JA, et al. cAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity. Blood. 2003 Aug 15;102(4):1458-65.
molnova catalog
related products
  • Dimetghyl 4-Hydroxyi...

    Dimetghyl 4-Hydroxyisophthalate ?is a methyl salicylate analogue used as a building block in the chemical synthesis.

  • Bragsin2

    Bragsin2 is a hydration-resistant cell penetrant, selective and non-competitive inhibitor of Afr guanine nucleotide exchange factor BRAG2.

  • (R)-3-Hydroxybutanoi...

    3-hydroxybutyric acid is involved in the synthesis and degradation of ketone bodies. Like the other ketone bodies (acetoacetate and acetone) levels of beta-hydroxybutyrate are raised in the blood and urine in ketosis. Beta-hydroxybutyrate is a typical partial-degradation product of branched-chain amino acids (primarily valine) released from muscle for hepatic and renal gluconeogenesis.