SMI-16a

CAS No. 587852-28-6

SMI-16a( Pim1/2 Inhibitor IV | PIM1/2 Kinase Inhibitor VI )

Catalog No. M17550 CAS No. 587852-28-6

PIM1/2 Kinase Inhibitor VI, a cell-permeable thiazolidinedione compound, acts as an effective, ATP-competitive inhibitor against Pim-1/2 kinases (IC50: 150/20 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 36 In Stock
5MG 58 In Stock
10MG 80 In Stock
25MG 147 In Stock
50MG 222 In Stock
100MG 335 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SMI-16a
  • Note
    Research use only, not for human use.
  • Brief Description
    PIM1/2 Kinase Inhibitor VI, a cell-permeable thiazolidinedione compound, acts as an effective, ATP-competitive inhibitor against Pim-1/2 kinases (IC50: 150/20 nM).
  • Description
    SMI-16a, also known as Pim1/2 Inhibitor IV, is a potent, cell-permeable, ATP-competitive inhibitor of Pim-1/2 kinases (IC50 = 150 nM and 20 nM against Pim-1 and Pim-2, respectively).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Pim1/2 Inhibitor IV | PIM1/2 Kinase Inhibitor VI
  • Pathway
    GPCR/G Protein
  • Target
    GPCR19
  • Recptor
    Pim1| Pim2
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    587852-28-6
  • Formula Weight
    263.31
  • Molecular Formula
    C13H13NO3S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 150 mg/mL; 569.67 mM
  • SMILES
    CCCOC1=CC=C(C=C1)/C=C\2/C(=O)NC(=O)S2
  • Chemical Name
    (Z)-5-(4-Propoxybenzylidene)thiazolidine-2,4-dione

Shipping & Storage Information

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

Reference

1. Xia Z., et al. Synthesis and evaluation of novel inhibitors of Pim-1 and Pim-2 protein kinases. J Med Chem. 2009 Jan 8;52(1):74-86.
molnova catalog
related products
  • TGR5

    TGR5 Receptor Agonist, a potent TGR5(GPCR19) agonist, showed improved potency in the U2-OS cell assay (pEC50 = 6.8) and in melanophore cells (pEC50 = 7.5).

  • TC-G 1005

    TC-G 1005 is a potent and selective GPBA agonist (EC50 :0.72 nM; hTGR5). Selective for TGR5 over FXR (farnesoid X receptor). Increases plasma GLP-1 levels and reduces blood glucose in mice.

  • SBI-115

    SBI-115 is an?antagonist of?TGR5.?SBI-115 decreases hepatic cystogenesis with polycystic liver diseases via inhibiting TGR5.