SMIFH2

CAS No. 340316-62-3

SMIFH2( —— )

Catalog No. M27714 CAS No. 340316-62-3

SMIFH2 is formin homology 2 (FH2) domains inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 67 In Stock
2MG 38 In Stock
5MG 61 In Stock
10MG 92 In Stock
25MG 188 In Stock
50MG 367 In Stock
100MG 546 In Stock
200MG Get Quote In Stock
500MG 1070 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SMIFH2
  • Note
    Research use only, not for human use.
  • Brief Description
    SMIFH2 is formin homology 2 (FH2) domains inhibitor.
  • Description
    SMIFH2 is formin homology 2 (FH2) domains inhibitor.
  • In Vitro
    SMIFH2 (25 uM; 1-16 hours) induces dynamic cytoskeletal remodelling in U2OS cells. SMIFH2 (25 μM) reduces p300, mDia2 and p53 levels in a proteasome-independent manner.SMIFH2 reduces expression and activity of p53 through a post-transcriptional, proteasome-independent mechanism that influences remodelling of the cytoskeleton. Western Blot Analysis Cell Line:293T, A375, U2OS, and MDA-MB-231 cells Concentration:25 μM Incubation Time:5 hours for 293T, U2OS, MDA-MB-231 cells; 2.5 hours for A375 cells Result:Downregulated mDia2, p53 and p300 protein levels.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    mGluR5
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    340316-62-3
  • Formula Weight
    377.21
  • Molecular Formula
    C15H9BrN2O3S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (331.38 mM)
  • SMILES
    Brc1cccc(c1)N1C(=S)NC(=O)\C(=C/c2ccco2)C1=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Keck TM, et al. A novel mGluR5 antagonist, MFZ 10-7, inhibits cocaine-taking and cocaine-seeking behavior in rats. Addict Biol.
molnova catalog
related products
  • Licoarylcoumarin

    Licoarylcoumarin is a strong inhibitor of adenosine 3',5'-cyclic monophosphate (cAMP) phosphodiesterase. Licoarylcoumarin has antibacterial effects on the VRE strains; it has anti-HIV activity, and it has inhibitory effects on xanthine oxidase.

  • Pasakbumin B

    Pasakbumin B is a bioactive compound from Eurycoma longifolia Jack.

  • Gentiopicrin

    Gentiopicroside, a naturally occurring iridoid glycoside, extracted from Gentiana manshurica Kitag, inhibits P450 activity, with an IC50 and a Ki of 61 μM and 22.8 μM for CYP2A6.