CC618

CAS No. 1680204-90-3

CC618( —— )

Catalog No. M28891 CAS No. 1680204-90-3

CC618 is a selective PPARβ/δ antagonist with an IC50 of 10.0 μM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 314 In Stock
5MG 249 In Stock
10MG 369 In Stock
25MG 562 In Stock
50MG 770 In Stock
100MG 1032 In Stock
200MG 1376 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    CC618
  • Note
    Research use only, not for human use.
  • Brief Description
    CC618 is a selective PPARβ/δ antagonist with an IC50 of 10.0 μM.
  • Description
    CC618 is a selective PPARβ/δ antagonist with an IC50 of 10.0 μM.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    PPAR
  • Recptor
    Hedgehog
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1680204-90-3
  • Formula Weight
    523.47
  • Molecular Formula
    C20H15F6N3O3S2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Cc1c(C(NCCS(c2ncc(C(F)(F)F)cc2)(=O)=O)=O)sc(-c2ccc(C(F)(F)F)cc2)n1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Williams JA, et al. Identification of a small molecule inhibitor of the hedgehog signaling pathway: effects on basal cell carcinoma-like lesions.Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4616-21. Epub 2003 Apr 4.
molnova catalog
related products
  • Sakuranetin

    Sakuranetin, a flavanone phytoalexin from ultraviolet-irradiated rice leaves, it has antifungal, antimutagenic, anti-inflammatory and antioxidant effects.

  • Fucosterol

    Fucosterol is isolated from E. stolonifera with anti-diabetic anti-adipogenic and anti-cancer activities. It regulates adipogenesis via modulation of PPARα and C/EBPα expression.

  • (R)-(+)-Bay-K-8644

    (R)-(+)-Bay-K-8644 is a Ca2+ channel and dihydropyridine agonist that inhibits Ba2+ currents (IBa), induces central respiratory depression in cats, and inhibits platelet activation through competitive antagonism of thromboxane A2-prostaglandin H2 receptors.