CPDA

CAS No. 1415834-63-7

CPDA( —— )

Catalog No. M26128 CAS No. 1415834-63-7

CPDA is a new potent inhibitor of SH2 domain-containing inositol phosphatase 2 (SHIP2).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 43 In Stock
5MG 39 In Stock
10MG 65 In Stock
25MG 128 In Stock
50MG 211 In Stock
100MG 333 In Stock
200MG 458 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    CPDA
  • Note
    Research use only, not for human use.
  • Brief Description
    CPDA is a new potent inhibitor of SH2 domain-containing inositol phosphatase 2 (SHIP2).
  • Description
    CPDA is a new potent inhibitor of SH2 domain-containing inositol phosphatase 2 (SHIP2).(In Vitro):CPDA enhances insulin signaling.(In Vivo):CPDA greatly improves abnormal glucose metabolism in diabetic animals. In db/db mice, CPDA improves abnormal glucose metabolism.
  • In Vitro
    CPDA enhances insulin signaling.
  • In Vivo
    CPDA greatly improves abnormal glucose metabolism in diabetic animals. CPDA improves the abnormal glucose metabolism in db/db mice.
  • Synonyms
    ——
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Phosphatase
  • Recptor
    Smoothened
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1415834-63-7
  • Formula Weight
    388.8
  • Molecular Formula
    C20H15ClF2N2O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : ≥ 50 mg/mL (128.60 mM)
  • SMILES
    Fc1cccc(F)c1CC(=O)Nc1cc(OCc2ccc(Cl)cc2)ccn1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Solinas et al (2012) Acylthiourea, acylurea, and acylguanidine derivatives with potent hedgehog inhibiting activity. J.Med.Chem. 55 1559
molnova catalog
related products
  • Cyclosporin A

    Cyclosporin A is an immunosuppressive agent, binds to the cyclophilin and then inhibits calcineurin with IC50 of 7 nM, widely used in organ transplantation to prevent rejection.

  • KY-226

    KY-226 is a potent inhibitor of protein tyrosine phosphatase 1B (PTP1B)(IC50: 0.25 μM)

  • BCI hydrochloride

    BCI hydrochloride ((E)-BCI hydrochloride) is a selective dual-specificity phosphatase 6 (DUSP6) inhibitor that inhibits RANKL-mediated osteoclastogenesis and attenuates oophorectomy-induced bone loss.