CRT 0066101

Catalog # Availability Size / Price Qty
4975/10
CRT 0066101 | CAS No. 1883545-60-5 | Protein Kinase D Inhibitors
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Description: Potent protein kinase D (PKD) inhibitor

Chemical Name: 2-[4-[[(2R)-2-aminobutyl]amino]-2-pyrimidinyl]-4-(1-methyl-1H-pyrazol-4-yl)phenol dihydrochloride

Purity: ≥98%

Product Details
Citations (7)
Reviews

Biological Activity

CRT 0066101 is a potent inhibitor of protein kinase D (PKD); inhibits all PKD isoforms (IC50 values are 1, 2 and 2.5 nM for PKD1, PKD3 and PKD2 respectively). Exhibits selectivity for PKD against a panel of >90 protein kinases, including PKCα, MEK, ERK, c-Raf and c-Src. Reduces proliferation and cell viability of pancreatic cancer cells expressing moderate levels of endogenous PKD1/2. Orally bioavailable.

Technical Data

M.Wt:
411.33
Formula:
C18H22N6O.2HCl
Solubility:
Soluble to 100 mM in water and to 20 mM in DMSO
Purity:
≥98%
Storage:
Store at -20°C
CAS No:
1883545-60-5

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.

Background References

  1. Insulin Receptor and GPCR Crosstalk Stimulates YAP via PI3K and PKD in Pancreatic Cancer Cells
    F Hao, Q Xu, Y Zhao, JV Stevens, SH Young, J Sinnett-Sm, E Rozengurt
    Mol. Cancer Res., 2017;0(0):.
  2. Protein kinase D1 (PKD1) phosphorylation on Ser(203) by type I p21-activated kinase (PAK) regulates PKD1 localization
    JK Chang, Y Ni, L Han, J Sinnett-Sm, R Jacamo, O Rey, SH Young, E Rozengurt
    J. Biol. Chem., 2017;0(0):.
  3. PKD1 mediates negative feedback of PI3K/Akt activation in response to G protein-coupled receptors.
    Ni et al.
    PLoS ONE, 2013;9:e73149
  4. A novel small molecule inhibitor of protein kinase D blocks pancreatic cancer growth in vitro and in vivo.
    Harikumar et al.
    Mol.Cancer Ther., 2010;9:1136

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Citations for CRT 0066101

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