926240-77-9Relevant academic research and scientific papers
From Pyrazolones to Azaindoles: Evolution of Active-Site SHP2 Inhibitors Based on Scaffold Hopping and Bioisosteric Replacement
Mostinski, Yelena,Heynen, Guus J. J. E.,López-Alberca, Maria Pascual,Paul, Jerome,Miksche, Sandra,Radetzki, Silke,Schaller, David,Shanina, Elena,Seyffarth, Carola,Kolomeets, Yuliya,Ziebart, Nandor,De Schryver, Judith,Oestreich, Sylvia,Neuenschwander, Martin,Roske, Yvette,Heinemann, Udo,Rademacher, Christoph,Volkamer, Andrea,Von Kries, Jens Peter,Birchmeier, Walter,Nazaré, Marc
, p. 14780 - 14804 (2020/12/23)
The tyrosine phosphatase SHP2 controls the activity of pivotal signaling pathways, including MAPK, JAK-STAT, and PI3K-Akt. Aberrant SHP2 activity leads to uncontrolled cell proliferation, tumorigenesis, and metastasis. SHP2 signaling was recently linked to drug resistance against cancer medications such as MEK and BRAF inhibitors. In this work, we present the development of a novel class of azaindole SHP2 inhibitors. We applied scaffold hopping and bioisosteric replacement concepts to eliminate unwanted structural motifs and to improve the inhibitor characteristics of the previously reported pyrazolone SHP2 inhibitors. The most potent azaindole 45 inhibits SHP2 with an IC50 = 0.031 μM in an enzymatic assay and with an IC50 = 2.6 μM in human pancreas cells (HPAF-II). Evaluation in a series of cellular assays for metastasis and drug resistance demonstrated efficient SHP2 blockade. Finally, 45 inhibited proliferation of two cancer cell lines that are resistant to cancer drugs and diminished ERK signaling.
Aminopyrazoles with high affinity for the human neuropeptide Y5 receptor
Kordik, Cheryl P,Luo, Chi,Zanoni, Brian C,Dax, Scott L,McNally, James J,Lovenberg, Timothy W,Wilson, Sandy J,Reitz, Allen B
, p. 2283 - 2286 (2007/10/03)
1,3-Disubstituted-5-aminopyrazoles were prepared based on a lead compound found through high-throughput screening of our corporate compound library in an assay measuring affinity for the human neuropeptide Y5 receptor. The target compounds were prepared b
