A series of novel pyrazole-5-carboxamide and pyrazole-pyrimidine derivatives were designed and synthesized. All compounds have been screened for their antiproliferative activity against MGC-803, SGC-7901 and Bcap-37 cell lines in vitro. The results revealed that compounds 8a, 8c and 8e exhibited strong inhibitory activity against MGC-803 cell line. The flow cytometric analysis result showed that compound 8e could inhibit MGC-803 proliferation. Some title compounds were tested against telomerase, and compound 8e showed the most potent inhibitory activity with IC50 value at 1.02 ± 0.08 μM. The docking simulation of compound 8e was performed to get the probable binding model, among them, LYS 189, LYS 372, LYS 249 and ASP 254 may be the key residues for the telomerase activity.
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http://dx.doi.org/10.1016/j.ejmech.2014.12.013 | DOI Listing |
Bioorg Med Chem
June 2024
School of Pharmacy, Changzhou University, Jiangsu 213164, China. Electronic address:
19 derivatives of 1-benzyl-3-arylpyrazole-5-carboxamides (H-H) and 5 derivatives of 1-benzyl-5-arylpyrazole-3-carboxamides (J-J) have been designed and synthesized as potential negative allosteric modulators (NAMs) for the β-adrenergic receptor (βAR). The new pyrazole derivatives were screened on the classic G-protein dependent signaling pathway at βAR. The majority of 1-benzyl-3-aryl-pyrazole-5-carboxamide derivatives show more potent allosteric antagonistic activity against βAR than Cmpd-15, the first reported βAR NAM.
View Article and Find Full Text PDFJ Agric Food Chem
February 2024
College of Science, China Agricultural University, Beijing 100193, China.
Pyrazole carboxamide is widely utilized in agricultural crop protection. In this research, we synthesized two classes of compounds, namely, pyrazole-5-carboxamide () and pyrazole-4-carboxamide (), which are distinguished by the inclusion of the -1-(6-aryloxypyridin-3-yl) ethylamine skeleton. This design was inspired by the frequent occurrence of diaryl ether modules in pesticide molecules.
View Article and Find Full Text PDFJ Agric Food Chem
October 2023
College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014, China.
J Mol Struct
August 2023
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Gazi University, 06330, Ankara, Turkey.
Structurally diverse indole-3-pyrazole-5-carboxamide analogues () were designed, synthesized, and evaluated for their antiproliferative activity against three cancer cell lines (Huh7, MCF-7, and HCT116) using the sulforhodamine B assay. Some of the derivatives showed anticancer activities equal to or better than sorafenib against cancer cell lines. Compounds showed potent activity against the hepatocellular cancer (HCC) cell lines, with IC values in the range 0.
View Article and Find Full Text PDFCurr Org Synth
March 2023
Innovation Center of Pesticide Research, Department of Applied Chemistry, College of Science, China Agricultural University, Beijing 100193, China.
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