Novel pyrazole-5-carboxamide and pyrazole-pyrimidine derivatives: synthesis and anticancer activity.

Eur J Med Chem

School of Pharmacy, Anhui Medical University, Hefei 230032, PR China; State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing 210093, PR China. Electronic address:

Published: January 2015

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.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejmech.2014.12.013DOI Listing

Publication Analysis

Top Keywords

novel pyrazole-5-carboxamide
8
pyrazole-5-carboxamide pyrazole-pyrimidine
8
pyrazole-pyrimidine derivatives
8
activity mgc-803
8
inhibitory activity
8
activity
5
derivatives synthesis
4
synthesis anticancer
4
anticancer activity
4
activity series
4

Similar Publications

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 PDF

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 PDF
Article Synopsis
  • New insecticides with unique mechanisms are needed to combat rising pesticide resistance.
  • Researchers designed and tested novel aryl isoxazoline derivatives, confirming their structures and finding excellent insecticidal activity against certain pests.
  • One specific compound showed promising results comparable to an existing insecticide, with potential for further development based on structure-activity relationships and molecular analysis.
View Article and Find Full Text PDF

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 PDF

A Potential Fungicide against Pseudoperonospora Cubensis: Design, Synthesis and 3D-QSAR of New Pyrazole-5-Carboxamide Derivatives.

Curr Org Synth

March 2023

Innovation Center of Pesticide Research, Department of Applied Chemistry, College of Science, China Agricultural University, Beijing 100193, China.

Article Synopsis
  • Downy mildew is a significant fungal threat to crops, with increasing resistance to current fungicides, highlighting the need for new treatments.
  • Researchers developed and tested a series of pyrazole amide derivatives for their effectiveness against the fungus Pseudoperonospora cubensis, responsible for cucumber downy mildew.
  • Among the compounds, T24 showed the best fungicidal activity and was further analyzed to understand how its structure contributes to its effectiveness, suggesting it could be a promising new fungicide.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!