A review: Biological activities of novel cyanopyridine derivatives

Y Wu, T Wu, Y Huang - Archiv der Pharmazie, 2023 - Wiley Online Library
The discovery of new therapeutic drugs is heavily reliant on the structural diversity and
pharmacological properties of heterocyclic compounds. Pyridine heterocyclic‐related …

Identification of 3‐(5‐cyano‐6‐oxo‐pyridin‐2‐yl) benzenesulfonamides as novel anticancer agents endowed with EGFR inhibitory activity

MA Shaldam, AF Khalil, H Almahli… - Archiv der …, 2024 - Wiley Online Library
Abstract New 5‐cyano‐6‐oxo‐pyridine‐based sulfonamides (6a–m and 8a–d) were
designed and synthesized to potentially inhibit both the epidermal growth factor receptor …

New 2-alkoxycyanopyridine derivatives as inhibitors of EGFR, HER2, and DHFR: Synthesis, anticancer evaluation, and molecular modeling studies

SS Hawas, SM El-Sayed, PA Elzahhar… - Bioorganic Chemistry, 2023 - Elsevier
New series of substituted 2-alkoxycyanopyridine derivatives were synthesized and
evaluated for their in vitro and in vivo anticancer activities. Comparing the evaluated …

Design and Synthesis of Novel Pyridine-Based Compounds as Potential PIM-1 Kinase Inhibitors, Apoptosis, and Autophagy Inducers Targeting MCF-7 Cell Lines: In …

SM Shaban, EH Eltamany, ATA Boraei, MS Nafie… - ACS …, 2023 - ACS Publications
2-((3-Cyano-4, 6-dimethylpyridin-2-yl) oxy) acetohydrazide 1 was used as the precursor for
the synthesis of 5-thioxo-1, 3, 4-oxadiazol-2-yl) methoxy) nicotinonitrile 2. The latter was …

PIM Kinase Inhibitors as Novel Promising Therapeutic Scaffolds in Cancer Therapy

D Karati, A Saha, S Roy… - Current Topics in …, 2024 - benthamdirect.com
Cancer involves the uncontrolled, abnormal growth of cells and affects other tissues. Kinase
has an impact on proliferating the cells and causing cancer. For the purpose of treating …

Mimicry of sorafenib: novel diarylureas as VEGFR2 inhibitors and apoptosis inducers in breast cancer

MMF Ismail, EM Husseiny, MH Ibrahim - New Journal of Chemistry, 2023 - pubs.rsc.org
Thirteen diarylurea derivatives were designed and synthesized as sorafenib mimetics. The
cytotoxic activity of the newly synthesized entities towards human breast cancer cell …

Design, synthesis, and anti-breast cancer activity evaluation of novel 3-cyanopyridine derivatives as PIM-1 inhibitors

BRM Hussein, HH Mohammed, EA Ahmed… - Molecular Diversity, 2024 - Springer
A novel series of cyanopyridines 7a-j were synthesized via a one-pot multicomponent
reaction of arylidene 4 with ammonium acetate 5 and respective methylaryl/heterylketones …

Combining machine learning and structure-based approaches to develop oncogene PIM kinase inhibitors

H Almukadi, GA Jadkarim, A Mohammed… - Frontiers in …, 2023 - frontiersin.org
Introduction: PIM kinases are targets for therapeutic intervention since they are associated
with a number of malignancies by boosting cell survival and proliferation. Over the past …

Design, synthesis, biological evaluation and molecular docking study of new pyrazolo [1, 5-a] pyrimidines as PIM kinase inhibitors and apoptosis inducers

FG Abdulrahman, R Sabour, SM Abd El-Gilil… - Journal of Molecular …, 2024 - Elsevier
This study involved designing and synthesizing new derivatives of pyrazolo [1, 5-a]
pyrimidine 5a-l, which were prepared via reaction of 4-Arylazo-1H-pyrazole-3, 5-diamines …

Assessment of structural and activity-related contributions of various PIM-1 kinase inhibitors in the treatment of leukemia and prostate cancer

A Sharma, R Dubey, V Asati, GS Baweja, S Gupta… - Molecular Diversity, 2024 - Springer
One of the most perilous illnesses in the world is cancer. The cancer may be associated with
the mutation of different genes inside the body. The PIM kinase, also known as the …