PIM kinase inhibitors: Structural and pharmacological perspectives

V Asati, DK Mahapatra, SK Bharti - European journal of medicinal chemistry, 2019 - Elsevier
The PIM kinase, also known as serine/threonine kinase plays an important role in cancer
biology and is found in three different isoforms namely PIM-1, PIM-2, and PIM-3. They are …

Topical advances in PIM kinases and their inhibitors: Medicinal chemistry perspectives

V Walhekar, C Bagul, D Kumar, A Muthal… - … et Biophysica Acta (BBA …, 2022 - Elsevier
Cytosolic PIM kinases are the members of serine/threonine family play a crucial role in the
cancer progression and development. Overexpression of PIM kinases is observed in various …

Design, synthesis and docking study of pyridine and thieno [2, 3-b] pyridine derivatives as anticancer PIM-1 kinase inhibitors

ME Abdelaziz, MMM El-Miligy, SM Fahmy… - Bioorganic …, 2018 - Elsevier
A series of pyridine and thieno [2, 3-b] pyridine derivatives have been designed and
synthesized as anticancer PIM-1 kinase inhibitors. Thirty-seven compounds were selected …

Application of Zr-MOFs based copper complex in synthesis of pyrazolo[3, 4-b]pyridine-5-carbonitriles via anomeric-based oxidation

E Tavakoli, H Sepehrmansourie, M Zarei… - Scientific Reports, 2023 - nature.com
In this research article, Zr-MOFs based copper complex as a novel heterogeneous and
porous catalyst was designed and prepared. The structure of catalyst has verified by various …

Utilization of cyanopyridine in design and synthesis of first-in-class anticancer dual acting PIM-1 kinase/HDAC inhibitors

AKA Bass, ESM Nageeb, MS El-Zoghbi… - Bioorganic …, 2022 - Elsevier
Herein, we report design and synthesis of twenty-one dual PIM-1/HDAC inhibitors utilizing 3-
cyanopyridines as a novel cap moiety linked with aliphatic/aromatic linker bearing carboxylic …

Development of novel cyanopyridines as PIM-1 kinase inhibitors with potent anti-prostate cancer activity: Synthesis, biological evaluation, nanoparticles formulation …

MH Ibrahim, MF Harras, SK Mostafa, SM Mohyeldin… - Bioorganic …, 2022 - Elsevier
Recently, inhibition of PIM-1 enzyme is found as an effective route in the fight against
proliferation of cancer. Herein, new cyano pyridines that target PIM-1 kinase were designed …

Discovery of new pyridine-quinoline hybrids as competitive and non-competitive PIM-1 kinase inhibitors with apoptosis induction and caspase 3/7 activation …

MMM El-Miligy, ME Abdelaziz, SM Fahmy… - Journal of Enzyme …, 2023 - Taylor & Francis
New quinoline-pyridine hybrids were designed and synthesised as PIM-1/2 kinase
inhibitors. Compounds 5b, 5c, 6e, 13a, 13c, and 14a showed in-vitro low cytotoxicity against …

[HTML][HTML] Bio-physical and computational studies on serum albumin/target protein binding of a potential anti-cancer agent

S SreedharanNair, KK Unni, S Sasidharanpillai… - European Journal of …, 2022 - Elsevier
The successful evolution of an effective drug depends on its pharmacokinetics, efficiency
and safety and these in turn depend on the drug-target/drug-carrier protein binding. This …

3-Cyano-2-oxa-pyridines: a promising template for diverse pharmacological activities

AK Bass, E Abdelhafez, M El-Zoghbi… - Journal of advanced …, 2021 - journals.ekb.eg
Pyridines have occupied a unique place in medicinal chemistry as it is widely profound as
natural products and formed the integral backbone of great number of drugs in the market. In …

Synthesis and in vitro evaluation of novel tetralin‐pyrazolo[3,4‐b]pyridine hybrids as potential anticancer agents

EK Hamza, NA Hamdy, ES Zarie… - Journal of …, 2020 - Wiley Online Library
New hybrids of tetralin‐pyrazolo [3, 4‐b] pyridine were synthesized in good yields. The
structures of newly synthesized compounds were confirmed by IR, NMR, MS, and elemental …