CDK inhibitors from past to present: A new wave of cancer therapy

MJ Mughal, K Bhadresha, HF Kwok - Seminars in cancer biology, 2023 - Elsevier
Deregulation of the cell cycle machinery, which has been linked to dysregulation of cyclin-
dependent kinases (CDKs), is a defining characteristic of cancer, eventually promoting …

[HTML][HTML] 1, 3, 4-Oxadiazole-containing hybrids as potential anticancer agents: Recent developments, mechanism of action and structure-activity relationships

S Nayak, SL Gaonkar, EA Musad… - Journal of Saudi Chemical …, 2021 - Elsevier
Chemotherapy is an important therapeutic approach for the treatment of cancer. Currently,
many anticancer drugs are available in the market that plays an important role in cancer …

Rational approaches, design strategies, structure activity relationship and mechanistic insights for therapeutic coumarin hybrids

H Singh, JV Singh, K Bhagat, HK Gulati… - Bioorganic & medicinal …, 2019 - Elsevier
Hybrid molecules, furnished by combining two or more pharmacophores is an emerging
concept in the field of medicinal chemistry and drug discovery that has attracted substantial …

[HTML][HTML] Small molecule therapeutics for tauopathy in Alzheimer's disease: walking on the path of most resistance

L Wang, R Kumar, PF Pavlov, B Winblad - European journal of medicinal …, 2021 - Elsevier
Alzheimer's disease (AD) is the most common form of dementia characterized by presence
of extracellular amyloid plaques and intracellular neurofibrillary tangles composed of tau …

Technologies of targeting histone deacetylase in drug discovery: Current progress and emerging prospects

J Ru, Y Wang, Z Li, J Wang, C Ren, J Zhang - European Journal of …, 2023 - Elsevier
Histone deacetylases (HDACs) catalyze the hydrolysis of acetyl-l-lysine side chains in
histones and non-histones, which are key to epigenetic regulation in humans. Targeting …

Triazole tethered isatin-coumarin based molecular hybrids as novel antitubulin agents: Design, synthesis, biological investigation and docking studies

H Singh, JV Singh, MK Gupta, AK Saxena… - Bioorganic & medicinal …, 2017 - Elsevier
In an attempt to develop potent anti-tubulin agents against most dreadful disease cancer, a
library of 28 novel triazole tethered isatin-coumarin hybrids were synthesized by click …

How selective are pharmacological inhibitors of cell-cycle-regulating cyclin-dependent kinases?

R Jorda, D Hendrychová, J Voller… - Journal of medicinal …, 2018 - ACS Publications
Cyclin-dependent kinases (CDKs) are an important and emerging class of drug targets for
which many small-molecule inhibitors have been developed. However, there is often …

Triazole tethered C5-curcuminoid-coumarin based molecular hybrids as novel antitubulin agents: Design, synthesis, biological investigation and docking studies

H Singh, M Kumar, K Nepali, MK Gupta… - European journal of …, 2016 - Elsevier
Kee** in view the confines allied with presently accessible antitumor agents and success
of C 5-curcuminoid based bifunctional hybrids as novel antitubulin agnets, molecular …

Determination of biological studies and molecular docking calculations of isatin-thiosemicarbazone hybrid compounds

ÜM Koçyiğit, M Doğan, H Muğlu, P Taslimi… - Journal of Molecular …, 2022 - Elsevier
Abstract Design, synthesis, structural elucidation, and investigation of cytotoxic and
antimicrobial activity, butyrylcholinesterase (BChE), and acetylcholinesterase (AChE) …