Monoamine oxidase inhibitors: A concise review with special emphasis on structure activity relationship studies

A Kumar, M Bhatia, A Kapoor, P Kumar… - European Journal of …, 2022 - Elsevier
Monoamine oxidase enzyme is necessary for the management of brain functions. It
oxidatively metabolizes monoamines and produces ammonia, aldehyde and hydrogen …

Effects of linkers and substitutions on multitarget directed ligands for Alzheimer's diseases: Emerging paradigms and strategies

N Pravin, K Jozwiak - International journal of molecular sciences, 2022 - mdpi.com
Alzheimer's disease (AD) is multifactorial, progressive and the most predominant cause of
cognitive impairment and dementia worldwide. The current “one-drug, one-target” approach …

Synthesis and biological evaluation of new pyrazolone Schiff bases as monoamine oxidase and cholinesterase inhibitors

F Tok, B Koçyiğit-Kaymakçıoğlu, BN Sağlık, S Levent… - Bioorganic …, 2019 - Elsevier
In the current work, Schiff base derivatives of antipyrine were synthesized. The chemical
characterization of the compounds was confirmed using IR, 1 H NMR, 13 C NMR and mass …

[HTML][HTML] Drug discovery and computational strategies in the multitarget drugs era

JO Viana, MB Félix, MS Maia, VL Serafim… - Brazilian Journal of …, 2018 - SciELO Brasil
The pharmaceutical industry is increasingly joining chemoinformatics in the search for the
development of new drugs to be used in the treatment of diseases. These computational …

QSAR models for nitrogen containing monophosphonate and bisphosphonate derivatives as human farnesyl pyrophosphate synthase inhibitors based on Monte …

P Kumar, A Kumar, J Sindhu, S Lal - Drug Research, 2019 - thieme-connect.com
Human farnesyl pyrophosphate synthase (hFPPS) is a well-settled therapeutic target and it
is an enzyme of the mevalonate pathway which catalyzes the biosynthesis of the C-15 …

Synthesis, characterization, enzyme inhibitory activity, and molecular docking analysis of a new series of thiophene-based heterocyclic compounds

A Cetin, F Türkan, E Bursal, M Murahari - Russian Journal of Organic …, 2021 - Springer
Phenyl-3-(thiophen-2-yl)-1 H-pyrazole-5-carboxamide derivatives were designed and
evaluated for their in vitro enzyme inhibitory activities against acetylcholinesterase (AChE) …

Homology model, molecular dynamics simulation and novel pyrazole analogs design of Candida albicans CYP450 lanosterol 14 α-demethylase, a target enzyme for …

S Jacob K, S Ganguly, P Kumar, R Poddar… - Journal of …, 2017 - Taylor & Francis
Candida albicans infections and their resistance to clinically approved azole drugs are
major concerns for human. The azole antifungal drugs inhibit the ergosterol synthesis by …

Recent advances in multi-target anti-Alzheimer disease compounds (2013 up to the present)

N Wang, P Qiu, W Cui, X Yan… - Current Medicinal …, 2019 - ingentaconnect.com
Since the last century, when scientists proposed the lock-and-key model, the discovery of
drugs has focused on the development of drugs acting on single target. However, single …

Therapeutic outlook of pyrazole analogs: A mini review

S Ganguly, S K. Jacob - Mini Reviews in Medicinal Chemistry, 2017 - benthamdirect.com
Background: Pyrazole is one of the excellent structural motifs in medicinal chemistry.
Various physiological and therapeutic possibilities have been exploited by incorporating …

Multi-targeting strategies for Alzheimer's disease therapeutics: pros and cons

S Das, S Basu - Current Topics in Medicinal Chemistry, 2017 - ingentaconnect.com
Alzheimer's Disease (AD) is a single major cause of dementia in middle to old age
individuals involving several different etiopathological mechanisms that are yet to be …