Antimalarial drug discovery: Progress and approaches
Recent antimalarial drug discovery has been a race to produce new medicines that
overcome emerging drug resistance, whilst considering safety and improving dosing …
overcome emerging drug resistance, whilst considering safety and improving dosing …
Dual-specificity, tyrosine phosphorylation-regulated kinases (DYRKs) and cdc2-like kinases (CLKs) in human disease, an overview
MF Lindberg, L Meijer - International Journal of Molecular Sciences, 2021 - mdpi.com
Dual-specificity tyrosine phosphorylation-regulated kinases (DYRK1A, 1B, 2-4) and cdc2-
like kinases (CLK1-4) belong to the CMGC group of serine/threonine kinases. These protein …
like kinases (CLK1-4) belong to the CMGC group of serine/threonine kinases. These protein …
Comparative efficacy and selectivity of pharmacological inhibitors of DYRK and CLK protein kinases
MF Lindberg, E Deau, J Arfwedson… - Journal of medicinal …, 2023 - ACS Publications
Dual-specificity, tyrosine phosphorylation-regulated kinases (DYRKs) and cdc2-like kinases
(CLKs) play a large variety of cellular functions and are involved in several diseases …
(CLKs) play a large variety of cellular functions and are involved in several diseases …
Small-molecule kinase inhibitors for the treatment of nononcologic diseases
Z Xie, X Yang, Y Duan, J Han… - Journal of medicinal …, 2021 - ACS Publications
Great successes have been achieved in developing small-molecule kinase inhibitors as
anticancer therapeutic agents. However, kinase deregulation plays essential roles not only …
anticancer therapeutic agents. However, kinase deregulation plays essential roles not only …
MalDA, accelerating malaria drug discovery
The Malaria Drug Accelerator (MalDA) is a consortium of 15 leading scientific laboratories.
The aim of MalDA is to improve and accelerate the early antimalarial drug discovery process …
The aim of MalDA is to improve and accelerate the early antimalarial drug discovery process …
Azaindole derivatives as potential kinase inhibitors and their SARs elucidation
G Fang, H Chen, Z Cheng, Z Tang, Y Wan - European Journal of Medicinal …, 2023 - Elsevier
Currently, heterocycles have occupied an important position in the fields of drug design.
Among them, azaindole moiety is regarded as one privileged scaffold to develop therapeutic …
Among them, azaindole moiety is regarded as one privileged scaffold to develop therapeutic …
Cdc-like kinases (CLKs): biology, chemical probes, and therapeutic potential
P Martín Moyano, V Němec, K Paruch - International Journal of Molecular …, 2020 - mdpi.com
Protein kinases represent a very pharmacologically attractive class of targets; however,
some members of the family still remain rather unexplored. The biology and therapeutic …
some members of the family still remain rather unexplored. The biology and therapeutic …
Trends of antimalarial marine natural products: Progresses, challenges and opportunities
Y Hai, ZM Cai, PJ Li, MY Wei, CY Wang, YC Gu… - Natural Product …, 2022 - pubs.rsc.org
Covering 1972 to 2021 Malaria remains a significant public health problem in some regions
of the world. The great efforts to control malaria have been severely compromised due to the …
of the world. The great efforts to control malaria have been severely compromised due to the …
Drug design targeting active posttranslational modification protein isoforms
Modern drug design aims to discover novel lead compounds with attractable chemical
profiles to enable further exploration of the intersection of chemical space and biological …
profiles to enable further exploration of the intersection of chemical space and biological …
Advances in omics-based methods to identify novel targets for malaria and other parasitic protozoan infections
AN Cowell, EA Winzeler - Genome medicine, 2019 - Springer
A major advance in antimalarial drug discovery has been the shift towards cell-based
phenotypic screening, with notable progress in the screening of compounds against the …
phenotypic screening, with notable progress in the screening of compounds against the …