Number of items: 4.
2024
Brettell, S. B. et al.
(2024)
Targeting PfCLK3 with covalent inhibitors: a novel strategy for malaria treatment.
Journal of Medicinal Chemistry, 67(21),
pp. 18895-18910.
(doi: 10.1021/acs.jmedchem.4c01300)
(PMID:39441986)
(PMCID:PMC11571108)
2021
Mahindra, A. et al.
(2021)
Peptides derived from the SARS-CoV-2 receptor binding motif bind to ACE2 but do not block ACE2-mediated host cell entry or pro-inflammatory cytokine induction.
PLoS ONE, 16(11),
e0260283.
(doi: 10.1371/journal.pone.0260283)
(PMID:34793553)
(PMCID:PMC8601423)
2020
Mahindra, Amit, Janha, Omar, Mapesa, Kopano, Sanchez Azqueta, Ana, Alam, Mahmood M.
ORCID: https://orcid.org/0000-0003-2148-4887, Amambua-Ngwa, Alfred, Nwakanma, Davis C., Tobin, Andrew B.
ORCID: https://orcid.org/0000-0002-1807-3123 and Jamieson, Andrew G.
ORCID: https://orcid.org/0000-0003-1726-7353
(2020)
Development of potent PfCLK3 inhibitors based on TCMDC-135051 as a new class of antimalarials.
Journal of Medicinal Chemistry, 63(17),
pp. 9300-9315.
(doi: 10.1021/acs.jmedchem.0c00451)
(PMID:32787140)
(PMCID:PMC7497403)
2019
Alam, M. M. et al.
(2019)
Validation of the protein kinase PfCLK3 as a multistage cross-species malarial drug target.
Science, 365(6456),
eaau1682.
(doi: 10.1126/science.aau1682)
(PMID:31467193)
This list was generated on Thu Jul 31 04:56:50 2025 BST.