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1.
Eur J Med Chem ; 268: 116162, 2024 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-38394930

RESUMO

Human African trypanosomiasis (HAT), or sleeping sickness, is a neglected tropical disease with current treatments marred by severe side effects or delivery issues. To identify novel classes of compounds for the treatment of HAT, high throughput screening (HTS) had previously been conducted on bloodstream forms of T. b. brucei, a model organism closely related to the human pathogens T. b. gambiense and T. b. rhodesiense. This HTS had identified a number of structural classes with potent bioactivity against T. b. brucei (IC50 ≤ 10 µM) with selectivity over mammalian cell-lines (selectivity index of ≥10). One of the confirmed hits was an aroyl guanidine derivative. Deemed to be chemically tractable with attractive physicochemical properties, here we explore this class further to develop the SAR landscape. We also report the influence of the elucidated SAR on parasite metabolism, to gain insight into possible modes of action of this class. Of note, two sub-classes of analogues were identified that generated opposing metabolic responses involving disrupted energy metabolism. This knowledge may guide the future design of more potent inhibitors, while retaining the desirable physicochemical properties and an excellent selectivity profile of the current compound class.


Assuntos
Parasitos , Tripanossomicidas , Trypanosoma brucei brucei , Trypanosoma , Tripanossomíase Africana , Animais , Humanos , Tripanossomicidas/química , Trypanosoma brucei rhodesiense , Guanidina/farmacologia , Tripanossomíase Africana/tratamento farmacológico , Tripanossomíase Africana/parasitologia , Guanidinas/farmacologia , Metabolismo Energético , Mamíferos
2.
Eur J Med Chem ; 226: 113822, 2021 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-34563964

RESUMO

MER tyrosine kinase (MERTK) upregulation is associated with M2 polarization of microglia, which plays a vital role in neuroregeneration following damage induced by neuroinflammatory diseases such as multiple sclerosis (MS). Therefore, a radiotracer specific for MERTK could be of great utility in the clinical management of MS, for the detection and differentiation of neuroregenerative and neurodegenerative processes. This study aimed to develop an [18F] ligand with high affinity and selectivity for MERTK as a potential positron emission tomography (PET) radiotracer. MIPS15691 and MIPS15692 were synthesized and kinase assays were utilized to determine potency and selectivity for MERTK. Both compounds were shown to be potent against MERTK, with respective IC50 values of 4.6 nM and 4.0 nM, and were also MERTK-selective. Plasma and brain pharmacokinetics were measured in mice and led to selection of MIPS15692 over MIPS15691. X-ray crystallography was used to visualize how MIPS15692 is recognized by the enzyme. [18F]MIPS15692 was synthesized using an automated iPHASE FlexLab module, with a molar activity (Am) of 49 ± 26 GBq/µmol. The radiochemical purity of [18F]MIPS15692 was >99% and the decay-corrected radiochemical yields (RCYs) were determined as 2.45 ± 0.85%. Brain MERTK protein density was measured by a saturation binding assay in the brain slices of a cuprizone mouse model of MS. High levels of specific binding of [18F]MIPS15692 to MERTK were found, especially in the corpus callosum/hippocampus (CC/HC). The in vivo PET imaging study of [18F]MIPS15692 suggested that its neuroPK is sub-optimal for clinical use. Current efforts are underway to optimize the neuroPK of our next generation PET radiotracers for maximal in vivo utility.


Assuntos
Desenvolvimento de Medicamentos , Doenças Neuroinflamatórias/tratamento farmacológico , Compostos Radiofarmacêuticos/farmacologia , c-Mer Tirosina Quinase/antagonistas & inibidores , Animais , Relação Dose-Resposta a Droga , Radioisótopos de Flúor , Camundongos , Estrutura Molecular , Doenças Neuroinflamatórias/diagnóstico por imagem , Tomografia por Emissão de Pósitrons , Compostos Radiofarmacêuticos/síntese química , Compostos Radiofarmacêuticos/química , Relação Estrutura-Atividade , c-Mer Tirosina Quinase/análise , c-Mer Tirosina Quinase/metabolismo
3.
Sci Total Environ ; 730: 138964, 2020 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-32402965

RESUMO

China has been implementing huge scale of urbanization in the past several decades and this will continue in the coming future years. Whilst the urbanization growth has presented good benefits to social and economic development in China, it has also brought severe challenges to the resource environment carrying capacity, such as air pollution, overloaded land resources. These challenges present differently in different provinces, which leads to the disparity in development between provinces. There has been growing concern whether the urbanization growth in different provinces is coordinated with resource environment carrying capacity (RECC), but this question has not been addressed in previous studies. This paper presents a critical analysis on the coordination between urbanization growth and resources environment carrying capacity (RECC) from provincial perspective in the context of China. A measurement of coordination degree (CD) is used to measure whether and to what extent that urbanization growth and RECC are coordinated by applying coupling coordination degree model (CCDM). The research data are collected from 30 provinces in China. The results suggest that the average coordination performance among the provinces experienced a steady growth during the period of 2005-2016, but there still exists big room for improvement towards well balanced coordination performance. From provincial perspective, the good performers are mainly economically developed provinces. The findings provide valuable references for the governments at both central and local level to adopt proper policy measures where necessary to improvement the coordination performance between urbanization and RECC.

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