[HTML][HTML] Receptors involved in mental disorders and the use of clozapine, chlorpromazine, olanzapine, and aripiprazole to treat mental disorders

R Mlambo, J Liu, Q Wang, S Tan, C Chen - Pharmaceuticals, 2023 - mdpi.com
Mental illnesses are a global health challenge, and effective medicines are needed to treat
these conditions. Psychotropic drugs are commonly prescribed to manage mental disorders …

[HTML][HTML] The gut microbiota in neurodegenerative diseases: revisiting possible therapeutic targets for cannabidiol

BSA de Oliveira, DS Milanezi, P do Val Gonzaga… - Heliyon, 2022 - cell.com
Understanding the pathophysiology of Alzheimer's disease (AD) is essential to improve the
efficacy of treatments and, consequently, patients' lives. Unfortunately, traditional therapeutic …

In vitro pharmacological profile of KW-6356, a novel adenosine A2A receptor antagonist/inverse agonist

Y Ohno, M Suzuki, H Asada, T Kanda, M Saki… - Molecular …, 2023 - ASPET
KW-6356 is a novel adenosine A2A (A2A) receptor antagonist/inverse agonist, and its
efficacy as monotherapy in Parkinson's disease (PD) patients has been reported …

[HTML][HTML] Anti-parkinsonian activity of the adenosine A2A receptor antagonist/inverse agonist KW-6356 as monotherapy in MPTP-treated common marmosets

Y Ohno, E Okita, M Kawai-Uchida, N Fukuda… - European Journal of …, 2023 - Elsevier
KW-6356 is a novel adenosine A 2A receptor antagonist/inverse agonist that not only blocks
binding of adenosine to adenosine A 2A receptor but also inhibits the constitutive activity of …

[HTML][HTML] The adenosine A2A receptor antagonist/inverse agonist, KW-6356 enhances the anti-parkinsonian activity of L-DOPA with a low risk of dyskinesia in MPTP …

Y Ohno, E Okita, M Kawai-Uchida, Y Shoukei… - Journal of …, 2023 - Elsevier
The adenosine A 2A receptor antagonist/inverse agonist, KW-6356 has been shown to be
effective in Parkinson's disease (PD) patients as monotherapy and as an adjunct therapy to …

[HTML][HTML] “Dual Anta-Inhibitors” of the A2A Adenosine Receptor and Casein Kinase CK1delta: Synthesis, Biological Evaluation, and Molecular Modeling Studies

A Spinaci, M Buccioni, D Catarzi, C Cui, V Colotta… - Pharmaceuticals, 2023 - mdpi.com
Based on a screening of a chemical library of A2A adenosine receptor (AR) antagonists, a
series of di-and tri-substituted adenine derivatives were synthesized and tested for their …

[HTML][HTML] Neuroprotection afforded by targeting G protein-coupled receptors in heteromers and by heteromer-selective drugs

R Franco, G Navarro - Frontiers in Pharmacology, 2023 - frontiersin.org
G protein-coupled receptors (GPCRs) are the target of hundreds of approved drugs.
Although these drugs were designed to target individual receptors, it is becoming …

8-Aminopurines in the Cardiovascular and Renal Systems and Beyond

EK Jackson, SP Tofovic, Y Chen, LA Birder - Hypertension, 2023 - Am Heart Assoc
Screening of compounds comprising 8-substituted guanine revealed that 8-aminoguanosine
and 8-aminoguanine cause diuresis/natriuresis/glucosuria, yet decrease potassium …

[HTML][HTML] Identification of metabolites reproducibly associated with Parkinson's Disease via meta-analysis and computational modelling

X Luo, Y Liu, A Balck, C Klein, RMT Fleming - npj Parkinson's Disease, 2024 - nature.com
Many studies have reported metabolomic analysis of different bio-specimens from
Parkinson's disease (PD) patients. However, inconsistencies in reported metabolite …

[HTML][HTML] The olfactory Olfr-78/51E2 receptor interacts with the adenosine A2A receptor. Effect of menthol and 1,8-cineole on A2A receptor-mediated signaling

J Lillo, I García-Pérez, A Lillo… - Frontiers in …, 2023 - frontiersin.org
Heteromer formation is unknown for the olfactory family of G protein-coupled receptors
(GPCRs). We here identified, in a heterologous system, heteromers formed by the …