Results 51 to 60 of about 3,571 (163)

Body fat reduction without cardiovascular changes in mice after oral treatment with the MAO inhibitor phenelzine

open access: yes, 2018
International audienceBackground and purpose: Phenelzine is an antidepressant drug known to increase the risk of hypertensive crisis when dietary tyramine is not restricted.
Sophie Le Gonidec   +13 more
core   +1 more source

Phenelzine: An old drug that may hold clues to the development of new neuroprotective agents

open access: yesPsychiatry and Clinical Psychopharmacology, 2021
The monoamine oxidase (MAO)-inhibiting antidepressant phenelzine (PLZ) is also used in the treatment of anxiety disorders such as panic disorder and social anxiety disorder and has been shown to have neuroprotective actions in an animal model of ...
Erin M. MacKenzie   +5 more
doaj  

Design, Synthesis of 3‐n‐Butylphthalide‐Hydrazine/Hydrazide Derivatives as Potential Anti‐Ischemic Stroke Agents

open access: yesChemistry &Biodiversity, Volume 23, Issue 10, October 2026.
A series of 3‐n‐butylphthalide hydrazine and hydrazide hybrids were synthesized. Among them, NBP‐HY exhibited superior antiplatelet activity compared to both NBP and aspirin. In vivo experiments confirmed that NBP‐HY possesses potent antithrombotic and anti‐ischemic stroke efficacy, coupled with moderate metabolic stability, favorable blood–brain ...
Yong Li   +7 more
wiley   +1 more source

Organoids in Precision Radiotherapy: Methodological Foundations, Tumor‐Specific Evidence, and Translational Roadmaps

open access: yesCancer Medicine, Volume 15, Issue 9, September 2026.
ABSTRACT Background Radiotherapy remains a cornerstone of cancer treatment, while its efficacy is often limited by tumor radioresistance and the risk of normal tissue toxicity. Conventional preclinical models, including two‐dimensional (2D) cell cultures and murine xenografts, exhibit significant limitations in recapitulating human tumor ...
Yixian Zhu   +4 more
wiley   +1 more source

Inhibitory effect of phenelzine on oxidative microsomal enzyme systems of rat liver

open access: yes, 1983
The inhibitory effects of phenelzine on the hepatic microsomal demethylation of aminopyrine, N,N-dimethylaniline, and p-nitroanisole on the hydroxylation of aniline and on the pharmacokinetics of antipyrine were investigated in the rat.
A. Atitsé-Gbeassor, P. M. Bélanger
core   +1 more source

Recent Advances in Luminescent Hydrogen‐Bonded Organic Frameworks (HOFs): Linker Design, Phosphorescence, and Smart Responsiveness

open access: yesInformation &Functional Materials, Volume 3, Issue 3, Page 321-353, September 2026.
Luminescent Hydrogen‐bonded organic frameworks (HOFs) provide an innovative platform for sensing and optoelectronic applications. This review outlines design principles, recent advances in synthesis and optical tuning, diverse sensing applications, and discusses current challenges and future directions for HOFs.
Heng Wu   +4 more
wiley   +1 more source

REVERSİBLE MAO İNHİBİTORS İN THE TREATMENT OF PANİC DISORDERS

open access: yesPsychiatry and Clinical Psychopharmacology, 2021
Members of three classes of drugs have been shown to have efficacy-tricyclic antidepressants,monoamine oxidase inhibitors and benzodiazepins. Imipramine and clomipramine have been the tricyclic antidepressants most extensively studied.
Nesrin DİLBAZ   +3 more
doaj  

Neurochemical effects of the monoamine oxidase inhibitor phenelzine on brain GABA and alanine: A comparison with vigabatrin

open access: yesJournal of Pharmacy & Pharmaceutical Sciences, 2008
PURPOSE. To compare phenelzine (PLZ), an antidepressant drug with anxiolytic properties which inhibits monoamine oxidase (MAO) but also elevates rat brain levels of the amino acids ?-aminobutyric acid (GABA) and alanine (ALA), with vigabatrin (VIG ...
Kathryn G. Todd, Glen B. Baker
doaj   +1 more source

From Fragments to Function: Novel Hydrazone Derivatives as Monoamine Oxidase Inhibitors

open access: yesChemMedChem, Volume 21, Issue 16, 27 August 2026.
Twelve N‐acylhydrazone derivatives (5a–f, 6a–f) were synthesized and characterized. Compounds displayed potent submicromolar inhibition against both MAO‐A and MAO‐B. Compound 6e exhibited the strongest activity (IC50 = 0.073 μM for MAO‐A; 0.064 μM for MAO‐B). Kinetic and docking analyses confirmed reversible, competitive inhibition via FAD interaction.
Hasan Erdinç Sellitepe   +5 more
wiley   +1 more source

Relationship Between Sexual Attitude and Sexual Function Among Iranian Women and Men During Pregnancy: A Cross‐Sectional Study

open access: yesHealth Science Reports, Volume 9, Issue 8, August 2026.
ABSTRACT Background and Aims Sexual function is considered an essential criterion for enhancing the quality of life, encompassing not only the genital component but also mental and physical factors. The present study was conducted to determine the relationship between sexual attitude and sexual function among Iranian women and men during pregnancy ...
Sepideh Mashayekh‐Amiri   +3 more
wiley   +1 more source

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