Improved Pharmacokinetic and Pharmacodynamic Profile of Deuterium-Reinforced Tricyclic Antidepressants Doxepin, Dosulepin, and Clomipramine in Animal …

S Moharir, L Akotkar, U Aswar, D Kumar… - European Journal of …, 2024 - Springer
Abstract Background and Objectives Doxepin, dosulepin, and clomipramine are tricyclic
antidepressants (TCAs) that act as serotonin and noradrenaline reuptake inhibitors. The …

The influence of cimetidine versus ranitidine on doxepin pharmacokinetics

DL Sutherland, AJ Remillard, KR Haight… - European journal of …, 1987 - Springer
The effect of cimetidine and ranitidine on doxepin pharmacokinetics was studied in 6 healthy
volunteers. Each subject completed 3 study phases: Treatment A, 9 consecutive doses of 50 …

Antidepressant-like activities of hispidol and decursin in mice and analysis of neurotransmitter monoamines

JM Oh, HS Lee, SC Baek, JP Lee, GS Jeong… - Neurochemical …, 2020 - Springer
The antidepressant activities of hispidol and decursin (both potent monoamine oxidase A
(MAO-A) inhibitors) were evaluated using the forced swimming test (FST) and the tail …

Altering metabolic profiles of drugs by precision deuteration: reducing mechanism-based inhibition of CYP2D6 by paroxetine

V Uttamsingh, R Gallegos, JF Liu, SL Harbeson… - … of Pharmacology and …, 2015 - ASPET
Selective deuterium substitution as a means of ameliorating clinically relevant
pharmacokinetic drug interactions is demonstrated in this study. Carbon-deuterium bonds …

Simultaneous determination of deuterated vortioxetine and its major metabolite in human plasma by UPLC-MS/MS and application to a pharmacokinetic study in …

Y Yi, G Ren, M Zheng, D Zhao, N Li, X Chen… - … of Chromatography B, 2020 - Elsevier
JJH201501, a deuterated modification for multi-target antidepressant vortioxetine, is
currently in phase I clinical trial. This study aimed to establish a sensitive and rapid UPLC …

Deuterated drugs

RH Howland - Journal of Psychosocial Nursing and Mental …, 2015 - journals.healio.com
Many drugs are carbon-based, and carbon–hydrogen bonding is particularly relevant for
understanding important properties of drug molecules. Deuteration refers to the selective …

Deuterated driven new chemical entities: An optimistic way to improve therapeutic efficacy

HMC Mouli, A Vinod, S Kumari, AK Tiwari… - Bioorganic …, 2023 - Elsevier
In organic chemistry, the use of deuterium exchange as a tool to study the mechanism of
chemical reaction has been well explored. Since two decades, the research focus on …

Deuterated drugs: where are we now?

GS Timmins - Expert opinion on therapeutic patents, 2014 - Taylor & Francis
Introduction: Deuterated versions of existing drugs can exhibit improved pharmacokinetic or
toxicological properties due the stronger deuterium–carbon bond modifying their …

Deuterated Drugs

N Rao, R Kini, P Kad - Pharmaceutical Chemistry Journal, 2022 - Springer
A deuterated drug comprises diminutive molecules in which deuterium replaces one or more
than one hydrogen atoms of the molecule. As deuterium and hydrogen possess almost …

Clinical Application and Synthesis Methods of Deuterated Drugs

XL Xu, W Zhang, GW Rao - Current Medicinal Chemistry, 2023 - ingentaconnect.com
Many drugs have adverse absorption, distribution, metabolism, and excretory (ADME)
properties that prevent their widespread use or limit their use in some indications. In addition …