We report the biological evaluation of a class of adamantane derivatives, which were achieved via modified telescoped machine-assisted flow procedure. Among the series of compounds tested in this work, <b>5</b> demonstrated outstanding analgesic properties. This compound showed that its action was not mediated through direct interaction with opioid and/or cannabinoid receptors. Moreover, it did not display any significant anti-inflammatory properties. Experiments carried out on rat cerebrocortical purified synaptosomes indicated that <b>5</b> inhibits the P2X<sub>7</sub>-evoked glutamate release, which may contribute to its antinociceptive properties. Nevertheless, further experiments are ongoing to characterize the pharmacological properti...
Abstract Adamantanyl benzamide 1 was identified as a potent P2X7R antagonist but failed to progress...
Anandamide (AEA) is an endogenous fatty acid which activates the same cannabinoid receptors as ∆9-te...
Cannabinoids have been shown to increase the release of aracha-donic acid, whereas nonsteroidal anti...
We report the biological evaluation of a class of adamantane derivatives, which were achieved via mo...
Copyright © 2014 Ruben S. Mirzoyan et al. This is an open access article distributed under the Creat...
Paracetamol also known as acetaminophen, is a widely used analgesic and antipyretic agent. We report...
Paracetamol also known as acetaminophen, is a widely used analgesic and antipyretic agent. We report...
The aqueous dissolution profile of the isomeric synthetic adamantane phenylalkylamine hydrochlorides...
<div><p>Paracetamol also known as acetaminophen, is a widely used analgesic and antipyretic agent. W...
Despite the varied approaches to the pain syndrome therapy with the changes and improvements of evol...
Two novel adamantane derivatives, adamantan-1-yl(1-pentyl-1<i>H</i>-indol-3-yl)methanone (AB-001) ...
The discovery of endocannabinoids opens up new perspectives in experimental pain research. Here we p...
Fentanyl is a powerful opiate analgesic typically used for the treatment of severe and chronic pain,...
Cannabinoid CB2 receptor activation by selective agonists has been shown to produce analgesic effect...
Improgan is a chemical congener of the H2 antagonist cimetidine which shows the profile of a highly ...
Abstract Adamantanyl benzamide 1 was identified as a potent P2X7R antagonist but failed to progress...
Anandamide (AEA) is an endogenous fatty acid which activates the same cannabinoid receptors as ∆9-te...
Cannabinoids have been shown to increase the release of aracha-donic acid, whereas nonsteroidal anti...
We report the biological evaluation of a class of adamantane derivatives, which were achieved via mo...
Copyright © 2014 Ruben S. Mirzoyan et al. This is an open access article distributed under the Creat...
Paracetamol also known as acetaminophen, is a widely used analgesic and antipyretic agent. We report...
Paracetamol also known as acetaminophen, is a widely used analgesic and antipyretic agent. We report...
The aqueous dissolution profile of the isomeric synthetic adamantane phenylalkylamine hydrochlorides...
<div><p>Paracetamol also known as acetaminophen, is a widely used analgesic and antipyretic agent. W...
Despite the varied approaches to the pain syndrome therapy with the changes and improvements of evol...
Two novel adamantane derivatives, adamantan-1-yl(1-pentyl-1<i>H</i>-indol-3-yl)methanone (AB-001) ...
The discovery of endocannabinoids opens up new perspectives in experimental pain research. Here we p...
Fentanyl is a powerful opiate analgesic typically used for the treatment of severe and chronic pain,...
Cannabinoid CB2 receptor activation by selective agonists has been shown to produce analgesic effect...
Improgan is a chemical congener of the H2 antagonist cimetidine which shows the profile of a highly ...
Abstract Adamantanyl benzamide 1 was identified as a potent P2X7R antagonist but failed to progress...
Anandamide (AEA) is an endogenous fatty acid which activates the same cannabinoid receptors as ∆9-te...
Cannabinoids have been shown to increase the release of aracha-donic acid, whereas nonsteroidal anti...