A series of 2-thio pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides were investigated as hTRPV1 antagonists. Among them, compound 24S showed stereospecific and excellent TRPV1 antagonism of capsaicin-induced activation. Further, it demonstrated strong anti-allodynic in a rat neuropathic pain model. Consistent with its action in vitro being through TRPV1, compound 24S blocked capsaicin-induced hypothermia in mice. Docking analysis of 24S with our hTRPV1 homology model was performed to identify its binding mode.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957258PMC
http://dx.doi.org/10.1016/j.bmc.2013.08.015DOI Listing

Publication Analysis

Top Keywords

2-thio pyridine
8
pyridine c-region
8
c-region analogues
8
analogues 2-3-fluoro-4-methylsulfonylaminophenylpropanamides
8
compound 24s
8
trpv1 antagonist
4
antagonist high
4
high analgesic
4
analgesic efficacy
4
efficacy 2-thio
4

Similar Publications

3-Phenyl-2-(thio-phen-3-yl)-2,3-di-hydro-4-pyrido[3,2-][1,3]thia-zin-4-one (CHNOS, ) and 2-(1-indol-3-yl)-3-phenyl-2,3-di-hydro-4-pyrido[3,2-][1,3]thia-zin-4-one 0.438-hydrate (CHNOS·0.438HO, ) crystallize in space groups 2/ and 2/, respectively.

View Article and Find Full Text PDF
Article Synopsis
  • Pyridine derivatives are important in medicinal chemistry due to their ability to bind biological targets, prompting research to create new thioalkyl derivatives for potential drug development.
  • The synthesis of these new compounds utilized classical organic chemistry methods, and various biological tests were conducted to analyze their neurotropic and psychotropic effects, including anticonvulsant and sedative activities.
  • Results showed that several synthesized derivatives had high gastro-intestinal absorption, low toxicity, and significant psychotropic effects, with some compounds demonstrating anxiolytic activity up to four times greater than diazepam.
View Article and Find Full Text PDF

The crystal structures of four thio-phene-carbohydrazide-pyridine derivatives, '-[()-pyridin-3-yl-methyl-idene]thio-phene-2-carbohydrazide, CHNOS, (I), '-[()-pyridin-2-yl-methyl-idene]thio-phene-2-carbohydrazide, CHNOS, (II), -methyl-'-[()-pyridin-2-yl-methyl-idene]thio-phene-2-carbohydrazide, CHNOS, (III) and '-[()-pyridin-2-yl-methyl-idene]-2-(thio-phen-2-yl)ethano-hydrazide, CHNOS, (IV) are described. The dihedral angles between the thio-phene ring and the pyridine ring are 21.4 (2), 15.

View Article and Find Full Text PDF

A new regioselective 3,4-difunctionalization of 3-chloropyridines 3,4-pyridyne intermediates is reported. Regioselective lithiation of 3-chloro-2-ethoxypyridine and a related 2-thio-derivative followed by treatment with aryl- and alkylmagnesium halides as well as magnesium thiolates at -78 °C produced 3,4-pyridynes during heating to 75 °C. Regioselective addition of the Grignard moiety in position 4 followed by an electrophilic quench in position 3 led to various 2,3,4-trisubstituted pyridines.

View Article and Find Full Text PDF

We have synthesized and characterized [F]--(4-chloro-3-((fluoromethyl-)thio)phenyl)-picolinamide ([F]) as a potential ligand for the positron emission tomography (PET) imaging of mGluR4 in the brain. Radioligand [F] displays central nervous system drug-like properties, including mGluR4 affinity, potent mGluR4 PAM activity, and selectivity against other mGluRs, as well as sufficient metabolic stability. Radiosynthesis was carried out in two steps.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!