Anti-Inflammatory Activity of Novel 12-N-methylcytisine Derivatives.

Autor:	Tsypysheva IP; Laboratory of Bioorganic Chemistry and Catalysis. Russian Federation., Borisevich SS; Laboratory of Chemical Physics Ufa Institute of Chemistry of RAS, 450054, Ufa. Russian Federation., Zainullina LF; Laboratory of Molecular Pharmacology and Immunology, Institute of Biochemistry and Genetics of RAS, 450054, Ufa. Russian Federation., Makara NS; Laboratory of Bioorganic Chemistry and Catalysis. Russian Federation., Koval'skaya AV; Laboratory of Bioorganic Chemistry and Catalysis. Russian Federation., Petrova PR; Department of Chemistry, Bashkir State University, 450077, Ufa. Russian Federation., Khursan SL; Laboratory of Chemical Physics Ufa Institute of Chemistry of RAS, 450054, Ufa. Russian Federation., Vakhitova YV; Laboratory of Molecular Pharmacology and Immunology, Institute of Biochemistry and Genetics of RAS, 450054, Ufa. Russian Federation., Zarudii FS; Department of Pharmacy, Bashkir State Medicinal University, 2a, Teatralnaya Str., Ground Floor, Ufa, 450000. Russian Federation.
Jazyk:	angličtina
Zdroj:	Anti-inflammatory & anti-allergy agents in medicinal chemistry [Antiinflamm Antiallergy Agents Med Chem] 2017; Vol. 16 (2), pp. 112-122.
DOI:	10.2174/1871523016666170616115252
Abstrakt:	Background and Objectives: Neurodegenerative diseases and inflammation are always linked to each other; therefore the elaboration of new chemical compounds, which interact with pharmacological targets involved into these two processes, can become one of ways of correction of these types of human CNS pathology. In the field of this problem the anti-inflammatory activity of ten 3-amino derivatives of quinolizidine alkaloid (.)-cytisine (the data about nootropic activity of these compounds are outlined by us previously) was studied by using in vivo, in vitro and in silico approaches. Methods: The anti-inflammatory activity of novel compounds was investigated on carrageenan- induced model of inflammation in Rat paw following an established protocol. COX-1 (ovin) and COX-2 (human recombinant) inhibition activities of tested compounds assessed using a COX Fluorescent Inhibitor Screening Assay Kit. And as part of an in silico screening the leading compounds were docked into the tyrosine sites of COX-1/COX-2 enzymes (PDB code: 1DIY and 1CVU). Results: It was established that ability of 3-(2-hydroxyphenyl)amino, 3-(4-hydroxyphenyl) amino and 3-(3-phenylprop-2-en-1-yl)amino derivatives of 12-N-metylcytisine to inhibit the carrageenan-induced paw oedema in rats is comparable with reference drug diclofenac. The results of in vitro COX-1/COX-2 inhibition assay showed no significant activity of tested compounds, except compounds with 2-hydroxyphenyl, 3-phenylprop-2-en-1-yl, furyl and thiophenyl fragments which slightly reduce the activity of COX-2. Conclusion: The tendency to occurrence of anti-inflammatory properties of synthesized derivatives of quinolizidine alkaloid (-)-cytisine can be explained on the basis of molecular docking results, which assume the possibility of interaction of more potent compounds with key amino acids of COX-1/COX-2 active sites. (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.)
Databáze:	MEDLINE
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