Synthesis of the N‐methyl Derivatives of 2‐Aminothiazol‐4(5H)‐one and Their Interactions with 11βHSD1‐Molecular Modeling and in Vitro Studies |
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| Authors: | Renata Studzi&#x;ska Renata Ko&#x;odziejska Wojciech P&#x;azi&#x;ski Daria Kupczyk Tomasz Kosmalski Katarzyna Jasieniecka Boena Modzelewska‐Banachiewicz |
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| Institution: | Renata Studzińska,Renata Ko?odziejska,Wojciech P?aziński,Daria Kupczyk,Tomasz Kosmalski,Katarzyna Jasieniecka,Bo?ena Modzelewska‐Banachiewicz |
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| Abstract: | 11β‐Hydroxysteroid dehydrogenase type 1 (11β‐HSD1) is an enzyme that affects the body's cortisol levels. The inhibition of its activity can be used in the treatment of Cushing's syndrome, metabolic syndrome and type 2 diabetes. In this study, we synthesized new derivatives of 2‐(methylamino)thiazol‐4(5H)‐one and tested their activity towards inhibition of 11β‐HSD1 and its isoform – 11β‐HSD2. The results were compared with the previously tested allyl derivatives. We found out that methyl derivatives are weaker inhibitors of 11β‐HSD1 in comparison to their allyl analogs. Due to significant differences in the activity of the compounds, molecular modeling was performed, which was aimed at comparing the interactions between 11β‐HSD1 and ligands differing by substituent at the amine group (allyl vs. methyl). Modeling showed that the absence of the allyl group can lead to the rotation of whole ligand molecule which affects its interaction with the enzyme. |
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| Keywords: | thiazolone derivatives 11β -hydroxysteroid dehydrogenase enzyme inhibitors molecular docking biological activity |
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