Introduction: Research among the Ukrainian (Carpatian) floras representatives is important for searching for new active compounds. Objective: The study aims to determine the potential of callus biomass of Delphinium elatum, Anemone nemorosa, and Pulsatilla alba to become an analog of medicinal plant raw material for the use in the pharmaceutical industry, to investigate the composition, antioxidant activity and antimicrobial activity of extracts of the callus biomass of the above-mentioned plants. Methods: The individual members of the family Ranunculaceae (Delphinium elatum L., Anemone nemorosa L., Pulsatilla alba Rchb.) were introduced into in vitro culture, and their callus induction was studied using the Folin-Ciocalteu spectrophotometric method, colorimetric analysis, antioxidant, and antimicrobial activity methods. Results: The maximum content of flavonoids and phenolic compounds was observed in 40% hydro-ethanolic extracts of callus biomass and plant raw materials of D. elatum. 90.0% and 70.0% D. elatum extracts showed significant activity against Gram-positive microorganisms. 90.0/70.0/40.0% extracts showed significant activity against Bacillus licheniformis. 70.0 % extract showed significant antifungal activity against clinical and reference strains of Candida albicans. Conclusion: Summarizing experimental results, it was proved that the callus biomass of D. elatum, A. nemorosa, and P. alba have potential as analogs of medicinal plant raw materials, both for the content of biologically active substances and biological activities. © 2023 Sciendo. All rights reserved.

UDC 547-327:547.821:54.057

The aim. The combination in one molecule of pharmacophore fragments of thieno[2,3-d]pyrimidine-4-carboxylic acids with the fragments of 2-or 4-aminopyrimidine by peptide coupling promoted acylation in order to develop the new drug-like molecules with antimicrobial activity. Materials and methods. The molecular docking studies were performed with the AutoDock Vina and AutoDock-Tools 1.5.6 programs; TrmD Pseudomonas aeruginosa PDB ID – 5ZHN was used as the protein target. Synthetic methods of peptide coupling were used. 1H and 13C NMR spectra were recorded with a Varian-400 spectrometer at 400 MHz and Bruker Avance DRX 500 device at 500 MHz and 125 MHz in DMSO-d6 as a solvent, using TMS as the internal standard. LC-MS analysis of the compounds was carried out with Agilent 1100 HPLC з with at-mospheric pressure chemical ionization (APCI). The studied derivates were tested in vitro for their antibacterial and anti-fungal activities using agar diffusion and serial dilutions resazurin-based microdilution assays (RBMA). Results and discussion. By the combination of the pharmacophore fragments of thieno[2,3-d]pyrimidine-4-carboxylic acids with the fragments of 2-of 4-aminopyrimidine, the combinatorial library of amides was constructed. For this library of compounds, the potential of antimicrobial activity was revealed using docking studies to the TrmD enzyme isolated from P. aeruginosa. The peptide coupling promoted by 1,1’-carbonyldiimidazole was found to be effective for the synthesis of pyridyl amides of thieno[2,3-d]pyrimidine-4-carboxylic acids, and it allowed to combine these phar-macophores in one molecule. The results of antimicrobial activity study revealed the broad spectrum of antimicrobial activity for N-(pyridin-4-yl)-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidine-4-carboxamide (2g), while 5,6-di-methyl-N-(6-methylpyridin-2-yl)thieno[2,3-d]pyrimidine-4-carboxamide (2c) showed the best MIC value against the reference strain of Pseudomonas aeruginosa ATCC 10145. N-(6-Methylpyridin-2-yl)-5,6,7,8-tetrahydro[1]benzothien-o[2,3-d]pyrimidine-4-carboxamide (2h) was also found to be active against Pseudomonas aeruginosa. Conclusions. An effective method for the synthesis of pyridyl amides of thieno[2,3-d]pyrimidine-4-carboxylic acid has been developed. The amides molecular docking method showed their ability to inhibit TrmD enzyme isolated from P. aeruginosa; the further in vitro studies of the compounds showed the rationality of the further studies of the derivatives with 2-ami-no-6-methylpyridine in amide substituent because this fragment favoured the selectivity against Pseudomonas aeruginosa. © The Author(s) 2023.

The analysis presented in this article is a continuation of a broader qualitative study examining the composition of the chloroform fraction of Caltha palustris. The study discovered 29 compounds, and 26 of them have been identified:paraffinic hydrocarbons, esters, fatty aldehydes, morphine derivatives, thiazole derivatives, benzodiazepines, naphthalene, and a small amount of terpene. It was figured out that the investigated lipophilic extract has an antioxidant impact. For the investigation, there were used such assays as the DPPH radical and the ABTS radical cation assays. Moreover the investigated lipophilic extract has an antimicrobial activity both in terms of gram-positive (Staphylococcus aureus (ATCC 25923 (F-49)), Bacillus cereus 34 (non-MDR), Enterococcus faecalis 26(MDR) and gram-negative, (Raoultella terrigena (ATCC 33257), Escherichia coli (ATCC 25922), Escherichia coli 168) microorganisms and yeast Candida spp. In addition, the significant content of biologically active substances in the lipophilic volatile fraction of Caltha palustris indicates the prospects for further study. © 2023, Research Journal of Pharmacy and Technology. All rights reserved.