Author:
Mukusheva Gulim Kenesbekovna,Seidakhmetova Roza Battalovna,Zhassymbekova Aigerim Rysbekovna,Nurkenov Oralgazy Aktaevich,Nurmaganbetov Zhangeldy Seitovich,Seilkhanov Tulegen Muratovich,Tazhybay Aizhan Maratovna,Mazhytov Alisher Sabyrovich
Abstract
The modern vegetable matter studies in the republic and abroad are devoted to a multi-faceted and comprehensive research of plant raw materials, including desorbing and structure of plant component chemical properties, the study of their biological activity, as well as the development of effective and environmentally friendly methods for соmprehensive mineral processing of plant raw materials.
The 1,2,3-triazoles attraction is due to their reactivity versatility, as well as practical application of 1,2,3-triazole derivatives as medicines. Modification of natural compound molecules by introducing such a substituent is one of promising directions in the search for new biologically active compounds.
According to the data obtained, the antimicrobial activity of sample (5) is higher than that of sample (3). Thus, sample (5) showed a moderate antibacterial activity against Escherichia coli, whereas sample (3) showed a weak antimicrobial activity against this test strain.
The analysis of test results concerning the analgesic activity assessment showed that samples (5) and (3) can reduce the rats ‘specific nociceptive responses severity when testing abdominal constriction. It is important to emphasize that when injecting a 1% acetic acid solution abdominally, all test animals developed “acetic writhing’s” (characteristic animal movements, including the abdominal muscles contraction, alternating with their relaxation, hind limbs stretching and back arching).
Subject
Organic Chemistry,Plant Science,Biomaterials
Reference23 articles.
1. Prakash B. Kujur A., Yadav A. Synthesis of Medicinal Agents from Plant. Elsevier Ltd., 2018, pp. 25–46. DOI: 10.1016/b978-0-08-102071-5.00002-7.
2. Thomford N.E., Senthebane D.A., Rowe A., Munro D., Seele P., Maroyi A., Dzobo K. Int. J. Mol. Sci., 2018, vol. 19, no. 6, p. 1578. DOI: 10.3390/ijms19061578.
3. Heinrich M., Mah J., Amirkia V. Molecules, 2021, vol. 26, no. 7, p. 1836. DOI: 10.3390/molecules26071836.
4. Ng Y.P., Or T.C.T., Ip N.Y. Neurochemistry International, 2015, vol. 89, pp. 260–270. DOI: 10.1016/j.neuint.2015.07.018.
5. Bondarenko S.P., Frasinyuk M.S., Vinogradova V.I., Khilya V.P. Khimiya prirodnykh soyedineniy, 2011, no. 4, pp. 536–538. (in Russ.).