Search for Monoamine Oxidase Inhibitors among Pyrazoline and Pyrimidine Derivatives and Studying Luminescent Properties of the Obtained Compounds
- Authors: Isakhanyan A.U.1, Hakobyan N.Z.1, Hovasyan Z.A.1, Grigoryan G.S.2, Mkhitaryan R.P.2, Yesayan D.L.2, Grigoryan A.S.1, Gasparyan H.V.1, Panosyan Н.A.1, Harutyunyan A.A.1
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Affiliations:
- Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
- Yerevan State University
- Issue: Vol 94, No 1 (2024)
- Pages: 80-91
- Section: Articles
- URL: https://cardiosomatics.ru/0044-460X/article/view/667235
- DOI: https://doi.org/10.31857/S0044460X24010065
- EDN: https://elibrary.ru/HLHZQA
- ID: 667235
Cite item
Abstract
Cyclization of the (E)-3-aryl-1-(4-alkoxyphenyl)prop-2-en-1-ones with phenylhydrazine in an acidic medium leads to the 5-aryl-3-(4-alkoxyphenyl)-1-phenyl-4,5-dihydro-1H-pyrazoles. Bubbling air through a solution of 5-(4-methoxyphenyl)-1-phenyl-3-(4-ethoxyphenyl)-4,5-dihydro-1H-pyrazole in ethylcellosolve resulted in an oxidation-dehydrogenation product, which characterized as the picrate of the corresponding pyrazole. The reaction of benzamidine and 4-methylbenzamidine hydrochlorides with substituted chalcones in а KOH–ethanol system leads to 2,4-diaryl-6-(4-alkoxyphenyl)pyrimidines. The luminescent and antimonoamine oxidase properties of the resulting systems were studied.
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About the authors
A. U. Isakhanyan
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Author for correspondence.
Email: anush.isakhanyan.51@mail.ru
ORCID iD: 0000-0002-1713-4908
Armenia, Yerevan
N. Z. Hakobyan
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Email: anush.isakhanyan.51@mail.ru
ORCID iD: 0000-0002-3095-5938
Armenia, Yerevan
Z. A. Hovasyan
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Email: anush.isakhanyan.51@mail.ru
ORCID iD: 0000-0001-6698-7184
Armenia, Yerevan
G. S. Grigoryan
Yerevan State University
Email: gevsgrig@ysu.am
ORCID iD: 0000-0002-0675-735X
Armenia, Yerevan
R. P. Mkhitaryan
Yerevan State University
Email: gevsgrig@ysu.am
ORCID iD: 0009-0009-6277-2747
Armenia, Yerevan
D. L. Yesayan
Yerevan State University
Email: gevsgrig@ysu.am
ORCID iD: 0009-0008-7243-6248
Russian Federation, Yerevan
A. S. Grigoryan
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Email: anush.isakhanyan.51@mail.ru
ORCID iD: 0000-0002-3834-3338
Russian Federation, Yerevan
H. V. Gasparyan
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Email: anush.isakhanyan.51@mail.ru
ORCID iD: 0000-0002-8555-3733
Russian Federation, Yerevan
Н. A. Panosyan
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Email: anush.isakhanyan.51@mail.ru
ORCID iD: 0000-0001-8311-6276
Russian Federation, Yerevan
A. A. Harutyunyan
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Email: anush.isakhanyan.51@mail.ru
ORCID iD: 0000-0003-0641-5453
Russian Federation, Yerevan
References
- Чиряпкин А.С. // Juvenis Scientia. 2022. Т. 8. № 5. С. 16. doi: 10.32415/jscientia_2022_8, 5,_16-30
- Varghese B., Al-Busafi S.N., Suliman F.O., Al-Kindy S.M.Z. // RSC Adv. 2017. Vol. 7. N 74. P. 46999. doi: 10.1039/c7ra08939b
- Kumar S., Bawa S., Drabu S., Kumar R., Gupta H. // Recent Pat. Antiinfect. Drug Discov. 2009. Vol. 4. N 3. P. 154. doi: 10.2174/157489109789318569
- Nehra B., Rulhania S., Jaswal S., Kumar B., Singh G., Monga V. // Eur. J. Med. Chem. 2020. Vol. 205. P. 112666. doi: 10.1016/j.ejmech.2020.112666
- Matiadis D., Sagnou M. // Int. J. Mol. Sci. 2020. Vol. 21. N 15. P. 5507. doi: 10.3390/ijms21155507
- Deng H., Yu Z.Y., Shi G.Y., Chen M.J., Tao K., Hou T.P. // Chem. Biol. Drug Des. 2012. Vol. 79. N 3. P. 279. doi: 10.1111/j.1747-0285.2011.01308.x
- Машковский М.Д. Лекарственные средства. М.: Новая волна, 2010. С. 851.
- Guglielmi P., Carradori S., Poli G., Secci D., Cirilli R., Rotondi G., Chimenti P., Petzer A., Petzer J.P. // Molecules. 2019. Vol. 24. N 3. Р. 484. doi: 10.3390/molecules24030484
- Исаханян А.У., Акопян Н.З., Овасян З.А., Григорян Г.С., Мхитарян Р.П., Аракелян А.Г., Сафарян А.С., Мурадян Р.Е., Паносян Г.А., Арутюнян А.А. // ЖОХ. 2023. Т. 93. № 9. С. 1335; Isakhanyan A.U., Hakobyan N.Z., Hovasyan Z.A., Grigoryan G.S., Mkhitaryan R.P., Aracelyan H.G., Safaryan A.S., Muradyan R.E., Panosyan Н.A., Harutyunyan A.A. // Russ. J. Gen. Chem. 2023. Vol. 93. N 9. P. 2210. doi: 10.1134/S1070363223090037
- Lakowicz J.R. Principles of Fluorescence Spectroscopy. New York: Springer, 2006. P. 954. doi: 10.1007/978-0-387-46312-4
- Brouwer A.M. // Pure Appl. Chem. 2011. Vol. 83. N 12. P. 2213. doi: 10.1351/PAC-REP-10-09-31
- Shivananda M.K., Holla B.S. // J. Chem. Pharm. Res. 2017. Vol. 9. N 6. P. 1.
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