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Rational Design of New Monoterpene-Containing Azoles and Their Antifungal Activity Научная публикация

Журнал Antibiotics
ISSN: 2079-6382
Вых. Данные Год: 2023, Том: 12, Номер: 5, Страницы: 818 Страниц : 1 DOI: 10.3390/antibiotics12050818
Ключевые слова triazole antifungals; monoterpenoids; hybrids; clinical isolates; CYP51; Candida spp.
Авторы Li-Zhulanov Nikolai S. 1 , Zaikova Nadezhda P. 1 , Sari Suat 2 , Gülmez Dolunay 3 , Sabuncuoğlu Suna 4 , Ozadali-Sari Keriman 2 , Arikan-Akdagli Sevtap 3 , Nefedov Andrey A. 1 , Rybalova Tatyana V. 1 , Volcho Konstantin P. 1 , Salakhutdinov Nariman F. 1
Организации
1 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Lavrentiev Ave., 9, 630090 Novosibirsk, Russia
2 Department of Pharmaceutical Chemistry, Hacettepe University Faculty of Pharmacy, Sihhiye, Ankara 06100, Turkey
3 Department of Medical Microbiology, Hacettepe University Faculty of Medicine, Sihhiye, Ankara 06100, Turkey
4 Department of Pharmaceutical Toxicology, Hacettepe University Faculty of Pharmacy, Sihhiye, Ankara 06100, Turkey

Информация о финансировании (1)

1 Российский Научный Фонд 22-73-00046

Реферат: Azole antifungals, including fluconazole, have long been the first-line antifungal agents in the fight against fungal infections. The emergence of drug-resistant strains and the associated increase in mortality from systemic mycoses has prompted the development of new agents based on azoles. We reported a synthesis of novel monoterpene-containing azoles with high antifungal activity and low cytotoxicity. These hybrids demonstrated broad-spectrum activity against all tested fungal strains, with excellent minimum inhibitory concentration (MIC) values against both fluconazole-susceptible and fluconazole-resistant strains of Candida spp. Compounds 10a and 10c with cuminyl and pinenyl fragments demonstrated up to 100 times lower MICs than fluconazole against clinical isolates. The results indicated that the monoterpene-containing azoles had much lower MICs against fluconazole-resistant clinical isolates of Candida parapsilosis than their phenyl-containing counterpart. In addition, the compounds did not exhibit cytotoxicity at active concentrations in the MTT assay, indicating potential for further development as antifungal agents.
Библиографическая ссылка: Li-Zhulanov N.S. , Zaikova N.P. , Sari S. , Gülmez D. , Sabuncuoğlu S. , Ozadali-Sari K. , Arikan-Akdagli S. , Nefedov A.A. , Rybalova T.V. , Volcho K.P. , Salakhutdinov N.F.
Rational Design of New Monoterpene-Containing Azoles and Their Antifungal Activity
Antibiotics. 2023. V.12. N5. P.818. DOI: 10.3390/antibiotics12050818 WOS РИНЦ
Даты:
Поступила в редакцию: 10 апр. 2023 г.
Принята к публикации: 25 апр. 2023 г.
Опубликована online: 27 апр. 2023 г.
Идентификаторы:
Web of science WOS:000994782500001
РИНЦ 61323887
OpenAlex W4367297954
Альметрики: