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http://dspace.nuph.edu.ua/handle/123456789/35539| Title: | Relation structure and action of antimicrobial activity α-arbutin, β-arbutin and hydroquinone |
| Authors: | Maslov, O. Yu. Komisarenko, M. A. Kolisnyk, S. V. Ponomarenko, S. V. Osolodchenko, T. P. |
| Keywords: | Arbutin (C12H16O7) |
| Issue Date: | 2025 |
| Publisher: | НФаУ |
| Bibliographic description (Ukraine): | Relation structure and action of antimicrobial activity α-arbutin, β-arbutin and hydroquinone / O. Yu. Maslov [et al.] //Проблеми та досягнення сучасної біотехнології : матеріали V міжнар. наук.-практ. інтернет-конф., м. Харків, 28 берез. 2025 р. – Харків : НФаУ, 2025. – C. 180-182. |
| Abstract: | Arbutin (C12H16O7) is aglucopyranoside of hydroquinone with two different configurations: alpha (α) and beta (β). The β-isomer can only be obtained from medicinal raw materials, and inturn, the α-isomer is its synthetic analog; the main difference between these isomers is that instead of β-glucose there is α-glucose. Hydroquinone is an aromatic compound which consists of benzyl and 2 OH groups in para-positions. Hydroquinone is a highly toxic compound and is carcinogenic. All over the world, arbutin-containing medicinal raw materials (lingonberry and bearberry leaves) are used for the treatment and prevention of cystitis, glomerulonephritis and pyelonephritis, as uroseptic, diuretic and antiazotemic agents |
| URI: | http://dspace.nuph.edu.ua/handle/123456789/35539 |
| Appears in Collections: | Тези доповідей співробітників НФаУ |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Проблеми та досягнення сучасної біотехнології 80-82.pdf | 88,64 kB | Adobe PDF | View/Open |
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