Journals / Türk Hijyen ve Deneysel Biyoloji Dergisi / 2021 / Cilt: 78 - Sayı: 2

Biological activity screening of some hydrazone and chalcone derivatives

Bazı hidrazon ve kalkon türevlerinin biyolojik aktivite taraması

Pages
159–166
Publication Date
2022-11-06
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

All compounds were observed to be more effective than gentamicin against methicillin-resistant Staphylococcus aureus.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: Today, the development of resistance to antibiotics is increasing rapidly.
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Key Findings & Data:Results: All compounds displayed the same activity against Mycobacterium tuberculosis (MIC: 64 μg/mL).
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Conclusion & Impact:All compounds were observed to be more effective than gentamicin against methicillin-resistant Staphylococcus aureus.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: Today, the development of resistance to antibiotics is increasing rapidly. Loss of antibiotics effectiveness due to the development of resistance causes serious hazards. Especially methicillinresistant Staphylococcus aureus and vancomycinresistant Enterococcus faecalis create life-threatening conditions in patients with a weak immune system. For this reason, it is important to develop new drug active substances against these microorganisms. In this article, hydrazones and chalcones were synthesized and some biological activities of these compounds such as antimicrobial and antituberculosis were investigated. This study was conducted to investigate new antimicrobial and antituberculous drug-active substances instead of antibiotics that lost their effectiveness due to the rapidly increasing resistance to existing antibiotics. Methods: The compounds were obtained by synthesis of chalcones via Claisen Schmidt condensation and then by reacting these chalcones with hydrazides to form hydrazone. Antimicrobial and antituberculosis activities of the compounds were evaluated by microdilution method and microplate alamar blue assays, respectively. Results: All compounds displayed the same activity against Mycobacterium tuberculosis (MIC: 64 μg/mL). E4, 4’-Bromo-4-methyl chalcone, displayed the best activity against Meticilline resistant-Staphylococcus aureus (MIC: 16 μg/mL). The most effective compounds against Enterococcus faecalis isolate and Enterococcus faecalis were found B26 (N-(1-(4fluorophenyl)-3-p-tolylallylidene) thiophene-2-carbohydrazide) and E8 (4’-fluoro-3-methyl chalcone), respectively (MIC: 32 μg/mL). Conclusion: Hydrazones have been found to be more effective than chalcones against S. aureus ATCC 29213. However, chalcones exhibited a remarkable effect against meticilline resistant-Staphylococcus aureus and Enterococcus faecalis. In terms of tuberculosis bacillus, it did not differ whether the compounds had a chalcone or hydrazone structure. Both chalcones and hydrazones exhibited the same activity against candida species. All compounds were observed to be more effective than gentamicin against methicillin-resistant Staphylococcus aureus.

Özet

Amaç: Günümüzde antibiyotiklere karşı direnç gelişimi hızla artmaktadır. Direnç gelişmesi nedeniyle antibiyotik etkinliğinin kaybı ciddi tehlikelere neden olmaktadır. Özellikle metisiline dirençli Staphylococcus aureus ve vankomisine dirençli Enterococcus faecalis izolatı, bağışıklık sistemi zayıf olan hastalarda yaşamı tehdit eden durumlar oluşturmaktadır. Bu nedenle, bu mikroorganizmalara karşı yeni ilaç etken maddeleri geliştirmek önemlidir. Bu makalede, hidrazonlar ve kalkonlar sentezlenmiş ve bu bileşiklerin antimikrobiyal ve antitüberküloz gibi bazı biyolojik aktivitelerinin araştırılması yapılmıştır. Bu çalışma, mevcut antibiyotiklere karşı hızla artan direnç nedeniyle etkinliğini kaybeden antibiyotiklerin yerine antimikrobiyal ve antitüberküloz etkili yeni ilaç etken maddelerinin araştırılması için yapılmıştır. Yöntem: Bileşikler, Claisen Schmidt kondensasyonu yoluyla kalkonların sentezi ve daha sonra bu kalkonların hidrazon oluşturmak üzere hidrazidlerle reaksiyona girmesiyle elde edilmiştir. Bileşiklerin antimikrobiyal ve antitüberküloz aktiviteleri, sırasıyla mikrodilüsyon yöntemi ve mikroplak alamar mavisi deneyleri ile değerlendirilmiştir. Bulgular: Tüm bileşikler Mycobacterium tuberculosis’e karşı aynı etkiyi göstermiştir (MİK: 64 ug/ mL). E4, 4’-Bromo-4-metil kalkon, metisiline dirençli- Staphylococcus aureus’a karşı en iyi etkinliği göstermiştir (MİK: 16 ug/mL). Enterococcus faecalis izolatı ve Enterococcus faecalis’e karşı en etkili bileşikler sırasıyla B26 (N-(1-(4-florofenil)-3-p-tolilaliliden)tiyofen-2- karbonhidrazit) ve E8 (4’-floro-3-metil kalkon) olarak bulunmuştur. Sonuç: Hidrazonların S. aureus ATCC 29213 suşu üzerine kalkonlardan daha etkili olduğu bulunmuştur. Bununla birlikte kalkonlar, metisiline dirençli- Staphylococcus aureus ve Enterococcus faecalis üzerine dikkate değer bir etki göstermiştir. Tüberküloz basili açısından, bileşiklerin kalkon veya hidrazon yapısında olması fark göstermemiştir. Hem kalkonlar hem de hidrazonlar kandida türlerine karşı aynı aktiviteyi sergilemiştir. Tüm bileşiklerin metisiline dirençli Staphylococcus aureus üzerine gentamisinden daha etkili olduğu gözlenmiştir.

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Cite This Article

AKSÖZ, B. E., ONURDAĞ, F. K., AKSÖZ, E., ÖZGACAR, S. Ö. (2022). Biological activity screening of some hydrazone and chalcone derivatives. Türk Hijyen ve Deneysel Biyoloji Dergisi, Cilt: 78 - Sayı: 2, 159–166. https://ajindex.com/articles/624960

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References (13)

  1. Lowy FD. Antimicrobial resistance: the example of Staphylococcus aureus. J Clin Invest, 2003; 111: 1265-73
  2. Monaco M, Araujo FP, Cruciani M, Coccia EM, Pantosti A. Worldwide epidemiology and antibiotic resistance of Staphylococcus aureus. Curr Top Microbiol Immunol, 2017; 409: 21–56
  3. Côté H, Pichette A, Simard F, Ouellette ME, Ripoll L, Mihoub M, et al. Balsacone C, a new antibiotic targeting bacterial cell membranes, inhibits clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA) without inducing resistance. Front Microbiol, 2019; 10: 2341
  4. Riviere C. Dihydrochalcones: Occurence in the plant kingdom, chemistry and biological activities. In: Atta-ur Rahman (Ed.). Studies in Natural Products Chemistry. John Fedor Publisher, Elsevier, Amsterdam, Netherlands, 2016; 253-373
  5. Osório TM, Monache FD, Chiaradia LD, Mascarello A, Stumpf TS, Zanetti CR, et al. Antibacterial activity of chalcones, hydrazones and oxadiazoles against methicillin-resistant Staphylococcus aureus. Bioorg Med Chem Lett, 2012; 22: 225-30
  6. De Oliveira KN, Costa P, Santin JR, Mazzambani L, Bürger C, Mora C, et al. Synthesis and antidepressant-like activity evaluation of sulphonamides and sulphonyl-hydrazones., 2011; 19(14): 4295-306
  7. Can ÖD, Altıntop MD, Özkay ÜD, Üçel UI, Doğruer B, Kaplancıklı ZA. Synthesis of thiadiazole derivatives bearing hydrazone moieties and evaluation of their pharmacological effects on anxiety, depression, and nociception parameters in mice. Arch Pharm Res, 2012; 35(4): 659-69
  8. Sridhar SK, Pandeya SN, Stables JP, Ramesh A. Anticonvulsant activity of hydrazones, schiff and mannich bases of isatin derivatives. Eur J Pharm Sci, 2002; 16: 129-32
  9. Angelova V, Karabeliov V, Andreeva-Gateva PA, Tchekalarova J. Recent developments of hydrazide/hydrazine derivatives and their analogs as anticonvulsant agents in animal models. Drug Dev Res, 2016; 77: 379-92
  10. Rollas S, Küçükgüzel ŞG. Biological activities of hydrazone derivatives. Molecules, 2007; 12: 1910- 39
  11. Asif M, Husain A. Analgesic, anti-inflammatory, and antiplatelet profile of hydrazones containing synthetic molecules. Journal of Applied Chemistry, 2013; 2013: Article ID 247203, 7 pages
  12. Verma G, Marella A, Shaquiquzzaman M, Akhtar M, Ali MR, Alam MM. A review exploring biological activities of hydrazones. J Pharm Bioallied Sci, 2014; 6(2): 69-80
  13. Sundaree S, Vaddula BR, Tantak MP, Khandagale SB, Shi C, Shah K, et al. Synthesis and anticancer activity study