Journals / Hacettepe Üniversitesi Eczacılık Fakültesi Dergisi / 2011 / Sayı: 1

Antimicrobial Screening of 2-Methyl-3- Acyl-4-Aryl-2,6,6 and / or 2,7,7-Trimethyl1,4,5,6,7,8-Hexahydroquinoline Derivatives

2-Metil-3-Acil-4-Aril-2,6,6 ve/veya 2,7,7-Trimetil-1,4,5,6,7,8-Hekzahidrokinolin Türevlerinin Antimikrobiyal Etkilerinin Araştırılması

Pages
51–58
Publication Date
2011-01-01
DOI
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AI Summary & Key Takeaways

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

Antimicrobial activities were determined as minimum inhibitory concentration MIC values by broth microdilution method against bacteria and fungi.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:In this study, thirty compounds having methyl ethyl 2,6,6- or 2,7,7-trimethyl-5-oxo-4- difluorosubstituted phenyl -1,4,5,6,7,8-hexahydroquinoline- 3-carboxylate and N,N-diethyl-2,6,6- or 2,7,7-trimethyl- 5-oxo-4- difluorosubstituted phenyl -1,4,5,6,7,8-hexahydroquinoline-3- carboxamide structure, have been screened for their antimicrobial activities.
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Key Findings & Data:In this study, thirty compounds having methyl ethyl 2,6,6- or 2,7,7-trimethyl-5-oxo-4- difluorosubstituted phenyl -1,4,5,6,7,8-hexahydroquinoline- 3-carboxylate and N,N-diethyl-2,6,6- or 2,7,7-trimethyl- 5-oxo-4- difluorosubstituted phenyl -1,4,5,6,7,8-hexahydroquinoline-3- carboxamide structure, have been screened for their antimicrobial activities.
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Conclusion & Impact:Antimicrobial activities were determined as minimum inhibitory concentration MIC values by broth microdilution method against bacteria and fungi.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:4-dihydropyridine · hexahydroquinoline · antimicrobial activity

Abstract

In this study, thirty compounds having methyl ethyl 2,6,6- or 2,7,7-trimethyl-5-oxo-4- difluorosubstituted phenyl -1,4,5,6,7,8-hexahydroquinoline- 3-carboxylate and N,N-diethyl-2,6,6- or 2,7,7-trimethyl- 5-oxo-4- difluorosubstituted phenyl -1,4,5,6,7,8-hexahydroquinoline-3- carboxamide structure, have been screened for their antimicrobial activities. Antimicrobial activities were determined as minimum inhibitory concentration MIC values by broth microdilution method against bacteria and fungi.

Özet

Bu çalışmada metil etil 2,6,6- veya 2,7,7-trimetil-5-okso-4- difluorosübstitüe fenil -1,4,5,6,7,8-hekzahidrokinolin-3-karboksilat ve N,N-dietil-2,6,6- veya 2,7,7-trimetil-5-okso-4- difluorosübstitüe fenil -1,4,5,6,7,8-hekzahidrokinolin-3-karboksamit yapısına sahip otuz bileşiğin antimikrobiyal aktivitesi taranmıştır. Bakteri ve funguslara karşı antimikrobiyal aktiviteleri broth mikrodilüsyon yöntemi kullanılarak minimum inhibitör konsantrasyonu MIC olarak saptanmıştır.

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Cite This Article

GÜNDÜZ, M. G., EKİZOĞLU, M., KART, D., ŞİMŞEK, R., ŞAFAK, C. (2011). Antimicrobial Screening of 2-Methyl-3- Acyl-4-Aryl-2,6,6 and / or 2,7,7-Trimethyl1,4,5,6,7,8-Hexahydroquinoline Derivatives. Hacettepe Üniversitesi Eczacılık Fakültesi Dergisi, Sayı: 1, 51–58. https://ajindex.com/articles/762396

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References (11)

  1. Edraki, N., Mehdipour, A. R., Khoshneviszadeh, M., Ramin, M.; Dihydropyridines: Evaluation of Their Current and Future Pharmacological Applications, Drug Discov. To- day, 14(21-22), 1058 (2009).
  2. Şafak, C., Şimşek, R.; Fused 1,4-Dihydropyridines as Potential Calcium Modulatory Compounds, Mini Rev. Med. Chem., 6, 747 ( 2006).
  3. Peri, R., Padmanabhan, S., Rutledge, A., Singh, S., Triggle, D.J.; Permanently Charged Chiral 1,4-Dihydropyridines: Molecular Probes of L-Type Calcium Channels. Synthesis and Pharmacological Characterization of Methyl (ω-Trimethylalkylammonium) 1,4-Di- hydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5- pyridinedicarboxylate Iodide, Calcium Channel Antagonists, J. Med. Chem, 43(15), 2906 ( 2000).
  4. Coburn, R. A., Wierzba, M., Suto, M. J., Solo, A. J., Triggle, A. M., Triggle, D.J.; 1,4-Di- hydropyridine Antagonist Activities at the Calcium Channel: A Quantitative Structure- Activity Relationship Approach, J. Med. Chem., 31(11), 2103 (1988).
  5. Wojewodzka, M., Gradzka, I., Buraczewska, I., Brzoska, K., Sochanowicz, B., Goncha- rov, R., et al.; Dihydropyridines Decrease X-ray-induced DNA Base Damage in Mam- malian Cells, Mutat. Res., 671(1-2), 45 (2009).
  6. Mehdipour, A. R., Javidnia, K., Hemmateenejad, B., Amirghofran, Z., Miri, R.; Dihy- dropyridine Derivatives to Overcome Atypical Multidrug Resistance: Design, Synthesis, QSAR Studies, and Evaluation of Their Cytotoxic and Pharmacological Activities, Chem. Biol. Drug Res., 70(4), 337 (2007).
  7. Samzadeh-Kermani, A., Shafaroodi, H., Miri, R., Mirkhani, H., Vosooghi, M., Shafiee, A.; Lipophilic 2-(4-chlorophenyl)-4-thiazolyl-1,4-dihydropyridines: Synthesis, Calcium Channel Antagonist Activity, and Protection Against Pentylenetetrazole-induced Seizu- re, Med. Chem. Res., 18, 112 (2009).
  8. Sirisha, K., Achaiah, G., Reddy, V.M.; Facile Synthesis and Antibacterial, Antitubercu- lar, and Anticancer Activities of Novel 1,4-Dihydropyridines, Arch. Pharm. Chem. Life Sci., 343, 342 (2010).
  9. Sirisha, K., Bikshapathi, D., Achaiah, G., Reddy, V.M.; Synthesis, Antibacterial and Antimycobacterial Activities of Some New 4-Aryl/heteroaryl-2,6-dimethyl-3,5-bis-N- (aryl)-carbamoyl-1,4-dihydropyridines, Eur. J. Med. Chem., 46, 1564 (2011).
  10. Desai, B., Sureja, D., Naliapara, Y., Shah, A., Saxena, A.K.; Synthesis and QSAR Stud- ies of 4-Substituted phenyl-2,6-dimethyl-3, 5-bis-N-(substituted phenyl)carbamoyl- 1,4-dihydropyridines as Potential Antitubercular Agents, Bioorg. Med. Chem., 9(8), 1993 (2001).
  11. Kumar, R. S., Idhayadhulla, A.