Journals / Journal of Ongoing Chemical Research / 2018 / Cilt: 3 - Sayı: 2

SYNTHESIS AND CHARACTERIZATION OF SOME NEW HYDRAZONES WITH ANTI‐UREASE ACTIVITIES

Pages
71–74
Publication Date
2018-06-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

This study has culminated in the identiŞcation of some compoundswhich can serve as leads for new potent urease inhibitors

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Hydrazones were considered as signiŞcant substrates in drug discovery process.
📊
Key Findings & Data:Therefore, a seriesof some new 1- 4- 1- 2- 4-substitutedphenyl hydrazono ethyl phenyl -3- 4-nitrophenyl ureaderivatives were synthesized as potential urease inhibitory agents.
💡
Conclusion & Impact:This study has culminated in the identiŞcation of some compoundswhich can serve as leads for new potent urease inhibitors
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:organic synthesis · Urease inhibition activity · Hydrazone

Abstract

Hydrazones were considered as signiŞcant substrates in drug discovery process. Therefore, a seriesof some new 1- 4- 1- 2- 4-substitutedphenyl hydrazono ethyl phenyl -3- 4-nitrophenyl ureaderivatives were synthesized as potential urease inhibitory agents. The synthesizedcompounds were characterized by FTIR, ¹H NMR, 13C NMR, and elemental analysis C, H, N . Allcompounds were evaluated in vitro for urease inhibitory potential. Among synthesized compounds,8, 7, 6, and 4 showed excellent activities IC50 i.e. 10.13±0.40, 12.15±0.22, 17.81±0.36, and22.95±0.47 µM, respectively. This study has culminated in the identiŞcation of some compoundswhich can serve as leads for new potent urease inhibitors

🔖

Cite This Article

SICAK, Y. (2018). SYNTHESIS AND CHARACTERIZATION OF SOME NEW HYDRAZONES WITH ANTI‐UREASE ACTIVITIES. Journal of Ongoing Chemical Research, Cilt: 3 - Sayı: 2, 71–74. https://ajindex.com/articles/778194

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (7)

  1. Pandey et al, 2000
  2. Pandey, Devendra; Kumar, Ajendra; Nag, AK (2000). Asian Journal of Chemistry, 12, 1361 Qu et al, 2015
  3. Qu, Dan; Niu, Fang; Zhao, Xinlu; Yan, Ke-Xiang; Ye, Yu-Ting; Wang, Jia; Zhang, Mei; You, Zhonglu (2015). Bioorganic & medicinal chemistry, 23, 1944-1949 Scavenging, 2015
  4. Scavenging, DPPH Radical (2015). J. Chem. Soc. Pak, 37, 479 Shakir et al, 2015
  5. Shakir, M; Abbasi, A (2015). Journal of Chemical and Pharmaceutical Research, 7, 375-382 Tan et al, 2013
  6. Tan, Lirong; Su, Jiyan; Wu, Dianwei; Yu, Xiaodan; Su, Zuqing; He, Jingjin; Wu, Xiaoli; Kong, Songzhi; Lai, Xiaoping; Lin, Ji; others (2013). The ScientiŞc World Journal, 2013 Verma et al, 2014
  7. Verma, Garima; Marella, Akranth; Shaquiquzzaman, Mohammad; Akhtar, Mymoona; Ali, Mohammad Rahmat; Alam, Mohammad Mumtaz (2014). Journal of pharmacy & bioallied sciences, 6, 69