Journal of Engineering and Applied Sciences

Year: 2019
Volume: 14
Issue: 6
Page No. 1760 - 1764

Antimicrobial Activity of Some Derivatives of 2-Arylidene-1-Benzosuberone

Authors : Nawal H.Al-Bahtiti

References

Al Bahtiti, H., 2008. Biological activity of alcoholic extract of Jordanian Propolis Nawal. Arabian J. Chem., 1: 333-336.

Al Bahtiti, N., 2005. Antimicrobial activity of some heterocyclic derivatives of chalcones. Jordan J. Appl. Sci. Nat., 7: 51-57.

Al-Bahtiti, N.H., 2007. Synthesis, characterization and antibacterial activity of some 5-aryl-1, 3-Diphenyl 1-4, 5-dihydro-1H-Pyrazoles. Arab Gulf J. Sci. Res., 25: 1-5.
Direct Link  |  

Alvarez-Builla, J. and J. Barluenga, 2011. An introduction of medical heterocyclic compounds. J. Heterocycl. Compd. Chem., 1: 1-9.

Azab, M.E., M.M. Youssef and E.A. El-Bordany, 2013. Synthesis and antibacterial evaluation of novel heterocyclic compounds containing a sulfonamido moiety. Mol., 18: 832-844.
CrossRef  |  PubMed  |  Direct Link  |  

Behbehani, H., K.M. Dawood and T.A. Farghaly, 2018. Biological evaluation of benzosuberones. Expert Opin. Ther. Pat., 28: 5-29.
CrossRef  |  PubMed  |  Direct Link  |  

El-Gohary, N.S., 2014. Arylidene derivatives as synthons in heterocyclic synthesis. Open Access Library J., 1: 1-47.
CrossRef  |  Direct Link  |  

El-Salam, O.I.A., A.S. Alsayed, K.A. Ali, A.A.A. Elwahab and A.E.G.E. Amr, et al., 2017. Antimicrobial activities of some newly synthesized substituted Benzosuberone and its related derivatives. Biomed. Res., 28: 157-163.
Direct Link  |  

El‐Rayyes, N.R. and H.M. Ramadan, 1987. Heterocycles part X. synthesis of new pyrimidine systems. J. Heterocycl. Chem., 24: 589-596.
CrossRef  |  Direct Link  |  

Farghaly, T.A., M.A. Abdallah and M.R. Abdel Aziz, 2012. Synthesis and antimicrobial activity of some new 1,3,4-thiadiazole derivatives. Molecules, 17: 14625-14636.
CrossRef  |  PubMed  |  Direct Link  |  

Farghaly, T.A., S.M. Gomha, K.M. Dawood and M.R. Shaaban, 2016. Synthetic routes to benzosuberone-based fused-and spiro-heterocyclic ring systems. RSC. Adv., 6: 17955-17979.
CrossRef  |  Direct Link  |  

Monostory, K., V. Tamasi, L. Vereczkey and P. Perjesi, 2003. A study on CYP1A inhibitory action of E-2-(4-methoxybenzylidene)-1-benzosuberone and some related chalcones and cyclic chalcone analogues. Toxicol., 184: 203-210.
CrossRef  |  PubMed  |  Direct Link  |  

Pati, H.N., U. Das, E.D. Clercq, J. Balzarini and J.R. Dimmock, 2007. Molecular modifications of 2-arylidene-1-indanones leading to increased cytotoxic potencies. J. Enzyme Inhib. Med. Chem., 22: 37-42.
CrossRef  |  Direct Link  |  

Stretton, R.J. and T.W. Manson, 1973. Some aspects of the mode of action of the antibacterial compound bronopol (2‐bromo‐2‐nitropropan‐1, 3‐diol). J. Appl. Bacteriol., 36: 61-76.
CrossRef  |  Direct Link  |  

Turek, M., D. Szczęsna, M. Koprowski and P. Balczewski, 2017. Synthesis of 1-indanones with a broad range of biological activity. Beilstein J. Org. Chem., 13: 451-494.
CrossRef  |  PubMed  |  Direct Link  |  

Verma, A. and S.K. Saraf, 2008. 4-Thiazolidinone-A biologically active scaffold. Eur. J. med. Chem., 43: 897-905.
CrossRef  |  PubMed  |  Direct Link  |  

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