Synthesis and antiurease & antioxidant activities of bis-Schiff bases of isophthalaldehyde

Bis-Schiff bases of iosophthalaldehyde were synthesized by reacting isophthalaldehyde with hydrazine hydrate in 1:2 ratio in ethanol for 2-3 h under reflux. Product of first step was again reacted in 1:2 ratio with different aldehyde or acetophenone yielding bis-Schiff bases (1-16). All compounds we...

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Main Authors: Abid, O.U.R (Author), Khan, A. (Author), Quereshi, M.T (Author), Rahim, F. (Author), Rehman, W. (Author), Shehzad, M. (Author), Taha, M. (Author), Tauseef, I. (Author), Waseeq-Ur-Rehamn (Author)
Format: Article
Language:English
Published: Chemical Publishing Co. 2016
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LEADER 01602nam a2200289Ia 4500
001 10.14233-ajchem.2016.19168
008 220120s2016 CNT 000 0 und d
020 |a 09707077 (ISSN) 
245 1 0 |a Synthesis and antiurease & antioxidant activities of bis-Schiff bases of isophthalaldehyde 
260 0 |b Chemical Publishing Co.  |c 2016 
520 3 |a Bis-Schiff bases of iosophthalaldehyde were synthesized by reacting isophthalaldehyde with hydrazine hydrate in 1:2 ratio in ethanol for 2-3 h under reflux. Product of first step was again reacted in 1:2 ratio with different aldehyde or acetophenone yielding bis-Schiff bases (1-16). All compounds were characterized by EI-MS and 1H NMR. All analogs were tested against antioxidant and urease inhibition. Few compounds were found to showed potent antiurease and antioxidant potential. 
650 0 4 |a Antioxidant potential 
650 0 4 |a Isophthalaldehyde 
650 0 4 |a Schiff bases 
650 0 4 |a Urease inhibition 
700 1 0 |a Abid, O.U.R.  |e author 
700 1 0 |a Khan, A.  |e author 
700 1 0 |a Quereshi, M.T.  |e author 
700 1 0 |a Rahim, F.  |e author 
700 1 0 |a Rehman, W.  |e author 
700 1 0 |a Shehzad, M.  |e author 
700 1 0 |a Taha, M.  |e author 
700 1 0 |a Tauseef, I.  |e author 
700 1 0 |a Waseeq-Ur-Rehamn  |e author 
773 |t Asian Journal of Chemistry  |x 09707077 (ISSN)  |g 28 1, 39-42 
856 |z View Fulltext in Publisher  |u https://doi.org/10.14233/ajchem.2016.19168 
856 |z View in Scopus  |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-84954126061&doi=10.14233%2fajchem.2016.19168&partnerID=40&md5=b087b7bde6d2a5b0d0c1c9993c1295a4