Acylhydrazide schiff bases: Synthesis and antiglycation activity

Acylhydrazide Schiff bases 1-27 were synthesized and their in vitro antiglycation potential was evaluated. Compounds 16 (IC50 = 199.82 ± 10.6 μM), 27 (IC50 = 234.83 ± 10.28 μM), 2 (IC50 = 240.99 ± 4.2 μM), and 14 (IC50 = 276.2 ± 2.3 μM) showed antiglycation potential comparable to the standard rutin...

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Published in:Journal of the Chemical Society of Pakistan
Main Author: Khan K.M.; Taha M.; Rahim F.; Fakhri M.I.; Jamil W.; Khan M.; Rasheed S.; Karim A.; Perveen S.; Choudhary M.I.
Format: Article
Language:English
Published: 2013
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84879727205&partnerID=40&md5=8a5fa6595cc3ce6d806bf70c4b71c2ba
id 2-s2.0-84879727205
spelling 2-s2.0-84879727205
Khan K.M.; Taha M.; Rahim F.; Fakhri M.I.; Jamil W.; Khan M.; Rasheed S.; Karim A.; Perveen S.; Choudhary M.I.
Acylhydrazide schiff bases: Synthesis and antiglycation activity
2013
Journal of the Chemical Society of Pakistan
35
3

https://www.scopus.com/inward/record.uri?eid=2-s2.0-84879727205&partnerID=40&md5=8a5fa6595cc3ce6d806bf70c4b71c2ba
Acylhydrazide Schiff bases 1-27 were synthesized and their in vitro antiglycation potential was evaluated. Compounds 16 (IC50 = 199.82 ± 10.6 μM), 27 (IC50 = 234.83 ± 10.28 μM), 2 (IC50 = 240.99 ± 4.2 μM), and 14 (IC50 = 276.2 ± 2.3 μM) showed antiglycation potential comparable to the standard rutin (IC50 = 294.50 ± 1.5 μM). From this study we identified a new series of potent antiglycating agents. A structure-activity relationship has been described, while all compounds were characterized by using different spectroscopic techniques.

2535106
English
Article

author Khan K.M.; Taha M.; Rahim F.; Fakhri M.I.; Jamil W.; Khan M.; Rasheed S.; Karim A.; Perveen S.; Choudhary M.I.
spellingShingle Khan K.M.; Taha M.; Rahim F.; Fakhri M.I.; Jamil W.; Khan M.; Rasheed S.; Karim A.; Perveen S.; Choudhary M.I.
Acylhydrazide schiff bases: Synthesis and antiglycation activity
author_facet Khan K.M.; Taha M.; Rahim F.; Fakhri M.I.; Jamil W.; Khan M.; Rasheed S.; Karim A.; Perveen S.; Choudhary M.I.
author_sort Khan K.M.; Taha M.; Rahim F.; Fakhri M.I.; Jamil W.; Khan M.; Rasheed S.; Karim A.; Perveen S.; Choudhary M.I.
title Acylhydrazide schiff bases: Synthesis and antiglycation activity
title_short Acylhydrazide schiff bases: Synthesis and antiglycation activity
title_full Acylhydrazide schiff bases: Synthesis and antiglycation activity
title_fullStr Acylhydrazide schiff bases: Synthesis and antiglycation activity
title_full_unstemmed Acylhydrazide schiff bases: Synthesis and antiglycation activity
title_sort Acylhydrazide schiff bases: Synthesis and antiglycation activity
publishDate 2013
container_title Journal of the Chemical Society of Pakistan
container_volume 35
container_issue 3
doi_str_mv
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-84879727205&partnerID=40&md5=8a5fa6595cc3ce6d806bf70c4b71c2ba
description Acylhydrazide Schiff bases 1-27 were synthesized and their in vitro antiglycation potential was evaluated. Compounds 16 (IC50 = 199.82 ± 10.6 μM), 27 (IC50 = 234.83 ± 10.28 μM), 2 (IC50 = 240.99 ± 4.2 μM), and 14 (IC50 = 276.2 ± 2.3 μM) showed antiglycation potential comparable to the standard rutin (IC50 = 294.50 ± 1.5 μM). From this study we identified a new series of potent antiglycating agents. A structure-activity relationship has been described, while all compounds were characterized by using different spectroscopic techniques.
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language English
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