dc.contributor.author |
Rehman, Saba Fazal-ur |
|
dc.contributor.author |
Wasim, Agha Arslan |
|
dc.contributor.author |
Iqbal, Sadaf |
|
dc.contributor.author |
Khan, Maria Aqeel |
|
dc.contributor.author |
Lateef, Mehreen |
|
dc.contributor.author |
Iqbal, Lubna |
|
dc.date.accessioned |
2022-12-07T07:40:04Z |
|
dc.date.available |
2022-12-07T07:40:04Z |
|
dc.date.issued |
2019-05-18 |
|
dc.identifier.citation |
Fazal-ur-Rehman, S., Wasim, A. A., Iqbal, S., Khan, M. A., Lateef, M., & Iqbal, L. (2019). Synthesis, lipoxygenase inhibition activity and molecular docking of oxamide derivative. Pakistan Journal of Pharmaceutical Sciences, 32(3), 1253-1259. |
en_US |
dc.identifier.issn |
1011-601X |
|
dc.identifier.uri |
http://142.54.178.187:9060/xmlui/handle/123456789/14846 |
|
dc.description.abstract |
In this study, a range of oxamide ligands were synthesized by the reaction of amines with oxalyl chloride in
basic medium. Spectroscopic and analytical techniques such as IR, 1H-NMR and ESI-MS techniques were used for characterization of the synthesized oxamides. The synthesized oxamides were screened for Lipoxygenase inhibition. Biological screening revealed that the oxamides possessed good lipoxygenase inhibition activities, whereas, the unsubstituted oxamide did not show any distinct lipoxygenase inhibition activity. Molecular docking studies of the oxamides were also carried out for lipoxygenase inhibition. The results obtained from molecular docking were well correlated with the empirical data. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Karachi: Faculty of Pharmacy & Pharmaceutical Sciences, Karachi |
en_US |
dc.subject |
Oxamide |
en_US |
dc.subject |
molecular docking |
en_US |
dc.subject |
lipoxygenase inhibition |
en_US |
dc.title |
Synthesis, lipoxygenase inhibition activity and molecular docking of oxamide derivative |
en_US |
dc.type |
Article |
en_US |