dc.contributor.author |
Hussain, Ghulam |
|
dc.contributor.author |
Ashfaq, Usman Ali |
|
dc.contributor.author |
Rahman, Mahmood-ur |
|
dc.contributor.author |
Masoud, Muhammad Shareef |
|
dc.contributor.author |
Nahid, Nazia |
|
dc.contributor.author |
Bhinder, Munir Ahmad |
|
dc.contributor.author |
Aslam, Nosheen |
|
dc.contributor.author |
Yousaf, Numan |
|
dc.contributor.author |
Ahmed, Uzair |
|
dc.contributor.author |
Qasim, Muhammad |
|
dc.date.accessioned |
2022-12-07T06:31:11Z |
|
dc.date.available |
2022-12-07T06:31:11Z |
|
dc.date.issued |
2019-05-04 |
|
dc.identifier.citation |
Hussain, G., Ashfaq, U. A., Masoud, M. S., Nahid, N., Bhinder, M. A., Aslam, N., ... & Qasim, M. (2019). Computational screening of phytochemicals against survivin protein: A potent target for cancer. Pakistan Journal of Pharmaceutical Sciences, 32. |
en_US |
dc.identifier.issn |
1011-601X |
|
dc.identifier.uri |
http://142.54.178.187:9060/xmlui/handle/123456789/14829 |
|
dc.description.abstract |
Survivin (IAP proteins) is considered as a significant target for anticancer drug research owing to its
upregulation in tumor cells to mediate resistance to apoptotic stimulus. The current study aimed to investigate
phytochemicals as inhibitors of survivin with caspases to reactivate the functioning of caspases through molecular docking. The compounds namely 2(R), 4(R)-dihydroxypyrrolidine, 4-hydroxy-2-(4-methoxyphenyl)-1,1-dioxo-3,4- dihydrothieno[3,2-e]thiazine-6-sulfonamide, 2,3-Diketo-L-gulonic acid, (3-hydroxy-2-octadeca-9,12-dienoyloxypropyl) octadecanoate, 2-[[4-[[4-[(4-formamido-1-methylimidazole-2-carbonyl)amino]-1-methylimidazole-2-carbonyl]amino]-1- methylimidazole-2-carbonyl]amino]ethyl-dimethylazanium, Picolinic acid and (2-Hydroxy-5-nitrophenyl) dihydrogen phosphate successfully bind inside the pocket of survivin. ADMETsar was used to evaluate the anticancer potential of selected compounds. These compounds can be proposed as effective inhibitors, disrupting the survivin-caspases interaction and reactivating the caspases function of apoptosis. The study might facilitate the development of costeffective and natural drugs against cancer. However, further validation is essential for confirmation of its drug efficacy
and bio-compatibility. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Karachi: Faculty of Pharmacy & Pharmaceutical Sciences, Karachi |
en_US |
dc.subject |
Survivin |
en_US |
dc.subject |
medicinal plants |
en_US |
dc.subject |
anticancer drugs |
en_US |
dc.subject |
computational drug design |
en_US |
dc.title |
Computational screening of phytochemicals against survivin protein: A potent target for cancer |
en_US |
dc.type |
Article |
en_US |