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dc.contributor.advisorYasmin, Hasina
dc.contributor.authorTabassum, Azwada
dc.date.accessioned2021-07-27T14:42:40Z
dc.date.available2021-07-27T14:42:40Z
dc.date.copyright2020
dc.date.issued2020-03
dc.identifier.otherID 16146004
dc.identifier.urihttp://hdl.handle.net/10361/14833
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2020.en_US
dc.descriptionCataloged from PDF version of thesis report.
dc.descriptionIncludes bibliographical references (pages 44-49).
dc.description.abstractBeing one of the leading cause of death worldwide, the fatality of colorectal cancer is increasing day by day causing approximately 862,000 deaths annually, according to IARC, 2020. As most of the conventional chemotherapeutics are becoming resistant, an in silico study was done using synthetic and natural small molecules to identify possible drug that may be proposed in the treatment of colorectal cancer. Because of having a significant role in the tumor progression of colorectal cancer, FAP-α was taken as the macromolecule. Molecular docking was performed and binding affinities were evaluated. Furthermore, the results were visualized by Discovery Studio to find out non-bonded ligand-protein interaction. At the end, admetSAR property of the drugs were assessed and compared with the standard drug. Therefore, analyzing all the in silico results, the selected drugs having the property of inhibiting FAP-α were proposed for the treatment of colorectal cancer.en_US
dc.description.statementofresponsibilityAzwada Tabassum
dc.format.extent50 pages
dc.language.isoenen_US
dc.publisherBrac Universityen_US
dc.rightsBrac University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission.
dc.subjectIn silicoen_US
dc.subjectMolecular dockingen_US
dc.subjectFAP-αen_US
dc.subjectBinding affinityen_US
dc.subject.lcshRectum--Cancer
dc.subject.lcshColon (Anatomy)--Cancer
dc.titleInhibition of Fibroblast Activation Protein alpha (FAP-α) in Colorectal Canceren_US
dc.typeThesisen_US
dc.contributor.departmentDepartment of Pharmacy, Brac University
dc.description.degreeB. Pharmacy


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