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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lawal, Hadiza Abdulrahman | vi |
dc.contributor.other | Uzairu, Adamu | vi |
dc.contributor.other | Uba, Sani | vi |
dc.date.accessioned | 2023-03-16T09:01:07Z | - |
dc.date.available | 2023-03-16T09:01:07Z | - |
dc.date.issued | 2021 | - |
dc.identifier.issn | 2522-8307 | vi |
dc.identifier.uri | http://tailieuso.tlu.edu.vn/handle/DHTL/12445 | - |
dc.description.abstract | The QSAR model of the derivatives was highly robust as it also conforms to the least minimum requirement for QSAR model from the statistical assessments of (R2) = 0.6715, (R2adj) = 0.61920, (Q2) = 0.5460 and (R2pred) of 0.5304, and the model parameters (AATS6i and VR1_Dze) were used in designing new derivative compounds with higher potency. The molecular docking studies between the derivative compounds and Maternal Embryonic Leucine Zipper Kinase (MELK) protein target revealed that ligand 2, 9 and 17 had the highest binding affinities of − 9.3, − 9.3 and − 8.9 kcal/mol which was found to be higher than the standard drug adriamycin with − 7.8 kcal/mol. The pharmacokinetics analysis carried out on the newly designed compounds revealed that all the compounds passed the drug-likeness test and also the Lipinski rule of five. | vi |
dc.description.uri | https://link.springer.com/article/10.1186/s42269-021-00541-x | vi |
dc.language | en_US | vi |
dc.relation.ispartofseries | Bulletin of the National Research Centre, Volume 45 (2021), Article number: 90 | vi |
dc.subject | QSAR | vi |
dc.subject | Molecular docking | vi |
dc.subject | Ligand-based design | vi |
dc.subject | Pharmacokinetic analysis | vi |
dc.title | QSAR, molecular docking studies, ligand-based design and pharmacokinetic analysis on Maternal Embryonic Leucine Zipper Kinase (MELK) inhibitors as potential anti-triple-negative breast cancer (MDA-MB-231 cell line) drug compounds | vi |
dc.type | BB | vi |
Appears in Collections: | Tài liệu mở |
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