THE MOLECULAR INTERACTION AND ADMET PREDICTION OF MODIFIED JPH203 AS A POTENTIAL RADIOPHARMACEUTICAL KIT FOR MOLECULAR IMAGING OF CANCER: AN IN SILICO RESEARCH
DOI:
https://doi.org/10.22159/ijap.2021.v13s4.43860Keywords:
JPH203, LAT-1, Molecular docking, ADMET, In silicoAbstract
Objective: In this study, various types of pharmacokinetic modifying linkers and chelators are combined with JPH203 to obtain the best-docked molecule for prospective radiopharmaceutical kits.
Methods: AutoDock 4.2.6 and AutoDockTools 1.5.6 programs was used to do the molecular docking simulation and ADMET prediction was done using VNN-ADMET to predict the pharmacokinetics and toxicity of the ligand.
Results: The result of this study showed that JPH203-linker K-NOTA has the best affinity with a docking score of about-10.7 kcal/mol and shows hydrogen interaction with Tyr259, which acts as key residue of the active site.
Conclusion: Based on the results, JPH203-linker K-NOTA has good potential as a radiopharmaceutical kit of cancer.
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Copyright (c) 2021 HOLIS ABDUL HOLIK, FAISAL MAULANA IBRAHIM, ELISHA WIANATALIE, ARIFUDIN ACHMAD, AHMAD FARIED, ACHMAD HUSSEIN SUNDAWA KARTAMIHARDJA
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