STUDI PENAMBATAN MOLEKUL SENYAWA-SENYAWA BIOAKTIF DARI KULIT AKAR MURBEI (Morus sp.) TERHADAP RESEPTOR TNF-α
Abstract
Tumor necrosis factor alfa (TNF)-α memiliki peranan penting dalam patogenesis beberapa penyakit inflamasi. Murbei dilaporkan memiliki efek penghambatan pada proses inflamasi. Penelitian ini ditujukan untuk mengetahui interaksi antara senyawa-senyawa bioaktif yang terdapat pada murbei terhadap reseptor TNF-α dengan metode simulasi docking molekuler. Docking dilakukan dengan menggunakan program AutoDock 4.2, dengan menambatkan senyawa pada sisi aktif reseptor TNF-α (PDB ID : 3EWJ) secara in silico. Hasil docking menunjukkan bahwa senyawa-senyawa bioaktif dari kulit akar murbei dapat berinteraksi dengan sisi aktif. Interaksi terbaik ditunjukkan oleh senyawa 86 dengan energi bebas ikatan -13,03 12kkal/mol, yang berinteraksi dengan residu asam amino yang penting pada reseptor TNF-α dan memiliki ikatan hidrogen yang sama pada Leu348, Glu406 dan Gly349 dengan menggunakan pembanding (1S, 3R, 6S)-4-oxo-6{4-[2-phenylquinolon-4-yl)methoxy]phenyl}-5-azaspiro [2.4]heptane-1-carboxylic acid sebagai ligan alami.
References
Levine, S.J., Tumor Necrosis Factor Alpha (TNF-α), National Institutes of Health, Bethesda, MD, USA, Published by Elsevier Ltd, 2017.
Kimura, Y., Okuda, H., Nomura, T., Fukai, T., & Arichi, S. Effects of phenolic constituents from the Mulberry tree on Arachidonate metabolism in Rat platelets. Journal of Natural Products, 1986; 49: 639–644.
Wei, H., Zhu, JJ., Liu, XQ., Feng, WH., Wang, ZM. and Yan, LH, Review Of Bioactive Compounds From Root Barks Of Morus Plants (Sang-Bai-Pi) And Their Pharmacological Effects, Cogent Chemistry 2016; 2: 1212320
Lestari, Tresna, Studi Interaksi Senyawa Turunan 1,3-Dibenzoiltiourea Sebagai Ribonukleotida Reduktase Inhibitor, Jurnal Farmasi Indonesia, 2015; 7(3):163-169
Pebriana, B. R., Romadhon, F. A., Yunianto, A., Rokhman, R. M., Fitriyah, Q. N., Jenie, I. R., et.al. Docking Kurkumin Dan Senyawa Analognya Pada Reseptor Progesteron: Studi Interaksinya Sebagai Selective Progesterone Receptor Modulators (SPRms), Pharmacon, 2008; 9 (1):14-20
Ferwadi, S., Gunawan, R., dan Astuti, W.., Studi Docking Molekular Senyawa Asam Sinamat Dan Derivatnya Sebagai Inhibitor Protein 1j4x Pada Sel Kanker Serviks, Jurnal Kimia Mulawarman, 2017; 14 (2):84-90
Bissantz, C. G., and Folkers, D. Rognan, Protein-based Virtual Screening of Chemical Databases : Evaluation of Different Docking/Scoring Combinations. Journal of Medicinal Chemistry, 2000; 43:4759-4767.
Pratama, F., R., Moh. 2016, Studi Docking Molekular Senyawa Turunan Kuinolin Terhadap Reseptor Estrogen-α, Jurnal Surya Medika, 2 (1):1-7.
Pranowo, H. D., Kimia Komputasi, Pusat Kimia Komputasi Indonesia Austria, Jurusan Kimia FMIPA, Universitas Gadjah Mada, Yogyakarta; 2006
Paul, J. Gane., and Philip, M. Dean., Recent Advances In Structure-Based Rational Drug Design, Current Opinion in Structural Biology, 2000; 10:401-404
Downloads
Published
Issue
Section
License
The copyright to this article is transferred to Universitas Hasanuddin (UNHAS) if and when the article is accepted for publication. The undersigned hereby transfers all rights in and to the paper including without limitation all copyrights to UNHAS. The undersigned hereby represents and warrants that the paper is original and that he/she is the author of the paper, except for material that is clearly identified as to its original source, with permission notices from the copyright owners where required. The undersigned represents that he/she has the power and authority to make and execute this assignment.
We declare that:
- This paper has not been published in the same form elsewhere.
- It will not be submitted anywhere else for publication prior to acceptance/rejection by this Journal.
- A copyright permission is obtained for materials published elsewhere and which require this permission for reproduction.
Furthermore, I/We hereby transfer the unlimited rights of publication of the above-mentioned paper in whole to UNHAS The copyright transfer covers the exclusive right to reproduce and distribute the article, including reprints, translations, photographic reproductions, microform, electronic form (offline, online) or any other reproductions of similar nature.
The corresponding author signs for and accepts responsibility for releasing this material on behalf of any and all co-authors. This agreement is to be signed by at least one of the authors who have obtained the assent of the co-author(s) where applicable. After submission of this agreement signed by the corresponding author, changes of authorship or in the order of the authors listed will not be accepted.