In-Silico Analysis of Momordica charantia L. As Antidiabetic Agents Through Activation of Human UDP-Galactose 4-Epimerase Receptors

Penulis

  • Asri Dwi Endah Dewi Pramesthi Universitas Muhammadiyah Kalimantan Timur https://orcid.org/0000-0002-0582-9139
  • Kafka Navisa Suwarno Universitas Muhammadiyah Kalimantan Timur
  • Aldo Pratama Universitas Muhammadiyah Kalimantan Timur
  • Jamiatur Rasyidah Universitas Muhammadiyah Kalimantan Timur
  • I Wayan Surya Rahadi Universitas Mahasaraswati Denpasar, Denpasar, Indonesia https://orcid.org/0009-0006-7858-4749
  • Rima Rasida Institut Teknologi Bandung, Bandung, Indonesia

DOI:

https://doi.org/10.32382/mf.v20i2.1002

Kata Kunci:

Momordica charantia, Metformin, Human UDP-Galactose 4-Epimerase Receptors, In silico analysis

Abstrak

Analisa In-Silico (Momordica charantia L.) Sebagai Senyawa Antidiabetes Melalui Aktivasi Reseptor UDP-Galactose 4-Epimerase Manusia

Potensi antidiabetes dari senyawa yang ditemukan dalam Momordica charantia L. yang dikenal sebagai pare diselidiki melalui docking molekuler dan analisis ADME. Beberapa senyawa bioaktif dari pare, seperti charantin, vicine, momordenol, momordicilin, dan momordikosida dianalisis secara in silico saat berinteraksi dengan reseptor UDP-4 manusia. Hasil docking menunjukkan bahwa senyawa-senyawa tersebut menunjukkan afinitas ikatan yang kuat dalam regulasi glukosa. Analisis ADME menunjukkan bahwa senyawa tersebut mematuhi Lipinski Rule of Five, dengan sifat yang menguntungkan seperti obat dan beberapa senyawa perlu dilakukan uji toksisitas. Hasil penelitian ini menunjukkan bahwa Momordica charantia L. memiliki potensi sebagai antidiabetes yang perlu dikonfirmasi secara in vivo dan uji klinis terkait efikasi dan keamanan dalam manajemen diabetes mellitus.

This study investigates the antidiabetic potential of compounds found in Momordica charantia L., commonly known as bitter melon, through molecular docking and ADME (Absorption, Distribution, Metabolism, and Excretion) analysis. Utilizing in silico methods, several bioactive compounds from bitter melon, such as charantin, vicine, momordenol, momordicilin, and momordicoside, were evaluated for their ability to interact with the human UDP-Galactose 4-Epimerase receptor, a key enzyme involved in glucose metabolism. The docking results indicate that these compounds exhibit strong binding affinities, suggesting their role in glucose regulation. Further ADME analysis revealed that the compounds generally comply with the Lipinski Rule of Five, indicating favorable drug-like properties, though some compounds exhibited potential toxicities requiring further investigation. These findings highlight the potential of Momordica charantia as a source of antidiabetic agents, warranting additional in vivo and clinical studies to confirm their efficacy and safety in managing diabetes mellitus.

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Unduhan

Diterbitkan

31-10-2024

Terbitan

Bagian

Terbitan Oktober 2024