IN SILICO INVESTIGATION OF ECHINODERMATA SECONDARY METABOLITES AS HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 (HIV-1) REVERSE TRANSCRIPTASE INHIBITORS

Authors

  • NURRAHMA NAZWIR Department of Pharmaceutical Chemistry, Biomedical Computation Laboratory, Faculty of Pharmacy, Universitas Indonesia, Depok 16424, Indonesia.
  • ARRY YANUAR Department of Pharmaceutical Chemistry, Biomedical Computation Laboratory, Faculty of Pharmacy, Universitas Indonesia, Depok 16424, Indonesia.
  • REZI RIADHI SYAHDI Department of Pharmaceutical Chemistry, Biomedical Computation Laboratory, Faculty of Pharmacy, Universitas Indonesia, Depok 16424, Indonesia

DOI:

https://doi.org/10.22159/ijap.2020.v12s1.FF006

Keywords:

Echinoderms, Human immunodeficiency virus, Reverse transcriptase inhibitor

Abstract

Objective: Human immunodeficiency virus (HIV) targets the immune system and weakens immune surveillance and defenses against infections,
leading to acute immunodeficiency syndrome. Recent trends in drug discovery from natural sources emphasize investigations of compounds from
marine ecosystems.
Methods: In this study, we compiled a database of chemical compounds from echinoderms and virtually screened for those that inhibit HIV-1 reverse
transcriptase (RT). The database was generated from literature searches. Virtual screening analyses for inhibitors of HIV-1 RT were then performed
using AutoDock software.
Results: Based on screening results, the top thirteen ranked compounds were nobilisidenol B, Ech_005, 17-deoxyholothurinogenin,
22,25-oxidoholothurinogenin, Ech_022, Ech_026, Ech_021, nobilisidenol A, Ech_025, 5α-cholest-8(14)-ene-3ß,7α-diol, astropecten A, Ech_004, and
phrygiasterol.
Conclusion: The present in silico screening analyses of compounds from marine ecosystems can be used to identify candidate compounds with high
potential as drugs for the treatment of refractory HIV infections.

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Published

23-03-2020

How to Cite

NAZWIR, N., YANUAR, A., & SYAHDI, R. R. (2020). IN SILICO INVESTIGATION OF ECHINODERMATA SECONDARY METABOLITES AS HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 (HIV-1) REVERSE TRANSCRIPTASE INHIBITORS. International Journal of Applied Pharmaceutics, 12(1), 51–55. https://doi.org/10.22159/ijap.2020.v12s1.FF006

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