Elucidating the Role of Santalol as a Potent Inhibitor of Tyrosinase: In Vitro and In Silico Approaches

Molecules. 2022 Dec 15;27(24):8915. doi: 10.3390/molecules27248915.

Abstract

This research work focuses on the potential application of an organic compound, santalol, obtained from santalum album, in the inhibition of the enzyme tyrosinase, which is actively involved in the biosynthesis of melanin pigment. Over-production of melanin causes undesirable pigmentation in humans as well as other organisms and significantly downgrades their aesthetic value. The study is designed to explain the purification of tyrosinase from the mushroom Agaricus bisporus, followed by activity assays and enzyme kinetics to give insight into the santalol-modulated tyrosinase inhibition in a dose-dependent manner. The multi-spectroscopic techniques such as UV-vis, fluorescence, and isothermal calorimetry are employed to deduce the efficiency of santalol as a potential candidate against tyrosinase enzyme activity. Experimental results are further verified by molecular docking. Santalol, derived from the essential oils of santalum album, has been widely used as a remedy for skin disorders and a potion for a fair complexion since ancient times. Based on enzyme kinetics and biophysical characterization, this is the first scientific evidence where santalol inhibits tyrosinase, and santalol may be employed in the agriculture, food, and cosmetic industries to prevent excess melanin formation or browning.

Keywords: melanogenesis; multi-spectroscopic techniques; mushroom tyrosinase; natural compounds; tyrosinase inhibitor.

MeSH terms

  • Enzyme Inhibitors / chemistry
  • Humans
  • Melanins*
  • Molecular Docking Simulation
  • Monophenol Monooxygenase*
  • Polycyclic Sesquiterpenes

Substances

  • santalol
  • Monophenol Monooxygenase
  • Melanins
  • Polycyclic Sesquiterpenes
  • Enzyme Inhibitors

Grants and funding

The authors extend their appreciation to the Deanship of Scientific Research at Imam Mohammad Ibn Saud Islamic University (IMSIU) for funding and supporting this work through Research Partnership Program no. RP-21-09-86.