New Class of Tyrosinase Inhibitors, Rotenoids, from Amorpha fruticosa

Si Won Moon; Jeong Yoon Kim; Seung Hwan Lee; Se Young Im; Gihwan Lee; Ki Hun Park

doi:10.1021/acsomega.3c03396

New Class of Tyrosinase Inhibitors, Rotenoids, from Amorpha fruticosa

ACS Omega. 2023 Aug 23;8(35):31870-31879. doi: 10.1021/acsomega.3c03396. eCollection 2023 Sep 5.

Authors

Si Won Moon¹, Jeong Yoon Kim², Seung Hwan Lee¹, Se Young Im¹, Gihwan Lee¹, Ki Hun Park¹

Affiliations

¹ Division of Applied Life Science (BK21 Four), IALS, Gyeongsang National University, Jinju 52828, Republic of Korea.
² Department of Pharmaceutical Engineering, IALS, Gyeongsang National University, Jinju 52725, Republic of Korea.

Abstract

A series of rotenoids including a new one from the seeds of Amorpha fruticosa were found to have significant potential as tyrosinase inhibitors. All of the isolated rotenoids (1-6) displayed inhibitory activity against tyrosinase, both as a monophenolase for the oxidation of l-tyrosine and as a diphenolase for the oxidation of l-DOPA. The three most active compounds (1, 5, and 6) showed significant monophenolase inhibition with IC₅₀ values of 2.1, 1.7, and 1.2 μM, respectively. They also inhibited diphenolase function with IC₅₀ values in the range of 9.5-21.5 μM. The inhibition kinetics established all compounds to be competitive inhibitors of both oxidation processes. All rotenoids formed the E_met·I complex effectively around their IC₅₀ values with long lag times. Tyrosinase inhibition of the new rotenoid 6 was additionally demonstrated using high-performance liquid chromatography (HPLC) analysis with N-acetyl-l-tyrosine. Molecular docking disclosed that the sugar moiety of 5 interacted with the bottom of the catalytic gorge.