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[DOI] [PMC free article] [PubMed] [Google Scholar] 87.Kuo Y., Ng I.W., Rajesh R

GSH exerts its action as skin whitening agent at various levels of melanogenesis which include the following: [1],[3] Interference with cellular transport of tyrosinase Direct inactivation of the enzyme tyrosinase by binding with the copper-containing active site of the enzyme Mediating the switch mechanism from eumelanin to phaeomelanin production as GSH is the major physiologic reservoir of cysteine and increase in cysteine levels results in switching of eumelanogenesis to pheomelanogenesis [Figure - 1] Quenching of free radicals and peroxides that contribute to tyrosinase activation and melanin formation Modulation of depigmenting abilities of melanocytotoxic agents

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The deal gave Lilly Loxo's oral TRK inhibitor, Vitrakvi (Larotrectinib), LOXO-292, an oral proto-oncogene receptor tyrosine kinase rearranged during transfection (RET) inhibitor, LOXO-305, an oral Bruton's tyrosine kinase (BTK) inhibitor, and LOXO-195, a follow-on TRK inhibitor