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Though the cosmetic-grade material is synthesized for purity and consistency

cerevisiae under five growth conditions tackled this gap (Fendt et al

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10.1016/s1525-5050(03)00121-5 94 HigginsA.NashM.LynchA

Since the discovery of the HGF/c-Met pathway in the mid-1980s, c-Met has attracted significant attention as an anticancer target with several agents have been marketed including Tepotinib [7,8,9], Altiratinib [10], Capmatinib [11], Savolitinib [12, 13], and the ALK/c-Met inhibitor Crizotinib [14], and the initial results are encouraging

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