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doi: 10.1111/jocs.1991.6.1s.270
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To investigate this hypothesis, we initiated theoretical studies (molecular docking) to compare the binding affinity of hypothetical CAT inhibitors containing heterocyclic substituents with that of the natural substrate L-carnitine and the inhibitors Meldonium and 4-(ethyldimethylammonio)butanoate (MeGBB—a drug candidate in phase III of clinical trials, Figure 1)
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