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The design of drug targets for ASCT2 typically follows a substrate analogue approach, wherein substrate analogues function as competitive inhibitors, thereby reducing the uptake of essential amino acids by cancer cells

Key findings Biochemical analysis demonstrated that paracetamol administration significantly increased ALT, AST, ALP, and MDA levels, along with a concomitant reduction in total protein, SOD and GSH levels, confirming hepatocellular injury

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It is always better to have them assessed