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Two synthetic des-thio analogues of glutathione, one featuring a serine hydroxyl group in place of the cysteine thiol, the other being the alanine analogue, devoid of any polar or chemically reactive group in the place of cysteine were synthesized and their efficiency as competitive inhibitors of glutathione- S -transferase iso-enzymes 3-3 and 4-4 was tested

Moreover, CUR inhibited NSCLC growth by regulating DMRT3 in vivo