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Asymmetric transfer hydrogenation by synthetic catalysts in cancer cells

13 , eabb0319 (2021)

Meanwhile, the incorporation of sulfonyl-morpholine and -piperazine aryl-substitution compromises the selectivity in compound 29b

However, the six most potent mAbs (from the same epitope community) did not inhibit DARC binding and lost GIA when tested against a heterologous strain of PvDBP