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- W2040349691 abstract "Substituted monocyclic β-lactam have recently been reported as inhibitors of human leukocyte elastase (HLE). Simple N-acetyl-2-azetidinone lead structures were found to undergo N-deacylation as well as β-lactam ring opening. The development of the N-carbamoyl-2-azetidinone nucleus was crucial to the stability of these compounds for effective oral bioavailability. Simple N-acetyl-2-azetidinone inhibitors of human leukocyte elastase ( I ) were found to undergo N-deacylation as well as β-lactam ring opening. The development of the N-carbamoyl-2-azetidinone nucleus in 5 was crucial to the stability of these compounds for effective oral bioavailability." @default.
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- W2040349691 date "1992-07-01" @default.
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- W2040349691 title "The effect of N-acyl substituents on the stability of monocyclic β-lactam inhibitors of human leukocyte elastase" @default.
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- W2040349691 doi "https://doi.org/10.1016/s0960-894x(00)80390-x" @default.
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