Synthesis of 2,3-dihydroxy-3-(N-substituted carbamoyl)propylphosphonic acid derivatives as hybrid DOXP-fosmidomycin analogues

Journal of Molecular Structure(2022)

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摘要
•Novel enzyme substrate-enzyme inhibitor hybrids synthesized.•Enzyme-binding capacity of novel hybrids demonstrated.•Computer modelling data support receptor-site docking potential.
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关键词
DOXP-fosmidomycin hybrid analogues,Synthesis,STD-NMR,In silico docking
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