,α-β-Galactosidases

Oluwafemi Akintola1, Sandeep Bhosale1, Andrew J Bennet1

  • 1Department of Chemistry, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.

PubMed
概括

新的循环烯基碳糖抑制剂与α-β-galactosidases形成可逆的共价键. 这些以机制为基础的抑制剂,向甘酸化酶,为化学生物学研究提供了一种通用的新工具.

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