尿素酶
幽门螺杆菌
化学
药理学
微生物学
酶
医学
生物化学
生物
内科学
作者
Özlen Güzel-Akdemir,Atilla Akdemir
标识
DOI:10.1080/13543776.2024.2423004
摘要
Increase in selectivity, affinity and potency of HPU inhibitors can be achieved by the design of compounds that interact with distinct regions within the enzyme active site. Especially, covalent interactions seem promising as they clearly effect the dose requirement of the drug candidate.
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