The Organic Chemistry of Drug Design and Drug Action 2014
DOI: 10.1016/b978-0-12-382030-3.00005-2
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Enzyme Inhibition and Inactivation

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Cited by 5 publications
(5 citation statements)
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References 278 publications
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“…Accuracy evaluation in accordance with the ICH guidelines [5] was performed through a bias % calculus as b(%) =…”
Section: Precision Evaluationmentioning
confidence: 99%
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“…Accuracy evaluation in accordance with the ICH guidelines [5] was performed through a bias % calculus as b(%) =…”
Section: Precision Evaluationmentioning
confidence: 99%
“…The complete pathway of OA biosynthesis is reported in Figure 1. The step (5), represented in Figure 1, is directly involved in the metabolism of 5-FU because this anticancer drug is a competitive substrate of OPRTase [4]. In particular, the transferase activity of OPRTase multicomplex enzyme is inhibited by 5-FU at 59% level of control [5].…”
Section: Introductionmentioning
confidence: 99%
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“…Development of affinity labeling agents 98 led to the discovery of 1,2,3-triazole ureas (1,2,3-TUs) as potent and selective irreversible inhibitors that inactivate SHs through carbamoylation of the catalytic serine 20 , 88 , 95 , 99 104 ( Fig. 1 ).…”
Section: Development Of Sutex Chemistrymentioning
confidence: 99%
“…It is therefore not surprising that thousands of different SA drugs, analogs and derivatives have been prepared so far. 5 However, the natural consequence of the use of these substances is their presence in the environment, where they cause serious concern, especially in soil and water. 6 In addition to directly affecting biota, including animals, they can have a major impact on microbial communities and can also lead to the development of antimicrobial resistance, with a significant impact on human health.…”
Section: ■ Introductionmentioning
confidence: 99%