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	Novel 2-arylthiopropanoyl-CoA inhibitors of α-methylacyl-CoA racemase 1A (AMACR; P504S) as potential anti-prostate cancer agents
	Yevglevskis M.; Nathubhai A.; Wadda K.; Lee G.L.; Al-Rawi S.; Jiao T.; Mitchell P.J.; James T.D.; 等 更多
刊名	Bioorganic Chemistry
	2019
卷号	92
关键词	Branched-chain fatty acid metabolism Castrate-resistant prostate cancer (CRPC) Drug lipophilicity Enzyme inhibitors Ibuprofen Mixed competitive inhibition Rational drug design Structure-activity relationships α-Methylacyl-CoA racemase (AMACR, P504S)
DOI	10.1016/j.bioorg.2019.103263
URL标识	查看原文
公开日期	[db:dc_date_available]
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4552898
专题	山东大学
作者单位	1.Drug & Target Discovery, Department of Pharmacy & Pharmacology, University of Bath, Claverton Down, Bath, BA2 7AY, United Kingdom 2.[ N
推荐引用方式 GB/T 7714	Yevglevskis M.,Nathubhai A.,Wadda K.,et al. Novel 2-arylthiopropanoyl-CoA inhibitors of α-methylacyl-CoA racemase 1A (AMACR; P504S) as potential anti-prostate cancer agents[J]. Bioorganic Chemistry,2019,92.
APA	Yevglevskis M..,Nathubhai A..,Wadda K..,Lee G.L..,Al-Rawi S..,...&等 更多.(2019).Novel 2-arylthiopropanoyl-CoA inhibitors of α-methylacyl-CoA racemase 1A (AMACR; P504S) as potential anti-prostate cancer agents.Bioorganic Chemistry,92.
MLA	Yevglevskis M.,et al."Novel 2-arylthiopropanoyl-CoA inhibitors of α-methylacyl-CoA racemase 1A (AMACR; P504S) as potential anti-prostate cancer agents".Bioorganic Chemistry 92(2019).

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