期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 44, 期 21, 页码 3351-3354出版社
AMER CHEMICAL SOC
DOI: 10.1021/jm0155502
关键词
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SAR exploration at P1' using an anti-succinate-based macrocyclic hydroxamic acid as a template led to the identification of several bulky biphenylmethyl P1' derivatives which confer potent porcine TACE and anti-TNF-alpha cellular activities with high selectivity versus most of the MMPs screened. Our studies demonstrate for the first time that TACE has a larger S1' pocket in comparison to MMPs and that potent and selective TACE inhibitors can be achieved by incorporation of sterically bulky P1' residues.
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