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Each member of these classes of drugs is designed to reduce AT 1 receptor activation and control hypertension
10.1016/j.ydbio.2010.01.009 144
As expected, the hydrocarbon-staple moiety did not interact with FAT but pointed outward from the complex interface
Agusti A, Hernndez-Rabaza V, Balzano T, TaoroGonzalez L, IbaezGrau A, CabreraPastor A, et al
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