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CP 80794

Known as: CP 80,794, CP-80,794, CP-80794 
National Institutes of Health

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Broader (1)

terlakiren

Papers overview

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2002
2002
Five atomic resolution structures of endothiapepsin inhibitor complexes: implications for the aspartic proteinase mechanism.
1997
1997
Quantitation of 4-cyclohexyl-2-hydroxy-3-(3-methylsulfanyl-2- [2-[(morpholine-4-carbonyl)amino]-3-phenylpropionylamino]propi onylamino ) butyric acid isopropyl ester (CP-80,794), a renin inhibitor…
1995
1995
The three-dimensional X-ray crystal structure of the aspartic proteinase native to Trichoderma reesei complexed with a renin inhibitor CP-80794.
Aspartic proteinases comprise a family of proteolytic enzymes found in a diverse range of species, from vertebrates, to lower… 
1992
1992
Synergistic Effect on Reduction in Blood Pressure with Coadministration of the Renin Inhibitor, CP‐80,794, and the Angiotensin Converting Enzyme Inhibitor, Captopril
Summary: The effects of coadministration of a renin inhibitor, CP-80,794, and an angiotensin converting enzyme inhibitor… 
Highly Cited
1991
Highly Cited
1991
Quantitative analysis by high-performance liquid chromatography atmospheric pressure chemical ionization mass spectrometry: The determination of the renin inhibitor CP-80,794 in human serum
1991
1991
Renin inhibitors containing esters at the P2-position. Oral activity in a derivative of methyl aminomalonate.
A series of renin inhibitors containing ester side chains at the P2 subsite are potent inhibitors of primate renin. Derivatives… 
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