Design of potent competitive inhibitors of angiotensin-converting enzyme. Carboxyalkanoyl and mercaptoalkanoyl amino acids von Cushman, D. W, Cheung, H. S, Sabo, E. F, Ondetti, M. A

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Angiotensin Converting Enzyme Inhibitors An Overview von Ondetti, Miguel A

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O-Sulfated .beta.-lactam hydroxamic acids (monosulfactams). Novel monocyclic .beta.-lactam antibiotics of synthetic origin von Gordon, E. M, Ondetti, M. A, Pluscec, Jelka, Cimarusti, C. M, Bonner, D. P, Sykes, R. B

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Design of Specific Inhibitors of Angiotensin-Converting Enzyme: New Class of Orally Active Antihypertensive Agents von Ondetti, Miguel A., Rubin, Bernard, Cushman, David W.

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Design of protease inhibitors von Ondetti, M. A., Cushman, D. W.

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Angiotensin‐converting enzyme inhibitors: Medicinal chemistry and biological actions von Petrillo, Edward W., Ondetti, Miguel A.

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Angiotensin-Converting Enzyme Inhibitors: Accomplishments and Challenges von Petrillo, E. W., Powell, J. R., Cushman, D. W., Ondetti, M. A.

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Inhibition of the renin-angiotensin system. A new approach to the therapy of hypertension von Ondetti, Miguel A, Cushman, David W

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From peptides to peptidases: a chronicle of drug discovery von Ondetti, M A

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Inhibitors of angiotensin-converting enzyme for treatment of hypertension von Cushman, David W., Ondetti, Miguel A.

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Diastereomeric 7-ureidoacetyl cephalosporins. II. 7beta [[[(Aminocarbonyl) amino]-2-thienylacetyl] amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl) thio] methyl]-8-oxo-5-thia-1-aza... von Applegate, H E, Cimarusti, C M, Dolfini, J E, Koster, W H, Ondetti, M A, Slusarchyk, W A, Young, M G, Breuer, H, Treuner, U D

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Rational Design and Biochemical Utility of Specific Inhibitors of Angiotensin-Converting Enzyme von Cushman, D W, Ondetti, M A, Gordon, E M, Natarajan, S, Karanewsky, D S, Krapcho, J, Petrillo, E W

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Bradykinin analogs containing .beta.-homoamino acids von Ondetti, Miguel A, Engel, Stanford L

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Design of new antihypertensive drugs: Potent and specific inhibitors of angiotensin-converting enzyme von Cushman, David W., Cheung, Hong Son, Sabo, Emily F., Ondetti, Miguel A.

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Synthesis of a Peptide Lactone Related to Vernamycin Bα von Ondetti, Miguel A, Thomas, Patsy L

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Chemical modifications of the active site of Streptomyces R61 DD-carboxypeptidase von GEORGOPAPADAKOU, Nafsika H., LIU, Fung Y., RYONO, Dennis E., NEUBECK, Richard, ONDETTI, Miguel A.

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The synthesis of secretin. 3. The fragment-condensation approach von Ondetti, M A, Narayanan, V L, von Saltza, M, Sheehan, J T, Sabo, E F, Bodanszky, M

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Inhibition of angiotensin-converting enzyme by analogs of peptides fromBothrops jararaca venom von Cushman, D. W., Pluščec, J., Williams, N. J., Weaver, E. R., Sabo, E. F., Kocy, O., Cheung, H. S., Ondetti, M. A.

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Design of potent and specific inhibitors of carboxypeptidases A and B von Ondetti, Miguel A, Condon, Michael E, Reid, Joyce, Sabo, Emily F, Cheung, Hong S, Cushman, David W

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Carbacyclic isosteres of penicillanic and carbapenemic acids. Synthesis of bicyclo[3.2.0]Heptan-6-ones as potential enzyme inhibitors von Gordon, E.M., Pluščec, Jelka, Ondetti, M.A.

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