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M A Ondetti

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Biochemistry|April 17, 1979
Design of potent and specific inhibitors of carboxypeptidases A and BM A Ondetti, M E Condon, J Reid, et al.
The Journal of Antibiotics|September 1, 1977
N-substituted derivatives of EM 49 structure-activity relationshipsJ Pluscec, E F Sabo, R O Neubeck, et al.
Biochemistry|October 26, 1971
Angiotensin-converting enzyme inhibitors from the venom of Bothrops jararaca. Isolation, elucidation of structure, and synthesisM A Ondetti, N J Williams, E F Sabo, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Inhibitors of angiotensin-converting enzymeD W Cushman, M A Ondetti, H S Cheung, et al.
Journal of Cardiovascular Pharmacology|January 1, 1987
Rational design and biochemical utility of specific inhibitors of angiotensin-converting enzymeD W Cushman, M A Ondetti, E M Gordon, et al.
Experientia|August 15, 1973
Inhibition of angiotensin-coverting enzyme by analogs of peptides from Bothrops jararaca venomD W Cushman, J Pluscec, N J Williams, et al.
The Journal of Antibiotics|June 1, 1978
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-azabicyclo [4.2.0] oct-2-ene-2-carboxylic acidH E Applegate, C M Cimarusti, J E Dolfini, et al.
Journal of Medicinal Chemistry|March 1, 1982
Angiotensin-converting enzyme inhibitors: importance of the amide carbonyl of mercaptoacyl amino acids for hydrogen bonding to the enzymeM E Condon, E W Petrillo, D E Ryono, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Biochemistry|April 17, 1979
Design of potent and specific inhibitors of carboxypeptidases A and BM A Ondetti, M E Condon, J Reid, et al.
The Journal of Antibiotics|September 1, 1977
N-substituted derivatives of EM 49 structure-activity relationshipsJ Pluscec, E F Sabo, R O Neubeck, et al.
Biochemistry|October 26, 1971
Angiotensin-converting enzyme inhibitors from the venom of Bothrops jararaca. Isolation, elucidation of structure, and synthesisM A Ondetti, N J Williams, E F Sabo, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Inhibitors of angiotensin-converting enzymeD W Cushman, M A Ondetti, H S Cheung, et al.
Journal of Cardiovascular Pharmacology|January 1, 1987
Rational design and biochemical utility of specific inhibitors of angiotensin-converting enzymeD W Cushman, M A Ondetti, E M Gordon, et al.
Experientia|August 15, 1973
Inhibition of angiotensin-coverting enzyme by analogs of peptides from Bothrops jararaca venomD W Cushman, J Pluscec, N J Williams, et al.
The Journal of Antibiotics|June 1, 1978
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-azabicyclo [4.2.0] oct-2-ene-2-carboxylic acidH E Applegate, C M Cimarusti, J E Dolfini, et al.
Journal of Medicinal Chemistry|March 1, 1982
Angiotensin-converting enzyme inhibitors: importance of the amide carbonyl of mercaptoacyl amino acids for hydrogen bonding to the enzymeM E Condon, E W Petrillo, D E Ryono, et al.
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