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A A Patchett

Showing results (31-40 of 66) with videos related to

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The Journal of Biological Chemistry|November 15, 1991
Mechanism-based inactivation of alanine racemase by 3-halovinylglycinesN A Thornberry, H G Bull, D Taub, et al.
Biochemical and Biophysical Research Communications|November 30, 1983
Benzolactams. A new class of converting enzyme inhibitorsW H Parsons, J L Davidson, D Taub, et al.
Bioorganic & Medicinal Chemistry Letters|May 26, 1999
Synthesis and biological activities of spiroheterocyclic growth hormone secretagoguesM H Chen, P P Pollard, A A Patchett, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Tripeptide growth hormone secretagoguesL Yang, G Morriello, Y Pan, et al.
Journal of Medicinal Chemistry|September 1, 1991
Design and synthesis of P2-P1'-linked macrocyclic human renin inhibitorsA E Weber, T A Halgren, J J Doyle, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1992
In vitro pharmacology of L-158,809, a new highly potent and selective angiotensin II receptor antagonistR S Chang, P K Siegl, B V Clineschmidt, et al.
Biochemistry|June 27, 1989
Design of a selective insulin receptor tyrosine kinase inhibitor and its effect on glucose uptake and metabolism in intact cellsR Saperstein, P P Vicario, H V Strout, et al.
Journal of Medicinal Chemistry|September 1, 1988
Phosphinic acid inhibitors of D-alanyl-D-alanine ligaseW H Parsons, A A Patchett, H G Bull, et al.
Experientia|January 15, 1991
1-(substituted)benzyl-5-aminoimidazole-4-carboxamides are potent orally active inhibitors of Trypanosoma cruzi in miceJ C Chabala, V B Waits, T Ikeler, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 1995
Design and biological activities of L-163,191 (MK-0677): a potent, orally active growth hormone secretagogueA A Patchett, R P Nargund, J R Tata, et al.
Pageof 7

Showing results (31-40 of 66) with videos related to

Sort By:
Pageof 7
The Journal of Biological Chemistry|November 15, 1991
Mechanism-based inactivation of alanine racemase by 3-halovinylglycinesN A Thornberry, H G Bull, D Taub, et al.
Biochemical and Biophysical Research Communications|November 30, 1983
Benzolactams. A new class of converting enzyme inhibitorsW H Parsons, J L Davidson, D Taub, et al.
Bioorganic & Medicinal Chemistry Letters|May 26, 1999
Synthesis and biological activities of spiroheterocyclic growth hormone secretagoguesM H Chen, P P Pollard, A A Patchett, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Tripeptide growth hormone secretagoguesL Yang, G Morriello, Y Pan, et al.
Journal of Medicinal Chemistry|September 1, 1991
Design and synthesis of P2-P1'-linked macrocyclic human renin inhibitorsA E Weber, T A Halgren, J J Doyle, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1992
In vitro pharmacology of L-158,809, a new highly potent and selective angiotensin II receptor antagonistR S Chang, P K Siegl, B V Clineschmidt, et al.
Biochemistry|June 27, 1989
Design of a selective insulin receptor tyrosine kinase inhibitor and its effect on glucose uptake and metabolism in intact cellsR Saperstein, P P Vicario, H V Strout, et al.
Journal of Medicinal Chemistry|September 1, 1988
Phosphinic acid inhibitors of D-alanyl-D-alanine ligaseW H Parsons, A A Patchett, H G Bull, et al.
Experientia|January 15, 1991
1-(substituted)benzyl-5-aminoimidazole-4-carboxamides are potent orally active inhibitors of Trypanosoma cruzi in miceJ C Chabala, V B Waits, T Ikeler, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 1995
Design and biological activities of L-163,191 (MK-0677): a potent, orally active growth hormone secretagogueA A Patchett, R P Nargund, J R Tata, et al.
Pageof 7