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J K Coward

Showing results (1-10 of 62) with videos related to

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Journal of Medicinal Chemistry|July 1, 1991
Stereospecific synthesis of (R)- and (S)-S-adenosyl-1,8-diamino-3-thiooctane, a potent inhibitor of polyamine biosynthesis. Comparison of asymmetric induction vs enantiomeric synthesisC Liu, J K Coward
Biochemistry|December 16, 1997
13C- and 15N-labeled peptide substrates as mechanistic probes of oligosaccharyltransferaseT Xu, J K Coward
Biochemistry|July 6, 1993
Oligosaccharyltransferase: synthesis and use of deuterium-labeled peptide substrates as mechanistic probesJ Lee, J K Coward
Bioorganic & Medicinal Chemistry Letters|June 20, 2001
N-Me-pAB-Glu-gamma-Glu-gamma-Tyr(3-NO(2)): an internally quenched fluorogenic gamma-glutamyl hydrolase substrateJ J Pankuch, J K Coward
Bioorganic & Medicinal Chemistry|September 1, 1996
Synthesis of complex delta-acetylenic amino acids as potential multisubstrate adduct inhibitors of methyltransferasesM R Burns, J K Coward
The Journal of Organic Chemistry|December 26, 2001
Electrophilic fluorination of pyroglutamic acid derivatives: application of substrate-dependent reactivity and diastereoselectivity to the synthesis of optically active 4-fluoroglutamic acidsD W Konas, J K Coward
Journal of Medicinal Chemistry|May 1, 1976
Analogues of S-adenosylhomocysteine as potential inhibitors of biological transmethylation. Synthesis of analogues with modifications at the 5'-thioether linkageC D Chang, J K Coward
Biochemical Pharmacology|August 17, 1993
Effect of N-(n-butyl)-1,3-diaminopropane on polyamine metabolism, cell growth and sensitivity to chloroethylating agentsA E Pegg, J K Coward
Bioorganic & Medicinal Chemistry|April 29, 1999
Dolichylpyrophosphate oligosaccharides: large-scale isolation and evaluation as oligosaccharyltransferase substratesB S Gibbs, J K Coward
Organic Letters|June 3, 2000
Synthesis of L-4,4-difluoroglutamic acid via electrophilic difluorination of a lactamD W Konas, J K Coward
Pageof 7

Showing results (1-10 of 62) with videos related to

Sort By:
Pageof 7
Journal of Medicinal Chemistry|July 1, 1991
Stereospecific synthesis of (R)- and (S)-S-adenosyl-1,8-diamino-3-thiooctane, a potent inhibitor of polyamine biosynthesis. Comparison of asymmetric induction vs enantiomeric synthesisC Liu, J K Coward
Biochemistry|December 16, 1997
13C- and 15N-labeled peptide substrates as mechanistic probes of oligosaccharyltransferaseT Xu, J K Coward
Biochemistry|July 6, 1993
Oligosaccharyltransferase: synthesis and use of deuterium-labeled peptide substrates as mechanistic probesJ Lee, J K Coward
Bioorganic & Medicinal Chemistry Letters|June 20, 2001
N-Me-pAB-Glu-gamma-Glu-gamma-Tyr(3-NO(2)): an internally quenched fluorogenic gamma-glutamyl hydrolase substrateJ J Pankuch, J K Coward
Bioorganic & Medicinal Chemistry|September 1, 1996
Synthesis of complex delta-acetylenic amino acids as potential multisubstrate adduct inhibitors of methyltransferasesM R Burns, J K Coward
The Journal of Organic Chemistry|December 26, 2001
Electrophilic fluorination of pyroglutamic acid derivatives: application of substrate-dependent reactivity and diastereoselectivity to the synthesis of optically active 4-fluoroglutamic acidsD W Konas, J K Coward
Journal of Medicinal Chemistry|May 1, 1976
Analogues of S-adenosylhomocysteine as potential inhibitors of biological transmethylation. Synthesis of analogues with modifications at the 5'-thioether linkageC D Chang, J K Coward
Biochemical Pharmacology|August 17, 1993
Effect of N-(n-butyl)-1,3-diaminopropane on polyamine metabolism, cell growth and sensitivity to chloroethylating agentsA E Pegg, J K Coward
Bioorganic & Medicinal Chemistry|April 29, 1999
Dolichylpyrophosphate oligosaccharides: large-scale isolation and evaluation as oligosaccharyltransferase substratesB S Gibbs, J K Coward
Organic Letters|June 3, 2000
Synthesis of L-4,4-difluoroglutamic acid via electrophilic difluorination of a lactamD W Konas, J K Coward
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