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B R Baker

Showing results (11-20 of 66) with videos related to

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Journal of Medicinal Chemistry|May 1, 1970
Irreversible enzyme inibitiors. CLXXII. Proteolytic enzymes. XVI. Covalent bonding of the sulfonyl fluoride group to serine outside the active site of alpha-chymotrypsin by exo-type active-site directed irreversible inhibitorsR Cardinaud, B R Baker
Journal of Medicinal Chemistry|February 1, 1971
Irreversible enzyme inhibitors. 180. Irreversible inhibitors of the C'la component of complement derived from m-(phenoxypropoxy)benzamidine and phenoxyacetamideB R Baker, M Cory
Journal of Medicinal Chemistry|December 22, 2011
Irreversible Enzyme Inhibitors. LXXIX.(1,2) Inhibitors of Thymidine Phosphorylase. V.(2) Mode of Pyrimidine BindingB R Baker, M Kawazu
The Journal of Organic Chemistry|March 19, 2010
Biotin; penthiane-3,4-dicarboxylic acidB R BAKER, F ABLONDI
The Journal of Organic Chemistry|March 19, 2010
Biotin; a second synthesis of 2-delta-carboxybutyl)-thiophane-3,4-dicarboxylic acidB R BAKER, M V QUERRY
The Journal of Organic Chemistry|March 19, 2010
Biotin; cis-3,4-diaminothiophaneB R BAKER, M V QUERRY
Journal of Medicinal Chemistry|May 1, 1970
Irreversible enzyme inhibitors. CLXIX. Inhibition of FUDR phosphorylase from Walker 256 rat tumor by 6-substituted uracilsB R Baker, J L Kelley
Journal of Medicinal Chemistry|May 1, 1970
Irreversible enzyme inhibitors. CLXX. Inhibition of FUDR phosphorylase from Walker 256 rat tumor by 1-substituted uracilsB R Baker, J L Kelley
Journal of Medicinal Chemistry|May 1, 1982
Irreversible enzyme inhibitors. 202. Candidate active-site-directed irreversible inhibitors of 5-fluoro-2'-deoxyuridine phosphorylase from Walker 256 rat tumor derived from 1-benzyl-5-(3-ethoxybenzyl)uracilJ L Kelley, B R Baker
Journal of Medicinal Chemistry|November 1, 1970
Irreversible enzyme inhibitors. CLXXVI. Active-site-directed irreversible inhibitors of dihydrofolate reductase derived from 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-phenyl-s-triazine by ether bridging to a terminal sulfonyl fluorideB R Baker, W T Ashton
Pageof 7

Showing results (11-20 of 66) with videos related to

Sort By:
Pageof 7
Journal of Medicinal Chemistry|May 1, 1970
Irreversible enzyme inibitiors. CLXXII. Proteolytic enzymes. XVI. Covalent bonding of the sulfonyl fluoride group to serine outside the active site of alpha-chymotrypsin by exo-type active-site directed irreversible inhibitorsR Cardinaud, B R Baker
Journal of Medicinal Chemistry|February 1, 1971
Irreversible enzyme inhibitors. 180. Irreversible inhibitors of the C'la component of complement derived from m-(phenoxypropoxy)benzamidine and phenoxyacetamideB R Baker, M Cory
Journal of Medicinal Chemistry|December 22, 2011
Irreversible Enzyme Inhibitors. LXXIX.(1,2) Inhibitors of Thymidine Phosphorylase. V.(2) Mode of Pyrimidine BindingB R Baker, M Kawazu
The Journal of Organic Chemistry|March 19, 2010
Biotin; penthiane-3,4-dicarboxylic acidB R BAKER, F ABLONDI
The Journal of Organic Chemistry|March 19, 2010
Biotin; a second synthesis of 2-delta-carboxybutyl)-thiophane-3,4-dicarboxylic acidB R BAKER, M V QUERRY
The Journal of Organic Chemistry|March 19, 2010
Biotin; cis-3,4-diaminothiophaneB R BAKER, M V QUERRY
Journal of Medicinal Chemistry|May 1, 1970
Irreversible enzyme inhibitors. CLXIX. Inhibition of FUDR phosphorylase from Walker 256 rat tumor by 6-substituted uracilsB R Baker, J L Kelley
Journal of Medicinal Chemistry|May 1, 1970
Irreversible enzyme inhibitors. CLXX. Inhibition of FUDR phosphorylase from Walker 256 rat tumor by 1-substituted uracilsB R Baker, J L Kelley
Journal of Medicinal Chemistry|May 1, 1982
Irreversible enzyme inhibitors. 202. Candidate active-site-directed irreversible inhibitors of 5-fluoro-2'-deoxyuridine phosphorylase from Walker 256 rat tumor derived from 1-benzyl-5-(3-ethoxybenzyl)uracilJ L Kelley, B R Baker
Journal of Medicinal Chemistry|November 1, 1970
Irreversible enzyme inhibitors. CLXXVI. Active-site-directed irreversible inhibitors of dihydrofolate reductase derived from 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-phenyl-s-triazine by ether bridging to a terminal sulfonyl fluorideB R Baker, W T Ashton
Pageof 7