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J L Dallas

Showing results (11-20 of 17) with videos related to

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Science (New York, N.Y.)|August 2, 1985
trans-4-Hydroxy-2-hexenal: a reactive metabolite from the macrocyclic pyrrolizidine alkaloid senecionineH J Segall, D W Wilson, J L Dallas, et al.
Archives of Biochemistry and Biophysics|October 1, 1983
Mg-2,4-divinyl pheoporphyrin a5: the product of a reaction catalyzed in vitro by developing chloroplastsB M Chereskin, P A Castelfranco, J L Dallas, et al.
Biochimica Et Biophysica Acta|January 4, 1982
High-field 1H NMR studies of synthetic analogs of somatostatin. Structural features involving aromatic residues in an active eight-membered ring analogJ D Cutnell, G N La Mar, J L Dallas, et al.
The Journal of Biological Chemistry|September 15, 1988
Exclusive A-ring linkage for singly attached phycocyanobilins and phycoerythrobilins in phycobiliproteins. Absence of singly D-ring-linked bilinsJ C Lagarias, A V Klotz, J L Dallas, et al.
Journal of Medicinal Chemistry|October 3, 1999
Conformations of trypsin-bound amidine inhibitors of blood coagulant factor Xa by double REDOR NMR and MD simulationsL M McDowell, M A McCarrick, D R Studelska, et al.
Bioorganic & Medicinal Chemistry Letters|June 15, 2000
Design, synthesis, and in vitro biological activity of benzimidazole based factor Xa inhibitorsZ Zhao, D O Arnaiz, B Griedel, et al.
Journal of Medicinal Chemistry|January 20, 2000
Synthesis, characterization, and structure-activity relationships of amidine-substituted (bis)benzylidene-cycloketone olefin isomers as potent and selective factor Xa inhibitorsW J Guilford, K J Shaw, J L Dallas, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Science (New York, N.Y.)|August 2, 1985
trans-4-Hydroxy-2-hexenal: a reactive metabolite from the macrocyclic pyrrolizidine alkaloid senecionineH J Segall, D W Wilson, J L Dallas, et al.
Archives of Biochemistry and Biophysics|October 1, 1983
Mg-2,4-divinyl pheoporphyrin a5: the product of a reaction catalyzed in vitro by developing chloroplastsB M Chereskin, P A Castelfranco, J L Dallas, et al.
Biochimica Et Biophysica Acta|January 4, 1982
High-field 1H NMR studies of synthetic analogs of somatostatin. Structural features involving aromatic residues in an active eight-membered ring analogJ D Cutnell, G N La Mar, J L Dallas, et al.
The Journal of Biological Chemistry|September 15, 1988
Exclusive A-ring linkage for singly attached phycocyanobilins and phycoerythrobilins in phycobiliproteins. Absence of singly D-ring-linked bilinsJ C Lagarias, A V Klotz, J L Dallas, et al.
Journal of Medicinal Chemistry|October 3, 1999
Conformations of trypsin-bound amidine inhibitors of blood coagulant factor Xa by double REDOR NMR and MD simulationsL M McDowell, M A McCarrick, D R Studelska, et al.
Bioorganic & Medicinal Chemistry Letters|June 15, 2000
Design, synthesis, and in vitro biological activity of benzimidazole based factor Xa inhibitorsZ Zhao, D O Arnaiz, B Griedel, et al.
Journal of Medicinal Chemistry|January 20, 2000
Synthesis, characterization, and structure-activity relationships of amidine-substituted (bis)benzylidene-cycloketone olefin isomers as potent and selective factor Xa inhibitorsW J Guilford, K J Shaw, J L Dallas, et al.
Pageof 2