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Results: 1-7 |
Results: 7
NOVEL CONSTRAINED CCK-B DIPEPTOID ANTAGONISTS DERIVED FROM PIPECOLIC ACID
Authors: BELLIER B DANASCIMENTO S MEUDAL H GINCEL E ROQUES BP GARBAY C
Citation: B. Bellier et al., NOVEL CONSTRAINED CCK-B DIPEPTOID ANTAGONISTS DERIVED FROM PIPECOLIC ACID, Bioorganic & medicinal chemistry letters, 8(11), 1998, pp. 1419-1424
2,4-DINITROPHENYL 4-METHOXYBENZYL DISULFIDE - A NEW EFFICIENT REAGENTFOR THE ELECTROPHILIC SULFENYLATION OF BETA-AMINO ESTER ENOLATES
Authors: BISCHOFF L DAVID C MARTIN L MEUDAL H ROQUES BP FOURNIEZALUSKI MC
Citation: L. Bischoff et al., 2,4-DINITROPHENYL 4-METHOXYBENZYL DISULFIDE - A NEW EFFICIENT REAGENTFOR THE ELECTROPHILIC SULFENYLATION OF BETA-AMINO ESTER ENOLATES, Journal of organic chemistry, 62(14), 1997, pp. 4848-4850
SYNTHESIS AND BIOLOGICAL PROPERTIES OF NEW CONSTRAINED CCK-B ANTAGONISTS - DISCRIMINATION OF 2 AFFINITY STATES OF THE CCK-B RECEPTOR ON TRANSFECTED CHO CELLS
Authors: BELLIER B MCCORTTRANCHEPAIN I DUCOS B DANASCIMENTO S MEUDAL H NOBLE F GARBAY C ROQUES BP
Citation: B. Bellier et al., SYNTHESIS AND BIOLOGICAL PROPERTIES OF NEW CONSTRAINED CCK-B ANTAGONISTS - DISCRIMINATION OF 2 AFFINITY STATES OF THE CCK-B RECEPTOR ON TRANSFECTED CHO CELLS, Journal of medicinal chemistry, 40(24), 1997, pp. 3947-3956
SYNTHESIS OF CONSTRAINED 4-(PHOSPHONOMETHYL)PHENYLALANINE DERIVATIVESAS HYDROLYTICALLY STABLE ANALOGS OF O-PHOSPHOTYROSINE
Authors: LIU WQ CARREAUX F MEUDAL H ROQUES BP GARBAYJAUREGUIBERRY C
Citation: Wq. Liu et al., SYNTHESIS OF CONSTRAINED 4-(PHOSPHONOMETHYL)PHENYLALANINE DERIVATIVESAS HYDROLYTICALLY STABLE ANALOGS OF O-PHOSPHOTYROSINE, Tetrahedron, 52(12), 1996, pp. 4411-4422
OPTIMAL RECOGNITION OF NEUTRAL ENDOPEPTIDASE AND ANGIOTENSIN-CONVERTING ENZYME ACTIVE-SITES BY MERCAPTOACYLDIPEPTIDES AS A MEANS TO DESIGN POTENT DUAL INHIBITORS
Authors: CORIC P TURCAUD S MEUDAL H ROQUES BP FOURNIEZALUSKI MC
Citation: P. Coric et al., OPTIMAL RECOGNITION OF NEUTRAL ENDOPEPTIDASE AND ANGIOTENSIN-CONVERTING ENZYME ACTIVE-SITES BY MERCAPTOACYLDIPEPTIDES AS A MEANS TO DESIGN POTENT DUAL INHIBITORS, Journal of medicinal chemistry, 39(6), 1996, pp. 1210-1219
DESIGN OF ORALLY-ACTIVE DUAL INHIBITORS OF NEUTRAL ENDOPEPTIDASE AND ANGIOTENSIN-CONVERTING ENZYME WITH LONG-DURATION OF ACTION
Authors: FOURNIEZALUSKI MC CORIC P THERY V GONZALEZ W MEUDAL H TURCAUD S MICHEL JB ROQUES BP
Citation: Mc. Fourniezaluski et al., DESIGN OF ORALLY-ACTIVE DUAL INHIBITORS OF NEUTRAL ENDOPEPTIDASE AND ANGIOTENSIN-CONVERTING ENZYME WITH LONG-DURATION OF ACTION, Journal of medicinal chemistry, 39(13), 1996, pp. 2594-2608
INVESTIGATION OF THE STRUCTURAL PARAMETERS INVOLVED IN THE DELTA-OPIOID SELECTIVITY OF SEVERAL FAMILIES OF OPIOID-PEPTIDES
Authors: GUIS C BRUETSCHY L MEUDAL H ROQUES BP GACEL GA
Citation: C. Guis et al., INVESTIGATION OF THE STRUCTURAL PARAMETERS INVOLVED IN THE DELTA-OPIOID SELECTIVITY OF SEVERAL FAMILIES OF OPIOID-PEPTIDES, International journal of peptide & protein research, 41(6), 1993, pp. 576-586
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