Bioorganic and Medicinal Chemistry Letters
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
Table of contents
- 957
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Contributors to this issue| 1993
- 961
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Graphical abstracts| 1993
- 983
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Optical isomers of RP 64406: New potent antiglutamate agentsJimonet, Patrick / Beaudoin, François / Chevé, Michel et al. | 1993
- 989
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a,b-Didehydrotryptophan as a surrogate for a-methyltryptophan in CCK 'peptoids' related to Cl-988Eden, J.M. et al. | 1993
- 989
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,-Didehydrotryptophan as a surrogate for -methyltryptophan in CCK `peptoids' related to Cl-988Eden, J. M. / Horwell, D. C. / Pritchard, M. C. et al. | 1993
- 989
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α-β-didehydrotryptophan as a surrogate for α-methyltryptophan in CCK ‘peptoids’ related to CI-988.Eden, J.M. / Horwell, D.C. / Pritchard, M.C. et al. | 1993
- 993
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Synthesis, biological activity and electrostatic properties of 3-[2-(dimethylamino)ethyl]-5-[(3-amino-1,2,4-thiadiazol-5-yl)methyl]-1H-indole, a novel 5-HT1D receptor agonist.Castro, Jose L. / Matassa, Victor G. / Broughton, Howard B. et al. | 1993
- 999
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Benzopyran potassium channel activators related to cromakalim - amide replacements at position 4.Burrell, Gordon / Evans, John M. / Hicks, Frances et al. | 1993
- 1003
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Biocompatible non -ionic surfactants for biomedical utilization: double- tailed hydrocarbon and/or fluorocarbon synthetic glycolipidsPucci, B. / Guedj, C. / Pavia, A.A. et al. | 1993
- 1007
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Design of novel agents for the therapy of non-insulin dependent diabetes mellitus (NIDDM)Bell, P. / Cheon, S.H. / Fillers, S. et al. | 1993
- 1013
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Synthesis of nucleoside analogues with a 1,5-anhydrohexitol moietyVan Aerschot, A. / Verheggen, I. / Herdewijn, P. et al. | 1993
- 1019
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The synthesis of heterosubstituted benzimidazole derivatives with potent angiotensin II antagonist activityGibson, K.H. / Wood, R / Oldham, A.A. et al. | 1993
- 1019
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The synthesis of heterosubstituted benzimidazoie derivatives with potent angiotensin li antagonist activityGibson, K. H. / Wood, R. / Oldham, A. A. et al. | 1993
- 1025
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A convenient method for the synthesis of peptides acylated with palmitic acid specifically at cysteine thiolJoseph, Mercy / Nagaraj, Ramakrishnan et al. | 1992
- 1029
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The conserved acid binding domain model of inhibitors of protein phosphatases 1 and 2A: Molecular modelling aspects.Quinn, Ronald J. / Taylor, Cherie / Suganuma, Masami et al. | 1992
- 1035
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Stable isosteres of neurotensin c-terminal pentapeptides derived by modification of the amide functionChristos, Thomas E. / Arvanitis, Argyrios / Cain, Gary A. et al. | 1992
- 1041
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Kinetic Resolution of p-hydroxyphenyl acetamides by hydrolysis with Pen-G acylaseGuy, Alain / Dumant, Anna / Sziraky, Patrick et al. | 1992
- 1045
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Induction of reversible protein-linked DNA breaks in human osteogenic sarcoma cells by novel cytocidal colchicine derivatives which inhibit DNA topoisomerase II in vitro: Absence of cross-resistance in a colchicine-resistant sub-cloneBastow, Kenneth F. / Tatematsu, Hiroshi / Bori, Ibrahim D. et al. | 1993
- 1051
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A new designed tumor selective daunomycin derivativeMaligres, P.E. / Nicolaou, K.C. / Wrasidlo, W. et al. | 1992
- 1055
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N1-Stencally hindered 2H-imidazol-2 one angiotensin II receptor antagonists: the conversion of surmountable antagonists to insurmountable antagonistsReitz, D.B. et al. | 1993
- 1055
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N1-sterically hindered 2H-imidazol-2-one angiotensin II receptor antagonists: The conversion of surmountable antagonists to insurmountable antagonistsReitz, David B. / Garland, Danny J. / Norton, Monica B. et al. | 1993
- 1061
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An unusual oxetane nudeoside as a potent antiviral agentPratap, R. et al. | 1993
- 1061
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An unusual oxetane nucleoside as a potent antiviral agentPratap, Ram / Gulati, D. / Bhakuni, D.S. et al. | 1992
- 1067
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Synthesis of 2-(p-aminobenzyl) derivatives of 1,4,7-triazacyclononane-N,N′,N″-triacetic acid (NOTA) and 1,4,7,10-tetraazacyclododecane-N,N′,N″,N″′-tetraacetic acid (DOTA): macrocyclic bifunctional chelating agents useful for antibodies labelingAnsari, Mohammad H / Ahmada, Mashood / Dicke, Karel A et al. | 1993
- 1071
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Synthesis of N-(3-(p-aminophenyl)-1 carboxypropyl) derivatives of 1,4,7-trazacydononane-N,N' diacetic acid and 1,4,7,10-tetraazacyclododecane-N,N',N"-triacetic acid: macrocyclic bifunctional chelating agents useful for antibodies labellingAnsari, M.H. et al. | 1993
- 1071
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Synthesis of N-[3-(p-aminophenyl)-1-carboxypropyl] derivatives of 1,4,7-triazacyclononane-N,N′-diacetic acid and 1,4,7,10-tetraazacyclododecane-N,N′,N″-triacetic acid: macrocyclic bifunctional chelating agents useful for antibodies labellingAnsari, Mohammad H / Ahmad, Mashood / Dicke, Karel A et al. | 1993
- 1073
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Dual antagonists of platelet activating factor and histamine-II. Pyridine ring substitution of N-acetyl-4-(8-chloro-5,6 dihydro-11H-benzo(5,6)cycloheta(1,2b) pyridin-11-ylidene)piperidinesWong, J.K. et al. | 1993
- 1073
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Dual antagonists of platelet activating factor and histamine. 2. pyridine ring substitution of N-acetyl-4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidinesWong, Jesse K. / Piwinski, John J. / Green, Michael J. et al. | 1993
- 1073
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Dual antagonists of platelet activating factor and histamine - II. Pyridine ring substitution of N-acetyl-4-(8-chloro-5,6-dihydro-11 H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidinesWong, J. K. / Piwinski, J. J. / Green, M. J. et al. | 1993
- 1079
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A convenient degradation of polyoxin D to uracil polyoxin C: access to key intermediates and synthesis of antifungal a-aminoacyl derivatives of UPOCCooper, A.B. et al. | 1993
- 1079
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A convenient degradation of polyoxin D to uracil polyoxin C: access to key intermediates and synthesis of antifungal α-aminoacyl derivatives of UPOCCooper, Alan B. / Desai, Jagdish / Lovey, Raymond G. et al. | 1993
- 1085
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Cytotoxicity of ent-udoteatrial diacetate and its analoguesGe, Yuting / Nakatani, Kazuhiko / Isoe, Sachihiko et al. | 1993
- 1089
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A multifunctional plasmid for protein expression by ECPCR: over-production of the p50 subunit of NF-kappaBSodeoka, M. / Larson, C. J. / Chen, L. et al. | 1993
- 1089
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A multifunctional plasmid for protein expression by ECPCR: overproduction- of the p50 subunit of NF-kBSodeoka, M. et al. | 1993
- 1089
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A multifunctional plasmid for protein expression by ECPCR: overproduction of the p50 subunit of NF-κBSodeoka, Mikiko / Larson, Christopher J. / Chen, Lin et al. | 1993
- 1095
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Limited proteolysis and site-directed mutagenesis of the NF-kB p50 DNA-binding subunitSodeoka, M. et al. | 1993
- 1095
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Limited proteolysis and site-directed mutagenesis of the NF-κB p50 DNA-binding subunitSodeoka, Mikiko / Larson, Christopher J. / Chen, Lin et al. | 1993
- 1095
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Limited proteolysis and site-directed mutagenesis of the NF-kappaB p50 DNA-binding subunitSodeoka, M. / Larson, C. J. / Chen, L. et al. | 1993
- 1101
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Conformationally constrained analogues of diacylglycerol (DAG). 3. Interaction of α-alkyl-γ-lactones with protein kinase C (PK-C)Lee, Jeewoo / Marquez, Victor E. / Lewin, Nancy E. et al. | 1993
- 1101
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Conformationally constrained analogues of diacylglycerol (DAG) - III. Interaction of -alkyl-gamma-lactones with protein kinase C (PK-C)Lee, J. / Marquez, V. E. / Lewin, N. E. et al. | 1993
- 1101
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Conformationally constrained analogues of diacylglycerol (DAG)- III. Interaction of a-alkyl-g-lactones with protein kinase C (PK-C)Lee, J. et al. | 1993
- 1107
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Conformationally constrained analoques of diacylglycerol (DAG)-IV. Interaction of a-alkylidene-g-lactones with protein kinase C (PK-C)Lee, J. et al. | 1993
- 1107
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Conformationally constrained analogues of diacylglycerol (DAG). 4. Interaction of α-alkylidene-γ-lactones with protein kinase C (PK-C)Lee, Jeewoo / Marquez, Victor E. / Lewin, Nancy E. et al. | 1993
- 1107
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Conformationally constrained analogues of diacylglycerol (DAG) - IV. Interaction of -alkylidene-gamma-lactones with protein kinase C (PK-C)Lee, J. / Marquez, V. E. / Lewin, N. E. et al. | 1993
- 1111
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N,N-disubstituted benzopyran-4-(N′-cyano)carboxamidines, cromakalim analogs with selective activity for guinea pig trachealisKoga, Hiroshi / Sato, Haruhiko / Ishizawa, Takenori et al. | 1993
- 1115
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Benzopyran-4-carboxamide K+ channel openersKoga, Hiroshi / Sato, Haruhiko / Ishizawa, Takenori et al. | 1993
- 1119
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New potent angiotensin II receptor antagonists containing phenylthiophenes and phenylfurans in place of the biphenyl moiety.Rivero, R.A. / Kevin, N.J. / Allen, E.E. et al. | 1993
- 1125
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A new series of potent LTD4 antagonists in the styrylquinoline class.Guay, D. / Gauthier, J.Y. / Metters, K.M. et al. | 1993
- 1131
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4-Aminomethyl chromans: dependence of serotonin and dopamine binding upon aromatic ring substitutionEnnis, Michael D. / Hoffman, Robert L. / Lahti, Robert A. et al. | 1992
- 1137
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Pentamidine congeners-I. Synthesis of cis and trans-butamidine analogues as anti-Pneumocystis carinii pneumonia agentsDonkor, I.O. et al. | 1993
- 1137
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Pentamidine congeners 1: Synthesis of Cis- and Trans-butamidine analogues as anti-Pneumocystis carinii pneumonia agents.Donkor, Isaac O. / Jones, Susan K. / Tidwell, Richard R. et al. | 1993
- 1141
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Composition and antiviral activities of a sulfated polysaccharide from schizymenia dubyi (rhodophyta, gigartinales)Bourgougnon, Nathalie / Lahaye, Marc / Chermann, Jean-Claude et al. | 1992
- 1147
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Acid unit modifications of 1,2,4,5-substituted hydroxyacetophenones and the effect on in vitro and in vivo LTB4 receptor antagonismSofia, Michael J. / Floreancig, Paul / Jackson, William T. et al. | 1993
- 1153
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A new type of cytotoxic annonaceous acetogenin: Giganin from goniothalamus giganteusFang, Xin-ping / Song, Rong / Gu, Zhe-ming et al. | 1993
- 1153
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A new type of cytotoxic Annonaceous acetoqenin: giganin from Goniothalamus giganteusFang, X. et al. | 1993
- 1157
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QSAR study of benzoquinolinones as inhibitors of human type 1 5-α-reductase.Wikel, James H. / Bemis, Kerry G. / Audia, James E. et al. | 1993
- 1157
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OSAR Study of benzoquinolinones as inhibitors of human type 1 5-a-reductase reductaseWikel, J.H. et al. | 1993
- 1163
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Heterocyclic inhibitors of human leukocyte elastase: 3-hydroxypyridazo-pyrimidine, 3-hydroxypyridopyrimidine and 3-hydroxyquinazoline-2.4- 1H,3H)dione derivativesGroutas, W.C. et al. | 1993
- 1163
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Heterocyclic inhibitors of human leukocyte elastase: 3-Hydroxypyridazopyrimidine, 3-hydroxypyridopyrimidine and 3-hydroxyquinazoline-2,4-1H,3H0dione derivativesGroutas, William C. / Castrisos, James C. / Stanga, Michael A. et al. | 1992
- 1169
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Difunctional enols of N-protected amino acids as low molecular weight and novel inhibitors of HIV-1 protease.Vaillancourt, Marc / Vanasse, Benoit / Cohen, Eric et al. | 1993
- 1175
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Inhibition of 2,3-oxidosqualene cyclase by N-alkylpiperidinesWannamaker, M.Woods / Waid, Philip P. / Moore, William R. et al. | 1993
- 1179
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Preparation and Properties of a fibrinogen receptor antagonist containing the Arg-Gly-Asp sequence and nitroxide radicalsCheng, H.-Y. / Davis, L.L. / Holl, W.W. et al. | 1993
- 1185
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Directed evolution of novel biosynthetic pathways: growth of an Escherichia coli proline auxotroph on cap delta^1-pyrroline-2-carboxylic acidSutherland, J. D. / Wilson, E. J. / Wright, M. C. et al. | 1993
- 1185
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Directed evolution of novel biosynthetic pathways: qrowth of an Escherichia coli proline auxotroph on D1-pyrroline-2-carboxylic acidSutherland, J.D. et al. | 1993
- 1185
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Directed evolution of novel biosynthetic pathways: growth of an escherichia coli proline auxotroph on Δ1-pyrroline-2-carboxylic acid.Sutherland, John D. / Wilson, Esther J. / Wright, Martin C. et al. | 1993
- 1189
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Reduction of Δ1-pyrroline-2-carboxylic acid to proline by an escherichia coli proline auxotroph.Lewis, Mark L. / Martin, Steve L. / Rowe, Christine J. et al. | 1993
- 1189
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Reduction of D1-pyrroline-2-carboxylic acid to proline by an Escherichia coliproline auxotrophLewis, M.L. et al. | 1993
- 1189
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Reduction of cap delta^1-pyrroline-2-carboxylic acid to proline by an Escherichia coli proline auxotrophLewis, M. L. / Martin, S. L. / Rowe, C. J. et al. | 1993
- 1193
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The effect of pH on the solution structure of Δ1-pyrroline-2-carboxylic acid as revealed by NMR and electrospray mass spectroscopy.Lewis, Mark L. / Rowe, Christine J. / Sewald, Norbert et al. | 1993
- 1193
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The effect of pH on the solution structure of cap delta^1-pyrroline-2-carboxylic acid as revealed by NMR and electrospray mass spectroscopyLewis, M. L. / Rowe, C. J. / Sewald, N. et al. | 1993
- 1193
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The effect of pH on the solution structure of D1-pyrroline-2-carboxylic acid as revealed by NMR and electrospray mass spectroscopyLewis, M.L. et al. | 1993
- 1197
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Reduction of cap delta^1-pyrroline-2-carboxylic acid to proline in Escherichia coli lack of involvement of glutamate dehydrogenase and cap delta^1-pyrroline-5-carboxylate reductaseLewis, M. L. / Martin, S. L. / Rowe, C. J. et al. | 1993
- 1197
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Reduction of D1-pyrroline-2-carboxylic acid to proline in Escherichia coli: lack of involvement of glutamate dehydrogenase and D1-pyrroline-5-carboxylate reductaseLewis, M.L. et al. | 1993
- 1197
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Reduction of Δ1-pyrroline-2-carboxylic acid to proline in escherichia coli: lack of involvement of glutamate dehydrogenase and Δ1-pyrroline-5-carboxylate reductase.Lewis, Mark L. / Martin, Steve L. / Rowe, Christine J. et al. | 1993
- 1203
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Phosphate derivatives of d4T as inhibitors of HIVMcGuigan, Christopher / Sheeka, Hendrika M. / Mahmood, Naheed et al. | 1993
- 1207
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Kinase bypass: A new strategy for anti-HIV drug designMcGuigan, Christopher / Kinchington, Derek / Nicholls, Simon R. et al. | 1993
- 1211
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Differences in antiviral activities for isomers of a fluorinated cyclobutane nucleoside analogVite, G.D. / Tino, J.A. / Zahler, R. et al. | 1993
- 1215
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Optically active fluorinated cyclobutane nucleoside analogs with potent anti-herpes activityAhmad, Saleem / Bisacchi, Gregory S. / Field, A.Kirk et al. | 1993
- 1219
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β-Glucan biosynthesis inhibitors isolated from fungi as hyphal malformation inducerFukushima, Yoshito / Sakagami, Youji / Marumo, Shingo et al. | 1993
- 1219
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b-Glucan biosynthesis inhibitors isolated from fungi as hyphal malformation inducerFukushima, Y. et al. | 1993
- 1223
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Anti-HIV activities and physicochemical properties of phosphorothioate analogues complementary to HIV sequencesKim, Sang-Gug / Kanbara, Kenji / Nakashima, Hideki et al. | 1993
- 1229
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Synthetic pterocarpans with anti-HIV activityEngler, Thomas A. / Lynch, Kenneth O. Jr. / Reddy, Jayachandra P. et al. | 1993
- 1233
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Determination of the active conformation of 6-amino-α-[(4-diphenylmethyl-1-piperazinyl)methyl-9H-purine]-9-ethanol: a positive inotropic agentMiltz, Wolfgang / Zierhurt, Wolfgang / Buccheri, Elena et al. | 1993
- 1233
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Determination of the active conformation of 6-amino-a-1(4-diphenylmethyl-1-piperazinyl) methyl-9H-purine)-9-ethanol: a positive inotropic agentMiltz, W. et al. | 1993
- 1241
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Enhancement of binding of quaternary ammonium derivatives of chlorpromazine to dopamine D-2 receptors by the addition of a H-bonding groupMarkovich, K.M. et al. | 1993
- 1241
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Enhancement of binding of quaternary ammonium derivatives of chlorpromaxine to dopamine D-2 receptors by the addition of a H-bonding groupMarkovich, Kimberly M. / Farooqui, Tahira / Wallace, Lane J. et al. | 1993
- 1245
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Cu(II)-catalysis in the reduction of , -dibenzoylhydroxylamine by a tertiary amineWathen, Steven P. / Czarnik, Anthony W. et al. | 1993
- 1247
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Simplified analogs of himbacine displaying potent binding affinity for muscannic receptorsMalaska, M.J. et al. | 1993
- 1247
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Simplified analogs of himbacine displaying potent binding affinity for muscarinic receptorsMalaska, Michael J. / Fauq, Abdul H. / Kozikowski, Alan P. et al. | 1993
- 1253
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Endothelin receptor ligands Multiple D-amino acid replacement net approachSpellmeyer, D.C. et al. | 1993
- 1253
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Endothelin eceptor Ligands. Multiple D-Amino acid replacement net approachSpellmeyer, David C. / Brown, Suzy / Stauber, Gregory B. et al. | 1993
- 1257
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Syntheis of TRP-VAL non-cleavable dipeptide transition state isosteresKornberg, B.E. / Doherty, A.M. et al. | 1992
- 1257
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Synthesis of Trp-Val non-cleavable dipeptide transition state isosteresKornberg, B.E. et al. | 1993
- 1263
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Synthesis of pyrrolidine oxazoles as thromboxane A2/endoperoxide receptor antagonistsHall, Steven E. / Han, Wen-Ching / Harris, Don H. et al. | 1993
- 1267
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Syntheses of Cyclopentane, Cyclohexene and Olefin Oxazoles as Thromboxane A2/Endoperoxide Receptor AntagonistsDas, Jagabandhu / Hall, Steven E. / Reid, Joyce A. et al. | 1993
- 1271
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Thromboxane A2-endoperoxide receptor antagonists 1,3-dioxane and 1,3-dioxolane analogsDas, J. et al. | 1993
- 1271
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Thoromboxane A2/endoperoxide receptor antagonists: 1,3-Dioxane and 1,3-dioxolane analogsDas, Jagabandhu / Reid, Joyce A. / Harris, Don N. et al. | 1993
- 1277
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Design and synthesis of hypertrehalosemic hormone mimeticsSato, M. et al. | 1993
- 1277
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Design and synthesis of hypertrehalosemic hormoe mimeticsSato, Michito / Kahn, Michael / Lin, ZhaoLan et al. | 1992
- 1283
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Double-headed molecules based on linear or angular psoralen and a-methylene-g-butyrolactone a search for non-phototoxic potential anti-proliferative compoundsBussey, C. et al. | 1993
- 1283
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Double-headed molecules based on linear or angular psoralen and α-methylene-ψ-butyrolactone: a search for non-phototoxic potential antiproliferative compoundsBussey, Cécile / Lepoittevin, Jean-Pierre / Benezra, Claude et al. | 1993
- 1283
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Double-headed molecules based on linear or angular psoralen and -methylene-gamma-butyrolactone: a search for non-phototoxic potential anti-proliferative compoundsBussey, C. / Lepoittevin, J.-P. / Benezra, C. et al. | 1993
- 1287
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The synthesis of novel Ba-aza-Ba-homoerythromycin derivatives via the Beckmann rearrangement of (9Z)-erythromycin A oximeWilkening, R. R. / Ratcliffe, R. W. / Doss, G. A. et al. | 1993
- 1287
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The synthesis of novel 8a-aza-8a-homoerythromycin derivatives via the beckmann rearrangement of (9z)-erythromycin a oximeWilkening, Robert R. / Ratcliffe, Ronald W. / Doss, George A. et al. | 1993
- 1293
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Quinazolinones 1: design and synthesis of potent quinazolinone- containing AT1-selective angiotensin-II receptor antagonistsAllen, Eric E. / de Laszlo, Stephen E. / Huang, Song X. et al. | 1992
- 1293
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Quinazolinones-I. Design and synthesis of potent quinazolinone-containing AT~1-selective angiotensin-II receptor antagonistsAllen, E. E. / De Laszlo, S. E. / Huang, S. X. et al. | 1993
- 1293
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Quinazolinones-I. Design and synthesis of potent quinazolinone-containing containing AT1-selective angiotensin-II receptor antagonistsAllen, E.E. et al. | 1993
- 1299
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Quinazolinones-II. QSAR and in vivo characterization of AT1 selective All antagonistsLaszio, S.E.de et al. | 1993
- 1299
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Quinazolinones 2: QSAR and in vivo characterization of AT1 selective AII antagonistsde Laszlo, Stephen E. / Allen, Eric E. / Quagliato, Carol S. et al. | 1992
- 1305
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Antibacterial activity of long-chain alcohols: the role of hydrophobic alkyl groupsKubo, Isao / Muroi, Hisae / Masaki, Himejima et al. | 1993
- 1309
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Covalent hydration: a side reaction for dihydropyridine-derived chemical delivery systems. an example with GABAergic compounds.Linget, J.M. / Schlewer, G. / Wermuth, C.G. et al. | 1993
- 1313
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A proposal for a three-dimensional representation of the S1 subsite of α-chymotrypsinKim, Dong H. et al. | 1993
- 1313
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A proposal for a three-dimensional representation of the S1 subsite of a-chymotrypsinKim, D.H. et al. | 1993
- 1319
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Trisnorsqualene methyl hydroxylamine: a potent dual inhibitor of mammalian squalene epoxidase and oxidosqualene cyclaseAnstead, Gregory M. / Lin, Hung-Kuei / Prestwich, Glenn D. et al. | 1993
- 1323
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Synthesis of D-3-deoxy-3-phosphonomethyl-myo-inositol and its dimethyl ester-compounds of use in studying the Ptdlns-3'-kinase signalling pathwayKozikowski, A.P. et al. | 1993
- 1323
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Synthesis of D-3-deoxy-3-phosphonomethyl-myo-inositol and its dimethyl ester - compounds of use in studying the ptdins-3′-kinase signalling pathwayKozikowski, Alan P. / Powis, Garth / Gallegos, Alfred et al. | 1993
- 1327
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SAR of cocaine: further exploration of structural variations at the C-2 center provides compounds of subnanomolar binding potencyKozikowski, Alan P. / Roberti, Marinella / Johnson, Kenneth M. et al. | 1993
- 1333
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Synthesis of Galb1-->3(Fuca1-->4)GlcNAcb-OR as potential acceptors for a new member of the a-1,2-L-fucosyltransferase familyJaln, R.K. et al. | 1993
- 1333
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Synthesis of Galβ1→3 (Fucα1→4) GlcNAcβ-OR as potential acceptors for a new member of the α-1,2-L-fucosyltransferase familyJain, Rakesh K. / Pawar, Sushama M. / Chandrasekaran, E.V. et al. | 1992
- 1339
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Chemical synthesis of 15-ketosterolsKim, Hong-Seok / Oh, Sang Ho et al. | 1993
- 1343
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The total synthesis of sarmentosin, a potent GPT lowering agentChu, Guohua / Zhou, Qiting / Bai, Donglu et al. | 1993
- 1345
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A reinvestigation of the taxol content of himalayan taxus wallichiana zucc. and a revision of the structure of brevifoliol.Georg, Gunda I. / Gollapudi, Sitaraghav R. / Grunewald, Gary L. et al. | 1993
- 1345
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A reinvestigation of the taxol content of Himalayan Taxus wallichiana Zucc. and a revision of the stnucture of brevifoliolGeorg, G.I. et al. | 1993
- 1349
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Semisynthesis and biological evaluation of brevifoliol 13-[N-benzoyl-(-2′R,3′S)-3′-phenylisoserinate]Georg, Gunda I. / Cheruvallath, Zacharia S. / Velde, David Vander et al. | 1993
- 1351
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Protein damage caused by a synthetic enediyne coreZein, Nada / Solomon, Wyle / Casazza, Anna Maria et al. | 1993
- 1357
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Synthesis and antitumor evaluation of water soluble taxol phosphatesVyas, Dolatrai M. / Wong, Henry / Crosswell, Alfred R. et al. | 1993
- 1361
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Quinuclidine-based NK-1 antagonists I: 3-benzyloxy-1-azabicyclo[2.2.2]octanesSeward, Eileen M. / Swain, Christopher J. / Merchant, Kevin J. et al. | 1993
- 1361
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Quinuclidine-based NK-1 antagonists-1. 3-Benzyloxy-1-azabicyclo[2,2,2]-octanesSeward, E. M. / Swain, C. J. / Merchant, K. J. et al. | 1993
- 1361
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Quinuclidine-based NK-1 antagonists-I 3-Benzyloxy-1-azabicydol2.2 2)-octanesSeward, E.M. et al. | 1993
- 1367
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Synthesis of iron-binding oligonucleotides and their reactions wibh single-stranded DNAKady, I.O. et al. | 1993
- 1367
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Synthesis of iron-binding oligonucleotides and their reactions with single-stranded DNAKady, Ismail O. / Groves, John T. et al. | 1992
- 1371
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Solid phase synthesis of oligonucleotides carrying puromycin at 3′-terminalNyilas, Agnes / Agrawal, Sudhir / Zamecnik, Paul et al. | 1993
- 1375
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N-(quinuclidin-3-YL)-1,8,-naphthalimides with 5-HT3 receptor antagonist and 5-HT4 receptor agonist propertiesClark, R.D. / Weinhardt, K.K. / Berger, J. et al. | 1993
- 1379
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Investigation of side-chain sar, formulation and injection site toleration of pyrazolo[3,4-f]quinoline derivatives: a potent series of in vivo active immunostimulantsMoyer, Mikel P. / Weber, Frederick H. / Canning, Peter C. et al. | 1993
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Investigation of side-chain SAR, formulation and injection site toleration of pyrazolo[3,4-f]Aquinoline derivatives: a potent series of in vivo active immunostimulantsMoyer, M. P. / Weber, F. H. / Canning, P. C. et al. | 1993
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Thiophene systems-XV Synthesis and antihypertensive activity of 7-(substituted benzamido)-6-hydroxythieno(3,2-b)pyrans as new potassium channel activatorsSanfilippo, P.J. et al. | 1993
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Thiopene systems. 15. Synthesis and antihypertensive activity of 7- (subsituted benzamido)-6-hydroxythieno[3,2,-b]pyrans as nwe potassium channel activitorsSanfilippo, Pauline J. / McNally, James J. / Press, Jeffery B. et al. | 1993
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Additions and Corrections| 1993
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Preparation and IN VITRO biological evaluation of the enantiomers of the dihydropyrodine BMY 20014, a combination calcium and a1- adrenoreceptor antagonistL. Cavanagh, Robert / D. Goggins, Gregory / George Sarmiento, J. et al. | 1993
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Instructions to Contributors| 1993
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Announcements| 1993