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
- 3847
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Graphical contents list| 2004
- 3861
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Estrogen receptor ligands. Part 7: Dihydrobenzoxathiin SERAMs with bicyclic amine side chainsBlizzard, Timothy A / DiNinno, Frank / Morgan, Jerry D II et al. | 2004
- 3865
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Estrogen receptor ligands. Part 8: Dihydrobenzoxathiin SERAMs with heteroatom-substituted side chainsBlizzard, Timothy A / DiNinno, Frank / Morgan, Jerry D II et al. | 2004
- 3869
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Synthesis of benzoylpyrimidines as antagonists of the corticotropin-releasing factor-1 receptorWebb, Thomas R / Moran, Terry / Huang, Charles Q et al. | 2004
- 3875
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Privileged scaffolds for blocking protein–protein interactions: 1,4-disubstituted naphthalene antagonists of transcription factor complex HOX–PBX/DNAJi, Tao / Lee, Madison / Pruitt, Steven C. et al. | 2004
- 3881
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Synthesis and antibacterial activity of arylpiperazinyl oxazolidinones with diversification of the N-substituentsJang, Sun-Young / Ha, Young Hwan / Ko, Seung Whan et al. | 2004
- 3885
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Synthesis and biological activity of 22-oxa CD-ring modified analogues of 1α,25-dihydroxyvitamin D3: cis-perhydrindane CE-ring analoguesDemin, Samuël / Haver, Dirk Van / Vandewalle, Maurits et al. | 2004
- 3885
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Synthesis and biological activity of 22-oxa CD-ring modified analogues of 1a,25-dihydroxyvitamin D3: cis-perhydrindane CE-ring analoguesDemin, Samue͏̈l et al. | 2004
- 3889
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Synthesis and biological activity of 22-oxa CD-ring modified analogues of 1a,25-dihydroxyvitamin D3: spiro(5.5)undecane CF-ring analoguesSchepens, Wim et al. | 2004
- 3889
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Synthesis and biological activity of 22-oxa CD-ring modified analogues of 1α,25-dihydroxyvitamin D3: spiro[5.5]undecane CF-ring analoguesSchepens, Wim / Haver, Dirk Van / Vandewalle, Maurits et al. | 2004
- 3893
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Synthesis of symmetrical bis-alkynyl or alkyl pyridine and thiophene derivatives and their antiangiogenic activitiesAhn, Chan Mug / Shin, Woon-Seob / Bum Woo, Ho et al. | 2004
- 3897
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Detection of DNA hybridization on a liposome surface using ultrasound velocimetry and turbidimetry methodsHianik, Tibor / Rybar, Peter / Andreev, Sergej Yu et al. | 2004
- 3901
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Application of multi-component reactions to antimalarial drug discovery. Part 1: Parallel synthesis and antiplasmodial activity of new 4-aminoquinoline Ugi adductsMusonda, Chitalu C / Taylor, Dale / Lehman, Julie et al. | 2004
- 3907
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4-Acylamino-6-arylfuro[2,3-d]pyrimidines: potent and selective glycogen synthase kinase-3 inhibitorsMaeda, Yutaka / Nakano, Masato / Sato, Hideyuki et al. | 2004
- 3913
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A convenient and biogenetic type synthesis of few naturally occurring chromeno dihydrochalcones and their in vitro antileishmanial activityNarender, Tadigoppula / Shweta / Gupta, Suman et al. | 2004
- 3917
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Intrinsic factor-mediated modulation of cyanocobalamin–N-sulfonyl-acridinium-9-carboxamide chemiluminescenceAdamczyk, Maciej / Johnson, Donald D / Mattingly, Phillip G et al. | 2004
- 3923
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Antituberculous activity of some aryl semicarbazone derivativesSriram, Dharmarajan / Yogeeswari, Perumal / Thirumurugan, Rathinasabapathy et al. | 2004
- 3925
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Preparation of novel aza-1,7-annulated indoles and their conversion to potent indolocarbazole kinase inhibitorsAl-awar, Rima S / Ray, James E / Hecker, Kyle A et al. | 2004
- 3929
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Synthesis and structure–activity relationships of 1,5-diazaanthraquinones as antitumour compoundsAvendaño, Carmen / Pérez, José Marı́a / Blanco, Ma̱ del Mar et al. | 2004
- 3933
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Cinnamic acid esters as potent inhibitors of fungal 17b-hydroxysteroid dehydrogenase--a model enzyme of the short-chain dehydrogenase-reductase superfamilyGobec, Stanislav et al. | 2004
- 3933
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Cinnamic acid esters as potent inhibitors of fungal 17β-hydroxysteroid dehydrogenase––a model enzyme of the short-chain dehydrogenase/reductase superfamilyGobec, Stanislav / Sova, Matej / Kristan, Katja et al. | 2004
- 3937
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Definition of the heterocyclic pharmacophore of bacterial methionyl tRNA synthetase inhibitors: potent antibacterially active non-quinolone analoguesJarvest, Richard L / Armstrong, Sula A / Berge, John M et al. | 2004
- 3943
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Design and synthesis of 3-(2-pyridyl)pyrazolo[1,5-a]pyrimidines as potent CRF1 receptor antagonistsHuang, Charles Q / Wilcoxen, Keith M / Grigoriadis, Dimitri E et al. | 2004
- 3949
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Synthesis and biological evaluation of flavonoids as vasorelaxant agentsChen, Zhiwei / Hu, Yongzhou / Wu, Haohao et al. | 2004
- 3953
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Oxamides as novel NR2B selective NMDA receptor antagonistsBarta-Szalai, Gizella / Borza, István / Bozó, Éva et al. | 2004
- 3957
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Solution phase parallel synthesis and evaluation of MAPK inhibitory activities of close structural analogues of a Ras pathway modulatorLu, Yingchun / Sakamuri, Sukumar / Chen, Quin-Zene et al. | 2004
- 3963
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Synthesis and radioiodination of selective ligands for the dopamine D3 receptor subtypeHocke, Carsten / Prante, Olaf / Löber, Stefan et al. | 2004
- 3967
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Himbacine analogs as muscarinic receptor antagonists––effects of tether and heterocyclic variationsChackalamannil, Samuel / Doller, Darı́o / McQuade, Robert et al. | 2004
- 3971
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Lysine sulfonamides as novel HIV-protease inhibitors: Nε-disubstituted ureasStranix, Brent R / Sauvé, Gilles / Bouzide, Abderrahim et al. | 2004
- 3971
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Lysine sulfonamides as novel HIV-protease inhibitors: Ne-disubstituted ureasStranix, Brent R. et al. | 2004
- 3975
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Rhodanine-3-acetic acid derivatives as inhibitors of fungal protein mannosyl transferase 1 (PMT1)Orchard, Michael G / Neuss, Judi C / Galley, Carl M.S et al. | 2004
- 3979
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Aza-boronic acids as non-b-lactam inhibitors of AmpC-b-lactamaseBuzzoni, Valentina et al. | 2004
- 3979
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Aza-boronic acids as non-β-lactam inhibitors of AmpC-β-lactamaseBuzzoni, Valentina / Blazquez, Jesus / Ferrari, Stefania et al. | 2004
- 3985
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Synthesis, characterization, and direct aqueous superoxide anion scavenging of a highly water-dispersible astaxanthin-amino acid conjugateJackson, Henry L / Cardounel, Arturo J / Zweier, Jay L et al. | 2004
- 3993
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5-[(2-Methyl-1,3-thiazol-4-yl)ethynyl]-2,3′-bipyridine: a highly potent, orally active metabotropic glutamate subtype 5 (mGlu5) receptor antagonist with anxiolytic activityRoppe, Jeffrey R / Wang, Bowei / Huang, Dehua et al. | 2004
- 3993
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5-[(2-Methyl-1,3-thiazol-4-yl)ethynyl]-2,3prime-bipyridine: a highly potent, orally active metabotropic glutamate subtype 5 (mGlu5) receptor antagonist with anxiolytic activityRoppe, J. R. / Wang, B. / Huang, D. et al. | 2004
- 3997
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Analogs of sub-nanomolar hMC1R agonist LK-184 [Ph(CH2)3CO-His-d-Phe-Arg-Trp-NH2]. An additional binding site within the human melanocortin receptor 1?Koikov, L.N / Ebetino, F.H / Solinsky, M.G et al. | 2004
- 4001
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Aptamer selection for the inhibition of cell adhesion with fibronectin as targetOgawa, Atsushi / Tomita, Naotoshi / Kikuchi, Naoko et al. | 2004
- 4005
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Quantitative structure–activity relationship analysis of a series of 2,3-diaryl benzopyran analogues as novel selective cyclooxygenase-2 inhibitorsPrasanna, S / Manivannan, E / Chaturvedi, S.C et al. | 2004
- 4013
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Synthesis and structure–activity relationships of novel IKK-β inhibitors. Part 2: Improvement of in vitro activityMurata, Toshiki / Shimada, Mitsuyuki / Kadono, Hiroshi et al. | 2004
- 4013
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Synthesis and structure-activity relationships of novel IKK-b inhibitors. Part 2: Improvement of in vitro activityMurata, Toshiki et al. | 2004
- 4019
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Synthesis and structure-activity relationships of novel IKK-b inhibitors. Part 3: Orally active anti-inflammatory agentsMurata, Toshiki et al. | 2004
- 4019
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Synthesis and structure–activity relationships of novel IKK-β inhibitors. Part 3: Orally active anti-inflammatory agentsMurata, Toshiki / Shimada, Mitsuyuki / Sakakibara, Sachiko et al. | 2004
- 4023
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Synthesis and cytotoxicity of water soluble quaternary salt derivatives of camptothecinZu, Yuan-gang / Li, Qing-yong / Fu, Yu-jie et al. | 2004
- 4027
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The synthesis and SAR of 2-arylsulfanyl-phenyl piperazinyl acetic acids as glyT-1 inhibitorsSmith, Garrick / Ruhland, Thomas / Mikkelsen, Gitte et al. | 2004
- 4031
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Defining determinant molecular properties for the blockade of the apamin-sensitive SKCa channel in guinea-pig hepatocytes: the influence of polarizability and molecular geometryGalanakis, Dimitrios / Ganellin, C.Robin et al. | 2004
- 4037
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Novel thiophenes and analogues with anthelmintic activity against Haemonchus contortusGonzález, Isabel C / Davis, Leon N / Smith, Charles K II et al. | 2004
- 4045
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Parallel synthesis and structure–activity relationships of a series of highly potent, selective, and neutral factor Xa inhibitorsBauer, Shawn M / Goldman, Erick A / Huang, Wenrong et al. | 2004
- 4051
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Synthesis of oligodeoxynucleotides containing a single diastereoisomer of α-(N2-2′-deoxyguanosinyl)-N-desmethyltamoxifenSantosh Laxmi, Y.R / Suzuki, Naomi / Kim, Sung Yeon et al. | 2004
- 4051
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Synthesis of oligodeoxynucleotides containing a single diastereoisomer of a-(N2-2'-deoxyguanosinyl)-N-desmethyltamoxifenSantosh Laxmi, Y.R. et al. | 2004
- 4051
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Synthesis of oligodeoxynucleotides containing a single diastereoisomer of a-(N2-2prime-deoxyguanosinyl)-N-desmethyltamoxifenSantosh Laxmi, Y. R. / Suzuki, N. / Kim, S. Y. et al. | 2004
- 4055
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Leishmanicidal activity of phenylene bridged C2 symmetric glycosyl ureidesTewari, Neetu / Ramesh / Mishra, R.C et al. | 2004
- 4061
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Change in liver and plasma ceramides during d-galactosamine-induced acute hepatic injury by LC–MS/MSYamaguchi, Miho / Miyashita, Yayoi / Kumagai, Yumi et al. | 2004
- 4065
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Flow cytometric screening of aldolase catalytic antibodiesShim, Hyunbo / Karlström, Amelie / Touami, Sofia M et al. | 2004
- 4069
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A novel series of 2-pyridyl-containing compounds as lysophosphatidic acid receptor antagonists: development of a nonhydrolyzable LPA3 receptor-selective antagonistHeasley, Brian H / Jarosz, Renata / Carter, Karen M et al. | 2004
- 4075
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Synthesis and antiviral activity of P1prime arylsulfonamide azacyclic urea HIV protease inhibitorsHuang, P. P. / Randolph, J. T. / Klein, L. L. et al. | 2004
- 4075
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Synthesis and antiviral activity of P1′ arylsulfonamide azacyclic urea HIV protease inhibitorsHuang, Peggy P / Randolph, John T / Klein, Larry L et al. | 2004
- 4079
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Synthesis of potent taxoids for tumor-specific delivery using monoclonal antibodiesMiller, Michael L / Roller, Elizabeth E / Wu, Xinyaun et al. | 2004
- 4083
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Synthesis and biological evaluation of the major metabolite of atomoxetine: elucidation of a partial κ-opioid agonist effectCreighton, Christopher J / Ramabadran, Kris / Ciccone, Patrick E et al. | 2004
- 4083
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Synthesis and biological evaluation of the major metabolite of atomoxetine: elucidation of a partial k-opioid agonist effectCreighton, Christopher J. et al. | 2004
- 4087
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Synthesis and cytotoxic activity of 3-O-acyl/3-hydrazine /2-bromo/20,29-dibromo betulinic acid derivativesMukherjee, Rama / Jaggi, Manu / Siddiqui, Mohammad J.A et al. | 2004
- 4093
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Synthesis of new coumarin 3-(N-aryl) sulfonamides and their anticancer activityReddy, Natala Srinivasa / Mallireddigari, Muralidhar Reddy / Cosenza, Stephen et al. | 2004
- 4099
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Structure–activity relationships of a novel series of melanin-concentrating hormone (MCH) receptor antagonistsArienzo, Rosa / Clark, David E / Cramp, Sue et al. | 2004
- 4103
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Fluorinated quinoid inhibitor: possible `pure' arylator predicted by the simple theoretical calculationWook Ham, Seung / Choe, Jong-In / Wang, Mei-Fang et al. | 2004
- 4103
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Fluorinated quinoid inhibitor: possible 5pure' arylator predicted by the simple theoretical calculationWook Ham, Seung et al. | 2004
- 4107
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Synthesis of C8-linked pyrrolo[2,1-c][1,4]benzodiazepine-acridone/acridine hybrids as potential DNA-binding agentsKamal, Ahmed / Srinivas, O / Ramulu, P et al. | 2004
- CO2
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Editorial board| 2004
- I
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Contributors to this issue| 2004
- III
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Instructions to contributors| 2004