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Publisher: Elsevier

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Volume 10, Number 9, 1 May 2000

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The synthesis and evaluation of 2-substituted-7-(alkylidene)cephalosporin sulfones as -lactamase inhibitors
pp. 847-851(5)
Authors: Buynak, J.D.; Doppalapudi, V.R.; Rao, A.S.; Nidamarthy, S.D.; Adam, G.

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Synthesis of NF-B activation inhibitors derived from epoxyquinomicin C
pp. 865-869(5)
Authors: Matsumoto, N.; Ariga, A.; To-e, S.; Nakamura, H.; Agata, N.; Hirano, S.; Inoue, J.; Umezawa, K.

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quinonic derivatives active against a virulent strain of toxoplasma gondii. synthesis of 2-methylfuro[2,3-g]- and [3,2-g]isoquinolinetriones
pp. 871-873(3)
Authors: Nebois, P.; Sarciron, M.; Bibal, B.; Bouammali, B.; Cherkaoui, O.; Pautet, F.; Petavy, A.; Walchshofer, N.; Fillion, H.

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Novel phenylpiperazine derivatives as dual cytokine regulators with TNF-α suppressing and IL-10 augmenting activity
pp. 875-879(5)
Authors: Hanano, T.; Adachi, K.; Aoki, Y.; Morimoto, H.; Naka, Y.; Hisadome, M.; Fukuda, T.; Sumichika, H.

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Novel DMARDs on the basis of a new concept of dual cytokine regulation, TNF-α suppression and IL-10 augmentation
pp. 881-884(4)
Authors: Hanano, T.; Adachi, K.; Aoki, Y.; Morimoto, H.; Naka, Y.; Hisadome, M.; Fukuda, T.; Sumichika, H.

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Thiol-dependent DNA cleavage by 3H-1,2-benzodithiol-3-one 1,1-dioxide
pp. 885-889(5)
Authors: Breydo, L.; Gates, K.S.

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Synthesis and evaluation of vitamin D-based cationic lipids for gene delivery in vitro
pp. 891-894(4)
Authors: Ren, T.; Zhang, G.; Liu, F.; Liu, D.

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Structural analogues of some highly active non-competitive AMPA antagonists
pp. 899-902(4)
Authors: Hamori, T.; Solyom, S.; Berzsenyi, P.; Andrasi, F.; Tarnawa, I.

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5-Thienyltryptamine derivatives as serotonin 5-HT1B/1D receptor agonists: potential treatments for migraine
pp. 903-905(3)
Authors: Meng?, C.Q.; Rakhit, S.; Lee, D.K.H.; Kamboj, R.; McCallum, K.L.; Mazzocco, L.; Dyne, K.; Slassi, A.

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Incorporation of 4-thiothymidine into DNA by the klenow fragment and HIV-1 reverse transcriptase
pp. 907-910(4)
Authors: Rao, T.V.S.; Haber, M.T.; Sayer, J.M.; Jerina, D.M.

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Non-electrostatic complexes with DNA: towards novel synthetic gene delivery systems
pp. 911-914(4)
Authors: Soto, J.; Bessodes, M.; Pitard, B.; Mailhe, P.; Scherman, D.; Byk, G.

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Pyrrolo[3,2,1-ij]quinoline derivatives, a 5-HT2c receptor agonist with selectivity over the 5-HT2a receptor: potential therapeutic applications for epilepsy and obesity
pp. 919-921(3)
Authors: Isaac, M.; Slassi, A.; O'Brien, A.; Edwards, L.; MacLean, N.; Bueschkens, D.; Lee?, D.K.H.; McCallum, K.; Lannoy?, I.D.; demchyshyn, L.; Kamboj, R.

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New quinolinic derivatives as centrally active antioxidants
pp. 935-939(5)
Authors: Dorey, G.; Lockhart, B.; Lestage, P.; Casara, P.

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Inhibition of neuraminidase with neuraminic acid C-glycosides
pp. 941-944(4)
Authors: Wang, Q.; Wolff, M.; Polat, T.; Du, Y.; Linhardt, R.J.

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Substituted 5,7-diphenyl-pyrrolo[2,3d]pyrimidines: potent inhibitors of the tyrosine kinase c-Src
pp. 945-949(5)
Authors: Missbach, M.; Altmann, E.; Widler, L.; Susa, M.; Buchdunger, E.; Mett, H.; Meyer, T.; Green, J.

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A simple, solid-phase binding assay for the nuclear import receptor karyopherin α. Part 1: direct binding
pp. 951-954(4)
Authors: Connolly, M.D.; Park, S.B.; Reedy, B.M.; Standaert, R.F.

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Design, synthesis, and in vitro biological activity of indole-based factor Xa inhibitors
pp. 957-961(5)
Authors: Arnaiz, D.O.; Zhao, Z.; Liang, A.; Trinh, L.; Whitlow, M.; Koovakkat, S.K.; Shaw, K.J.

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Design, synthesis, and in vitro biological activity of benzimidazole based factor Xa inhibitors
pp. 963-966(4)
Authors: Zhao, Z.; Arnaiz, D.O.; Griedel, B.; Sakata, S.; Dallas, J.L.; Whitlow, M.; Trinh, L.; Post, J.; Liang, A.; Morrissey, M.M.; Shaw, K.J.

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New fluorogenic substrate for the first continuous steroid sulfatase assay
pp. 967-969(3)
Authors: Bilban, M.; Billich, A.; Auer, M.; Nussbaumer, P.

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Stereo-random synthesis of highly functionalized proline analogues by azomethine cycloaddition
pp. 975-977(3)
Authors: Henkel, B.; Stenzel, W.; Schotten, T.

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-Carbonyl substituted glutathione conjugates as inhibitors of O. Volvulus GST2
pp. 979-981(3)
Authors: Brophy, P.M.; Campbell, A.M.; van Eldik, A.J.; Teesdale-Spittle, P.H.; Liebau, E.; Wang, M.F.

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Synthesis and biological activity of peptidyl aldehyde urokinase inhibitors
pp. 983-987(5)
Authors: Tamura?, S.Y.; Weinhouse, M.I.; Roberts, C.A.; Goldman?, E.A.; Masukawa, K.; Anderson, S.M.; Cohen?, C.R.; Bradbury, A.E.; Bernardino, V.T.; Dixon, S.A.; Ma, M.G.; Nolan, T.G.; Brunck?, T.K.

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Discovery and evaluation of potent, cysteine-based α41 integrin antagonists
pp. 993-995(3)
Authors: Archibald, S.C.; Head, J.C.; Linsley, J.M.; Porter, J.R.; Robinson, M.K.; Shock, A.; Warrellow, G.J.

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Discovery and evaluation of potent, tyrosine-based α41 integrin antagonists
pp. 997-999(3)
Authors: Archibald, S.C.; Head, J.C.; Gozzard, N.; Howat, D.W.; Parton, T.A.H.; Porter, J.R.; Robinson, M.K.; Shock, A.; Warrellow, G.J.; Abraham, W.M.

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Corrigendum to ''2,6,9-trisubstituted purines: optimization towards highly potent and selective CDK1 inhibitors''?
pp. 1001-1001(1)
Authors: Imbach, P.; Capraro, H.; Furet, P.; Mett, H.; Meyer, T.; Zimmermann, J.

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