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Publisher: Elsevier

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Volume 9, Number 18, 20 September 1999

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Asymmetric synthesis and antitumor activity of cycloalkanin
pp. 2635-2638(4)
Authors: Wu, X.; Xu, L.; Cai, J.

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Incorrectly folded aromatic polyketides from polyketide reductase deficient mutants
pp. 2639-2642(4)
Authors: Kunnari, T.; Ylihonko, K.; Hautala, A.; Klika, K.D.; Mantsala, P.; Hakala, J.

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Syntheses of novel antitumor dihydroxanthone derivatives with inhibitory activity against DNA topoisomerase II
pp. 2653-2656(4)
Authors: Sato, S.; Suga, Y.; Yoshimura, T.; Nakagawa, R.; Tsuji, T.; Umemura, K.; Ando, T.

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Selective recognition of a C-G base-pair in the parallel DNA triple-helical binding motif
pp. 2657-2660(4)
Authors: Prevot-Halter, I.; Leumann, C.J.

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[35S]S-[5-(4-benzoylphenyl)pentyl]glutathione: A Versatile Radioligand Targeting GS-X Pumps with the Ability of Photoaffinity Labeling
pp. 2661-2666(6)
Authors: Furuta, K.; Hosoya, T.; Tomokiyo, K.; Okuda, S.; Kuniyasu, A.; Nakayama, H.; Ishikawa, T.; Suzuki, M.

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Synthesis and in vitro activity of new oxazolidinone antibacterial agents having substituted isoxazoles
pp. 2679-2684(6)
Authors: Pae, A.N.; Kim, H.Y.; Joo, H.J.; Kim, B.H.; Cho, Y.S.; Choi, K.I.; Choi, J.H.; Koh, H.Y.

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3D QSAR studies on new oxazolidinone antibacterial agents by comparative molecular field analysis
pp. 2685-2690(6)
Authors: Pae, A.N.; Kim, S.Y.; Kim, H.Y.; Joo, H.J.; Cho, Y.S.; Choi, K.I.; Choi, J.H.; Koh, H.Y.

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Synthesis and SAR studies of 1-substituted-n-(4-alkoxycarbonylpiperidin-1-yl)alkanes as potent antiarrhythmic agents
pp. 2693-2698(6)
Authors: Tripathi, R.C.; Pandey, S.K.; Kar, K.; Dikshit, M.; Saxena, A.K.

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New class of biphenylene dibenzazocinones as potent ligands for the human EP1 prostanoid receptor
pp. 2699-2704(6)
Authors: Ruel, R.; Lacombe, P.; Abramovitz, M.; Godbout, C.; Lamontagne, S.; Rochette, C.; Sawyer, N.; Stocco, R.; Tremblay, N.M.; Metters, K.M.; Labelle, M.

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Combinatorial search of substituted -cyclodextrins for phosphatase-like activity
pp. 2705-2710(6)
Authors: Yu, J.; Zhao, Y.; Holterman, M.J.; Venton, D.L.

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Leishmanicidal activity of combretastatin analogues and heteroanalogues
pp. 2711-2714(4)
Authors: del Rey, B.; Ramos, A.C.; Caballero, E.; Inchaustti, A.; Yaluff, G.; Medarde, M.; de Arias, A.R.; San Feliciano, A.

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Heterocyclic analogues of 2-aminotetralins with high affinity and selectivity for the dopamine D3 receptor
pp. 2715-2720(6)
Authors: Avenell, K.Y.; Boyfield, I.; Hadley, M.S.; Johnson, C.N.; Nash, D.J.; Riley, G.J.; Stemp, G.

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Synthesis and antitumour activity of novel diterpenequinone salvicine and the analogs
pp. 2731-2736(6)
Authors: Zhang, J.; Ding, J.; Tang, Q.; Li, M.; Zhao, M.; Lu, L.; Chen, L.; Yuan, S.

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Structure-activity relationships of biphenyl tetrazoles as metallo--lactamase inhibitors
pp. 2741-2746(6)
Authors: Toney, J.H.; Cleary, K.A.; Hammond, G.G.; Yuan, X.; May, W.J.; Hutchins, S.M.; Ashton, W.T.; vanderwall, D.E.

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Structure-activity studies on a novel series of cholinergic channel activators based on a heteroaryl ether framework
pp. 2747-2752(6)
Authors: Lin, N.; Abreo, M.A.; Gunn, D.E.; Lebold, S.A.; Lee, E.L.; Wasicak, J.T.; Hettinger, A.; Daanen, J.F.; Garvey, D.S.; Campbell, J.E.; Sullivan, J.P.; Williams, M.; Arneric, S.P.

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Synthesis, SAR and in vivo activity of novel thienopyridine sulfonamide pyrrolidinones as factor Xa inhibitors
pp. 2753-2758(6)
Authors: Becker, M.R.; Ewing, W.R.; Davis, R.S.; Pauls, H.W.; Ly, C.; Li, A.; Mason, H.J.; Choi-Sledeski, Y.M.; Spada, A.P.; Chu, V.; Brown, K.D.; Colussi, D.J.; Leadley, R.J.; Bentley, R.; Bostwick, J.; Kasiewski, C.; Morgan, S.

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Biological activity of fragments and analogues of the potent dimeric opioid peptide, biphalin
pp. 2763-2766(4)
Authors: Lipkowski, A.W.; Misicka, A.; Davis, P.; Stropova, D.; Janders, J.; Lachwa, M.; Porreca, F.; Yamamura, H.I.; Hruby, V.J.

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The design of potent, selective, non-covalent, peptide thrombin inhibitors utilizing imidazole as a S1 binding element
pp. 2767-2772(6)
Authors: Wiley, M.R.; Weir, L.C.; Briggs, S.L.; Chirgadze, N.Y.; Clawson, D.; Gifford-Moore, D.S.; Schacht, A.L.; Smith, G.F.; Vasudevan, V.; Zornes, L.I.; Klimkowski, V.J.

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Discovery of CP-199,330 and CP-199,331: two potent and orally efficacious cysteinyl LT1 recepto antagonists devoid of live toxicity
pp. 2773-2778(6)
Authors: Chambers, R.J.; Marfat, A.; Antognoli, G.W.; Cheng, J.B.; Damon, D.B.; Kuperman, A.V.; Liston, T.C.; Mebus, C.; Pillarr, J.S.; Shirley, J.T.; Watson, J.W.

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