Publisher: Elsevier

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Volume 11, Number 19, 8 October 2001

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Graphical Abstracts
pp. vii-xii(6)

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Combinatorial synthesis of SSAO inhibitors using sonogashira coupling: SAR of aryl propargylic amines
pp. 2565-2568(4)
Authors: Conn, C.; Shimmon, R.; Cordaro, F.; Hargraves, T.; Ibrahim, P.

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Novel 3-dodecanoylindole-2-carboxylic acid inhibitors of cytosolic phospholipase A2
pp. 2569-2572(4)
Authors: Lehr, M.; Klimt, M.; Elfringhoff, A.S.

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Solid-Phase synthesis of a library constructed of aromatic phosphate, long alkyl chains and tryptophane components, and identification of potent dipeptide telomerase inhibitors
pp. 2581-2584(4)
Authors: Sasaki, S.; Ehara, T.; Rowshon Alam, M.; Fujino, Y.; Harada, N.; Kimura, J.; Nakamura, H.; Maeda, M.

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Asymmetric synthesis of bb-3497-A potent peptide deformylase inhibitor
pp. 2585-2588(4)
Authors: Pratt, L.M.; Beckett, R.P.; Davies, S.J.; Launchbury, S.B.; Miller, A.; Spavold, Z.M.; Todd, R.S.; Whittaker, M.

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Synthesis and in vitro evaluation of a series of diketopiperazine inhibitors of plasminogen activator inhibitor-1
pp. 2589-2592(4)
Authors: Folkes, A.; Roe, M.B.; Sohal, S.; Golec, J.; Faint, R.; Brooks, T.; Charlton, P.

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Isoxazolyl, oxazolyl, and thiazolylpropionic acid derivatives as potent α41 integrin antagonists
pp. 2593-2596(4)
Authors: Duplantier, A.J.; Beckius, G.E.; Chambers, R.J.; Chupak, L.S.; Jenkinson, T.H.; Klein, A.S.; Kraus, K.G.; Kudlacz, E.M.K.; McKechney, M.W.M.; Pettersson, M.P.; Whitney, C.A.W.; Milici, A.J.M.

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Orally bioavailable, indole-based nonpeptide GnRH receptor antagonists with high potency and functional activity
pp. 2597-2602(6)
Authors: Ashton, W.T.; Sisco, R.M.; Kieczykowski, G.R.; Yang, Y.T.; Yudkovitz, J.B.; Cui, J.; Mount, G.R.; Ren, R.N.; Wu, T.; Shen, X.; Lyons, K.A.; Mao, A.; Carlin, J.R.; Karanam, B.V.; Vincent, S.H.; Cheng, K.; Goulet, M.T.

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Robinlin: A novel bioactive homo-monoterpene from Robinia pseudoacacia L. (Fabaceae)
pp. 2603-2606(4)
Authors: Tian, F.; Chang, C.; Grutzner, J.B.; Nichols, D.E.; McLaughlin, J.L.

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Inhibition of hiv-1 infection by synthetic peptide analogues derived from the nh2-Terminal extracellular region of gpr1
pp. 2607-2609(3)
Authors: Ikeda, K.; Konishi, K.; Sato, M.; Hoshino, H.; Tanaka, K.

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Novel lipophilic chloroquine analogues for a highly efficient gene transfer into gynecological tumors
pp. 2611-2613(3)
Authors: Keil, O.; Bojar, H.; Prisack, H.; Dall, P.

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Potent peptide α-Ketohydroxamate inhibitors of recombinant human calpain I
pp. 2615-2617(3)
Authors: Josef, K.A.; Kauer, F.W.; Bihovsky, R.

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1,2,4-Triazolo[3,4-a]pyridine as a novel, constrained template for fibrinogen receptor (GPIIb/IIIa) antagonists
pp. 2619-2622(4)
Authors: Lawson, E.C.; Hoekstra, W.J.; Addo, M.F.; Andrade-Gordon, P.; Damiano, B.P.; Kauffman, J.A.; Mitchell, J.A.; Maryanoff, B.E.

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RNA-DNA Hybrids Containing Damaged DNA are Substrates for RNase H
pp. 2623-2626(4)
Authors: Shiels, J.C.; Jerkovic, B.; Baranger, A.M.; Bolton, P.H.

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Synthesis and acetylcholinesterase inhibition of 5-desamino huperzine A derivatives
pp. 2627-2630(4)
Authors: Hogenauer, K.; Baumann, K.; Enz, A.; Mulzer, J.

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Design, synthesis and characterisation of a peptide with oxaloacetate decarboxylase activity
pp. 2631-2635(5)
Authors: Taylor, S.E.; Rutherford, T.J.; Allemann, R.K.

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New inhibitors of the thioredoxin-thioredoxin reductase system based on a naphthoquinone spiroketal natural product lead
pp. 2637-2641(5)
Authors: Wipf, P.; Hopkins, T.D.; Jung, J.; Rodriguez, S.; Birmingham, A.; Southwick, E.C.; Lazo, J.S.; Powis, G.

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Synthesis of a reported calpain inhibitor isolated from Streptomyces griseus
pp. 2647-2649(3)
Authors: Donkor, I.O.; Sanders, M.L.

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Selective heterocyclic amidine inhibitors of human inducible nitric oxide synthase
pp. 2651-2653(3)
Authors: Moormann, A.E.; Metz, S.; Toth, M.V.; Moore, W.M.; Jerome, G.; Kornmeier, C.; Manning, P.; Hansen, D.W.; Pitzele, B.S.; Webber, R.K.

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Antiprotozoal and cytotoxicity evaluation of sulfonamide and urea analogues of quinacrine
pp. 2655-2657(3)
Authors: Chibale, K.; Haupt, H.; Kendrick, H.; Yardley, V.; Saravanamuthu, A.; Fairlamb, A.H.; Croft, S.L.

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Synthesis, topoisomerase I inhibition and antitumor cytotoxicity of 2,2':6',2''-, 2,2':6',3''- and 2,2':6',4''-Terpyridine derivatives
pp. 2659-2662(4)
Authors: Zhao, L.; Kim, T.S.; Ahn, S.; Kim, T.; Kim, E.; Cho, W.; Choi, H.; Lee, C.; Kim, J.; Jeong, T.C.; Chang, C.; Lee E.-S.

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Synthesis of diaminobutane derivatives as potent Ca2+-Permeable AMPA receptor antagonists
pp. 2663-2666(4)
Authors: Yoneda, Y.; Kawajiri, S.; Sugimura, M.; Osanai, K.; Kito, F.; Ota, E.; Mimura, T.

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