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Publisher: Elsevier

Volume 12, Number 9, 6 May 2002

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Graphical Abstracts
pp. vii-xii(6)

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Synthesis of a molecular mimic of the Glc1Man9 oligoside as potential inhibitor of calnexin binding to ΔF508 CFTR protein
pp. 1237-1240(4)
Authors: Cherif, S.; Leach, M.R.; Williams, D.B.; Monneret, C.

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Enantioselective synthesis of S-(+)-2-carboalkoxy-3α-[bis(4-fluorophenyl)methoxy]tropanes as novel probes for the dopamine transporter
pp. 1249-1252(4)
Authors: Zou, M.; Agoston, G.E.; Belov, Y.; Kopajtic, T.; Katz, J.L.; Newman, A.H.

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Synthesis of aminoglycoside-DNA conjugates
pp. 1259-1262(4)
Authors: Charles, I.; Xue, L.; Arya, D.P.

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Induction of apoptosis by aryl-substituted diamines: role of aromatic group substituents and distance between nitrogens
pp. 1263-1267(5)
Authors: Burns, M.R.; LaTurner, S.; Ziemer, J.; McVean, M.; Devens, B.; Carlson, C.L.; Graminski, G.F.; Vanderwerf, S.M.; Weeks, R.S.; Carreon, J.

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Potent inhibitors of farnesyltransferase and geranylgeranyltransferase-I
pp. 1269-1273(5)
Authors: Nguyen, D.N.; Stump, C.A.; Walsh, E.S.; Fernandes, C.; Davide, J.P.; Ellis-Hutchings, M.; Robinson, R.G.; Williams, T.M.; Lobell, R.B.; Huber, H.E.; Buser, C.A.

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Design, synthesis and biological activity of novel non-peptidyl endothelin converting enzyme inhibitors, 1-phenyl-tetrazole-formazan analogues
pp. 1275-1278(4)
Authors: Yamazaki, K.; Hasegawa, H.; Umekawa, K.; Ueki, Y.; Ohashi, N.; Kanaoka, M.

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Synthesis of a novel fluorescent probe for estrogen receptor
pp. 1283-1285(3)
Authors: Adamczyk, M.; Reddy, R.E.; Yu, Z.

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Imidazole-based ligands of the Src SH2 protein
pp. 1287-1289(3)
Authors: Deprez, P.; Mandine, E.; Vermond, A.; Lesuisse, D.

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Discovery of highly potent Src SH2 binders: Structure-activity studies and X-ray structures
pp. 1291-1294(4)
Authors: Deprez, P.; Baholet, I.; Burlet, S.; Lange, G.; Amengual, R.; Schoot, B.; Vermond, A.; Mandine, E.; Lesuisse, D.

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Small ligands interacting with the phosphotyrosine binding pocket of the Src SH2 protein
pp. 1295-1298(4)
Authors: Deprez, P.; Mandine, E.; Gofflo, D.; Meunier, S.; Lesuisse, D.

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Optimization of the 4-aryl group of 4-aryl-pyridine glucagon antagonists: development of an efficient, alternative synthesis
pp. 1303-1306(4)
Authors: Smith, R.A.; Hertzog, D.L.; Osterhout, M.H.; Ladouceur, G.H.; Korpusik, M.; Bobko, M.A.; Jones, J.H.; Phelan, K.; Romero, R.H.; Hundertmark, T.; MacDougall, M.L.; Livingston, J.N.; Schoen, W.R.

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Design and synthesis of aminophenol-Based factor xa inhibitors
pp. 1307-1310(4)
Authors: Wu, S.; Guilford, W.J.; Chou, Y.; Griedel, B.D.; Liang, A.; Sakata, S.; Shaw, K.J.; Trinh, L.; Xu, W.; Zhao, Z.; Morrissey, M.M.

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Benzimidazole-Based fXa inhibitors with improved thrombin and trypsin selectivity
pp. 1311-1314(4)
Authors: Shaw, K.J.; Guilford, W.J.; Griedel, B.D.; Sakata, S.; Trinh, L.; Wu, S.; Xu, W.; Zhao, Z.; Morrissey, M.M.

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Enantiospecific, selective cyclooxygenase-2 inhibitors
pp. 1315-1318(4)
Authors: Kozak, K.R.; Prusakiewicz, J.J.; Rowlinson, S.W.; Marnett, L.J.

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Novel diamide-Based inhibitors of IMPDH
pp. 1323-1326(4)
Authors: Gu, H.H.; Iwanowicz, E.J.; Guo, J.; Watterson, S.H.; Shen, Z.; Pitts, W.J.; Dhar, T.G.M.; Fleener, C.A.; Rouleau, K.; Sherbina, N.Z.; Witmer, M.; Tredup, J.; Hollenbaugh, D.

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