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Publisher: Elsevier

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Volume 11, Number 20, 22 October 2001

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Graphical Abbstracts
pp. xi-xvii(7)

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Efficient synthesis of lactosaminylated core-2 O-glycans
pp. 2667-2669(3)
Authors: Misra, A.K.; Fukuda, M.; Hindsgaul, O.

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Microwave assisted synthesis of N-Arylphthalamic acids with hyperlipidemic activity
pp. 2671-2674(4)
Authors: Sena, V.L.M.; Srivastava, R.M.; Oliveira, S.P.; Lima, V.L.M.

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Synthesis, characterisation and antiamoebic activity of new thiophene-2-carboxaldehyde thiosemicarbazone derivatives and Their cyclooctadiene Ru(II) complexes
pp. 2675-2678(4)
Authors: Shailendra, N.S.; Bharti, N.; Gonzalez Garza, M.T.; Cruz-Vega, D.E.; Castro Garza, J.; Saleem, K.; Naqvi, F.; Azam, A.

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N,N'-Bis[4-(N-alkylamidino)phenyl]homopiperazines as anti-Pneumocystis carinii agents
pp. 2679-2681(3)
Authors: Huang, T.L.; Tao, B.; Quarshie, Y.; Queener, S.F.; Donkor, I.O.

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Design and synthesis of irreversible depsipeptidyl human rhinovirus 3C protease inhibitors
pp. 2683-2686(4)
Authors: Webber, S.E.; Marakovits, J.T.; Dragovich, P.S.; Prins, T.J.; Zhou, R.; Fuhrman, S.A.; Patick, A.K.; Matthews, D.A.; Lee, C.A.; Srinivasan, B.; Moran, T.; Ford, C.E.; Brothers, M.A.; Harr, J.E.V.; Meador, J.W.; Ferre, R.A.; Worland, S.T.

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Naphthalene derivatives: A new series of selective cyclooxygenase-2 inhibitors
pp. 2687-2690(4)
Authors: Feixas, J.; Jimenez J.-M.; Godessart, N.; Puig, C.; Soca, L.; Crespo, M.I.

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Discovery and initial structure-Activity relationships of trisubstituted ureas as thrombin receptor (PAR-1) antagonists
pp. 2691-2696(6)
Authors: Barrow, J.C.; Nantermet, P.G.; Selnick, H.G.; Glass, K.L.; Ngo, P.L.; Young, M.B.; Pellicore, J.M.; Breslin, M.J.; Hutchinson, J.H.; Freidinger, R.M.; Condra, C.; Karczewski, J.; Bednar, R.A.; Gaul, S.L.; Stern, A.; Gould, R.; Connolly, T.M.

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The synthesis and properties of new 2-pyrrolylthiones as chelating agents for transition metals and technetium
pp. 2697-2699(3)
Authors: Selivanova, S.V.; Dolphin, D.; Bruckner, C.; E. van Lier, J.E.; Kudrevich, S.V.

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Synthesis and biological evaluation of novel bisindolylmaleimides that inhibit vascular endothelial cell proliferation
pp. 2701-2703(3)
Authors: Brana, M.F.; Anorbe, L.; Tarrason, G.; Mitjans, F.; Piulats, J.

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The discovery of sulfonylated dipeptides as Potent VLA-4 antagonists
pp. 2709-2713(5)
Authors: Hagmann, W.K.; Durette, P.L.; Lanza, T.; Kevin, N.J.; de Laszlo, S.E.; Kopka, I.E.; Young, D.; Magriotis, P.A.; Li, B.; Lin, L.S.; Yang, G.; Kamenecka, T.; Chang, L.L.; Wilson, J.; MacCoss, M.; Mills, S.G.; van Riper, G.; McCauley, E.; Egger, L.A.; Kidambi, U.; Lyons, K.; Vincent, S.; Stearns, R.; Colletti, A.; Teffera, J.; Tong, S.; Fenyk-Melody, J.; Owens, K.; Levorse, D.; Kim, P.; Schmidt, J.A.; Mumford, R.A.

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Synthesis of N-propargylphenelzine and analogues as neuroprotective agents
pp. 2715-2717(3)
Authors: Ling, L.; Urichuk, L.J.; Sloley, B.D.; Coutts, R.T.; Baker, G.B.; Shan, J.J.; Pang, P.K.T.

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α-Amino--sulphone hydroxamates as potent MMP-13 inhibitors that spare MMP-1
pp. 2719-2722(4)
Authors: Becker, D.P.; Barta, T.E.; Bedell, L.; deCrescenzo, G.; Freskos, J.; Getman, D.P.; Hockerman, S.L.; Li, M.; Mehta, P.; Mischke, B.; Munie, G.E.; Swearingen, C.; Villamil, C.I.

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α-Alkyl-α-amino--sulphone hydroxamates as potent MMP inhibitors that spare MMP-1
pp. 2723-2725(3)
Authors: Becker, D.P.; deCrescenzo, G.; Freskos, J.; Getman, D.P.; Hockerman, S.L.; Li, M.; Mehta, P.; Munie, G.E.; Swearingen, C.

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Small molecule somatostatin receptor subtype-2 antagonists
pp. 2731-2734(4)
Authors: Hay, B.A.; Cole, B.M.; DiCapua, F.M.; Kirk, G.W.; Murray, M.C.; Nardone, R.A.; Pelletier, D.J.; Ricketts, A.P.; Robertson, A.S.; Siegel, T.W.

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Mixed  agonists and  agonists/Antagonists as potential pharmacotherapeutics for cocaine abuse: synthesis and opioid receptor binding affinity of N-substituted derivatives of morphinan
pp. 2735-2740(6)
Authors: Neumeyer, J.L.; Gu, X.; van Vliet, L.A.; denunzio, N.J.; Rusovici, D.E.; Cohen, D.J.; Negus, S.S.; Mello, N.K.; Bidlack, J.M.

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1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 2: lead optimization affording selective, orally bioavailable compounds with potent Anti-HIV activity
pp. 2741-2745(5)
Authors: Hale, J.J.; Budhu, R.J.; Holson, E.B.; Finke, P.E.; Oates, B.; Mills, S.G.; MacCoss, M.; Gould, S.L.; deMartino, J.A.; Springer, M.S.; Siciliano, S.; Malkowitz, L.; Schleif, W.A.; Hazuda, D.; Miller, M.; Kessler, J.; Danzeisen, R.; Holmes, K.; Lineberger, J.; Carella, A.; Carver, G.; Emini, E.

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Synthesis and progesterone receptor antagonist activities of 6-aryl benzimidazolones and benzothiazolones
pp. 2747-2750(4)
Authors: Zhang, P.; Terefenko, E.A.; Wrobel, J.; Zhang, Z.; Zhu, Y.; Cohen, J.; Marschke, K.B.; Mais, D.

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Synthesis and structure-activity relationships of thiotetronic acid analogues of thiolactomycin
pp. 2751-2754(4)
Authors: Sakya, S.M.; Suarez-Contreras, M.; Dirlam, J.P.; O'Connell, T.N.; Hayashi, S.F.; Santoro, S.L.; Kamicker, B.J.; George, D.M.; Ziegler, C.B.

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Anti-Trypanosoma activity of some natural stilbenoids and synthetic related heterocyclic compounds
pp. 2755-2757(3)
Authors: Olmo, E.; Armas, M.G.; Lopez-Perez, J.L.; Ruiz, G.; Vargas, F.; Gimenez, A.; deharo, E.; Feliciano, A.S.

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Potent second generation vinyl sulfonamide inhibitors of the trypanosomal cysteine protease cruzain
pp. 2759-2762(4)
Authors: Roush, W.R.; Cheng, J.; Knapp-Reed, B.; Alvarez-Hernandez, A.; McKerrow, J.H.; Hansell, E.; Engel, J.C.

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Simplified catechin-gallate inhibitors of HIV-1 reverse transcriptase
pp. 2763-2767(5)
Authors: Tillekeratne, L.M.V.; Sherette, A.; Grossman, P.; Hupe, L.; Hupe, D.; Hudson, R.A.

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Discovery of novel, orally active dual NK1/NK2 antagonists
pp. 2769-2773(5)
Authors: Bernstein, P.R.; Aharony, D.; Albert, J.S.; Andisik, D.; Barthlow, H.G.; Bialecki, R.; Davenport, T.; dedinas, R.F.; dembofsky, B.T.; Koether, G.; Kosmider, B.J.; Kirkland, K.; Ohnmacht, C.J.; Potts, W.; Rumsey, W.L.; Shen, L.; Shenvi, A.; Sherwood, S.; Stollman, D.; Russell, K.

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Discovery of heterocyclic ureas as a new class of raf kinase inhibitors: identification of a second generation lead by a combinatorial chemistry approach
pp. 2775-2778(4)
Authors: Smith, R.A.; Barbosa, J.; Blum, C.L.; Bobko, M.A.; Caringal, Y.V.; Dally, R.; Johnson, J.S.; Katz, M.E.; Kennure, N.; Kingery-Wood, J.; Lee, W.; Lowinger, T.B.; Lyons, J.; Marsh, V.; Rogers, D.H.; Swartz, S.; Walling, T.; Wild, H.

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Structure-based design of caspase-1 inhibitor containing a diphenyl ether sulfonamide
pp. 2779-2782(4)
Authors: Shahripour, A.B.; Plummer, M.S.; Lunney, E.A.; Sawyer, T.K.; Stankovic, C.J.; Connolly, M.K.; Rubinb?, J.R.; Walkerc?, N.P.C.; Brady, K.D.; Allen, H.J.; Talanian, R.V.; Wong, W.W.; Humblet, C.

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Total synthesis and antifungal activity of 9-methoxystrobilurin L as the originally proposed 1,4-Benzodioxan structure
pp. 2783-2786(4)
Authors: Aiba, Y.; Hasegawa, D.; Marunouchi, T.; Nagasawa, K.; Uchiro, H.; Kobayashi, S.

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NaBH4 in N-methylpyrrolidone: a safe alternative for hydride displacement reaction
pp. 2787-2789(3)
Authors: Torisawa, Y.; Nishi, T.; Minamikawa, J.

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