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Publisher: Elsevier

Volume 8, Number 22, 17 November 1998

Synthesis of Novel Fluorinated Coumarins: Excellent UV-Light Excitable Fluorescent Dyes
pp. 3107-3110(4)
Authors: Sun, W.; Gee, K.R.; Haugland, R.P.

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Pyrimidinylimidazole inhibitors of CSBP/P38 kinase demonstrating decreased inhibition of hepatic cytochrome P450 enzymes
pp. 3111-3116(6)
Authors: Adams, J.L.; Boehm, J.C.; Kassis, S.; Gorycki, P.D.; Webb, E.F.; Hall, R.; Sorenson, M.; Lee, J.C.; Ayrton, A.; Griswold, D.E.; Gallagher, T.F.

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Design and synthesis of a tetrahydropyran-based inhibitor of mammalian ribonucleotide reductase
pp. 3133-3136(4)
Authors: Smith, A.B.; Sasho, S.; Barwis, B.A.; Sprengeler, P.; Barbosa, J.; Hirschmann, R.; Cooperman, B.S.

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Design and synthesis of SH3 domain binding ligands: modifications of the consensus sequence XPpXP
pp. 3137-3142(6)
Authors: Witter, D.J.; Famiglietti, S.J.; Cambier, J.C.; Castelhano, A.L.

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Preparation of meta-amidino-N,N-disubstituted anilines as potent inhibitors of coagulation factor Xa
pp. 3143-3148(6)
Authors: Fevig, J.M.; Cacciola, J.; Alexander, R.S.; Knabb, R.M.; Lam, G.N.; Wong, P.C.; Wexler, R.R.

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N-substituted octahydro-4a-(3-hydroxyphenyl)-10a-methylbenzo[g]isoquinolines are opioid receptor pure antagonists
pp. 3149-3152(4)
Authors: Thomas, J.B.; Mascarella, S.W.; Burgess, J.P.; Xu, H.; McCullough, K.B.; Rothman, R.B.; Flippen-Anderson, J.L.; George, C.F.; Cantrell, B.E.; Zimmerman, D.M.; Carroll, F.I.

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Syntheses and antitumor activity of cis-restricted combretastatins: 5-membered heterocyclic analogues
pp. 3153-3158(6)
Authors: Ohsumi, K.; Hatanaka, T.; Fujita, K.; Nakagawa, R.; Fukuda, Y.; Nihei, Y.; Suga, Y.; Morinaga, Y.; Akiyama, Y.; Tsuji, T.

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Synthesis and biological evaluation of a water soluble phosphate prodrug of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP)
pp. 3159-3164(6)
Authors: Li, J.; Luo, X.; Wang, Q.; Zheng, L.; King, I.; Doyle, T.W.; Chen, S.

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Benzimidazole derivatives as arginine mimetics in 1,4-benzodiazepine nonpeptide vitronectin receptor (αv3) antagonists
pp. 3165-3170(6)
Authors: Keenan, R.M.; Miller, W.H.; Lago, M.A.; Ali, F.E.; Bondinell, W.E.; Callahan, J.F.; Calvo, R.R.; Cousins, R.D.; Hwang, S.; Jakas, D.R.; Ku, T.W.; Kwon, C.; Nguyen, T.T.; Reader, V.A.; Rieman, D.J.; Ross, S.T.; Takata, D.T.; Uzinskas, I.N.; Yuan, C.C.K.; Smith, B.R.

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Discovery of an imidazopyridine-containing 1,4-benzodiazepine nonpeptide vitronectin receptor (αv3) antagonist with efficacy in a restenosis model
pp. 3171-3176(6)
Authors: Keenan, R.M.; Lago, M.A.; Miller, W.H.; Ali, F.E.; Cousins, R.D.; Hall, L.B.; Hwang, S.; Jakas, D.R.; Kwon, C.; Louden, C.; Nguyen, T.T.; Ohlstein, E.H.; Rieman, D.J.; Ross, S.T.; Samanen, J.M.; Smith, B.R.; Stadel, J.; Takata, D.T.; Vickery, L.; Yuan, C.C.K.; Yue, T.

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Enantioselective synthesis of a 3'-dephenylcryptophycin synthon
pp. 3177-3180(4)
Authors: Eggen, M.; Georg, G.I.

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Synthesis and evaluation of paclitaxel C7 derivatives: solution phase synthesis of combinatorial libraries
pp. 3181-3186(6)
Authors: Bhat, L.; Liu, Y.; Victory, S.F.; Himes, R.H.; Georg, G.I.

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Resveratrol as a new type of DNA-cleaving agent
pp. 3187-3192(6)
Authors: Fukuhara, K.; Miyata, N.

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Potent bicyclic lactam inhibitors of thrombin: Part I: P3 modifications
pp. 3193-3198(6)
Authors: St-denis, Y.; Augelli-Szafran, C.E.; Bachand, B.; Berryman, K.A.; DiMaio, J.; Doherty, A.M.; Edmunds, J.J.; Leblond, L.; Levesque, S.; Narasimhan, L.S.; Penvose-Yi, J.R.; Rubin, J.R.; Tarazi, M.; Winocour, P.D.; Siddiqui, M.A.

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Gal(1->S-4)GlcNAc-OR: a galactosidase-stable substrate for α(1->3)fucosyltransferase
pp. 3199-3202(4)
Authors: Ding, Y.; Hindsgaul, O.; Li, H.; Palcic, M.M.

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Evaluation of a structure-based statine cyclic diamino amide encoded combinatorial library against plasmepsin II and cathepsin D
pp. 3203-3206(4)
Authors: Carroll, C.D.; Johnson, T.O.; Tao, S.; Lauri, G.; Orlowski, M.; Gluzman, I.Y.; Goldberg, D.E.; Dolle, R.E.

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Oligonucleotides Bearing 5-Formyl-2'-O-methyluridine: Preference in Binding Affinity to the NF-B (p50)2 Homo- and p50/p65 Heterodimers
pp. 3207-3210(4)
Authors: Kittaka, A.; Kuze, T.; Asakura, T.; Ito, K.; Miyasaka, T.; Inoue, J.

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Hydroindenic-guanylhydrazones. Synthesis and evaluation as inotropic agents
pp. 3217-3222(6)
Authors: Melero, C.P.; Sevillano, L.G.; Caballero, E.; Tome, F.; Carron, R.; Montero, M.J.; San Feliciano, A.; Medarde, M.

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Fluorescent probes for adenosine receptors: synthesis and biology of N6-dansylaminoalkyl-substituted NECA derivatives
pp. 3223-3228(6)
Authors: Macchia, M.; Salvetti, F.; Barontini, S.; Calvani, F.; Gesi, M.; Hamdan, M.; Lucacchini, A.; Pellegrini, A.; Soldani, P.; Martini, C.

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N-arylrolipram derivatives as potent and selective PDE4 inhibitors
pp. 3229-3234(6)
Authors: Bacher, E.; Boer, C.; Bray-French, K.; demnitz, F.W.J.; Keller, T.H.; Mazzoni, L.; Muller, T.; Walker, C.

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Ligands for the estrogen receptor, containing cyclopentadienyltricarbonylrhenium units
pp. 3235-3240(6)
Authors: Spradau, T.W.; Katzenellenbogen, J.A.

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Synthesis of diacylamines and the preparation of α-amino-acylureas, a new type of α-amino acid derivatives
pp. 3241-3244(4)
Authors: Weisz, I.; Roboz, J.; Wolf, I.; Szabo, J.; Bekesi, J.G.

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Synthesis and comparative evaluation of two antiviral agents: -L-Fd4C and -D-Fd4C
pp. 3245-3250(6)
Authors: Chen, S.; Lin, S.; King, I.; Spinka, T.; Dutschman, G.E.; Gullen, E.A.; Cheng, Y.; Doyle, T.W.

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Aryl ketones as novel replacements for the C-terminal amide bond of succinyl hydroxamate MMP inhibitors
pp. 3251-3256(6)
Authors: Sheppard, G.S.; Florjancic, A.S.; Giesler, J.R.; Xu, L.; Guo, Y.; Davidsen, S.K.; Marcotte, P.A.; Elmore, I.; Albert, D.H.; Magoc, T.J.; Bouska, J.J.; Goodfellow, C.L.; Morgan, D.W.; Summers, J.B.

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Growth inhibitory effect of juvenile hormone analogues on epimastigotes of Trypanosoma cruzi
pp. 3257-3260(4)
Authors: Rodriguez, J.B.; Zhong, L.; Docampo, R.; Wimmer, Z.; Gros, E.G.

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Novel phosphate mimetics for the design of non-peptidyl inhibitors of protein tyrosine phosphatases
pp. 3275-3280(6)
Authors: Kotoris, C.C.; Chen, M.; Taylor, S.D.

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