Publisher: Elsevier

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Volume 8, Number 7, 7 April 1998

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Syntheses and kinetic evaluation of hydroxamate-based peptide inhibitors of glyoxalase I
pp. 705-710(6)
Authors: Ly, H.D.; Clugston, S.L.; Sampson, P.B.; Honek, J.F.

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Synthesis and evaluation of a photolyzable derivative of sphingosine 1-phosphate--caged SPP
pp. 711-714(4)
Authors: Lixin, Q.; Kozikowski, A.P.; Olivera, A.; Spiegel, S.

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Potent cyclic urea HIV protease inhibitors with 3-aminoindazole P2/P2? groups
pp. 715-720(6)
Authors: Rodgers, J.D.; Johnson, B.L.; Haisheng, W.; Erickson-Viitanen, S.; Klabe, R.M.; Bacheler, L.; Cordova, B.C.; Chang, C.

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Synthesis of the Vancomycin CDE Ring System
pp. 721-724(4)
Authors: Boger, D.L.; Beresis, R.T.; Loiseleur, O.; Wu, J.H.; Castle, S.L.

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Synthesis, SAR and pharmacology of CP-293,019: a potent, selective dopamine D4 receptor antagonist
pp. 725-730(6)
Authors: Sanner, M.A.; Chappie, T.A.; Dunaiskis, A.R.; Fliri, A.F.; desai, K.A.; Zorn, S.H.; Jackson, E.R.; Johnson, C.G.; Morrone, J.M.; Seymour, P.A.; Majchrzak, M.J.; Faraci, W.S.; Collins, J.L.; Duignan, D.B.; Di Prete, C.C.; Lee, J.S.; Trozzi, A.

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A new antitumor agent: methyl sulfonium perchlorate of echinomycin
pp. 731-734(4)
Authors: Yil, S.P.; Yong, H.K.; Soo, K.K.; Choi, S.

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Solid phase synthesis of benzylamine-derived sulfonamide library
pp. 735-738(4)
Authors: Sang, W.K.; Chang, Y.H.; Koo, L.; Eun, J.L.; Jong, S.K.

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New nonsteroidal androgen receptor modulators based on 4-(trifluoromethyl)-2(1H)-pyrrolidino[3,2-g]quinolinone
pp. 745-750(6)
Authors: Edwards, J.P.; West, S.J.; Pooley, C.L.F.; Marschke, K.B.; Farmer, L.J.; Jones, T.K.

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On the preparative use of recombinant (1-3)galactosyl-transferase
pp. 751-754(4)
Authors: Baisch, G.; Ohrlein, R.; Streiff, M.; Kolbinger, F.

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Enzymatic synthesis of sialyl-lewisa-libraries with two non-natural monosaccharide units
pp. 755-758(4)
Authors: Baisch, G.; Ohrlein, R.; Streiff, M.; Kolbinger, F.

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Tripeptide growth hormone secretagogues
pp. 759-764(6)
Authors: Yang, L.; Morriello, G.; Pan, Y.; Nargund, R.P.; Barakat, K.; Prendergast, K.; Cheng, K.; Chan, W.W.; Smith, R.G.; Patchett, A.A.

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(2S,4S)-2-amino-4-(2,2-diphenylethyl)pentanedioic acid selective group 2 metabotropic glutamate receptor antagonist
pp. 765-770(6)
Authors: Escribano, A.; Ezquerra, J.; Pedregal, C.; Rubio, A.; Yruretagoyena, B.; Baker, S.R.; Wright, R.A.; Johnson, B.G.; Schoepp, D.D.

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Identification of a non peptidic rantes antagonist
pp. 771-774(4)
Authors: Bright, C.; Brown, T.J.; Cox, P.; Halley, F.; Lockey, P.; McLay, I.M.; Moore, U.; Porter, B.; Williams, R.J.

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Pyrazoles, 1,2,4-triazoles, and tetrazoles as surrogates for cis-amide bonds in boronate ester thrombin inhibitors
pp. 775-780(6)
Authors: Duncia, J.V.; Santella, J.B.; Higley, C.A.; vanAtten, M.K.; Weber, P.C.; Alexander, R.S.; Kettner, C.A.; Pruitt, J.R.; Liauw, A.Y.; Quan, M.L.; Knabb, R.M.; Wexler, R.R.

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Amygdalin binds to the CD4 receptor as suggested from molecular modeling studies
pp. 781-786(6)
Authors: Llorens, O.; Filizola, M.; Spisani, S.; Marastoni, M.; Herranz, C.; Perez, J.J.

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Affinity labelling of the tick-borne encephalitis virus RNA replicase proteins by 4-N-exo-base-substituted photoreactive CTP analogs
pp. 787-792(6)
Authors: Morozova, O.V.; Safronov, I.V.; Bahvalova, V.N.; Dobrikov, M.I.

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Synthesis of C2 alkynylated purines, a new family of potent inhibitors of cyclin-dependent kinases
pp. 793-798(6)
Authors: Legraverend, M.; Ludwig, O.; Bisagni, E.; Leclerc, S.; Meijer, L.

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Synthesis and biological activity of 3-substituted 3-desoxynaltrindole derivatives
pp. 799-804(6)
Authors: Kubota, H.; Rothman, R.B.; dersch, C.; McCullough, K.; Pinto, J.; Rice, K.C.

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Preparation of 9-deoxo-4?-deoxy-6,9-epoxyerythromycin lactams ?motilactides?: potent and orally active prokinetic agents
pp. 805-810(6)
Authors: Faghih, R.; Nellans, H.N.; Lartey, P.A.; Petersen, A.; Marsh, K.; Bennani, Y.L.; Plattner, J.J.

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An approach to use an unusual adenosine transporter to selectively deliver polyamine analogues to trypanosomes
pp. 811-816(6)
Authors: Tye, C.; Kasinathan, G.; Barrett, M.P.; Brun, R.; Doyle, V.E.; Fairlamb, A.H.; Weaver, R.; Gilbert, I.H.

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L-374,087, an efficacious, orally bioavailable, pyridinone acetamide thrombin inhibitor
pp. 817-822(6)
Authors: Sanderson, P.E.J.; Cutrona, K.J.; Dorsey, B.D.; Dyer, D.L.; McDonough, C.M.; Naylor-Olsen, A.M.; Chen, I.; Chen, Z.; Cook, J.J.; Gardell, S.J.; Krueger, J.A.; Lewis, S.D.; Lin, J.H.; Lucas, B.J.; Lyle, E.A.; Lynch, J.J.; Stranieri, M.T.; Vastag, K.; Shafer, J.A.; Vacca, J.P.

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The synthesis and evaluation of cyclic ureas as HIV protease inhibitors: modifications of the P1/P1? residues
pp. 823-828(6)
Authors: Patel, M.; Bacheler, L.T.; Rayner, M.M.; Cordova, B.C.; Klabe, R.M.; Erickson-Viitanen, S.; Seitz, S.P.

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Synthesis and pharmacological activity of the stereoisomers of GP-88, a propafenone-type modulator of multidrug resistance
pp. 829-832(4)
Authors: Chiba, P.; Rebitzer, S.; Richter, E.; Hitzler, M.; Ecker, G.

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Synthesis of a cosalane analog with an extended polyanionic pharmacophore conferring enhanced potency as an anti-HIV agent
pp. 833-836(4)
Authors: Cushman, M.; Insaf, S.; Ruell, J.A.; Schaeffer, C.A.; Rice, W.G.

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Structure-based design and synthesis of a series of hydroxamic acids with a quaternary-hydroxy group in P1 as inhibitors of matrix metalloproteinases
pp. 837-842(6)
Authors: Jacobson, I.C.; Reddy, P.G.; Wasserman, Z.R.; Hardman, K.D.; Covington, M.B.; Arner, E.C.; Copeland, R.A.; decicco, C.P.; Magolda, R.L.

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Syntheses and evaluation of benzodiazaborine compounds against M. tuberculosis H37RV in vitro
pp. 843-846(4)
Authors: Davis, M.C.; Franzblau, S.G.; Martin, A.R.

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Hydroxyl radical-induced cross-linking of thymine and lysine: identification of the primary structure and mechanism
pp. 865-870(6)
Authors: Morimoto, S.; Hatta, H.; Fujita, S.; Matsuyama, T.; Ueno, T.; Nishimoto, S.

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Organometallic photonucleases: a novel class of DNA-cleaving agents
pp. 871-874(4)
Authors: Mohler, D.L.; Dain, D.R.; Kerekes, A.D.; Nadler, W.R.; Scott, T.L.

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A labeled guanidine ligand for studying sweet taste
pp. 881-884(4)
Authors: Yangbo, F.; Burgess, K.; Pledger, D.; Cairns, N.; Linthicum, D.S.

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