Publisher: Elsevier

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Volume 5, Number 9, 4 May 1995

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The combinatorial synthesis of a 30,752-compound library: discovery of SAR around the endothelin antagonist, FR-139,317
pp. 917-922(6)
Authors: Terrett, N.K.; Brown, D.; Gardner, M.; Gordon, D.W.; Steele, J.; Bojanic, D.; Bungay, P.J.; Mayers, C.J.

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Preparation and Biological Evaluation of -Trifluoromethyl-α,-unsaturated Carbonyl Compounds
pp. 923-926(4)
Authors: Shinohara, N.; Yamazaki, T.; Kitazume, T.

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Peptides inhibit complexation of the bacterial chaperone PapD and reveal potential to block assembly of virulence associated pili
pp. 927-932(6)
Authors: Flemmer, K.; Xu, Z.; Pinkner, J.S.; Hultgren, S.J.; Kihlberg, J.

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Synthesis and antifungal activities of optically active isomers of SM-8668
pp. 933-936(4)
Authors: Miyauchi, H.; Tanio, T.; Ohashi, N.

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Acyloxymethyl as a Drug Protecting Group. Synthesis and Reactivity of N-Acyloxymethylsulfonamide Prodrugs.
pp. 937-940(4)
Authors: Calheiros, T.; Iley, J.; Lopes, F.; Moreira, R.

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Synthesis of Indane Derivatives as Mechanism-Based Inhibitors of Dopamine -Hydroxylase
pp. 941-944(4)
Authors: Eydoux, F.; Chlenov, M.A.; Reglier, M.

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The discovery and synthesis of 2-biphenylcarbapenems active against methicillin resistant staphylococci
pp. 945-948(4)
Authors: DiNinno, F.; Muthard, D.A.; Salzmann, T.N.; Huber, J.; Kahan, J.; Kropp, H.

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Conformationally constrained precursors to retinoic acid analogs which stabilize the 9Z-configuration
pp. 953-958(6)
Authors: Robinson, C.Y.; Waterhous, D.V.; Muccio, D.D.; Brouillette, W.J.

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Structural optimization of alkyl-substituted 2-(7-5H-[1]benzopyrano[2,3-b]pyridyl)propionic acid as anti-inflammatory agents
pp. 959-962(4)
Authors: Naka, Y.; Yamada, I.; Ochi, H.; Matsuura, M.; Nagamatsu, Y.; Oe, T.

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Structure-activity and biophysical studies of the C-terminal hexapeptide of endothelin
pp. 967-972(6)
Authors: Leonard, D.M.; Reily, M.D.; Dunbar, J.B.; Holub, K.E.; Cody, W.L.; Hill, K.E.; Welch, K.M.; Flynn, M.A.; Reynolds, E.E.; Doherty, A.M.

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Decomposition of FK 409, a new vasodilator: identification of nitric oxide as a metabolite
pp. 973-978(6)
Authors: Decout, J.; Roy, B.; Fontecave, M.; Muller, J.; Williams, P.H.; Loyaux, D.

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On the side chain conformation of 1α,25-dihydroxyvitamin D3 responsible for binding to the receptor
pp. 979-984(6)
Authors: Yamamoto, K.; DeLuca, H.F.; Yamada, S.; Ohta, M.

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3-pyridines as replacements for an isoxazole ring: the antirhinoviral activity of pyridine analogues related to disoxaril
pp. 985-990(6)
Authors: Bailey, T.R.; Diana, G.D.; Draper, T.L.; Vescio, N.; Nitz, T.J.; Pevear, D.C.; Dutko, F.J.

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Phenyl pyrrolidine analogues as potent nicotinic acetylcholine receptor (nAChR) ligands
pp. 991-996(6)
Authors: Elliott, R.L.; Ryther, K.B.; Anderson, D.J.; Raszkiewicz, J.L.; Campbell, J.E.; Sullivan, J.P.; Garvey, D.S.

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Reduced amide bond neurotensin 8-13 mimetics with potent in vivo activity.
pp. 997-1002(6)
Authors: Wustrow, D.J.; Davis, M.D.; Akunne, H.C.; Corbin, A.E.; Wiley, J.N.; Wise, L.D.; Heffner, T.G.

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Synthesis and Bioassay of a Protein Tyrosine Phosphatase Inhibitor, Dephostatin
pp. 1003-1006(4)
Authors: Yu, L.; McGill, A.; Ramirez, J.; Wang, P.G.; Zhang, Z.

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Selective inhibition of the tyrosine kinase pp60src by analogs of 5,10-dihydropyrimido[4,5-b]quinolin-4(1H)-one
pp. 1007-1010(4)
Authors: Dow, R.L.; Bechle, B.M.; Chou, T.T.; Goddard, C.; Larson, E.R.

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Resolution and comparative anti-HIV evaluation of the enantiomers of calanolides A and B
pp. 1011-1014(4)
Authors: Cardellina, J.H.; Bokesch, H.R.; McKee, T.C.; Boyd, M.R.

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Synthesis and pharmacological evaluation of a novel series of 5-aryl benzimidazole angiotensin II receptor antagonists
pp. 1015-1020(6)
Authors: Palkowitz, A.D.; Steinberg, M.I.; Zimmerman, K.M.; Thrasher, K.J.; Hauser, K.L.; Boyd, D.B.

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3-benzyl-quinolones: novel, potent inhibitors of mammalian topoisomerase II.
pp. 1021-1026(6)
Authors: Eissenstat, M.A.; Kuo, G.; Weaver, J.D.; Wentland, M.P.; Robinson, R.G.; Klingbeil, K.M.; Danz, D.W.; Corbett, T.H.; Coughlin, S.A.

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