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Publisher: Elsevier

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Volume 6, Number 10, 21 May 1996

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Synthesis and biological activity of conformationally restricted tricyclic analogs of the hormone melatonin
pp. 1071-1076(6)
Authors: Leclerc, V.; depreux, P.; Lesieur, D.; Caignard, D.H.; Renard, P.; delagrange, P.; Guardiola-Lemaitre, B.; Morgan, P.

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Synthesis, biological activity and quantitative structure-activity relationships of N-substituted-3,4-dihydro-2H-1-benzopyran derivatives
pp. 1077-1082(6)
Authors: Marot, C.; Comoy, C.; Viaud, M.C.; Rettori, M.C.; Pfeiffer, B.; Morin-Allory, L.; Guillaumet, G.

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Synthesis of (9S,12S)-cycloisodityrosine and its unnatural (9R,12S)-diastereomer
pp. 1089-1092(4)
Authors: Boger, D.L.; Jiacheng, Z.; Borzilleri, R.M.; Nukui, S.

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DNA cleavage of novel propargylic sulfones. Enhancement of potency via intercalating interaction
pp. 1093-1098(6)
Authors: Wei-Min, D.; Kin Chiu, F.; Solow, M.; Wing Leung, M.; Mau Lam, Y.; Danjo, H.; Sei-ichi, N.

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A topliss tree analysis of the HIV-protease inhibitory activity of 6-phenyl-4-hydroxy-pyran-2-ones
pp. 1099-1104(6)
Authors: Steinbaugh, B.A.; Hamilton, H.W.; Vara Prasad, J.V.N.; Para, K.S.; Tummino, P.J.; Ferguson, D.; Lunney, E.A.; Blankley, C.J.

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Synthesis and radical scavenging activity of 3,3-dialkyl-3,4-dihydro-isoquinoline 2-oxides
pp. 1105-1110(6)
Authors: Bernotas, R.C.; Thomas, C.E.; Carr, A.A.; Nieduzak, T.R.; Adams, G.; Ohlweiler, D.F.; Hay, D.A.

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Synthesis and in vitro cytotoxicity of cryptophycins and related analogs
pp. 1111-1116(6)
Authors: de Muys, J.; Rej, R.; Nguyen, D.; Go, B.; Fortin, S.; Lavallee, J.

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Synthesis of C2-symmetrical polyhydroxyazepanes as inhibitors of glycosidases
pp. 1117-1122(6)
Authors: Xinhua, Q.; Moris-Varas, F.; Chi-Huey, W.

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Synthesis of lactosamine derivatives using -d-galactosidase from Bacillus circulans
pp. 1123-1126(4)
Authors: Takayama, S.; Shimazaki, M.; Lei, Q.; Chi-Huey, W.

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Studies on irreversible inhibition of serine proteases by α-sulfonyloxyketone derivatives
pp. 1127-1132(6)
Authors: Ohba, T.; Wakayama, J.; Ikeda, E.; Takei, H.

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Nonpeptidic HIV protease inhibitors: 3-(S-benzyl substituted)-4-hydroxy-6-(phenyl substituted)-2H-pyran-2-one with an inverse mode of binding
pp. 1133-1138(6)
Authors: Prasad, J.V.N.V.; Pavlovsky, A.; Para, K.S.; Ellsworth, E.L.; Tummino, P.J.; Nouhan, C.; Ferguson, D.

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Suppression of morphine and cocaine self-administration in rats by a mixed mu antagonist-kappa agonist (N-CBM-TAMO) and a long-acting selective D1 antagonist (AS-300)
pp. 1139-1144(6)
Authors: Archer, S.; Glick, S.D.; Maisonneuve, I.M.; Bidlack, J.M.; Xu, J.Y.; Teitler, M.; Sebastian, A.; El-Hamouly, W.; Hutchinson, I.

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Synthesis and SAR of diiodotyrosine-derived glycine-site N-methyl-d-aspartate receptor ligands
pp. 1145-1150(6)
Authors: Curtis, N.R.; Kulagowski, J.J.; Leeson, P.D.; Mawer, I.M.; Ridgill, M.P.; Rowley, M.; Grimwood, S.; Marshall, G.R.

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Dipeptide mimetics can substitute for the receptor activation domain resulting in highly potent analogues of hPTH(1-36) fragment
pp. 1151-1156(6)
Authors: Waelchli, R.; Gamse, R.; Bauer, W.; Meigel, H.; Lier, E.; Feyen, J.H.M.

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Structural characterization of a flavin-specific RNA aptamer by chemical probing
pp. 1157-1162(6)
Authors: Burgstaller, P.; Famulok, M.

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2-Cyanopyrrolidides as potent, stable inhibitors of dipeptidyl peptidase IV
pp. 1163-1166(4)
Authors: Ashworth, D.M.; Atrash, B.; Baker, G.R.; Baxter, A.J.; Jenkins, P.D.; Jones, D.M.; Szelke, M.

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The phototrityl group. Photocrosslinking of oligonucleotides to BSA
pp. 1167-1170(4)
Authors: Bidaine, A.; Berens, C.; Sonveaux, E.

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The synthesis of a radioligand with high potency and selectivity for CCKB/gastrin receptors
pp. 1171-1174(4)
Authors: Kalindjian, S.B.; Harper, E.A.; Pether, M.J.

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Rapid synthesis and properties of (+/-)-6-deoxy-6-fluoro-myo-inositol-1,4,5-tris(phosphate) an analogue of myo-inositol-1,4,5-tris(phosphate).
pp. 1175-1178(4)
Authors: Guedat, P.; Poitras, M.; Spiess, B.; Guillemette, G.; Schlewer, G.

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Site-specific 15N-labelling of Adenine in DNA for NMR Studies
pp. 1179-1182(4)
Authors: Yao-Zhong, X.; Ramesh, V.; Swann, P.F.

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Phosphoramidate derivatives of d4T with improved anti-HIV efficacy retain full activity in thymidine kinase-deficient cells
pp. 1183-1186(4)
Authors: McGuigan, C.; Cahard, D.; Sheeka, H.M.; de Clercq, E.; Balzarini, J.

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1-o-, 2-o- and 3-o--glycosyl-sn-glycerols: structure - anti-tumor-promoting activity relationship
pp. 1187-1190(4)
Authors: Colombo, D.; Scala, A.; Taino, I.M.; Toma, L.; Ronchetti, F.; Tokuda, H.; Nishino, H.; Nagatsu, A.; Sakakibara, J.

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