Publisher: Elsevier

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Volume 5, Number 18, 21 September 1995

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Inhibitors of glucosidases with related structures and inverse specificity
pp. 2055-2058(4)
Authors: Therisod, M.; Therisod, H.; Lubineau, A.

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A New Deprotection Strategy for Automated Oligonucleotide Synthesis Using a Novel Silyl-Linked Solid Support
pp. 2059-2064(6)
Authors: Routledge, A.; Wallis, M.P.; Ross, K.C.; Fraser, W.

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Non-peptide neuropeptide Y antagonists derived from the histamine H2 agonist arpromidine: role of the guanidine group
pp. 2065-2070(6)
Authors: Knieps, S.; Michel, M.C.; Dove, S.; Buschauer, A.

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Uracil-based angiotensin II receptor antagonists
pp. 2071-2076(6)
Authors: Dorsch, D.; Mederski, W.W.K.R.; Osswald, M.; Beier, N.; Schelling, P.

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Synthesis and structure-activity relationships of new acetylcholinesterase inhibitors: morpholinoalkylcarbamoyloxyeseroline derivatives
pp. 2077-2080(4)
Authors: Alisi, M.A.; Brufani, M.; Filocamo, L.; Gostoli, G.; Licandro, E.; Cesta, M.C.; Lappa, S.; Marchesini, D.; Pagella, P.

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Incorporation of a pyrene nucleoside analogue into synthetic oligodeoxynucleotides using a nucleoside-like synthon
pp. 2081-2084(4)
Authors: Prokhorenko, I.A.; Korshun, V.A.; Petrov, A.A.; Gontarev, S.V.; Berlin, Y.A.

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Proctolin and related N-methylated pentapeptides selectively contract locust foregut but not rat ileum
pp. 2085-2088(4)
Authors: Osborne, R.H.; Odell, B.; Blagbrough, I.S.

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5,6,7,8-Tetrahydroquinolones as antagonists at the Glycine site of the NMDA receptor.
pp. 2089-2092(4)
Authors: Rowley, M.; Leeson, P.; Grimwood, S.; Marshall, G.; Saywell, K.

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Synthesis of Bisindolylmaleimide Macrocycles
pp. 2093-2096(4)
Authors: Jirousek, M.R.; Gillig, J.R.; Neel, D.A.; Rito, C.J.; O'Bannon, D.; Heath, W.F.; McDonald, J.H.; Faul, M.M.; Winneroski, L.L.; Melikian-Badalian, A.; Baevsky, M.; Ballas, L.M.; Hall, S.E.

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Synthesis and Antiplatelet Activity of DMP 757 Analogs
pp. 2097-2100(4)
Authors: Wityak, J.; Fevig, J.M.; Jackson, S.A.; Johnson, A.L.; Mousa, S.A.; Parthasarathy, A.; Wells, G.J.; DeGrado, W.F.; Wexler, R.R.

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Chiral spirocyclic benzopyran potassium channel openers: evidence for the active conformation of levcromakalim
pp. 2101-2104(4)
Authors: Gadwood, R.C.; Thomasco, L.M.; Groppi, V.E.; Burnett, B.; Humphrey, S.J.; Smith, M.P.; Watt, W.

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Synthesis and Evaluation of Nitro 5-Deazaflavins as Novel Bioreductive Antitumor Agents
pp. 2109-2114(6)
Authors: Kawamoto, T.; Ikeuchi, Y.; Hiraki, J.; Eikyu, Y.; Shimizu, K.; Tomishima, M.; Bessho, K.; Yoneda, F.; Mikata, Y.; Nishida, M.; Ikehara, K.; Sasaki, T.

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Evaluation of Differential Hypoxic Cytotoxicity and Electrochemical Studies of Nitro 5-Deazaflavins
pp. 2115-2118(4)
Authors: Kawamoto, T.; Ikeuchi, Y.; Hiraki, J.; Eikyu, Y.; Shimizu, K.; Tomishima, M.; Bessho, K.; Yoneda, F.; Mikata, Y.; Nishida, M.; Ikehara, K.

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RS-100235: a high affinity 5-HT4 receptor antagonist
pp. 2119-2122(4)
Authors: Clark, R.D.; Jahangir, A.; Flippin, L.A.; Langston, J.A.; Leung, E.; Bonhaus, D.W.; Wong, E.H.F.; Johnson, L.G.; Eglen, R.M.

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Synthesis and biological evaluation of 2,3-diarylthiophenes as selective Cox-2 and Cox-1 inhibitors
pp. 2123-2128(6)
Authors: Leblanc, Y.; Gauthier, J.Y.; Ethier, D.; Guay, J.; Mancini, J.; Riendeau, D.; Tagari, P.; Vickers, P.; Wong, E.; Prasit, P.

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Novel A-ring modified camptothecins as topoisomerase I inhibitors
pp. 2129-2132(4)
Authors: Peel, M.R.; Milstead, M.W.; Sternbach, D.D.; Besterman, J.M.; Leitner, P.; Morton, B.; Wall, M.E.; Wani, M.C.

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Increasing the cellular PKC inhibitory activity of balanol: a study of ester analogs
pp. 2133-2138(6)
Authors: Crane, H.M.; Menaldino, D.S.; Jagdmann, G.E.; Darges, J.W.; Buben, J.A.

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Synthetic inhibitors of interleukin-6 I: 2,3,7,8-tetrahydro-4-aryl-1h-cyclopent [e] imidazo [1,2-a]- pyridin-5(6H)-one and related compounds
pp. 2139-2142(4)
Authors: Tagat, J.R.; Nazareno, D.V.; McCombie, S.W.; Barton, B.E.; Shortall, J.; Jackson, J.

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Synthetic inhibitors of interleukin-6 II: 3,5-diaryl pyridines and meta-terphenyls
pp. 2143-2146(4)
Authors: Tagat, J.R.; McCombie, S.W.; Barton, B.E.; Jackson, J.; Shortall, J.

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Ring size effect in the PKC inhibitory activities of perhydroazepine analogs of balanol
pp. 2151-2154(4)
Authors: Yen-Shi, L.; Menaldino, D.S.; Nichols, J.B.; Jagdmann, G.E.; Mylott, F.; Gillespie, J.; Hall, S.E.

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Synthesis and PKC inhibitory activities of balanol analogs with a cyclopentane substructure
pp. 2155-2160(6)
Authors: Yen-Shi, L.; Mendoza, J.S.; Hubbard, F.; Kalter, K.

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1α,25-Dihydroxyvitamin D3 Hybrid Analogs with Structural Changes at Both the A-Ring and the C,D-Ring Side-chain. II
pp. 2163-2168(6)
Authors: Posner, G.H.; Jae, K.L.; Zhengong, L.; Takeuchi, K.; Guggino, S.E.; Dolan, P.; Kensler, T.W.

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Preparation of substituted chlorins and benzochlorins
pp. 2175-2178(4)
Authors: Kohli, D.H.; Morgan, A.R.

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Molecular design of novel PGI2 agonists without PG skeleton
pp. 2179-2179(1)
Authors: Hamanaka, N.; Takahashi, K.; Nagao, Y.; Torisu, K.; Tokumoto, H.; Kondo, K.

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