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Publisher: Elsevier

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Volume 8, Number 16, 18 August 1998

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Pyrazolo[1,5-a]pyrimidine CRF-1 receptor antagonists
pp. 2067-2070(4)
Authors: Wustrow, D.J.; Capiris, T.; Rubin, R.; Knobelsdorf, J.A.; Akunne, H.; Davis, M.D.; MacKenzie, R.; Pugsley, T.A.; Zoski, K.T.; Heffner, T.G.; Wise, L.D.

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Kampanols: novel Ras farnesyl-protein transferase inhibitors from Stachybotrys kampalensis
pp. 2071-2076(6)
Authors: Singh, S.B.; Zink, D.L.; Williams, M.; Polishook, J.D.; Sanchez, M.; Silverman, K.C.; Lingham, R.B.

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Design and synthesis of conformationally-constrained MMP inhibitors
pp. 2077-2080(4)
Authors: Natchus, M.G.; Cheng, M.; Wahl, C.T.; Pikul, S.; Almstead, N.G.; Bradley, R.S.; Taiwo, Y.O.; Mieling, G.E.; Dunaway, C.M.; Snider, C.E.; McIver, J.M.; Barnett, B.L.; McPhail, S.J.; Anastasio, M.B.; de, B.

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Biological properties of synthetic glycoconjugate mimics of heparin comprising different molecular spacers
pp. 2081-2086(6)
Authors: Dreef-Tromp, C.M.; Basten, J.E.M.; Broekhoven, M.A.; van Dinther, T.G.; Petitou, M.; van Boeckel, C.A.A.

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The design, synthesis, and structure-activity relationships of a series of macrocyclic MMP inhibitors
pp. 2087-2092(6)
Authors: Steinman, D.H.; Curtin, M.L.; Garland, R.B.; Davidsen, S.K.; Heyman, H.R.; Holms, J.H.; Albert, D.H.; Magoc, T.J.; Nagy, I.B.; Marcotte, P.A.; Li, J.; Morgan, D.W.; Hutchins, C.; Summers, J.B.

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Antineoplastic agents 397: isolation and structure of sesterstatins 4 and 5 from Hyrtios erecta (the Republic of Maldives)
pp. 2093-2098(6)
Authors: Pettit, G.R.; Tan, R.; Melody, N.; Cichacz, Z.A.; Herald, D.L.; Hoard, M.S.; Pettit, R.K.; Chapuis, J.

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Identification of N2-(1-carboxymethyl)guanine (CMG) as a guanine advanced glycation end product
pp. 2109-2110(2)
Authors: Al-Abed, Y.; Schleicher, E.; Voelter, W.; Liebich, H.; Papoulis, A.; Bucala, R.

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3-pyridyloxypropanolamine agonists of the 3 adrenergic receptor with improved pharmacokinetic properties
pp. 2111-2116(6)
Authors: Weber, A.E.; Ok, H.O.; Alvaro, R.F.; Candelore, M.R.; Cascieri, M.A.; Chiu, S.; deng, L.; Forrest, M.J.; Hom, G.J.; Hutchins, J.E.; Kao, J.; MacIntyre, D.E.; Mathvink, R.J.; McLoughlin, D.; Miller, R.R.; Newbold, R.C.; Olah, T.V.; Parmee, E.R.; Perkins, L.; Stearns, R.A.; Strader, C.D.; Szumiloski, J.; Tang, Y.S.; Tota, L.; Vicario, P.P.; Wyvratt, M.J.; Fisher, M.H.

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Synthesis of novel substituted pyridines as inhibitors of endothelin converting enzyme-1 (ECE-1)
pp. 2117-2122(6)
Authors: Massa, M.A.; Patt, W.C.; Ahn, K.; Sisneros, A.M.; Herman, S.B.; Doherty, A.

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Probing the Importance of Spacial and Conformational Domains in Captopril Analogs for Angiotensin Converting Enzyme Activity
pp. 2123-2128(6)
Authors: Hanessian, S.; Reinhold, U.; Saulnier, M.; Claridge, S.

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The structure-activity relationships of a series of suicide inhibitors of phospholipase A2
pp. 2129-2132(4)
Authors: Yu, L.; Ternansky, R.J.; Victoria, E.J.; Chang, J.; Coutts, S.M.

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Solid phase synthesis of oligomannopeptoids that mimic the concanavalin A-binding trimannoside
pp. 2139-2144(6)
Authors: Yuasa, H.; Kamata, Y.; Kurono, S.; Hashimoto, H.

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Synthesis and biological activity of 2-methyl-20-EPI analogues of 1α,25-dihydroxyvitamin D3
pp. 2145-2148(4)
Authors: Fujishima, T.; Liu, Z.; Miura, D.; Chokki, M.; Ishizuka, S.; Konno, K.; Takayama, H.

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Novel H3 receptor antagonists. Sulfonamide homologs of histamine
pp. 2157-2162(6)
Authors: Wolin, R.; Connolly, M.; Afonso, A.; Hey, J.A.; She, H.; Rivelli, M.A.; Williams, S.M.; West, R.E.

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Novel imidazole derivatives with subtype-selective antimuscarinic activity (2)
pp. 2163-2168(6)
Authors: Miyachi, H.; Kiyota, H.; Segawa, M.

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A dipyrido [2,3-b:3',2'-f]azepine analog of the HIV-1 reverse transcriptase inhibitor nevirapine
pp. 2169-2172(4)
Authors: Dyatkin, A.B.; Brickwood, J.R.; Proudfoot, J.R.

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Conformationally restricted analogues of nicotine and anabasine
pp. 2173-2178(6)
Authors: Vernier, J.; Holsenback, H.; Cosford, N.D.P.; Whitten, J.P.; Menzaghi, F.; Reid, R.; Rao, T.S.; Sacaan, A.I.; Lloyd, G.K.; Suto, C.M.; Chavez-Noriega, L.E.; Washburn, M.S.; Urrutia, A.; McDonald, I.A.

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In vitro anti-human immunodeficiency virus (HIV) activity of the chromanone derivative, 12-oxocalanolide A, a novel NNRTI
pp. 2179-2184(6)
Authors: Xu, Z.; Buckheit, R.W.; Stup, T.L.; Flavin, M.T.; Khilevich, A.; Rizzo, J.D.; Lin, L.; Zembower, D.E.

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Synthesis and structure-activity relationships of 7-(2-aminoalkyl)morpholinoquinolones as anti-helicobacter pylori agents
pp. 2185-2190(6)
Authors: Sakurai, N.; Sano, M.; Hirayama, F.; Kuroda, T.; Uemori, S.; Moriguchi, A.; Yamamoto, K.; Ikeda, Y.; Kawakita, T.

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Hepatoprotective and nitric oxide production inhibitory activities of coumarin and polyacetylene constituents from the roots of Angelica furcijuga
pp. 2191-2196(6)
Authors: Matsuda, H.; Murakami, T.; Kageura, T.; Ninomiya, K.; Toguchida, I.; Nishida, N.; Yoshikawa, M.

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Isoxazolylthioamides as potential immunosuppressants a combinatorial chemistry approach
pp. 2203-2208(6)
Authors: Albert, R.; Knecht, H.; Andersen, E.; Hungerford, V.; Schreier, M.H.; Papageorgiou, C.

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Requirement of the Glycosyl Parts in Platycodin D to Stimulate Pancreatic Exocrine Secretion
pp. 2209-2212(4)
Authors: Ida, Y.; Hirai, Y.; Kajimoto, T.; Shingu, K.; Miura, T.; Kuwahara, N.; Taguchi, S.; Sasaki, K.; Kuroiwa, Y.; Yamamoto, T.; Arai, I.; Amagaya, S.; Komatsu, Y.

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The first analogues of LNA (locked nucleic acids): phosphorothioate-LNA and 2'-thio-LNA
pp. 2219-2222(4)
Authors: Kumar, R.; Singh, S.K.; Koshkin, A.A.; Rajwanshi, V.K.; Meldgaard, M.; Wengel, J.

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Enantioselective Synthesis and Pharmacology of 11-Hydroxy-(1'S,2'R)-Dimethylheptyl-Δ8-THC
pp. 2223-2226(4)
Authors: Liddle, J.; Huffman, J.W.; Wiley, J.L.; Martin, B.R.

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Synthesis of a Paclitaxel Isomer: C-2-Acetoxy-C-4-Benzoate Paclitaxel
pp. 2227-2230(4)
Authors: Chen, S.; Farina, V.; Vyas, D.M.; Doyle, T.W.

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A simple procedure for solid-phase synthesis of peptide nucleic acids with N-terminal cysteine
pp. 2231-2234(4)
Authors: Goodwin, T.E.; Holland, R.D.; Lay, J.O.; Raney, K.D.

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Design, synthesis, and biological activity of novel purine and bicyclic pyrimidine factor Xa inhibitors
pp. 2235-2240(6)
Authors: Buckman, B.O.; Mohan, R.; Koovakkat, S.; Liang, A.; Trinh, L.; Morrissey, M.M.

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Discovery of IRL 3461: a novel and potent endothelin antagonist with balanced ETA/ETB affinity
pp. 2241-2246(6)
Authors: Sakaki, J.; Murata, T.; Yuumoto, Y.; Nakamura, I.; Frueh, T.; Pitterna, T.; Iwasaki, G.; Oda, K.; Yamamura, T.; Hayakawa, K.

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Stereoselective synthesis of a novel and bifunctional endothelin antagonist, IRL 3630
pp. 2247-2252(6)
Authors: Sakaki, J.; Murata, T.; Yuumoto, Y.; Nakamura, I.; Hayakawa, K.

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C32-O-imidazol-2-yl-methyl ether derivatives of the immunosuppressant ascomycin with improved therapeutic potential
pp. 2253-2258(6)
Authors: Goulet, M.T.; McAlpine, S.R.; Staruch, M.J.; Koprak, S.; Dumont, F.J.; Cryan, J.G.; Wiederrecht, G.J.; Rosa, R.; Wilusz, M.B.; Peterson, L.B.; Wyvratt, M.J.; Parsons, W.H.

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L-tryptophan urea amides as NK1/NK2 dual antagonists
pp. 2259-2262(4)
Authors: Qi, H.; Shah, S.K.; Cascieri, M.A.; Sadowski, S.J.; MaCcoss, M.

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4 - [(1H - imidazol - 4 - yl) methyl] benzamidines and benzylamidines: novel antagonists of the histamine H3 receptor
pp. 2263-2268(6)
Authors: Aslanian, R.; Brown, J.E.; Shih, N.; wa Mutahi, M.; Green, M.J.; She, S.; del Prado, M.; West, R.; Hey, J.

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Alkyl side-chain derivatives of sordaricin as potent antifungal agents against yeast
pp. 2269-2272(4)
Authors: Tse, B.; Balkovec, J.M.; Blazey, C.M.; Hsu, M.; Nielsen, J.; Schmatz, D.

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