Publisher: Elsevier

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Volume 6, Number 16, 20 August 1996

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Inactivation of serine protease, α-chymotrypsin by fluorinated phenylalanine analogues
pp. 1875-1880(6)
Authors: Ohba, T.; Ikeda, E.; Takei, H.

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Conformational analysis of meropenem and desmethyl meropenem: the effect of 1-methyl group on carbapenem antibiotics
pp. 1881-1886(6)
Authors: Igarashi, J.; Nishimura, T.; Sasaki, A.; Sunagawa, M.

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Synthesis and activity of staurosporine analogs with a lactone functionality
pp. 1893-1896(4)
Authors: Yamada, R.; Fukuda, K.; Kawanishi, M.; Ohmori, Y.; Nasu, M.; Seto, M.; Sasaki, Y.; Sunazuka, T.; Zhuorong, L.; Funato, N.; Iguchi, M.; Harigaya, Y.; Iwai, Y.; Omura, S.

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Synthesis of C-oxetanosyl-thiazole and its carbocyclic analog nucleosides as potential chemotherapeutic agents
pp. 1897-1900(4)
Authors: Kikuchi, Y.; Nishiyama, S.; Yamamura, S.; Kato, K.; Fujiwara, S.; Umezawa, K.; Terada, Y.

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Synthesis, characterization, and anti-HIV activity of some 2-p-X-phenyl-1,3-N,N'-diphenyl-amidines
pp. 1901-1904(4)
Authors: Echevarria, A.; Santos, L.H.; Miller, J.; Mahmood, N.

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Rapid synthesis of novel dipeptide inhibitors of human collagenase and gelatinase using solid phase chemistry
pp. 1905-1910(6)
Authors: Foley, M.A.; Hassman, A.S.; Drewry, D.H.; Greer, D.G.; Wagner, C.D.; Feldman, P.L.; Berman, J.; Bickett, D.M.; McGeehan, G.M.; Lambert, M.H.; Green, M.

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Thiono triester modified antisense oligonucleotides for inhibition of human cytomegalovirus in vitro
pp. 1911-1916(6)
Authors: Zhang, Z.; Smith, J.A.; Smyth, A.P.; Eisenberg, W.; Pari, G.S.; Tang, J.Y.

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Acyloxyaryl prodrugs of oligonucleoside phosphorothioates
pp. 1917-1922(6)
Authors: Iyer, R.P.; Dong, Y.; devlin, T.; Nan-hui, H.; Agrawal, S.

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Synthesis of azido derivatives of semotiadil, a novel 1,4-benzothiazine calcium antagonist, for photoaffinity probes of calcium channels
pp. 1923-1926(4)
Authors: Watanabe, Y.; Osanai, K.; Nishi, T.; Miyawaki, N.; Shii, D.; Honda, T.; Shibano, T.

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Synthesis and acetylcholinesterase inhibitory activity of fluorinated analogues of huperzine A
pp. 1927-1930(4)
Authors: Kaneko, S.; Nakajima, N.; Shikano, M.; Katoh, T.; Terashima, S.

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Design of MHC class II (DR4) ligands using conformationally restricted imino acids at p3 and p5
pp. 1931-1936(6)
Authors: Hanson, G.J.; Vuletich, J.L.; Bedell, L.J.; Bono, C.P.; Howard, S.C.; Welply, J.K.; Woulfe, S.L.; Zacheis, M.L.

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Aromatic P1 replacements for the highly potent HIV-1 protease inhibitor CRIXIVAN(R)
pp. 1937-1940(4)
Authors: Coburn, C.A.; Young, M.B.; Hungate, R.W.; Isaacs, R.C.A.; Vacca, J.P.; Huff, J.R.

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Stereoselective synthesis and biological activity of CIS azetidinones as cholesterol absorption inhibitors
pp. 1947-1950(4)
Authors: McKittrick, B.A.; Ke, M.; Dugar, S.; Clader, J.W.; Davis, H.; Czarniecki, M.; McPhail, A.T.

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Phosphonate-containing analogs of cholesteryl ester as novel inhibitors of cholesteryl ester transfer protein
pp. 1951-1954(4)
Authors: Pietzonka, T.; Damon, R.; Russell, M.; Wattanasin, S.

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Rapid assembly of ''subtiligase'' substrates to elucidate optimal ligation junctures
pp. 1961-1966(6)
Authors: Judice, J.K.; Namenuk, A.K.; Burnier, J.P.

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Target directed enediyne prodrugs: hER and AhR degradation by a synthetic oxo-enediyne
pp. 1971-1976(6)
Authors: Jones, G.B.; Kilgore, M.W.; Pollenz, R.S.; Li, A.; Mathews, J.E.; Wright, J.M.; Huber, R.S.; Tate, P.L.; Price, T.L.; Sticca, R.P.

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Synthesis of potential peptidomimetics based on highly substituted glucose and allose scaffolds.
pp. 1983-1988(6)
Authors: Le Diguarher, T.; Boudon, A.; Elwell, C.; Paterson, D.E.; Billington, D.C.

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p-Nitrophenyl 1,5-dithio-α-l-fucopyranoside: a novel sulfur based fucosidase inhibitor
pp. 1989-1992(4)
Authors: Tsuruta, O.; Yuasa, H.; Hashimoto, H.

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Utilization of wieland furoxan synthesis for preparation of 4-aryl-1,2,5-oxadiazole-3-yl carbamate derivatives having potent anti-HIV activity
pp. 1993-1996(4)
Authors: Takayama, H.; Shirakawa, S.; Kitajima, M.; Aimi, N.; Yamaguchi, K.; Hanasaki, Y.; Ide, T.; Katsuura, K.; Fujiwara, M.; Ijichi, K.; Konno, K.; Sigeta, S.; Yokota, T.; Baba, M.

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Synthesis of a chemiluminescent probe useful for the purification of steroid 5α-reductase
pp. 1997-2002(6)
Authors: Guarna, A.; Poletti, A.; Catrambone, F.; Danza, G.; Marrucci, A.; Serio, M.; Celotti, F.; Martini, L.

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Identification and stereochemistry of the product of 4-HPPD catalyzed oxidation of the ketoacid of methionine
pp. 2003-2006(4)
Authors: Adlington, R.M.; Baldwin, J.E.; Crouch, N.P.; Meng-Huee, L.; MacKinnon, C.H.

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Solid phase synthesis of peptides containing a phosphoserine - sulfur mustard adduct
pp. 2007-2012(6)
Authors: Noort, D.; Platenburg, D.H.J.M.; Benschop, H.P.

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Diphenylmethyl ethers: synthesis and histamine H3-receptor antagonist in vitro and in vivo activity
pp. 2013-2018(6)
Authors: Huls, A.; Purand, K.; Stark, H.; Ligneau, X.; Arrang, J.; Schwartz, J.; Schunack, W.

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Synthesis and biological evaluation of 4-alkoxy substituted trinems. Part I
pp. 2019-2024(6)
Authors: Andreotti, D.; Biondi, S.; Di Fabio, R.; Donati, D.; Piga, E.; Rossi, T.

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Synthesis and biological evaluation of 4-alkoxysubstituted trinems. Part II
pp. 2025-2030(6)
Authors: Di Fabio, R.; Andreotti, D.; Biondi, S.; Gaviraghi, G.; Rossi, T.

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Novel antifungal 2-aryl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol derivatives with high activity against aspergillus fumigatus.
pp. 2031-2036(6)
Authors: Dickinson, R.P.; Bell, A.S.; Hitchcock, C.A.; Narayanaswami, S.; Ray, S.J.; Richardson, K.; Troke, P.F.

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