Publisher: Elsevier

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Volume 12, Number 15, 5 August 2002

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Contents List
pp. ii

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Graphical Abstracts
pp. 1885-1894(10)

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Combinatorial synthesis and biological evaluation of isoxazole-based libraries as antithrombotic agents
pp. 1905-1908(4)
Authors: Batra, S.; Srinivasan, T.; Rastogi, S.K.; Kundu, B.; Patra, A.; Bhaduri, A.P.; Dixit, M.

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Synthesis and affinity studies of himbacine derived muscarinic receptor antagonists
pp. 1909-1912(4)
Authors: Gao, L.; Waelbroeck, M.; Hofman, S.; van Haver, D.; Milanesio, M.; Viterbo, D.; de Clercq, P.J.

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Synthesis of C-8 Alkylamino substituted pyrrolo[2,1-c][1,4]benzodiazepines as potential anti-Cancer agents
pp. 1917-1919(3)
Authors: Kamal, A.; Laxman, N.; Ramesh, G.; Srinivas, O.; Ramulu, P.

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Synthesis and anti-influenza virus activity of 4-guanidino-7-substituted Neu5Ac2en derivatives
pp. 1921-1924(4)
Authors: Honda, T.; Masuda, T.; Yoshida, S.; Arai, M.; Kobayashi, Y.; Yamashita, M.

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Synthesis and anti-Influenza virus activity of 7-O-Alkylated derivatives related to zanamivir
pp. 1925-1928(4)
Authors: Honda, T.; Masuda, T.; Yoshida, S.; Arai, M.; Kaneko, S.; Yamashita, M.

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Synthesis and anti-Influenza evaluation of polyvalent sialidase inhibitors bearing 4-guanidino-Neu5Ac2en derivatives
pp. 1929-1932(4)
Authors: Honda, T.; Yoshida, S.; Arai, M.; Masuda, T.; Yamashita, M.

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Design and synthesis of C-8 linked pyrrolobenzodiazepine-naphthalimide hybrids as anti-tumour agents
pp. 1933-1935(3)
Authors: Kamal, A.; Reddy, B.S.N.; Reddy, G.S.K.; Ramesh, G.

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Synthesis and PTP1B inhibition of 1,2-naphthoquinone derivatives as potent anti-diabetic agents
pp. 1941-1946(6)
Authors: Ahn, J.H.; Cho, S.Y.; Ha, J.D.; Chu, S.Y.; Jung, S.H.; Jung, Y.S.; Baek, J.Y.; Choi, I.K.; Shin, E.Y.; Kang, S.K.; Kim, S.S.; Cheon, H.G.; Yang, S.; Choi J.-K.

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Novel diphenylalkyl piperazine derivatives with dual calcium antagonistic and antioxidative activities
pp. 1947-1950(4)
Authors: Kimura, M.; Masuda, T.; Yamada, K.; Kubota, N.; Kawakatsu, N.; Mitani, M.; Kishii, K.; Inazu, M.; Namiki, T.

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The synthesis and effect of fluorinated chalcone derivatives on nitric oxide production
pp. 1951-1954(4)
Authors: Rojas, J.; Paya, M.; Dominguez, J.N.; Luisa Ferrandiz, M.

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Synthesis and anti-tumor activity of novel combretastatins: combretocyclopentenones and related analogues
pp. 1955-1958(4)
Authors: Nam, N.; Kim, Y.; You, Y.; Hong, D.; Kim, H.; Ahn B.-Z.

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Inhibition of ADP-triggered blood platelet aggregation by diadenosine polyphosphate analogues
pp. 1959-1962(4)
Authors: Walkowiak, B.; Baraniak, J.; Cierniewski, C.S.; Stec, W.

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Synthesis and application of an auxiliary group for chemical ligation at the X-gly site
pp. 1963-1965(3)
Authors: Vizzavona, J.; Dick, F.; Vorherr, T.

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Novel human metabolites of the angiotensin-II antagonist tasosartan and their pharmacological effects
pp. 1967-1971(5)
Authors: Elokdah, H.M.; Friedrichs, G.S.; Chai, S.; Harrison, B.L.; Primeau, J.; Chlenov, M.; Crandall, D.L.

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A solid-phase approach towards the synthesis of PDE5 inhibitors
pp. 1973-1976(4)
Authors: Beer, D.; Bhalay, G.; Dunstan, A.; Glen, A.; Haberthuer, S.; Moser, H.

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Base pairing properties of 8-oxo-7,8-dihydroadenosine in cDNA synthesis by reverse transcriptases
pp. 1977-1980(4)
Authors: Kim, S.K.; Kim, J.Y.; Baek, A.K.; Moon, B.J.

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A Convenient Synthesis of Δ7,8-Morphinan-6-one and Its Direct Oxidation to 14-Hydroxy-Δ7,8-morphinan-6-one
pp. 1981-1983(3)
Authors: Passarella, D.; Consonni, A.; Giardini, A.; Lesma, G.; Silvani, A.

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Discovery of non-Zwitterionic GABAA receptor full agonists and a superagonist
pp. 1985-1988(4)
Authors: Carlier, P.R.; Chow, E.S.; Barlow, R.L.; Bloomquist, J.R.

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A comparison of the binding of three series of nicotinic ligands
pp. 1989-1992(4)
Authors: Lee, M.; Dukat, M.; Liao, L.; Flammia, D.; Imad Damaj, M.; Martin, B.; Glennon, R.A.

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Novel cyclourethane-Derived HIV protease inhibitors: A ring-closing olefin metathesis based strategy
pp. 1993-1996(4)
Authors: Ghosh, A.K.; Swanson, L.M.; Liu, C.; Hussain, K.A.; Cho, H.; Walters, D.E.; Holland, L.; Buthod, J.

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N-[2-(Indan-1-yl)-3-mercapto-propionyl] amino acids as highly potent inhibitors of the three vasopeptidases (NEP, ACE, ECE): In vitro and In vivo activities
pp. 2001-2005(5)
Authors: Inguimbert, N.; Poras, H.; Teffo, F.; Beslot, F.; Selkti, M.; Tomas, A.; Scalbert, E.; Bennejean, C.; Renard, P.; Fournie-Zaluski, M.; Roques B.-P.

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Inhibition of feline immunodeficiency virus (FIV) replication by DNA binding polyamides
pp. 2007-2010(4)
Authors: Sharma, S.K.; Billaud, J.; Tandon, M.; Billet, O.; Choi, S.; Kopka, M.L.; Phillips, T.R.; Lown, J.W.

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Inhibition of Src kinase activity by 4-anilino-7-thienyl-3-quinolinecarbonitriles
pp. 2011-2014(4)
Authors: Boschelli, D.H.; Wang, D.Y.; Ye, F.; Yamashita, A.; Zhang, N.; Powell, D.; Weber, J.; Boschelli, F.

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Convergent synthesis of an inner core GPI of sperm CD52
pp. 2015-2018(4)
Authors: Xue, J.; Guo, Z.

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2-(2-Hydroxy-3-alkoxyphenyl)-1H-benzimidazole-5-carboxamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors
pp. 2019-2022(4)
Authors: Mackman, R.L.; Hui, H.C.; Breitenbucher, J.G.; Katz, B.A.; Luong, C.; Martelli, A.; McGee, D.; Radika, K.; Sendzik, M.; Spencer, J.R.; Sprengeler, P.A.; Tario, J.; Verner, E.; Wang, J.

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4-Aminoarylguanidine and 4-aminobenzamidine derivatives as potent and selective urokinase-type plasminogen activator inhibitors
pp. 2023-2026(4)
Authors: Spencer, J.R.; McGee, D.; Allen, D.; Katz, B.A.; Luong, C.; Sendzik, M.; Squires, N.; Mackman, R.L.

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The synthesis and biological evaluation of a series of potent dual inhibitors of farnesyl and geranyl-Geranyl protein transferases
pp. 2027-2030(4)
Authors: Tucker, T.J.; Abrams, M.T.; Buser, C.A.; Davide, J.P.; Ellis-Hutchings, M.; Fernandes, C.; Gibbs, J.B.; Graham, S.L.; Hartman, G.D.; Huber, H.E.; Liu, D.; Lobell, R.B.; Lumma, W.C.; Robinson, R.G.; Sisko, J.T.; Smith, A.M.

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Structure-activity relationships of non-imidazole H3 receptor ligands. Part 1
pp. 2031-2034(4)
Authors: Faghih, R.; Dwight, W.; Gentles, R.; Phelan, K.; Esbenshade, T.A.; Ireland, L.; Miller, T.R.; Kang, C.; Fox, G.B.; Gopalakrishnan, S.M.; Hancock, A.A.; Bennani, Y.L.

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Structure-Activity relationships of non-imidazole H3 Receptor ligands. Part 2: binding preference for d-Amino acids motifs
pp. 2035-2037(3)
Authors: Faghih, R.; Dwight, W.; Black, L.; Liu, H.; Gentles, R.; Phelan, K.; Esbenshade, T.A.; Ireland, L.; Miller, T.R.; Kang, C.; Krueger, K.M.; Fox, G.B.; Hancock, A.A.; Bennani, Y.L.

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Synthesis and biological evaluation of a spongistatin AB-spiroketal analogue
pp. 2039-2042(4)
Authors: Smith, A.B.; Corbett, R.M.; Pettit, G.R.; Chapuis, J.; Schmidt, J.M.; Hamel, E.; Jung, M.K.

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Substituted acrylamides as factor Xa inhibitors: improving bioavailability by P1 modification
pp. 2043-2046(4)
Authors: Song, Y.; Clizbe, L.; Bhakta, C.; Teng, W.; Li, W.; Wong, P.; Huang, B.; Sinha, U.; Park, G.; Reed, A.; Scarborough, R.M.; Zhu, B.

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Preparation of soluble and insoluble polymer supported IBX reagents
pp. 2047-2049(3)
Authors: Reed, N.N.; Delgado, M.; Hereford, K.; Clapham, B.; Janda, K.D.

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Erratum to ''Vitamin D3: Synthesis of seco C-9,11,21-trisnor-17-Methyl-1α,25-dihydroxyvitamin D3 Analogues'' [Bioorg. Med. Chem. Lett. 12 (2002) 1629]
pp. 2051-2051(1)
Authors: Wu, Y.; Sabbe, K.; de Clercq, P.; Vandewalle, M.; Bouillon, R.; Verstuyf, A.

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