Publisher: Elsevier

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Volume 8, Number 12, 16 June 1998

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Broad spectrum matrix metalloproteinase inhibitors: an examination of succinamide hydroxamate inhibitors with P1Cα gem-disubstitution
pp. 1443-1448(6)
Authors: Curtin, M.L.; Garland, R.B.; Davidsen, S.K.; Marcotte, P.A.; Albert, D.H.; Magoc, T.J.; Hutchins, C.

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Functionalization of a viscosity-sensitive fluorophore for probing of biological systems
pp. 1455-1460(6)
Authors: Petric, A.; Jacobson, A.F.; Barrio, J.R.

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5-alkyl-2-[(methylthiomethyl)thio]-6-(benzyl)-pyrimidin-4-(1H)-ones as potent non-nucleoside reverse transcriptase inhibitors of S-DABO series
pp. 1461-1466(6)
Authors: Vig, R.; Mao, C.; Venkatachalam, T.K.; Tuel-Ahlgren, L.; Sudbeck, E.A.; Uckun, F.M.

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Inhibition of electric eel acetylcholinesterase by porphin compounds
pp. 1467-1470(4)
Authors: Lee, B.H.; Park, M.B.; Soo Yu, B.

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2(1H)-Quinolinone derivatives as novel anti-arteriostenotic agents showing anti-thrombotic and anti-hyperplastic activities
pp. 1471-1476(6)
Authors: Koga, Y.; Kihara, Y.; Okada, M.; Inoue, Y.; Tochizawa, S.; Toga, K.; Tachibana, K.; Kimura, Y.; Nishi, T.; Hidaka, H.

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Peptidyl -homo-aspartals: specific inhibitors of interleukin-1 converting enzyme and its homologues (caspases)
pp. 1477-1482(6)
Authors: Bajusz, S.; Fauszt, I.; Nemeth, K.; Barabas, E.; Juhasz, A.; Patthy, M.

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8-Aminoquinolines as anticoccidials - II
pp. 1487-1492(6)
Authors: Armer, R.E.; Barlow, J.S.; Dutton, C.J.; Greenway, D.H.J.; Greenwood, S.D.W.; Lad, N.; Thompson, A.P.; Thong, K.; Tommasini, I.

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N-[4-(1,1?-biphenyl)methyl]-4-(4-thiomorpholinylmethyl) benzenamines as non-oxazolidinone analogues of antimycobacterial U-100480
pp. 1493-1498(6)
Authors: Artico, M.; Mai, A.; Sbardella, G.; Massa, S.; Lampis, G.; deidda, D.; Pompei, R.

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Isoindolinone enantiomers having affinity for the dopamine D4 receptor
pp. 1499-1502(4)
Authors: Belliotti, T.R.; Brink, W.A.; Kesten, S.R.; Rubin, J.R.; Wustrow, D.J.; Zoski, K.T.; Whetzel, S.Z.; Corbin, A.E.; Pugsley, T.A.; Heffner, T.G.; Wise, L.D.

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Syntheses of two enantiomeric pairs of myo-inositol(1,2,4,5,6) and -(1,2,3,4,5) pentakisphosphate
pp. 1503-1506(4)
Authors: Chung, S.; Chang, Y.; Eun, J.L.; Shin, B.; Kwon, Y.; Kim, K.; Dong, H.L.; Kim, M.

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Synthesis and Pharmacological Activities of 13-Dehydro Derivatives of Primary Prostaglandins
pp. 1507-1510(4)
Authors: Tanami, T.; Kameo, K.; Ono, N.; Nakagawa, T.; Annou, S.; Tsuboi, M.; Tani, K.; Okamoto, S.; Sato, F.

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Synthesis and anti-HIV activities of urea-PETT analogs belonging to a new class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors
pp. 1511-1516(6)
Authors: Sahlberg, C.; Noreen, R.; Engelhardt, P.; Hogberg, M.; Kangasmetsa, J.; Vrang, L.; Hong, Z.

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Evaluation of phosphorus-containing inhibitors of -glutamyl hydrolase
pp. 1521-1524(4)
Authors: Rodriguez, C.E.; Holmes, H.M.; Mlodnosky, K.L.; Lam, V.Q.; Berkman, C.E.

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Synthesis and in vitro cytotoxicity of lipophilic platinum(II) complexes
pp. 1525-1530(6)
Authors: Kokotos, G.; Theodorou, V.; Constantinou-Kokotou, V.; Gibbons, W.A.; Roussakis, C.

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Design and Synthesis of an Orally Active GPIIb/IIIa Antagonist Based on a Phenylpiperazine Scaffold
pp. 1531-1536(6)
Authors: van Maarseveen, J.H.; den Hartog, J.A.J.; Tipker, K.; Reinders, J.; Brakkee, J.; Schon, U.; Kehrbach, W.; Kruse, C.G.

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A Potent Dipeptide Inhibitor of Dipeptidyl Peptidase IV
pp. 1537-1540(4)
Authors: Yamada, M.; Okagaki, C.; Higashijima, T.; Tanaka, S.; Ohnuki, T.; Sugita, T.

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Synthesis and NK1 Receptor Antagonistic Activity of (±)-1-Acyl-3-(3,4-dichlorophenyl)-3-[2-(spiro-substituted piperidin-1?-yl)ethyl]piperidines
pp. 1541-1546(6)
Authors: Kubota, H.; Okamoto, Y.; Fujii, M.; Ikeda, K.; Takeuchi, M.; Shibanuma, T.; Isomura, Y.

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Synthesis and antitumor activity of 4-phenyl-1-arylsulfonyl imidazolidinones
pp. 1547-1550(4)
Authors: Jung, S.; Lee, H.; Song, J.; Kim, H.; Han, S.; Lee, C.; Moonsun, L.; Choi, D.; Lee, J.; Chung, Y.; Yoon, S.; Moon, E.; Hwang, H.; Seong, S.; Lee, D.

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Modulation of multidrug resistance by Taxuspine C and other taxoids from Japanese yew
pp. 1555-1558(4)
Authors: Kobayashi, J.; Hosoyama, H.; Wang, X.; Shigemori, H.; Sudo, Y.; Tsuruo, T.

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A New Class of Sulfoxide Surfactants derived from Tris. Synthesis and Preliminary Assessments of their Properties
pp. 1559-1562(4)
Authors: Barthelemy, P.; Maurizis, J.C.; Lacombe, J.M.; Pucci, B.

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Synthesis and pharmacology of N-alkylated derivatives of the excitotoxin ibotenic acid
pp. 1563-1568(6)
Authors: Madsen, U.; Dumpis, M.A.; Brauner-Osborne, H.; Piotrovsky, L.B.

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Synthesis and preliminary evaluation of (S)-2-(4?-carboxycubyl)glycine, a new selective mGluR1 antagonist
pp. 1569-1574(6)
Authors: Pellicciari, R.; Costantino, G.; Giovagnoni, E.; Mattoli, L.; Brabet, I.; Pin, J.

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On the Preparative Use of Recombinant Pig α(1-3)Galactosyl-Transferase
pp. 1575-1578(4)
Authors: Baisch, G.; Ohrlein, R.; Kolbinger, F.; Streiff, M.

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