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Publisher: Elsevier

Volume 5, Number 15, 3 August 1995

Methylenedioxyphenyl substituted compounds from piper species as inhibitors of liver microsome-mediated aflatoxin B1-DNA binding in vitro
pp. 1567-1572(6)
Authors: Raj, H.G.; Gupta, S.; Prasad, A.K.; Boll, P.M.; Wengel, J.; Biswas, G.; Singh, S.K.; Sharma, N.K.; Bisht, K.S.; Parmar, V.S.

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Preparation of Oligonucleotide-Dexamethasone conjugates
pp. 1577-1580(4)
Authors: Acedo, M.; Tarrason, G.; Piulats, J.; Mann, M.; Wilm, M.; Eritja, R.

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Synthesis and pharmacological profile of FCE 28654: A water-soluble and injectable ACAT inhibitor
pp. 1581-1586(6)
Authors: Chiari, A.; Fancelli, D.; Lovisolo, P.P.; Radice, A.; Savoia, L.; Severino, D.; Ghiselli, G.

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Synthesis of -keto and α,-unsaturated n-acetylcysteamine thioesters
pp. 1587-1590(4)
Authors: Gilbert, I.H.; Ginty, M.; O'Neill, J.A.; Simpson, T.J.; Staunton, J.; Willis, C.L.

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RES-701-1, comparative study of the synthetic and the microbial-origin compounds
pp. 1595-1600(6)
Authors: Katahira, R.; Shibata, K.; Yamasaki, M.; Matsuda, Y.; Yoshida, M.

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Effects of 10-n-Butyl-3-methyl-5-deazaflavo-6,9-quinone (5-dFlQ) on Mitochondrial Respiration
pp. 1601-1604(4)
Authors: Konobu, K.; Toyomoto, M.; Murai, Y.; Yamamoto, E.; Kimachi, T.; Bessho, K.; Yoneda, F.

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Substrate Specificity of Farnesyl Diphosphate Synthase from Bacillus stearothermophilus
pp. 1605-1608(4)
Authors: Maki, Y.; Masukawa, A.; Ono, H.; Endo, T.; Koyama, T.; Ogura, K.

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Specific affinity labeling of  opioid receptors in rat brain by S-activated sulfhydryldihydromorphine analogs
pp. 1609-1614(6)
Authors: Sagara, T.; Okamura, M.; Shimohigashi, Y.; Ohno, M.; Kanematsu, K.

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Evolution of a series of non-quinoline leukotriene D4 receptor antagonist; synthesis and sar of benzothiazoles and thiazoles substituted benzyl alcohols as potent ltd4 antagonists
pp. 1615-1620(6)
Authors: Lau, C.K.; Dufresne, C.; Gareau, Y.; Zamboni, R.; Labelle, M.; Young, R.N.; Metters, K.M.; Rochette, C.; Sawyer, N.; Slipetz, D.M.; Charette, L.; Jones, T.; McAuliffe, M.; McFarlane, C.; Ford-Hutchinson, A.W.

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Palladium-catalyzed synthesis of (E)-5-(2-acylvinyl)-2'-deoxyuridines and their antiviral and cytotoxic activities
pp. 1627-1632(6)
Authors: Kundu, N.G.; Mahanty, J.S.; Spears, C.P.; Andrei, G.; Snoeck, R.; Balzarini, J.; de Clercq, E.

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Inhibition of Metalloproteinase by Futoenone Derivatives
pp. 1637-1642(6)
Authors: Yeh, L.; Chen, J.; Baculi, F.; Gingrich, D.E.; Shen, T.Y.

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3,4-Diesters of Zaragozic Acid A
pp. 1643-1646(4)
Authors: Chiang, Y.; Kurtz, M.M.; Bergstrom, J.D.; Berger, G.D.

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Synthesis of Thymidine Dimers Containing a New Internucleosidic Amide Linkage and their Incorporation into Oligodeoxyribonucleotides
pp. 1647-1652(6)
Authors: de Napoli, L.; Iadonisi, A.; Montesarchio, D.; Varra, M.; Piccialli, G.

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Synthesis of a fluorescent labeled thromboxane A2 receptor antagonist
pp. 1653-1656(4)
Authors: Prakash, C.; Saleh, S.; Murray, R.; FitzGerald, G.A.; Blair, I.A.

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WIN 70197: A novel liver-targeted magnetic resonance imaging contrast agent
pp. 1657-1662(6)
Authors: Caulfield, T.J.; Guo, P.; Illig, C.R.; Kellar, K.E.; Liversidge, E.; Shen, J.; Wellons, J.; Ladd, D.; Peltier, N.; Toner, J.L.

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Inactivation of carboxypeptidase a by 2-benzyl-3,4-epithiobutanoic acid
pp. 1667-1672(6)
Authors: Kim, D.H.; Chung, S.J.

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Molecular modelling of inhibitors of aromatase - a novel approach
pp. 1673-1678(6)
Authors: Ahmed, S.; Davis, P.J.

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Enzymatic synthesis of 1-(2-deoxy--d-ribofuranosyl) imidazole-4-carboxamide, a simplified DNA building block
pp. 1679-1684(6)
Authors: Pochet, S.; Dugue, L.; Meier, A.; Marliere, P.

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Nucleosides and nucleotides. 142. An alternative synthesis of 9-(5,6-dideoxy--d-ribo-hex-5-ynofuranosyl) adenine and its antiviral activity
pp. 1685-1688(4)
Authors: Matsuda, A.; Kosaki, H.; Yoshimura, Y.; Shuto, S.; Ashida, N.; Konno, K.; Shigeta, S.

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9-Aminoacridine-EDTA conjugates as hydroxy radical footprinting reagents with no intrinsic cutting specificity
pp. 1689-1694(6)
Authors: Chiu, F.C.K.; Brownlee, R.T.C.; Mitchell, K.; Phillips, D.R.

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Enzymatic cyclization of 1,N6-etheno-nicotinamide adenine dinucleotide
pp. 1701-1706(6)
Authors: Fang-Jie, Z.; Sih, C.J.

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Symmetry-based HIV protease inhibitors: rational design of 2-methylbenzamides as novel P2/P2' ligands
pp. 1707-1712(6)
Authors: Randad, R.S.; Lubkowska, L.; Bhat, T.N.; Munshi, S.; Gulnik, S.V.; Yu, B.; Erickson, J.W.

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17-hydroxywortmannin: a potent inhibitor or bone resorption and phosphatidylinositol-3-kinase
pp. 1713-1718(6)
Authors: Dodge, J.A.; Bryant, H.U.; Kim, J.; Matter, W.F.; Norman, B.H.; Srinivasan, U.; Vlahos, C.J.; Sato, M.

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Design, Synthesis and X-ray Crystallographic Studies of Novel FKBP-12 Ligands
pp. 1719-1724(6)
Authors: Babine, R.E.; Bleckman, T.M.; Kissinger, C.R.; Showalter, R.; Pelletier, L.A.; Lewis, C.; Tucker, K.; Moomaw, E.; Parge, H.E.; Villafranca, J.E.

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Modifications of the MeBmt Side Chain of Cyclosporin A
pp. 1725-1728(4)
Authors: Eberle, M.K.; Jutzi-Eme, A.; Nuninger, F.

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α-hydroxyamide derived aminodiols as potent inhibitors of HIV protease
pp. 1729-1734(6)
Authors: Ahmad, S.; Ashfaq, A.; Alam, M.; Bisacchi, G.S.; Chen, P.; Cheng, P.T.W.; Greytok, J.A.; Hermsmeier, M.A.; Pin-Fang, L.; Lis, K.A.; Merchant, Z.; Mitt, T.; Skoog, M.; Spergel, S.H.; Tino, J.A.; Vite, G.D.; Colonno, R.J.; Zahler, R.; Barrish, J.C.

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Synthesis of racemic 2-phosphonomethyl-1,3-dioxolane nucleoside analogues as potential antiviral agents
pp. 1741-1744(4)
Authors: Bednarski, K.; Dixit, D.M.; Mansour, T.S.; Colman, S.G.; Walcott, S.M.; Ashman, C.

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Analogs of UK 14,304: structural features responsible for α2 adrenoceptor activity
pp. 1745-1750(6)
Authors: Munk, S.A.; Harcourt, D.; Arasasingham, P.; Gluchowski, C.; H., W.; Burke, J.; Kharlamb, A.; Manlapaz, C.; Padillo, E.; Williams, L.; Wheeler, L.; Garst, M.

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Design, synthesis and evaluation of C/D-ring analogs of the fungal metabolite K-76 as potential complement inhibitors
pp. 1751-1755(5)
Authors: Srivastava, R.P.; Xiaoyan, Z.; Walker, L.A.; Sindelar, R.D.

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