Anti-malarial activities of acylated bruceolide derivatives (English)
- New search for: Murakami, N.
- New search for: Murakami, N.
- New search for: Umezome, T.
- New search for: Mahmud, T.
- New search for: Sugimoto, M.
- New search for: Kobayashi, M.
- New search for: Wataya, Y.
- New search for: Kim, H.-S.
In:
Bioorganic & medicinal chemistry letters
;
8
, 5
; 459-462
;
1998
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ISSN:
- Article (Journal) / Print
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Title:Anti-malarial activities of acylated bruceolide derivatives
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Contributors:Murakami, N. ( author ) / Umezome, T. / Mahmud, T. / Sugimoto, M. / Kobayashi, M. / Wataya, Y. / Kim, H.-S.
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Published in:Bioorganic & medicinal chemistry letters ; 8, 5 ; 459-462
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Publisher:
- New search for: Elsevier
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Place of publication:Amsterdam [u.a.]
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Publication date:1998
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ISSN:
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ZDBID:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 35.70 / 44.33 / 44.42
- Further information on Basic classification
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Keywords:
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Classification:
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Source:
Table of contents – Volume 8, Issue 5
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 405
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Solid phase synthesis of a biased mini tetrapeptoid-library for the discovery of monodentate ITAM mimics as ZAP-70 inhibitorsRévész, L. et al. | 1998
- 409
-
Structure activity relationship study of known inhibitors of the enzyme 5a-reductase (5AR)Ahmed, S. et al. | 1998
- 409
-
Structure activity relationship study of known inhibitors of the enzyme 5-reductase (5AR)Ahmed, S. / Denison, S. et al. | 1998
- 415
-
Synthesis of a new class of camptothecin derivatives, the long-chain fatty acid esters of 10-hydroxycamptothecin, as a potent prodrug candidate, and their in vitro metabolic conversion by carboxylesterasesTakayama, H. et al. | 1998
- 419
-
Interpreting the effect of methyl group at the three carbon bridge of (-)-huperzine A on its anticholinesterase activity by molecular dynamics methodLiu, D. et al. | 1998
- 423
-
Stereoselective synthesis of 11Z-9-demethyl-9-benzyl- and 9-phenyl-retinals and their interaction with bovine opsinWada, A. et al. | 1998
- 427
-
Synthesis and cytotoxic activity of novel 10-alkylated docetaxel analogsNakayama, K. et al. | 1998
- 433
-
Solid phase synthesis of N-carboxy alkyl-containing peptides derived from enantiopure a-keto-b-aminoacidsFernández-Garcia, C. et al. | 1998
- 433
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Solid phase synthesis of N-carboxy alkyl-containing peptides derived from enantiopure -keto--aminoacidsFernandez-Garcia, C. / Prager, K. / McKervey, M. A. / Walker, B. / Williams, C. H. et al. | 1998
- 437
-
Synthetic arabinofuranosyl oligosaccharides as mycobacterial arabinosyltransferase substratesAyers, J.D. et al. | 1998
- 443
-
Bis(5-hydroxy-2-hydroxymethyl-pyran-4-one-6-yl)methane: A novel ligand for the intracellular mobilisation of ferritin-bound ironFox, R.C. et al. | 1998
- 447
-
a-Substituted quisqualic acid analogs: New metabotropic glutamate receptor group II selective antagonistsKozikowski, A.P. et al. | 1998
- 447
-
-Substituted quisqualic acid analogs: new metabotropic glutamate receptor group II selective antagonistsKozikowski, A. P. / Steensma, D. / Varasi, M. / Pshenichkin, S. / Surina, E. / Wroblewski, J. T. et al. | 1998
- 453
-
A series of non-quinoline cysLT1 receptor antagonists: SAR study on pyridyl analogs of Singulair(R)Guay, D. et al. | 1998
- 459
-
Anti-malarial activities of acylated bruceolide derivativesMurakami, N. et al. | 1998
- 463
-
Synthesis of 2,3,4a, 11b-tetrahydro-oxazino(2,3-c)benzopyran-9-carbonitriles as ATP-sensitive potassium channel openersCheng, C.-Y. et al. | 1998
- 469
-
Functionalized 1,3-teraryls as a new class of hepatoprotectants. Part 5Ram, V.J. et al. | 1998
- 473
-
Structure-activity relationships of a series of 1-substituted-4-methylbenzimidazole neuropeptide Y-1 receptor antagonistsZimmerman, D.M. et al. | 1998
- 477
-
New bronchodilators selected by molecular topologyRios-Santamarina, L. et al. | 1998
- 483
-
Nonpeptide glycoprotein IIb IIIa inhibitors: Substituted quinazolinediones and quinazolinones as potent fibrinogen receptor antagonistsLiverton, N.J. et al. | 1998
- 487
-
Synthesis of a potent wide-spectrum serotonin-, norepinephrine-, dopamine-reuptake inhibitor (SNDRI) and a species-selective dopamine-reuptake inhibitor based on the gamma-amino alcohol functional groupCarlier, P.R. et al. | 1998
- 493
-
5-Aminomethylquinoxaline-2,3-diones. Part 3: Arylamide derivatives as highly potent and selective glycine-site NMDA receptor antagonistsAcklin, P. et al. | 1998
- 493
-
5-Aminomethylquinoxaline-2,3-diones. Part 3: Arylamide derivatives as highly potent selective glycine-site NMDA receptor antagonistsAcklin, P. / Allgeier, H. / Auberson, Y. P. / Bischoff, S. / Ofner, S. / Sauer, D. / Schmutz, M. et al. | 1998
- 499
-
Recognition of 2'-deoxyisoguanosine triphosphate by HIV-1 reverse transcriptase and mammalian cellular DNA polymerasesLutz, M.J. et al. | 1998
- 505
-
Phosphodiesterase inhibitory properties of losartan. Design and synthesis of new lead compoundsSegarra, V. et al. | 1998
- 511
-
Solid-phase synthesis of peptidomimetic oligomers with a phosphodiester backboneLin, P. et al. | 1998
- 515
-
Novel bisphosphonate inhibitors of phosphoglycerate kinaseCaplan, N.A. et al. | 1998
- 521
-
2'-Deoxy-2'(S)-ethinyl oligonucleotides: A modification which selectively stabilizes oligoadenylate pairing to DNA complementsBuff, R. et al. | 1998
- 525
-
Novel quinolone derivatives as potent antibacterialsLohray, B.B. et al. | 1998
- 529
-
Discovery of a new cyclooxygenase-2 lead compound through 3-D database searching and combinatorial chemistryStewart, K.D. et al. | 1998
- 535
-
DNA cleavage by 7-methylbenzopentathiepin: A simple analog of the antitumor antibiotic varacinChatterji, T. et al. | 1998
- 539
-
Use of the 1,2,5-thiadiazolidin-3-one 1,1 dioxide and isothiazolidin-3-one 1,1 dioxide scaffolds in the design of potent inhibitors of serine proteinasesKuang, R. et al. | 1998
- 545
-
Indolequinone antitumor agents: Relationship between quinone structure and rate of metabolism by recombinant human NQO1Beall, H.D. et al. | 1998
- 549
-
Synthesis and antibacterial activity of o-methyl derivatives of azalide antibiotics: I. 4", 11 And 12-OMe derivatives via direct methylationWaddell, S. T. / Santorelli, G. M. / Blizzard, T. A. / Graham, A. / Occi, J. et al. | 1998
- 549
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Synthesis and antibacterial activity of O-methyl derivatives of azalide antibiotics. Part 1: 4",11 and 12-OMe derivatives via direct methylationWaddell, S.T. et al. | 1998
- 555
-
Modifications of the 4,4'-residues and SAR studies of Biphalin, a highly potent opioid receptor active peptideLi, G. et al. | 1998
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Graphical abstracts| 1998
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Contributors to this issue| 1998
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Tetrahedron prize for creativity in organic chemistry| 1998