Design, Synthesis and DNA-Cleavage of Gly-Gly-His-Naphthalene Diimide Conjugates (English)
- New search for: Steullet, V.
- New search for: Dixon, D.W.
- New search for: Steullet, V.
- New search for: Dixon, D.W.
In:
BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS
;
9
, 20
;
2935-2940
;
1999
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ISSN:
- Article (Journal) / Print
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Title:Design, Synthesis and DNA-Cleavage of Gly-Gly-His-Naphthalene Diimide Conjugates
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Contributors:Steullet, V. ( author ) / Dixon, D.W. ( author )
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Published in:BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS ; 9, 20 ; 2935-2940
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Publisher:
- New search for: PERGAMON PRESS
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Publication date:1999-01-01
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Size:6 pages
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ISSN:
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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: 572.5
- Further information on Dewey Decimal Classification
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Classification:
DDC: 572.5 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 9, Issue 20
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.
- 2903
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Studies on the synthesis and properties of new PNA analogs consisting of L- and D-lysine backbonesZhang, L. et al. | 1999
- 2909
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3-Acyloxy-2-phenalkylpropyl amides and esters of homovanillic acid as novel vanilloid receptor agonistsLee, J. et al. | 1999
- 2915
-
Mapping the X+1 binding site of the Grb2-SH2 domain with a,a-disubstituted cyclic a-amino acidsGarcia-Echeverria, C. et al. | 1999
- 2921
-
Spiro-Imidazo[1,2-a]Indeno[1,2-e]Pyrazine-4-One Derivatives are Mixed AMPA and NMDA Glycine-Site Antagonists Active in vivoJimonet, P. / Boireau, A. / Cheve, M. / Damour, D. / Genevois-Borella, A. / Imperato, A. / Pratt, J. / Randle, J.C.R. / Ribeill, Y. / Stutzmann, J.-M. et al. | 1999
- 2921
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Spiro-imidazo(1,2-e)lindeno(1,2-e)pyrazine-4-one derivatives are mixed AMPA and NIVIDA glycine-site antagonists active in vivoJimonet, P. et al. | 1999
- 2927
-
Stabilization of microtubules by combretastatin D derivativesCouladouros, E.A. et al. | 1999
- 2929
-
Synthesis of novel orthoalkylaminophenol derivatives as potent neuroprotective agents in vitroLarget, R. et al. | 1999
- 2935
-
Design, synthesis and DNA-cleavage of Gly-Gly-His-naphthalene diimide conjugatesSteullet, V. et al. | 1999
- 2941
-
An efficient synthesis of two monosulfated trisaccharides with the Galb-1,3GIcNAcb1,3Galb-O-allyl backboneXia, J. et al. | 1999
- 2941
-
An Efficient Synthesis of Two Monosulfated Trisaccharides with the Gal@b1,3GlcNAc@b1,3Gal@b-O-Allyl BackboneXia, J. / Piskorz, C.F. / Locke, R.D. / Chandrasekaran, E.V. / Alderfer, J.L. / Matta, K.L. et al. | 1999
- 2947
-
6-Oxa isosteres of anacardic acids as potent inhibitors of bacterial histidine protein kinase (HPK)-mediated two-component regulatory systemsKanojia, R.M. et al. | 1999
- 2953
-
Guanidine-substituted imidazoles as inhibitors of nitric oxide synthaseAtkinson, R.N. et al. | 1999
- 2959
-
Inhibition of E coli growth by fullerene derivatives and inhibition mechanismMashino, T. et al. | 1999
- 2963
-
Synthesis and Biological Characterization of SQBAzide, a Novel Biotinylated Photoaffinity Probe for the Study of the Human Platelet Thromboxane A"2 ReceptorHalmos, T. / Turek, J.W. / Le Breton, G.C. / Antonakis, K. et al. | 1999
- 2963
-
Synthesis and biological characterization of SQBAzicle, a novel biotinylated photoaffinity probe for the study of the human platelet thromboxane A2 receptorHalmos, T. et al. | 1999
- 2969
-
Structure and antimalarial activity of adducts of 11-azaartemisinin with conjugated terminal acetylenesKatz, E. et al. | 1999
- 2973
-
The synthesis and anti-MRSA activity of amidinium-substituted 2- dibenzofuranylcarbapenemsLaub, J.B. et al. | 1999
- 2977
-
First systematic chiral syntheses of two pairs of enantiomers with 3,5-dihydroxyheptenoic acid chain, associated with a potent synthetic statin NK-104Suzuki, M. et al. | 1999
- 2983
-
New pyrrole derivatives as antimycobacterial agents analogs of BM212Biava, M. et al. | 1999
- 2989
-
Synthesis and fluorescence properties of Oregon Green 514 labeled peptidesDelmotte, C. et al. | 1999
- 2995
-
Synthesis and antitumor activity of water-soluble duocarmycin B1 prodrugsAsai, A. et al. | 1999
- 2999
-
A novel class of Na+ and Ca2+ channel dual blockers with highly potent anti-ischemic effectsAnnoura, H. et al. | 1999
- 3003
-
Design, synthesis and antimuscarinic activity of some imidazolium derivativesMiyachi, H. et al. | 1999
- 3009
-
Nonpeptidic SH2 inhibitors of the tyrosine kinase ZAP-70Vu, C.B. et al. | 1999
- 3015
-
Wasalexins A and B1 new phytoalexins from wasabi: Isolation, synthesis, and antifungal activityPedras, M.S.C. et al. | 1999
- 3015
-
Wasalexins A and B, New Phytoalexins from Wasabi: Isolation, Synthesis, and Antifungal ActivityPedras, M.S.C. / Sorensen, J.L. / Okanga, F.I. / Zaharia, I.L. et al. | 1999
- 3021
-
A new efficient synthesis of efaroxanMayer, P. et al. | 1999
- 3023
-
A new approach to the synthesis of efaroxanCouture, K. et al. | 1999
- 3027
-
Stereoselective synthesis of non symmetric dihydroxyethylene dipeptide isosteres via epoxyalcohols derived from a-amino acidsBenedetti, F. et al. | 1999
- 3031
-
Quinolizidinyl derivatives of 5,11-dihydro-6H- pyrido(2,3-b)(1,4)benzodiazepin-6-one as ligands for muscarinic receptorsNovelli, F. et al. | 1999
- 3035
-
Partition coefficients (free ligands and their iron(III) complexes) and lipophilic behavior of new abiotic chelators. Correlation to biological activityThomas, F. et al. | 1999
- 3041
-
The oxetane conformational lock of paclitaxel: Structural analysis of D-secopaclitaxelBoge, T.C. et al. | 1999
- 3047
-
Conformationally restricted paclitaxel analogues: Macrocyclic mimics of the 'hydrophobic collapse' conformationBoge, T.C. et al. | 1999
- 3053
-
((plus-minus))-4-((N-allyl-cis-3-methyl-4-piperidinyl)phenylamino)- N,N-diethylbenzamide displays selective binding for the delta opioid receptorThomas, J.B. et al. | 1999
- 3053
-
(+/-)-4-[(N-Allyl-Cis-3-Methyl-4-Piperidinyl)Phenylamino]-N,N-Diethylbenzami de Displays Selective Binding for the Delta Opioid ReceptorThomas, J.B. / Herault, X.M. / Rothman, R.B. / Burgess, J.P. / Mascarella, S.W. / Xu, H. / Horel, R.B. / Dersch, C.M. / Carroll, F.I. et al. | 1999
- 3057
-
Antitumor agents. Part 200: Cytotoxicity of naturally occurring resveratrol oligomers and their acetate derivativesOhyama, M. et al. | 1999
- 3057
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Antitumor Agents 200. Cytotoxicity of Naturally Occurring Resveratrol Oligomers and their Acetate DerivativesOhyama, M. / Tanaka, T. / Ito, T. / Iinuma, M. / Bastow, K.F. / Lee, K.-H. et al. | 1999
- 3061
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From histamine to imidazolylalkyl-sulfonamides: the design of a novel series of histamine H"3-receptor antagonistsTozer, M.J. / Harper, E.A. / Kalindjian, S.B. / Pether, M.J. / Shankley, N.P. / Watt, G.F. et al. | 1999
- 3061
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CorrigendumTozer, M.J. et al. | 1999
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Graphical abstracts| 1999
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Instructions to contributors| 1999
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Contributors| 1999