6,7-Dihydroxyisoquinoline-3-carboxylic acids are potent inhibitors on the binding of insulin-Like growth factor (IGF) to IGF-binding proteins: optimization of the 1-position benzoyl side chain (English)
- New search for: Zhu, Y. F.
- New search for: Wilcoxen, K.
- New search for: Gross, T.
- New search for: Connors, P.
- New search for: Strack, N.
- New search for: Gross, R.
- New search for: Huang, C. Q.
- New search for: McCarthy, J. R.
- New search for: Xie, Q.
- New search for: Ling, N.
- New search for: Zhu, Y. F.
- New search for: Wilcoxen, K.
- New search for: Gross, T.
- New search for: Connors, P.
- New search for: Strack, N.
- New search for: Gross, R.
- New search for: Huang, C. Q.
- New search for: McCarthy, J. R.
- New search for: Xie, Q.
- New search for: Ling, N.
In:
BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS
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13
, 11
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1927-1930
;
2003
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ISSN:
- Article (Journal) / Print
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Title:6,7-Dihydroxyisoquinoline-3-carboxylic acids are potent inhibitors on the binding of insulin-Like growth factor (IGF) to IGF-binding proteins: optimization of the 1-position benzoyl side chain
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Contributors:Zhu, Y. F. ( author ) / Wilcoxen, K. ( author ) / Gross, T. ( author ) / Connors, P. ( author ) / Strack, N. ( author ) / Gross, R. ( author ) / Huang, C. Q. ( author ) / McCarthy, J. R. ( author ) / Xie, Q. ( author ) / Ling, N. ( author )
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Published in:BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS ; 13, 11 ; 1927-1930
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Publisher:
- New search for: Elsevier Science B.V., Amsterdam.
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Publication date:2003-01-01
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Size:4 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 13, Issue 11
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.
- 1839
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Graphical Abstracts| 2003
- 1845
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Inhibition of HIV tat-TAR interactions by an antisense oligo-2prime-O-methylribonucleoside methylphosphonateHamma, T. / Saleh, A. / Huq, I. / Rana, T. M. / Miller, P. S. et al. | 2003
- 1845
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Inhibition of HIV tat–TAR interactions by an antisense oligo-2′-O-methylribonucleoside methylphosphonateHamma, Tomoko / Saleh, Anthony / Huq, Ikramul / Rana, Tariq M / Miller, Paul S et al. | 2003
- 1849
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Synthesis and biological evaluation of some novel 4′-Thio-l-ribonucleosides with modified nucleobase moietiesPejanović, Vjera / Stokić, Zdenka / Stojanović, Biljana / Piperski, Vesna / Popsavin, Mirjana / Popsavin, Velimir et al. | 2003
- 1849
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Synthesis and biological evaluation of some novel 4prime-Thio-l-ribonucleosides with modified nucleobase moietiesPejanovic, V. / Stokic, Z. / Stojanovic, B. / Piperski, V. / Popsavin, M. / Popsavin, V. et al. | 2003
- 1853
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Synthesis and biological evaluation of new UDP-GalNAc analogues for the study of polypeptide-a-GalNAc-transferasesBusca, Patricia et al. | 2003
- 1853
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Synthesis and biological evaluation of new UDP-GalNAc analogues for the study of polypeptide-α-GalNAc-transferasesBusca, Patricia / Piller, Véronique / Piller, Friedrich / Martin, Olivier R. et al. | 2003
- 1857
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Acyclic N-(azacycloalkyl)bisindolylmaleimides: isozyme selective inhibitors of PKCβFaul, Margaret M / Gillig, James R / Jirousek, Michael R / Ballas, Lawrence M / Schotten, Theo / Kahl, Astrid / Mohr, Michael et al. | 2003
- 1857
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Acyclic N-(azacycloalkyl)bisindolylmaleimides: isozyme selective inhibitors of PKCbFaul, Margaret M. et al. | 2003
- 1861
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Amide analogues of TSA: synthesis, binding mode analysis and HDAC inhibitionVan Ommeslaeghe, K / Elaut, G / Brecx, V / Papeleu, P / Iterbeke, K / Geerlings, P / Tourwé, D / Rogiers, V et al. | 2003
- 1865
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Binding mode of 6ECDCA, a potent bile acid agonist of the farnesoid X receptor (FXR)Costantino, Gabriele / Macchiarulo, Antonio / Entrena-Guadix, Antonio / Camaioni, Emidio / Pellicciari, Roberto et al. | 2003
- 1869
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Density functional theory calculations for resveratrolCao, Huai / Pan, Xulin / Li, Cong / Zhou, Chun / Deng, Fengyi / Li, Taohong et al. | 2003
- 1873
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Synthesis, pharmacology and pharmacokinetics of 3-(4-Aryl-piperazin-1-ylalkyl)-uracils as uroselective a1A-antagonistsLopez, F.J. et al. | 2003
- 1873
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Synthesis, pharmacology and pharmacokinetics of 3-(4-Aryl-piperazin-1-ylalkyl)-uracils as uroselective α1A-antagonistsLopez, F.J. / Arias, L. / Chan, R. / Clarke, D.E. / Elworthy, T.R. / Ford, A.P.D.W. / Guzman, A. / Jaime-Figueroa, S. / Jasper, J.R. / Morgans, D.J. Jr. et al. | 2003
- 1879
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Design and synthesis of novel pyrrolidine-containing bradykinin antagonistsLee, Jung / Reynolds, Charles / Jetter, Michele C / Youngman, Mark A / Hlasta, Dennis J / Dax, Scott L / Stone, Dennis J / Zhang, Sui-Po / Codd, Ellen E et al. | 2003
- 1883
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Optimization of α-acylaminoketone ecdysone agonists for control of gene expressionTice, Colin M. / Hormann, Robert E. / Thompson, Christine S. / Friz, Jennifer L. / Cavanaugh, Caitlin K. / Saggers, Jessica A. et al. | 2003
- 1883
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Optimization of a-acylaminoketone ecdysone agonists for control of gene expressionTice, Colin M. et al. | 2003
- 1887
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Potent, selective inhibitors of protein tyrosine phosphatase 1BXin, Zhili / Oost, Thorsten K / Abad-Zapatero, Cele / Hajduk, Philip J / Pei, Zhonghua / Szczepankiewicz, Bruce G / Hutchins, Charles W / Ballaron, Steve J / Stashko, Mike A / Lubben, Tom et al. | 2003
- 1891
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N-Isonicotinoyl-(l)-4-aminophenylalanine derivatives as tight binding VLA-4 antagonistsDoherty, George A. / Yang, Ginger X. / Borges, Edite / Tong, Sharon / McCauley, Ermengilda D. / Treonz, Kelly M. / Van Riper, Gail / Pacholok, Stephen / Si, Qian / Koo, Gloria C. et al. | 2003
- 1897
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Indole amide hydroxamic acids as potent inhibitors of histone deacetylasesDai, Yujia / Guo, Yan / Guo, Jun / Pease, Lori J / Li, Junling / Marcotte, Patrick A / Glaser, Keith B / Tapang, Paul / Albert, Daniel H / Richardson, Paul L et al. | 2003
- 1903
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Advances toward new antidepressants beyond SSRIs: 1-aryloxy-3-piperidinylpropan-2-ols with dual 5-HT1A receptor antagonism/SSRI activities. Part 1Takeuchi, Kumiko / Kohn, Todd J / Honigschmidt, Nicholas A / Rocco, Vincent P / Spinazze, Patrick G / Koch, Daniel J / Nelson, David L / Wainscott, D.Bradley / Ahmad, Laura J / Shaw, Janice et al. | 2003
- 1907
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Tetrahydroquinoline-Based selective estrogen receptor modulators (SERMs)Wallace, Owen B / Lauwers, Kenneth S / Jones, Scott A / Dodge, Jeffrey A et al. | 2003
- 1911
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Redefining the structure–activity relationships of 2,6-methano-3-benzazocines. Part 2: 8-formamidocyclazocine analoguesWentland, Mark P. / Sun, Xufeng / Ye, Yingchun / Lou, Rongliang / Bidlack, Jean M. et al. | 2003
- 1915
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Polyacylated neohesperidosides From Geranium caespitosum: bacterial multidrug resistance pump inhibitorsStermitz, Frank R / Cashman, Kevin K / Halligan, Kathleen M / Morel, Cécile / Tegos, George P / Lewis, Kim et al. | 2003
- 1919
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A novel estrogen receptor ligand templateSibley, Robert / Hatoum-Mokdad, Holia / Schoenleber, Robert / Musza, Laszlo / Stirtan, William / Marrero, Diana / Carley, William / Xiao, Hong / Dumas, Jacques et al. | 2003
- 1923
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Substituted 2-Pyridinemethanol derivatives as potent and selective phosphodiesterase-4 inhibitorsDucharme, Yves / Friesen, Richard W / Blouin, Marc / Côté, Bernard / Dubé, Daniel / Ethier, Diane / Frenette, Richard / Laliberté, France / Mancini, Joseph A / Masson, Paul et al. | 2003
- 1927
-
6,7-Dihydroxyisoquinoline-3-carboxylic acids are potent inhibitors on the binding of insulin-Like growth factor (IGF) to IGF-binding proteins: optimization of the 1-position benzoyl side chainZhu, Yun-Fei / Wilcoxen, Keith / Gross, Timothy / Connors, Patrick / Strack, Nathalie / Gross, Raymond / Huang, Charles Q. / McCarthy, James R. / Xie, Qiu / Ling, Nicholas et al. | 2003
- 1931
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Quinoline-Carboxylic acids are potent inhibitors that inhibit the binding of insulin-Like growth factor (IGF) to IGF-Binding proteinsZhu, Yun-Fei / Wang, Xiao-Chuan / Connors, Patrick / Wilcoxen, Keith / Gao, Yinghong / Gross, Raymond / Strack, Nathalie / Gross, Timothy / McCarthy, James R. / Xie, Qiu et al. | 2003
- 1935
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Antifungal activity of a Candida albicans GGTase I inhibitor-Alanine conjugate. inhibition of Rho1p prenylation in C. albicansMurthi, Krishna K / Smith, Susan E / Kluge, Arthur F / Bergnes, Gustave / Bureau, Patrick / Berlin, Vivian et al. | 2003
- 1939
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Novel pyrrolyllactone and pyrrolyllactam indolinones as potent cyclin-Dependent kinase 2 inhibitorsLi, Xiaoyuan / Huang, Ping / Cui, Jingrong Jean / Zhang, Jennifer / Tang, Cho et al. | 2003
- 1943
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Synthesis and SAR of cis-1-Benzoyl-1,2,3,4-tetrahydroquinoline ligands for control of gene expression in ecdysone responsive systemsSmith, Howard C / Cavanaugh, Caitlin K / Friz, Jennifer L / Thompson, Christine S / Saggers, Jessica A / Michelotti, Enrique L / Garcia, Javier / Tice, Colin M et al. | 2003
- CO2
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Editorial board| 2003
- I
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Instructions to Contributors and GA example| 2003
- iii
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Contents List| 2003
- v
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Contributors to this Issue| 2003