Antituberculosis drugs: Ten years of research (English)
- New search for: Janin, Yves L.
- New search for: Janin, Yves L.
In:
Bioorganic and Medicinal Chemistry
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15
, 7
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2479-2513
;
2007
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ISSN:
- Article (Journal) / Electronic Resource
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Title:Antituberculosis drugs: Ten years of research
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Contributors:Janin, Yves L. ( author )
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Published in:Bioorganic and Medicinal Chemistry ; 15, 7 ; 2479-2513
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Publisher:
- New search for: Elsevier Ltd
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Publication date:2007-01-17
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Size:35 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:
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Source:
Table of contents – Volume 15, Issue 7
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.
- 2471
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Graphical contents list| 2007
- 2479
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Antituberculosis drugs: Ten years of researchJanin, Yves L. et al. | 2007
- 2514
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N6-[(Hetero)aryl/(cyclo)alkyl-carbamoyl-methoxy-phenyl]-(2-chloro)-5prime-N-ethylcarboxamido-adenosines: The first example of adenosine-related structures with potent agonist activity at the human A2B adenosine receptorBaraldi, P. G. / Preti, D. / Tabrizi, M. A. / Fruttarolo, F. / Saponaro, G. / Baraldi, S. / Romagnoli, R. / Moorman, A. R. / Gessi, S. / Varani, K. et al. | 2007
- 2514
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N6-[(Hetero)aryl/(cyclo)alkyl-carbamoyl-methoxy-phenyl]-(2-chloro)-5′-N-ethylcarboxamido-adenosines: The first example of adenosine-related structures with potent agonist activity at the human A2B adenosine receptorBaraldi, Pier Giovanni / Preti, Delia / Tabrizi, Mojgan Aghazadeh / Fruttarolo, Francesca / Saponaro, Giulia / Baraldi, Stefania / Romagnoli, Romeo / Moorman, Allan R. / Gessi, Stefania / Varani, Katia et al. | 2007
- 2528
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Exploration of the correlation between the structure, hemolytic activity, and cytotoxicity of steroid saponinsWang, Yibing / Zhang, Yichun / Zhu, Ziyan / Zhu, Shilei / Li, Yingxia / Li, Ming / Yu, Biao et al. | 2007
- 2533
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Novel chiral isoxazole derivatives: Synthesis and pharmacological characterization at human β-adrenergic receptor subtypesDallanoce, Clelia / Frigerio, Fabio / De Amici, Marco / Dorsch, Sandra / Klotz, Karl-Norbert / De Micheli, Carlo et al. | 2007
- 2533
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Novel chiral isoxazole derivatives: Synthesis and pharmacological characterization at human b-adrenergic receptor subtypesDallanoce, C. / Frigerio, F. / De Amici, M. / Dorsch, S. / Klotz, K. N. / De Micheli, C. et al. | 2007
- 2544
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On the applicability of QSAR for recognition of miRNA bioorganic structures at early stages of organism and cell development: Embryo and stem cellsGonzález-Díaz, Humberto / Vilar, Santiago / Santana, Lourdes / Podda, Gianni / Uriarte, Eugenio et al. | 2007
- 2551
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A new modification of anti-tubercular active moleculesImramovský, Aleš / Polanc, Slovenko / Vinšová, Jarmila / Kočevar, Marijan / Jampílek, Josef / Rečková, Zuzana / Kaustová, Jarmila et al. | 2007
- 2560
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Synthesis, structural characterization, and in vitro antitumor activity of novel N-(6-chloro-1,1-dioxo-1,4,2-benzodithiazin-3-yl)arylsulfonamidesBrzozowski, Zdzisław / Sączewski, Franciszek / Sławiński, Jarosław / Bednarski, Patrick J. / Grünert, Renate / Gdaniec, Maria et al. | 2007
- 2573
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Novel 3-iodo-8-ethoxypyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide as promising lead for design of a5-inverse agonist useful tools for therapy of mnemonic damageGuerrini, G. / Ciciani, G. / Cambi, G. / Bruni, F. / Selleri, S. / Besnard, F. / Montali, M. / Martini, C. / Ghelardini, C. / Galeotti, N. et al. | 2007
- 2573
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Novel 3-iodo-8-ethoxypyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide as promising lead for design of α5-inverse agonist useful tools for therapy of mnemonic damageGuerrini, Gabriella / Ciciani, Giovanna / Cambi, Giovanni / Bruni, Fabrizio / Selleri, Silvia / Besnard, François / Montali, Marina / Martini, Claudia / Ghelardini, Carla / Galeotti, Nicoletta et al. | 2007
- 2587
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Design, synthesis, and evaluation of non-steroidal farnesoid X receptor (FXR) antagonistKainuma, Masahiko / Makishima, Makoto / Hashimoto, Yuichi / Miyachi, Hiroyuki et al. | 2007
- 2601
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Clubbed thiazoles by MAOS: A novel approach to cyclin-dependent kinase 5/p25 inhibitors as a potential treatment for Alzheimer’s diseaseShiradkar, Mahendra Ramesh / Akula, Kalyan Chakravarthy / Dasari, Varaprasad / Baru, Vijayakumar / Chiningiri, Bhoomeshwar / Gandhi, Santosh / Kaur, Ranjit et al. | 2007
- 2611
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Comparative rates of sialylation by recombinant trans-sialidase and inhibitor properties of synthetic oligosaccharides from Trypanosoma cruzi mucins-containing galactofuranose and galactopyranoseAgustí, Rosalía / Giorgi, M. Eugenia / Mendoza, Verónica M. / Gallo-Rodriguez, Carola / de Lederkremer, Rosa M. et al. | 2007
- 2617
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Amphipathic benzoic acid derivatives: Synthesis and binding in the hydrophobic tunnel of the zinc deacetylase LpxCShin, Hyunshun / Gennadios, Heather A. / Whittington, Douglas A. / Christianson, David W. et al. | 2007
- 2624
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Actions between neonicotinoids and key residues of insect nAChR based on an ab initio quantum chemistry study: Hydrogen bonding and cooperative π–π interactionWang, Yanli / Cheng, Jiagao / Qian, Xuhong / Li, Zhong et al. | 2007
- 2624
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Actions between neonicotinoids and key residues of insect nAChR based on an ab initio quantum chemistry study: Hydrogen bonding and cooperative p-p interactionWang, Y. / Cheng, J. / Qian, X. / Li, Z. et al. | 2007
- 2631
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Design and synthesis of new potent dipeptidyl peptidase IV inhibitors with enhanced ex vivo durationKondo, Takashi / Nekado, Takahiro / Sugimoto, Isamu / Ochi, Kenya / Takai, Shigeyuki / Kinoshita, Atsushi / Tajima, Yohei / Yamamoto, Susumu / Kawabata, Kazuhito / Nakai, Hisao et al. | 2007
- 2651
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Naphthoindole-based analogues of tryptophan and tryptamine: Synthesis and cytotoxic propertiesShchekotikhin, Andrey E. / Dezhenkova, Lyubov G. / Susova, Olga Yu. / Glazunova, Valeria A. / Luzikov, Yuri N. / Sinkevich, Yuri B. / Buyanov, Vladimir N. / Shtil, Alexander A. / Preobrazhenskaya, Maria N. et al. | 2007
- 2660
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Synthesis of S-dialkylarsino-3-mercapto-1,2-propanediols and evaluation of their anticancer activityGao, Mingzhang / Tan, Songde / Chen, Yiwen / Zingaro, Ralph A. et al. | 2007
- 2667
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Synthesis of dioxane-based antiviral agents and evaluation of their biological activities as inhibitors of Sindbis virus replicationKim, Ha Young / Kuhn, Richard J. / Patkar, Chinmay / Warrier, Ranjit / Cushman, Mark et al. | 2007
- 2680
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QSAR analysis for heterocyclic antifungalsDuchowicz, Pablo R. / Vitale, Martín G. / Castro, Eduardo A. / Fernández, Michael / Caballero, Julio et al. | 2007
- 2690
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Optimization and determination of the absolute configuration of a series of potent inhibitors of human papillomavirus type-11 E1–E2 protein–protein interaction: A combined medicinal chemistry, NMR and computational chemistry approachGoudreau, Nathalie / Cameron, Dale R. / Déziel, Robert / Haché, Bruno / Jakalian, Araz / Malenfant, Eric / Naud, Julie / Ogilvie, William W. / O’Meara, Jeff / White, Peter W. et al. | 2007
- 2701
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The synthesis of a,b-unsaturated carbonyl derivatives with the ability to inhibit both glutathione S-transferase P1-1 activity and the proliferation of leukemia cellsZhao, G. / Liu, C. / Wang, R. / Song, D. / Wang, X. / Lou, H. / Jing, Y. et al. | 2007
- 2701
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The synthesis of α,β-unsaturated carbonyl derivatives with the ability to inhibit both glutathione S-transferase P1-1 activity and the proliferation of leukemia cellsZhao, Guisen / Liu, Chuan / Wang, Rui / Song, Dandan / Wang, Xiaobing / Lou, Hongxiang / Jing, Yongkui et al. | 2007
- 2708
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Identification of tyrosinase inhibitors from Marrubium velutinum and Marrubium cylleneumKarioti, Anastasia / Protopappa, Anastasia / Megoulas, Nikolaos / Skaltsa, Helen et al. | 2007
- 2715
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Design and synthesis of long-acting inhibitors of dipeptidyl peptidase IVKondo, Takashi / Sugimoto, Isamu / Nekado, Takahiro / Ochi, Kenya / Ohtani, Tazumi / Tajima, Yohei / Yamamoto, Susumu / Kawabata, Kazuhito / Nakai, Hisao / Toda, Masaaki et al. | 2007
- 2736
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Synthesis of dl-standishinal and its related compounds for the studies on structure–activity relationship of inhibitory activity against aromataseKatoh, Takahiro / Akagi, Taichi / Noguchi, Chie / Kajimoto, Tetsuya / Node, Manabu / Tanaka, Reiko / Nishizawa (née Iwamoto), Manabu / Ohtsu, Hironori / Suzuki, Noriyuki / Saito, Koichi et al. | 2007
- 2749
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Design, synthesis, inhibitory activity, and SAR studies of pyrrolidine derivatives as neuraminidase inhibitorsZhang, Jie / Wang, Qiang / Fang, Hao / Xu, Wenfang / Liu, Ailin / Du, Guanhua et al. | 2007
- 2759
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Discovery of 1,4-dihydroindeno[1,2-c]pyrazoles as a novel class of potent and selective checkpoint kinase 1 inhibitorsTong, Yunsong / Claiborne, Akiyo / Stewart, Kent D. / Park, Chang / Kovar, Peter / Chen, Zehan / Credo, Robert B. / Gu, Wen-Zhen / Gwaltney, Stephen L. II / Judge, Russell A. et al. | 2007
- 2768
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Second generation of 5-ethenylbenzofuroxan derivatives as inhibitors of Trypanosoma cruzi growth: Synthesis, biological evaluation, and structure–activity relationshipsPorcal, Williams / Hernández, Paola / Aguirre, Gabriela / Boiani, Lucía / Boiani, Mariana / Merlino, Alicia / Ferreira, Ana / Maio, Rossanna Di / Castro, Ana / González, Mercedes et al. | 2007
- 2782
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Synthesis and antiplasmodial activity of new N-[3-(4-{3-[(7-chloroquinolin-4-yl)amino]propyl}piperazin-1-yl)propyl]carboxamidesFreitag, Marcus / Kaiser, Marcel / Larsen, Tim / Zohrabi-Kalantari, Vida / Heidler, Philipp / Link, Andreas et al. | 2006
- 2789
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Dibenzothiazoles as novel amyloid-imaging agentsWu, Chunying / Wei, Jingjun / Gao, Kuanqiang / Wang, Yanming et al. | 2006
- 2797
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Bioorganic & Medicinal Chemistry Reviews and Perspectives| 2007
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Instructions to contributors| 2007
- IFC
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Editorial board| 2007