BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS
Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
Inhaltsverzeichnis
- 1
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Graphical contents list| 2006
- 17
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Publisher’s Announcement: New Chairman of the Executive Board of Editors for Tetrahedron Publications| 2006
- 18
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Samarium(II) promoted stereoselective synthesis of antiproliferative cis-b-alkoxy-g-alkyl-g-lactonesDonadel, O. J. / Martin, T. / Martin, V. S. et al. | 2007
- 18
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Samarium(II) promoted stereoselective synthesis of antiproliferative cis-β-alkoxy-γ-alkyl-γ-lactonesDonadel, Osvaldo J. / Martín, Tomás / Martín, Víctor S. et al. | 2006
- 22
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Acyclic, orally bioavailable ketone-based cathepsin K inhibitorsBarrett, David G. / Catalano, John G. / Deaton, David N. et al. | 2006
- 28
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Isothiazoles as active-site inhibitors of HCV NS5B polymeraseYan, Shunqi / Appleby, Todd / Gunic, Esmir et al. | 2006
- 34
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Identification of potent and selective TACE inhibitors via the S1 pocketCondon, Jeffrey S. / Joseph-McCarthy, Diane / Levin, Jeremy I. et al. | 2006
- 40
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Parallel strategies for the preparation and selection of liver-targeted glucocorticoid receptor antagonistsBackes, Bradley J. / Hamilton, Gregory L. / Nguyen, Phong et al. | 2006
- 45
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Kojic acid and its manganese and zinc complexes as potential radioprotective agentsEmami, Saeed / Hosseinimehr, Seyed Jalal / Taghdisi, Seyed Mohammad et al. | 2006
- 49
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(3R)-4-[(3R)-3-Amino-4-(2,4,5-trifluorophenyl)butanoyl]-3-(2,2,2-trifluoroethyl)-1,4-diazepan-2-one, a selective dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetesBiftu, Tesfaye / Feng, Dennis / Qian, Xiaoxia et al. | 2006
- 53
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Antibiotic-conjugated polyacrylate nanoparticles: New opportunities for development of anti-MRSA agentsTuros, Edward / Shim, Jeung-Yeop / Wang, Yang et al. | 2006
- 57
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2,6-Disubstituted N-arylsulfonyl piperidines as γ-secretase inhibitorsPissarnitski, Dmitri A. / Asberom, Theodros / Bara, Thomas A. et al. | 2006
- 57
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2,6-Disubstituted N-arylsulfonyl piperidines as g-secretase inhibitorsPissarnitski, D. A. / Asberom, T. / Bara, T. A. et al. | 2007
- 63
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Novel thiazolones as HCV NS5B polymerase allosteric inhibitors: Further designs, SAR, and X-ray complex structureYan, Shunqi / Larson, Gary / Wu, Jim Z. et al. | 2006
- 68
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Equilibrium shift by target DNA substrates for determination of DNA binding ligandsTsujita, Saori / Tanada, Mikimasa / Kataoka, Tomonobu et al. | 2006
- 73
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Design of potent inhibitors of human b-secretase. Part 1Freskos, J. N. / Fobian, Y. M. / Benson, T. E. et al. | 2007
- 73
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Design of potent inhibitors of human β-secretase. Part 1Freskos, John N. / Fobian, Yvette M. / Benson, Timothy E. et al. | 2006
- 78
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Design of potent inhibitors of human β-secretase. Part 2Freskos, John N. / Fobian, Yvette M. / Benson, Timothy E. et al. | 2006
- 78
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Design of potent inhibitors of human b-secretase. Part 2Freskos, J. N. / Fobian, Y. M. / Benson, T. E. et al. | 2007
- 82
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Structure–activity delineation of quinones related to the biologically active Calothrixin BBernardo, Paul H. / Chai, Christina L.L. / Guen, Maurice Le et al. | 2006
- 86
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Microwave prompted multigram synthesis, structural determination, and photo-antiproliferative activity of fluorinated 4-hydroxyquinolinonesArya, Kapil / Agarwal, Manish et al. | 2006
- 94
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Formation of the intermediate nitronyl nitroxide–anthracene dyad sensing saccharidesYu, Yanxin / Zhang, Deqing / Tan, Wei et al. | 2006
- 97
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Synthesis and structure–activity studies of antofine analogues as potential anticancer agentsFu, Ye / Lee, Sang Kook / Min, Hye-Young et al. | 2006
- 101
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Ezetimibe analogs with a reorganized azetidinone ring: Design, synthesis, and evaluation of cholesterol absorption inhibitionsXu, Xianxiu / Fu, Renzhong / Chen, Jin et al. | 2006
- 105
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Intermediate analogue inhibitors of mandelate racemase: N-Hydroxyformanilide and cupferronBourque, Jennifer R. / Burley, Rodney K.M. / Bearne, Stephen L. et al. | 2006
- 109
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Ponapensin, a cyclopenta[bc]benzopyran with potent NF-κB inhibitory activity from Aglaia ponapensisSalim, Angela A. / Pawlus, Alison D. / Chai, Hee-Byung et al. | 2006
- 109
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Ponapensin, a cyclopenta[bc]benzopyran with potent NF-kB inhibitory activity from Aglaia ponapensisSalim, A. A. / Pawlus, A. D. / Chai, H. B. et al. | 2007
- 113
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Synthesis and surface activity of diether-linked phosphoglycerols: Potential applications for exogenous lung surfactantsNotter, Robert H. / Wang, Zhongyi / Wang, Zhengdong et al. | 2006
- 118
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Estrogen receptor b ligands: Design and synthesis of new 2-phenyl-isoindole-1,3-dionesUllrich, J. W. / Unwalla, R. J. / Singhaus, R. R. et al. | 2007
- 118
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Estrogen receptor β ligands: Design and synthesis of new 2-phenyl-isoindole-1,3-dionesUllrich, John W. / Unwalla, Rayomand J. / Singhaus, Robert R. Jr. et al. | 2006
- 123
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The discovery of a potent orally efficacious indole androgen receptor antagonist through in vivo screeningLanter, James C. / Fiordeliso, James J. / Jiang, Weiqin et al. | 2006
- 127
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Synthesis and antifungal activity of 1H-indole-4,7-dionesRyu, Chung-Kyu / Lee, Jung Yoon / Park, Rae-Eun et al. | 2006
- 132
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Structure–activity relationships of the ultrapotent vanilloid resiniferatoxin (RTX): The homovanillyl moietyAppendino, Giovanni / Ech-Chahad, Abdellah / Minassi, Alberto et al. | 2006
- 136
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Structure–activity relationships of aryloxyalkanoic acid hydroxyamides as potent inhibitors of histone deacetylaseMarson, Charles M. / Mahadevan, Thevaki / Dines, Jon et al. | 2006
- 142
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2,6-Quinolinyl derivatives as potent VLA-4 antagonistsLassoie, Marie-Agnès / Broeders, Fabienne / Collart, Philippe et al. | 2006
- 147
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ATP-conjugated peptide inhibitors for calmodulin-dependent protein kinase IIAhn, Dae-Ro / Han, Ki-Cheol / Kwon, Hyuk Sung et al. | 2006
- 152
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Mono, di and tri-mannopyranosyl phosphates as mannose-1-phosphate prodrugs for potential CDG-Ia therapyHardré, Renaud / Khaled, Amira / Willemetz, Alexandra et al. | 2006
- 156
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Synthesis of bisdesmosidic kryptogenyl saponins using the ‘random glycosylation’ strategy and evaluation of their antitumor activityLiu, Yang / Zhao, Dong-Mei / Lu, Xue-Hua et al. | 2006
- 161
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N6-Cycloalkyl-2-substituted adenosine derivatives as selective, high affinity adenosine A1 receptor agonistsElzein, Elfatih / Kalla, Rao / Li, Xiaofen et al. | 2006
- 167
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Screening of α-helical peptide ligands controlling a calcineurin-phosphatase activityUsui, Kenji / Tomizaki, Kin-ya / Mihara, Hisakazu et al. | 2006
- 167
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Screening of a-helical peptide ligands controlling a calcineurin-phosphatase activityUsui, K. / Tomizaki, K. y. / Mihara, H. et al. | 2007
- 172
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Identification of novel, selective and potent Chk2 inhibitorsLarson, Gary / Yan, Shunqi / Chen, Huanming et al. | 2006
- 176
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N-Substituted carbazolyloxyacetic acids modulate Alzheimer associated γ-secretaseNarlawar, Rajeshwar / Pérez Revuelta, Blanca I. / Baumann, Karlheinz et al. | 2006
- 176
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N-Substituted carbazolyloxyacetic acids modulate Alzheimer associated g-secretaseNarlawar, R. / Perez Revuelta, B. I. / Baumann, K. et al. | 2007
- 183
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Phosphate transfer from inositol pyrophosphates InsP5PP and InsP4(PP)2: A semi-empirical investigationHand, Christine E. / Honek, John F. et al. | 2006
- 189
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SAR studies of 6-(arylamino)-4,4-disubstituted-1-methyl-1,4-dihydro-benzo[d][1,3]oxazin-2-ones as progesterone receptor antagonistsKern, Jeffrey C. / Terefenko, Eugene A. / Fensome, Andrew et al. | 2006
- 193
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Identification of a series of highly potent activators of the Nurr1 signaling pathwayHintermann, Samuel / Chiesi, Michele / von Krosigk, Ulrike et al. | 2006
- 197
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Species marker for developing novel and safe pesticidesPang, Yuan-Ping et al. | 2006
- 200
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Syntheses of F-18 labeled fluoroalkyltyrosine derivatives and their biological evaluation in rat bearing 9L tumorMoon, Byung Seok / Lee, Tae Sup / Lee, Kyo Chul et al. | 2006
- 205
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Tetrahydroquinoline sulfonamides as γ-secretase inhibitorsAsberom, Theodros / Bara, Thomas A. / Clader, John W. et al. | 2006
- 205
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Tetrahydroquinoline sulfonamides as g-secretase inhibitorsAsberom, T. / Bara, T. A. / Clader, J. W. et al. | 2007
- 208
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2-Arylidenedihydroindole-3-ones: Design, synthesis, and biological activity on bladder carcinoma cell linesGerby, Bastien / Boumendjel, Ahcène / Blanc, Madeleine et al. | 2006
- 214
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Halogenation of 4-hydroxy-3-methoxybenzyl thiourea TRPV1 agonists showed enhanced antagonism to capsaicinKang, Dong Wook / Ryu, HyungChul / Lee, Jeewoo et al. | 2006
- 220
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Design, synthesis, and biological evaluation of new (2E,6E)-10-(dimethylamino)-3,7-dimethyl-2,6-decadien-1-ol ethers as inhibitors of human and Trypanosoma cruzi oxidosqualene cyclaseGalli, Ubaldina / Oliaro-Bosso, Simonetta / Taramino, Silvia et al. | 2006
- 225
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Discovery of potent and selective PKC-θ inhibitorsCywin, Charles L. / Dahmann, Georg / Prokopowicz, Anthony S. III et al. | 2006
- 231
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CCR5 receptor antagonists: Discovery and SAR study of guanylhydrazone derivativesWei, Robert G. / Arnaiz, Damian O. / Chou, Yuo-Ling et al. | 2006
- 235
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Glucose-specific poly(allylamine) hydrogels—A reassessmentFazal, Furqan M. / Hansen, David E. et al. | 2006
- 239
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New antifungal flavonoid glycoside from Vitex negundoSathiamoorthy, B. / Gupta, Prasoon / Kumar, Manmeet et al. | 2006
- 243
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Farnesyltransferase pharmacophore model derived from diverse classes of inhibitorsLu, Aijun / Zhang, Jian / Yin, Xiaojin et al. | 2006
- 250
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Design and effective synthesis of novel templates, 3,7-diphenyl-4-amino-thieno and furo-[3,2-c]pyridines as protein kinase inhibitors and in vitro evaluation targeting angiogenetic kinasesMiyazaki, Yasushi / Nakano, Masato / Sato, Hideyuki et al. | 2006
- 255
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Synthesis and anticonvulsant activity of sulfonamide derivatives-hydrophobic domainSiddiqui, Nadeem / Pandeya, Surendra N. / Khan, Suroor A. et al. | 2006
- 260
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4-Aminopyrimidines as novel HIV-1 inhibitorsGadhachanda, Venkat R. / Wu, Baogen / Wang, Zhiwei et al. | 2006
- 266
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Discovery of low nanomolar non-hydroxamate inhibitors of tumor necrosis factor-a converting enzyme (TACE)Duan, J. J. / Chen, L. / Lu, Z. et al. | 2007
- 266
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Discovery of low nanomolar non-hydroxamate inhibitors of tumor necrosis factor-α converting enzyme (TACE)Duan, James J.-W. / Chen, Lihua / Lu, Zhonghui et al. | 2006
- 272
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Arylsulfonamides as a new class of cannabinoid CB1 receptor ligands: Identification of a lead and initial SAR studiesLambeng, N. / Lebon, F. / Christophe, B. et al. | 2006
- 278
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Nitrogen-containing flavonoids as CDK1/Cyclin B inhibitors: Design, synthesis, and biological evaluationLiu, Tao / Xu, Zhongmiao / He, Qiaojun et al. | 2006
- 282
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Evolution of thiazolidine-based blockers of human Kv1.5 for the treatment of atrial arrhythmiasJackson, Chris M. / Blass, Benjamin / Coburn, Keith et al. | 2006
- CO2
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Editorial board| 2006
- I
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Instructions to contributors| 2006