4-[6-(2-Aminoethyl)naphthalen-2-yl]benzonitriles are potent histamine H3 receptor antagonists with high CNS penetration (English)
- New search for: Black, Lawrence A.
- New search for: Nersesian, Diana L.
- New search for: Sharma, Padam
- New search for: Ku, Yi-Yin
- New search for: Bennani, Youssef L.
- New search for: Marsh, Kennan C.
- New search for: Miller, Thomas R.
- New search for: Esbenshade, Timothy A.
- New search for: Hancock, Arthur A.
- New search for: Cowart, Marlon
- New search for: Black, Lawrence A.
- New search for: Nersesian, Diana L.
- New search for: Sharma, Padam
- New search for: Ku, Yi-Yin
- New search for: Bennani, Youssef L.
- New search for: Marsh, Kennan C.
- New search for: Miller, Thomas R.
- New search for: Esbenshade, Timothy A.
- New search for: Hancock, Arthur A.
- New search for: Cowart, Marlon
In:
Bioorganic and Medicinal Chemistry Letters
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17
, 5
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1443-1446
;
2006
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ISSN:
- Article (Journal) / Electronic Resource
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Title:4-[6-(2-Aminoethyl)naphthalen-2-yl]benzonitriles are potent histamine H3 receptor antagonists with high CNS penetration
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Contributors:Black, Lawrence A. ( author ) / Nersesian, Diana L. ( author ) / Sharma, Padam ( author ) / Ku, Yi-Yin ( author ) / Bennani, Youssef L. ( author ) / Marsh, Kennan C. ( author ) / Miller, Thomas R. ( author ) / Esbenshade, Timothy A. ( author ) / Hancock, Arthur A. ( author ) / Cowart, Marlon ( author )
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Published in:Bioorganic and Medicinal Chemistry Letters ; 17, 5 ; 1443-1446
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Publisher:
- New search for: Elsevier Ltd
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Publication date:2006-11-29
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Size:4 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 17, 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.
- 1131
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Graphical contents list| 2007
- 1149
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Synthesis of O-prenylated and O-geranylated derivatives of 5-benzylidene2,4-thiazolidinediones and evaluation of their free radical scavenging activity as well as effect on some phase II antioxidant/detoxifying enzymesHossain, Sk. Ugir / Bhattacharya, Sudin et al. | 2006
- 1155
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Synthesis and structure evaluation of a novel cantharimide and its cytotoxicity on SK-Hep-1 hepatoma cellsKok, Stanton Hon Lung / Chui, Chung Hin / Lam, Wing Sze / Chen, Jien / Lau, Fung Yi / Wong, Raymond Siu Ming / Cheng, Gregory Yin Ming / Lai, Paul Bo San / Leung, Thomas Wai Tong / Yu, Michael Wing Yiu et al. | 2006
- 1160
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Opioids and efflux transporters. Part 1: P-Glycoprotein substrate activity of N-substituted analogs of meperidineMercer, Susan L. / Hassan, Hazem E. / Cunningham, Christopher W. / Eddington, Natalie D. / Coop, Andrew et al. | 2006
- 1163
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Synthesis of new xanthone analogues and their biological activity test—Cytotoxicity, topoisomerase II inhibition, and DNA cross-linking studyWoo, Sangwook / Jung, Ji / Lee, Chongsoon / Kwon, Youngjoo / Na, Younghwa et al. | 2006
- 1167
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Discovery of thienopyridines as Src-family selective Lck inhibitorsAbbott, Lily / Betschmann, Patrick / Burchat, Andrew / Calderwood, David J. / Davis, Heather / Hrnciar, Peter / Hirst, Gavin C. / Li, Biqin / Morytko, Michael / Mullen, Kelly et al. | 2006
- 1172
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A new visual screening assay for catalytic antibodies with retro-aldol retro-Michael activityShamis, Marina / Barbas, Carlos F. III / Shabat, Doron et al. | 2006
- 1176
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Chiral tetrahydroquinoline derivatives as potent anti-hyperalgesic agents in animal models of sustained inflammation and chronic neuropathic painDi Fabio, Romano / Alvaro, Giuseppe / Bertani, Barbara / Donati, Daniele / Pizzi, Domenica Maria / Gentile, Gabriella / Pentassuglia, Giorgio / Giacobbe, Simone / Spada, Simone / Ratti, Emiliangelo et al. | 2006
- 1181
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Synthesis and antibacterial evaluation of a novel series of rifabutin-like spirorifamycinsKim, In Ho / Combrink, Keith D. / Ma, Zhenkun / Chapo, Katrina / Yan, Dalai / Renick, Paul / Morris, Timothy W. / Pulse, Mark / Simecka, Jerry W. / Ding, Charles Z. et al. | 2006
- 1185
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Synthesis and evaluation of aryl thioxothiazolidinone inhibitors of ADAMTS-5 (Aggrecanase-2)Bursavich, Matthew G. / Gilbert, Adam M. / Lombardi, Sabrina / Georgiadis, Katy E. / Reifenberg, Erica / Flannery, Carl R. / Morris, Elisabeth A. et al. | 2006
- 1189
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5-((1H-Pyrazol-4-yl)methylene)-2-thioxothiazolidin-4-one inhibitors of ADAMTS-5Gilbert, Adam M. / Bursavich, Matthew G. / Lombardi, Sabrina / Georgiadis, Katy E. / Reifenberg, Erica / Flannery, Carl R. / Morris, Elisabeth A. et al. | 2006
- 1193
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Novel pyridinyl and pyrimidinylcarbazole sulfonamides as antiproliferative agentsHu, Laixing / Li, Zhuo-rong / Wang, Yue-ming / Wu, Yanbin / Jiang, Jian-Dong / Boykin, David W. et al. | 2006
- 1197
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Hydrolytic cleavage of DNA by quercetin zinc(II) complexJun, Tan / Bochu, Wang / Liancai, Zhu et al. | 2006
- 1200
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Discovery of novel, non-acidic 1,5-biaryl pyrrole EP1 receptor antagonistsHall, Adrian / Atkinson, Stephen / Brown, Susan H. / Chessell, Iain P. / Chowdhury, Anita / Giblin, Gerard M.P. / Goldsmith, Paul / Healy, Mark P. / Jandu, Karamjit S. / Johnson, Matthew R. et al. | 2006
- 1206
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Synthesis and SAR of 3,5-diamino-piperidine derivatives: Novel antibacterial translation inhibitors as aminoglycoside mimeticsZhou, Yuefen / Gregor, Vlad E. / Ayida, Benjamin K. / Winters, Geoffrey C. / Sun, Zhongxiang / Murphy, Douglas / Haley, Greg / Bailey, Dwight / Froelich, Jamie M. / Fish, Sarah et al. | 2006
- 1211
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Discovery and preliminary evaluation of 5-(4-phenylbenzyl)oxazole-4-carboxamides as prostacyclin receptor antagonistsBrescia, Marc-Raleigh / Rokosz, Laura L. / Cole, Andrew G. / Stauffer, Tara M. / Lehrach, John M. / Auld, Douglas S. / Henderson, Ian / Webb, Maria L. et al. | 2006
- 1216
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In vitro selection of RNA aptamer against Escherichia coli release factor 1Sando, Shinsuke / Ogawa, Atsushi / Nishi, Teruyuki / Hayami, Masayoshi / Aoyama, Yasuhiro et al. | 2006
- 1221
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Discovery of uracil-based histone deacetylase inhibitors able to reduce acquired antifungal resistance and trailing growth in Candida albicansMai, Antonello / Rotili, Dante / Massa, Silvio / Brosch, Gerald / Simonetti, Giovanna / Passariello, Claudio / Palamara, Anna Teresa et al. | 2006
- 1226
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Simple criterion for selection of flavonoid compounds with anti-HIV activityVeljkovic, Veljko / Mouscadet, Jean-François / Veljkovic, Nevena / Glisic, Sanja / Debyser, Zeger et al. | 2006
- 1233
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Synthesis and biological evaluation of 4-amino derivatives of benzimidazoquinoxaline, benzimidazoquinoline, and benzopyrazoloquinazoline as potent IKK inhibitorsBeaulieu, Francis / Ouellet, Carl / Ruediger, Edward H. / Belema, Makonen / Qiu, Yuping / Yang, Xuejie / Banville, Jacques / Burke, James R. / Gregor, Kurt R. / MacMaster, John F. et al. | 2006
- 1238
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Synthesis, characterization, antibacterial activity, and interaction with DNA of the vanadyl-enrofloxacin complexEfthimiadou, Eleni K. / Katsaros, Nikos / Karaliota, Alexandra / Psomas, George et al. | 2006
- 1243
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Synthesis of 3-(1H-benzimidazol-2-yl)-5-isoquinolin-4-ylpyrazolo[1,2-b]pyridine, a potent cyclin dependent kinase 1 (CDK1) inhibitorHuang, Shenlin / Lin, Ronghui / Yu, Yang / Lu, Yanhua / Connolly, Peter J. / Chiu, George / Li, Shengjian / Emanuel, Stuart L. / Middleton, Steven A. et al. | 2006
- 1246
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Thienopyridine urea inhibitors of KDR kinaseHeyman, H. Robin / Frey, Robin R. / Bousquet, Peter F. / Cunha, George A. / Moskey, Maria D. / Ahmed, Asma A. / Soni, Niru B. / Marcotte, Patrick A. / Pease, Lori J. / Glaser, Keith B. et al. | 2006
- 1250
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Development of new pyrrolopyrimidine-based inhibitors of Janus kinase 3 (JAK3)Clark, Michael P. / George, Kelly M. / Bookland, Roger G. / Chen, Jack / Laughlin, Steven K. / Thakur, Kumar D. / Lee, Wenlin / Davis, Jan R. / Cabrera, Ed J. / Brugel, Todd A. et al. | 2006
- 1254
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Bicyclic carbamates as inhibitors of papain-like cathepsin proteasesEpple, Robert / Urbina, Hugo D. / Russo, Ross / Liu, Hong / Mason, Daniel / Bursulaya, Badry / Tumanut, Christine / Li, Jun / Harris, Jennifer L. et al. | 2006
- 1260
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Weak base dispiro-1,2,4-trioxolanes: Potent antimalarial ozonidesTang, Yuanqing / Dong, Yuxiang / Wittlin, Sergio / Charman, Susan A. / Chollet, Jacques / Chiu, Francis C.K. / Charman, William N. / Matile, Hugues / Urwyler, Heinrich / Dorn, Arnulf et al. | 2006
- 1266
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A novel diketo phosphonic acid that exhibits specific, strand-transfer inhibition of HIV integrase and anti-HIV activityChi, Guochen / Nair, Vasu / Semenova, Elena / Pommier, Yves et al. | 2006
- 1270
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Identification of arylsulfonamides as Aquaporin 4 inhibitorsHuber, Vincent J. / Tsujita, Mika / Yamazaki, Maya / Sakimura, Kenji / Nakada, Tsutomu et al. | 2006
- 1274
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3-[2-((2S)-2-Cyano-pyrrolidin-1-yl)-2-oxo-ethylamino]-3-methyl-butyramide analogues as selective DPP-IV inhibitors for the treatment of type-II diabetesCoumar, Mohane Selvaraj / Chang, Chung-Nien / Chen, Chiung-Tong / Chen, Xin / Chien, Chia-Hui / Tsai, Ting-Yueh / Cheng, Jai-Hong / Wu, Hsin-Yi / Han, Chia-Hung / Wu, Ssu-Hui et al. | 2006
- 1280
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High-throughput screening affords novel and selective trypanothione reductase inhibitors with anti-trypanosomal activityMartyn, Derek C. / Jones, Deuan C. / Fairlamb, Alan H. / Clardy, Jon et al. | 2006
- 1284
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3-Hydroxychromones as cyclin-dependent kinase inhibitors: Synthesis and biological evaluationLee, Jinho / Park, Taesik / Jeong, Shinwu / Kim, Kyoung-Hee / Hong, Changyong et al. | 2006
- 1288
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Synthesis, structural revision, and antioxidant activities of antimutagenic homoisoflavonoids from Hoffmanosseggia intricataSiddaiah, Vidavalur / Maheswara, Muchchintala / Venkata Rao, Chunduri / Venkateswarlu, Somepalli / Subbaraju, Gottumukkala V. et al. | 2006
- 1291
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3-Substituted-(5-arylfuran-2-ylcarbonyl)guanidines as NHE-1 inhibitorsLee, Sunkyung / Kim, Taemi / Lee, Byung Ho / Yoo, Sung-eun / Lee, Kyunghee / Yi, Kyu Yang et al. | 2006
- 1296
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N-(3-Cyano-4,5,6,7-tetrahydro-1-benzothien-2-yl)amides as potent, selective, inhibitors of JNK2 and JNK3Angell, Richard M. / Atkinson, Francis L. / Brown, Murray J. / Chuang, Tsu Tshen / Christopher, John A. / Cichy-Knight, Maria / Dunn, Allison K. / Hightower, Kendra E. / Malkakorpi, Susanna / Musgrave, James R. et al. | 2006
- 1302
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Rational design, synthesis, and structure–activity relationship of benzoxazolones: New potent mglu5 receptor antagonists based on the fenobam structureCeccarelli, Simona M. / Jaeschke, Georg / Buettelmann, Bernd / Huwyler, Jörg / Kolczewski, Sabine / Peters, Jens-Uwe / Prinssen, Eric / Porter, Richard / Spooren, Will / Vieira, Eric et al. | 2006
- 1307
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Synthesis and biological evaluation of fenobam analogs as mGlu5 receptor antagonistsJaeschke, Georg / Porter, Richard / Büttelmann, Bernd / Ceccarelli, Simona M. / Guba, Wolfgang / Kuhn, Bernd / Kolczewski, Sabine / Huwyler, Jörg / Mutel, Vincent / Peters, Jens-Uwe et al. | 2006
- 1312
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Structure–activity relationships of 3-aminoquinazolinediones, a new class of bacterial type-2 topoisomerase (DNA gyrase and topo IV) inhibitorsTran, Tuan P. / Ellsworth, Edmund L. / Sanchez, Joseph P. / Watson, Brian M. / Stier, Michael A. / Showalter, H.D. Hollis / Domagala, John M. / Shapiro, Martin A. / Joannides, E. Themis / Gracheck, Stephen J. et al. | 2006
- 1321
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Diastereoselective synthesis of glycosylated prolines as a-glucosidase inhibitors and organocatalyst in asymmetric aldol reactionPandey, J. / Dwivedi, N. / Singh, N. / Srivastava, A. K. / Tamarkar, A. / Tripathi, R. P. et al. | 2007
- 1321
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Diastereoselective synthesis of glycosylated prolines as α-glucosidase inhibitors and organocatalyst in asymmetric aldol reactionPandey, Jyoti / Dwivedi, Namrata / Singh, Nimisha / Srivastava, A.K. / Tamarkar, A. / Tripathi, R.P. et al. | 2006
- 1326
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Amino acid-based enantiomerically pure 3-substituted 1,4-benzodiazepin-2-ones: A new class of anti-ischemic agentsMishra, Jitendra Kumar / Garg, Puja / Dohare, Preeti / Kumar, Ashutosh / Siddiqi, Mohammad Imran / Ray, Madhur / Panda, Gautam et al. | 2006
- 1332
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Novel antiproliferative analogs of the Taq DNA polymerase inhibitor catalpolPungitore, Carlos R. / León, Leticia G. / García, Celina / Martín, Víctor S. / Tonn, Carlos E. / Padrón, José M. et al. | 2006
- 1336
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Carbonic anhydrase activators: An activation study of the human mitochondrial isoforms VA and VB with amino acids and aminesVullo, Daniela / Nishimori, Isao / Innocenti, Alessio / Scozzafava, Andrea / Supuran, Claudiu T. et al. | 2006
- 1341
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Synthesis and biological evaluation of new conformationally biased integrin ligands based on a tetrahydroazoninone scaffoldBanfi, Luca / Basso, Andrea / Damonte, Gianluca / Pellegrini, Federico De / Galatini, Andrea / Guanti, Giuseppe / Monfardini, Ilaria / Riva, Renata / Scapolla, Carlo et al. | 2006
- 1346
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Synthesis and antitubercular activity of quaternized promazine and promethazine derivativesBate, Aaron B. / Kalin, Jay H. / Fooksman, Eric M. / Amorose, Erica L. / Price, Cristofer M. / Williams, Heather M. / Rodig, Michael J. / Mitchell, Miguel O. / Cho, Sang Hyun / Wang, Yuehong et al. | 2006
- 1349
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3-Mercaptopropionic acids as efficacious inhibitors of activated thrombin activatable fibrinolysis inhibitor (TAFIa)Islam, Imadul / Bryant, Judi / May, Karen / Mohan, Raju / Yuan, Shendong / Kent, Lorraine / Morser, John / Zhao, Lei / Vergona, Ron / White, Kathy et al. | 2006
- 1355
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Anti-mycobacterial activity of a bis-sulfonamideWilkinson, Brendan L. / Bornaghi, Laurent F. / Wright, Anthony D. / Houston, Todd A. / Poulsen, Sally-Ann et al. | 2006
- 1358
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Inhibition of Src kinase activity by 7-ethynyl-4-phenylamino-3-quinolinecarbonitriles: Identification of SKS-927Boschelli, Diane H. / Barrios Sosa, Ana Carolina / Golas, Jennifer M. / Boschelli, Frank et al. | 2006
- 1362
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Synthesis and HIV-1 integrase inhibitory activity of spiroundecane(ene) derivativesShults, Elvira E. / Semenova, Elena A. / Johnson, Allison A. / Bondarenko, Svetlana P. / Bagryanskaya, Irina Y. / Gatilov, Yuri V. / Tolstikov, Genrikh A. / Pommier, Yves et al. | 2006
- 1369
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ortho-Substituted azoles as selective and dual inhibitors of VEGF receptors 1 and 2Kiselyov, Alexander S. / Piatnitski, Evgueni L. / Samet, Alexander V. / Kisliy, Victor P. / Semenov, Victor V. et al. | 2006
- 1376
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Potent, selective, and orally active adenosine A2A receptor antagonists: Arylpiperazine derivatives of pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidinesNeustadt, Bernard R. / Hao, Jinsong / Lindo, Neil / Greenlee, William J. / Stamford, Andrew W. / Tulshian, Deen / Ongini, Ennio / Hunter, John / Monopoli, Angela / Bertorelli, Rosalia et al. | 2006
- 1381
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Structural simplification of bioactive natural products with multicomponent synthesis: Dihydropyridopyrazole analogues of podophyllotoxinMagedov, Igor V. / Manpadi, Madhuri / Rozhkova, Elena / Przheval’skii, Nikolai M. / Rogelj, Snezna / Shors, Scott T. / Steelant, Wim F.A. / slambrouck, Severine Van / Kornienko, Alexander et al. | 2006
- 1386
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Challenges in the development of mGluR5 positive allosteric modulators: The discovery of CPPHAZhao, Zhijian / Wisnoski, David D. / O’Brien, Julie A. / Lemaire, Wei / Williams, David L. Jr. / Jacobson, Marlene A. / Wittman, Marion / Ha, Sookhee N. / Schaffhauser, Herve / Sur, Cyrille et al. | 2006
- 1392
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A potent and orally active HIV-1 integrase inhibitorEgbertson, Melissa S. / Moritz, H. Marie / Melamed, Jeffrey Y. / Han, Wei / Perlow, Debra S. / Kuo, Michelle S. / Embrey, Mark / Vacca, Joseph P. / Zrada, Matthew M. / Cortes, Amanda R. et al. | 2006
- 1399
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Dopamine/serotonin receptor ligands. Part 15: Oxygenation of the benz-indolo-azecine LE 300 leads to novel subnanomolar dopamine D1/D5 antagonistsEnzensperger, Christoph / Kilian, Susann / Ackermann, Marit / Koch, Anne / Kelch, Kristin / Lehmann, Jochen et al. | 2006
- 1403
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Quinazoline and benzimidazole MCH-1R antagonistsArienzo, Rosa / Cramp, Sue / Dyke, Hazel J. / Lockey, Peter M. / Norman, Dennis / Roach, Alan G. / Smith, Phil / Wong, Melanie / Wren, Stephen P. et al. | 2006
- 1408
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A molecular modeling analysis of novel non-hydroxamate inhibitors of TACESheppeck, James E. II / Tebben, Andrew / Gilmore, John L. / Yang, Anle / Wasserman, Zelda R. / Decicco, Carl P. / Duan, James J.-W. et al. | 2006
- 1413
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Discovery of novel hydantoins as selective non-hydroxamate inhibitors of tumor necrosis factor-a converting enzyme (TACE)Sheppeck, J. E. / Gilmore, J. L. / Yang, A. / Chen, X. T. / Xue, C. B. / Roderick, J. / Liu, R. Q. / Covington, M. B. / Decicco, C. P. / Duan, J. J. et al. | 2007
- 1413
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Discovery of novel hydantoins as selective non-hydroxamate inhibitors of tumor necrosis factor-α converting enzyme (TACE)Sheppeck, James E. II / Gilmore, John L. / Yang, Anle / Chen, Xiao-Tao / Xue, Chu-Biao / Roderick, John / Liu, Rui-Qin / Covington, Maryanne B. / Decicco, Carl P. / Duan, James J.-W. et al. | 2006
- 1418
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Synthesis and evaluation of novel chromogenic aminopeptidase substrates for microorganism detection and identificationJames, Arthur L. / Perry, John D. / Rigby, Annette / Stanforth, Stephen P. et al. | 2006
- 1422
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Discovery of 2-iminobenzimidazoles as a new class of trypanothione reductase inhibitor by high-throughput screeningHolloway, Georgina A. / Baell, Jonathan B. / Fairlamb, Alan H. / Novello, Patrizia M. / Parisot, John P. / Richardson, John / Watson, Keith G. / Street, Ian P. et al. | 2006
- 1428
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Ac2-DPD, the bis-(O)-acetylated derivative of 4,5-dihydroxy-2,3-pentanedione (DPD) is a convenient stable precursor of bacterial quorum sensing autoinducer AI-2Frezza, Marine / Soulère, Laurent / Balestrino, Damien / Gohar, Michel / Deshayes, Christian / Queneau, Yves / Forestier, Christiane / Doutheau, Alain et al. | 2006
- 1432
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Pyrazole-based factor Xa inhibitors containing N-arylpiperidinyl P4 residuesQiao, Jennifer X. / Cheng, Xuhong / Smallheer, Joanne M. / Galemmo, Robert A. / Drummond, Spencer / Pinto, Donald J.P. / Cheney, Daniel L. / He, Kan / Wong, Pancras C. / Luettgen, Joseph M. et al. | 2006
- 1438
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Synthesis and structure–activity relationship of N-acyl-Gly-, N-acyl-Sar- and N-blocked-boroPro inhibitors of FAP, DPP4, and POPTran, Thuy / Quan, Clifford / Edosada, Conrad Yap / Mayeda, Mark / Wiesmann, Christian / Sutherlin, Dan / Wolf, Beni B. et al. | 2006
- 1443
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4-[6-(2-Aminoethyl)naphthalen-2-yl]benzonitriles are potent histamine H3 receptor antagonists with high CNS penetrationBlack, Lawrence A. / Nersesian, Diana L. / Sharma, Padam / Ku, Yi-Yin / Bennani, Youssef L. / Marsh, Kennan C. / Miller, Thomas R. / Esbenshade, Timothy A. / Hancock, Arthur A. / Cowart, Marlon et al. | 2006
- 1447
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N-Alkyl-N-alkyloxycarbonylaminomethyl (NANAOCAM) prodrugs of carboxylic acid containing drugsMajumdar, Susruta / Sloan, Kenneth B. et al. | 2006
- 1451
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Novel membrane-localizing TEMPO derivatives for measurement of cellular oxidative stress at the cell membraneBan, Shizuka / Nakagawa, Hidehiko / Suzuki, Takayoshi / Miyata, Naoki et al. | 2006
- 1455
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Structure–activity relationship analysis of a novel necroptosis inhibitor, Necrostatin-5Wang, Ke / Li, Jinfeng / Degterev, Alexei / Hsu, Emily / Yuan, Junying / Yuan, Chengye et al. | 2006
- 1466
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Bis-styrylpyridine and bis-styrylbenzene derivatives as inhibitors for Aβ fibril formationByeon, Seong Rim / Lee, Ji Hoon / Sohn, Ji-Hoon / Kim, Dong Chan / Shin, Kye Jung / Yoo, Kyung Ho / Mook-Jung, Inhee / Lee, Won Koo / Kim, Dong Jin et al. | 2006
- 1466
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Bis-styrylpyridine and bis-styrylbenzene derivatives as inhibitors for Ab fibril formationByeon, S. R. / Lee, J. H. / Sohn, J. H. / Kim, D. C. / Shin, K. J. / Yoo, K. H. / Mook-Jung, I. / Lee, W. K. / Kim, D. J. et al. | 2007
- 1471
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Discovery of novel phosphorus-containing steroids as selective glucocorticoid receptor antagonistJiang, Weiqin / Fiordeliso, James J. / Allan, George / Linton, Olivia / Tannenbaum, Pamela / Xu, Jun / Zhu, Peifang / Gunnet, Joseph / Demarest, Keith / Lundeen, Scott et al. | 2006
- 1475
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Synthesis and cytotoxic activity of 17-carboxylic acid modified 23-hydroxy betulinic acid ester derivativesBi, Yi / Xu, Jinyi / Wu, Xiaoming / Ye, Wencai / Yuan, Shengtao / Zhang, Luyong et al. | 2006
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Editorial board| 2007
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Instructions to contributors| 2007