1,2,3-Thiadiazole substituted pyrazolones as potent KDR/VEGFR-2 kinase inhibitors (English)
- New search for: Tripathy, Rabindranath
- New search for: Ghose, Arup
- New search for: Singh, Jasbir
- New search for: Bacon, Edward R.
- New search for: Angeles, Thelma S.
- New search for: Yang, Shi X.
- New search for: Albom, Mark S.
- New search for: Aimone, Lisa D.
- New search for: Herman, Joseph L.
- New search for: Mallamo, John P.
- New search for: Tripathy, Rabindranath
- New search for: Ghose, Arup
- New search for: Singh, Jasbir
- New search for: Bacon, Edward R.
- New search for: Angeles, Thelma S.
- New search for: Yang, Shi X.
- New search for: Albom, Mark S.
- New search for: Aimone, Lisa D.
- New search for: Herman, Joseph L.
- New search for: Mallamo, John P.
In:
Bioorganic and Medicinal Chemistry Letters
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17
, 6
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1793-1798
;
2006
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ISSN:
- Article (Journal) / Electronic Resource
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Title:1,2,3-Thiadiazole substituted pyrazolones as potent KDR/VEGFR-2 kinase inhibitors
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Contributors:Tripathy, Rabindranath ( author ) / Ghose, Arup ( author ) / Singh, Jasbir ( author ) / Bacon, Edward R. ( author ) / Angeles, Thelma S. ( author ) / Yang, Shi X. ( author ) / Albom, Mark S. ( author ) / Aimone, Lisa D. ( author ) / Herman, Joseph L. ( author ) / Mallamo, John P. ( author )
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Published in:Bioorganic and Medicinal Chemistry Letters ; 17, 6 ; 1793-1798
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Publisher:
- New search for: Elsevier Ltd
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Publication date:2006-12-13
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Size:6 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 6
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.
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Graphical contents list| 2007
- 1499
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Synthesis of a coumarin-based europium complex for bioanalyte labelingFéau, Clémentine / Klein, Emmanuel / Kerth, Paul / Lebeau, Luc et al. | 2007
- 1504
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The role of fluorine substitution in the structure–activity relationships (SAR) of classical cannabinoidsCrocker, Peter J. / Mahadevan, Anu / Wiley, Jenny L. / Martin, Billy R. / Razdan, Raj K. et al. | 2007
- 1508
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High-affinity carbamate analogues of morphinan at opioid receptorsPeng, Xuemei / Knapp, Brian I. / Bidlack, Jean M. / Neumeyer, John L. et al. | 2007
- 1512
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Probing binding requirements of NAD kinase with modified substrate (NAD) analoguesBonnac, Laurent / Chen, Liqiang / Pathak, Rashmi / Gao, Guangyao / Ming, Qian / Bennett, Eric / Felczak, Krzysztof / Kullberg, Martin / Patterson, Steven E. / Mazzola, Francesca et al. | 2007
- 1516
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Novel hydroxamic acid-related phosphinates: Inhibition of neutral aminopeptidase N (APN)Drag, Marcin / Grzywa, Renata / Oleksyszyn, Jozef et al. | 2007
- 1520
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Quinuclidines as selective agonists for alpha-7 nicotinic acetylcholine receptorsLeonik, Fedra M. / Papke, Roger L. / Horenstein, Nicole A. et al. | 2007
- 1523
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Discovery of an androgen receptor modulator pharmacophore based on 2-quinolinonesvan Oeveren, Arjan / Pio, Barbara A. / Tegley, Christopher M. / Higuchi, Robert I. / Wu, Min / Jones, Todd K. / Marschke, Keith B. / Negro-Vilar, Andrés / Zhi, Lin et al. | 2007
- 1527
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Novel selective androgen receptor modulators: SAR studies on 6-bisalkylamino-2-quinolinonesvan Oeveren, Arjan / Motamedi, Mehrnoush / Martinborough, Esther / Zhao, Shuo / Shen, Yixing / West, Sarah / Chang, William / Kallel, Adam / Marschke, Keith B. / López, Francisco J. et al. | 2007
- 1532
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Carbonic anhydrase inhibitors. Inhibition of transmembrane isozymes XII (cancer-associated) and XIV with anionsInnocenti, Alessio / Vullo, Daniela / Pastorek, Jaromir / Scozzafava, Andrea / Pastorekova, Silvia / Nishimori, Isao / Supuran, Claudiu T. et al. | 2006
- 1538
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Carbonic anhydrase inhibitors: Inhibition of cytosolic/tumor-associated isoforms I, II, and IX with iminodiacetic carboxylates/hydroxamates also incorporating benzenesulfonamide moietiesSantos, M. Amelia / Marques, Sergio / Vullo, Daniela / Innocenti, Alessio / Scozzafava, Andrea / Supuran, Claudiu T. et al. | 2006
- 1544
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In vitro antimalarial activity of hyperforin, a prenylated acylphloroglucinol. A structure–activity studyVerotta, Luisella / Appendino, Giovanni / Bombardelli, Ezio / Brun, Reto et al. | 2006
- 1549
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Antibody catalyzed hydrolysis of a quorum sensing signal found in Gram-negative bacteriaDe Lamo Marin, Sandra / Xu, Yang / Meijler, Michael M. / Janda, Kim D. et al. | 2006
- 1553
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Bile acid-based receptors containing 2,6-bis(acylamino)pyridine for recognition of uracil derivativesChattopadhyay, Prosenjit / Pandey, Pramod S. et al. | 2006
- 1558
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Identification of a potent and stable antiproliferative agent by the prodrug formation of a thiolate histone deacetylase inhibitorSuzuki, Takayoshi / Hisakawa, Shinya / Itoh, Yukihiro / Maruyama, Sakiko / Kurotaki, Mineko / Nakagawa, Hidehiko / Miyata, Naoki et al. | 2006
- 1562
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Antiviral activity of berberine and related compounds against human cytomegalovirusHayashi, Kyoko / Minoda, Kazuki / Nagaoka, Yasuo / Hayashi, Toshimitsu / Uesato, Shinichi et al. | 2006
- 1565
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Synthesis and in vitro binding studies of substituted piperidine naphthamides. Part I: Influence of the substitution on the basic nitrogen and the position of the amide on the affinity for D2L, D4.2, and 5-HT2A receptorsCarato, Pascal / Graulich, Amaury / Jensen, Niels / Roth, Bryan L. / Liégeois, Jean-François et al. | 2006
- 1570
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Synthesis and in vitro binding studies of substituted piperidine naphthamides. Part II: Influence of the substitution on the benzyl moiety on the affinity for D2L, D4.2, and 5-HT2A receptorsCarato, Pascal / Graulich, Amaury / Jensen, Niels / Roth, Bryan L. / Liégeois, Jean-François et al. | 2006
- 1575
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Synthesis and evaluation of prodrugs for anti-angiogenic pyrrolylmethylidenyl oxindolesMaskell, Lesley / Blanche, Emilie A. / Colucci, Marie A. / Whatmore, Jacqueline L. / Moody, Christopher J. et al. | 2006
- 1579
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Synthesis and biological evaluation of new taxoids derived from 2-deacetoxytaxinine JBotta, Maurizio / Armaroli, Silvia / Castagnolo, Daniele / Fontana, Gabriele / Pera, Paula / Bombardelli, Ezio et al. | 2006
- 1584
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Solid phase synthesis and SAR of small molecule agonists for the GPR40 receptorMcKeown, Stephen C. / Corbett, David F. / Goetz, Aaron S. / Littleton, Thomas R. / Bigham, Eric / Briscoe, Celia P. / Peat, Andrew J. / Watson, Steve P / Hickey, Deirdre M.B. et al. | 2006
- 1590
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Antitrypanosomal activity of quaternary naphthalimide derivativesMuth, Mathias / Hoerr, Verena / Glaser, Melanie / Ponte-Sucre, Alicia / Moll, Heidrun / Stich, August / Holzgrabe, Ulrike et al. | 2006
- 1594
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Pharmacophore mapping of diverse classes of farnesyltransferase inhibitorsEqubal, Tabish / Silakari, Om / Rambabu, Gundla / Ravikumar, Muttineni et al. | 2006
- 1601
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Synthesis of pseudopeptides based l-tryptophan as a potential antimicrobial agentLv, Jian / Yin, Liang / Liu, Tingting / Wang, Yongmei et al. | 2006
- 1608
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Immunomodulatory effects of two sapogenins 1 and 2 isolated from Luffa cylindrica in Balb/C miceKhajuria, Anamika / Gupta, Amit / Garai, Saraswati / Wakhloo, Basanti Purinima et al. | 2006
- 1613
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Synthesis and cytotoxicity of novel fatty acid-nucleoside conjugatesZhang, Yun-Xiao / Dai, Gui-Fu / Wang, Le / Tao, Jing-Chao et al. | 2006
- 1616
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Novel 4-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-2-yl)methylbenzofuran derivatives as selective a2C-adrenergic receptor antagonistsHagihara, K. / Kashima, H. / Iida, K. / Enokizono, J. / Uchida, S. i. / Nonaka, H. / Kurokawa, M. / Shimada, J. et al. | 2007
- 1616
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Novel 4-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-2-yl)methylbenzofuran derivatives as selective α2C-adrenergic receptor antagonistsHagihara, Koji / Kashima, Hajime / Iida, Kyoichiro / Enokizono, Junichi / Uchida, Shin-ichi / Nonaka, Hiromi / Kurokawa, Masako / Shimada, Junichi et al. | 2006
- 1622
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Efficient synthesis and biological evaluation of ω-oxygenated analogues of vitamin K2: Study of modification and structure–activity relationship of vitamin K2 metabolitesSuhara, Yoshitomo / Murakami, Aya / Kamao, Maya / Mimatsu, Shino / Nakagawa, Kimie / Tsugawa, Naoko / Okano, Toshio et al. | 2006
- 1626
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A new class of anti-MRSA and anti-VRE agents: Preparation and antibacterial activities of indole-containing compoundsYamamoto, Yasuo / Kurazono, Mizuyo et al. | 2006
- 1629
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Design and synthesis of BACE1 inhibitors containing a novel norstatine derivative (2R,3R)-3-amino-2-hydroxy-4-(phenylthio)butyric acidZiora, Zyta / Kasai, Soko / Hidaka, Koushi / Nagamine, Ayaka / Kimura, Tooru / Hayashi, Yoshio / Kiso, Yoshiaki et al. | 2006
- 1634
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Synthesis and biological evaluation of phosphonate derivatives as autotaxin (ATX) inhibitorsCui, Peng / Tomsig, Jose L. / McCalmont, William F. / Lee, Sangderk / Becker, Christopher J. / Lynch, Kevin R. / Macdonald, Timothy L. et al. | 2006
- 1641
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Pyrazolo[1,5-a]pyrimidin-7-yl phenyl amides as novel antiproliferative agents: Exploration of core and headpiece structure–activity relationshipsPowell, Dennis / Gopalsamy, Ariamala / Wang, Yanong D. / Zhang, Nan / Miranda, Miriam / McGinnis, John P. / Rabindran, Sridhar K. et al. | 2006
- 1646
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1-Arylpiperazinyl-4-cyclohexylamine derived isoindole-1,3-diones as potent and selective α-1a/1d adrenergic receptor ligandsLi, Shengjian / Chiu, George / Pulito, Virginia L. / Liu, Jingchun / Connolly, Peter J. / Middleton, Steven A. et al. | 2006
- 1646
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1-Arylpiperazinyl-4-cyclohexylamine derived isoindole-1,3-diones as potent and selective a-1a/1d adrenergic receptor ligandsLi, S. / Chiu, G. / Pulito, V. L. / Liu, J. / Connolly, P. J. / Middleton, S. A. et al. | 2007
- 1651
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Structural modifications of (1S,3S)-3-amino-4-difluoromethylenecyclopentanecarboxylic acid, a potent irreversible inhibitor of GABA aminotransferaseYuan, Hai / Silverman, Richard B. et al. | 2006
- 1655
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Synthesis and evaluation of 4-O-alkylated 2-deoxy-2,3-didehydro-N-acetylneuraminic acid derivatives as inhibitors of human parainfluenza virus type-3 sialidase activityTindal, David J. / Dyason, Jeffrey C. / Thomson, Robin J. / Suzuki, Takashi / Ueyama, Hiroo / Kuwahara, Yohta / Maki, Naoyoshi / Suzuki, Yasuo / Itzstein, Mark von et al. | 2006
- 1659
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3H-[1,2,4]-Triazolo[5,1-i]purin-5-amine derivatives as adenosine A2A antagonistsSilverman, Lisa S. / Caldwell, John P. / Greenlee, William J. / Kiselgof, Eugenia / Matasi, Julius J. / Tulshian, Deen B. / Arik, Leyla / Foster, Carolyn / Bertorelli, Rosalia / Monopoli, Angela et al. | 2006
- 1663
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Structure–activity relationship (SAR) studies of quinoxalines as novel HCV NS5B RNA-dependent RNA polymerase inhibitorsRong, Frank / Chow, Suetying / Yan, Shunqi / Larson, Gary / Hong, Zhi / Wu, Jim et al. | 2006
- 1667
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Inhibition of the mitochondrial F1F0-ATPase by ligands of the peripheral benzodiazepine receptorCleary, Joanne / Johnson, Kathryn M. / Opipari, Anthony W. Jr. / Glick, Gary D. et al. | 2006
- 1671
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Solid-phase analogue synthesis of caspase-3 inhibitors via palladium-catalyzed amination of 3-bromopyrazinonesIsabel, Elise / Aspiotis, Renee / Black, W. Cameron / Colucci, John / Fortin, Réjean / Giroux, André / Grimm, Erich L. / Han, Yongxin / Mellon, Christophe / Nicholson, Donald W. et al. | 2006
- 1675
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A novel, non-substrate-based series of glycine type 1 transporter inhibitors derived from high-throughput screeningLowe, J. / Drozda, S. / Qian, W. / Peakman, M.-C. / Liu, J. / Gibbs, J. / Harms, J. / Schmidt, C. / Fisher, K. / Strick, C. et al. | 2006
- 1679
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Identification and structure–activity relationships of substituted pyridones as inhibitors of Pim-1 kinaseCheney, I. Wayne / Yan, Shunqi / Appleby, Todd / Walker, Heli / Vo, Todd / Yao, Nanhua / Hamatake, Robert / Hong, Zhi / Wu, Jim Z. et al. | 2006
- 1684
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Discovery of anticonvulsant activity of abietic acid through application of linear discriminant analysisTalevi, Alan / Cravero, Mariana Sella / Castro, Eduardo A. / Bruno-Blanch, Luis E. et al. | 2006
- 1691
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Further studies on the binding of N1-substituted tryptamines at h5-HT6 receptorsNyandege, Abner / Kolanos, Renata / Roth, Bryan L. / Glennon, Richard A. et al. | 2006
- 1695
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Synthesis, antimycobacterial activity evaluation, and QSAR studies of chalcone derivativesSivakumar, P.M. / Seenivasan, S. Prabu / Kumar, Vanaja / Doble, Mukesh et al. | 2006
- 1701
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A spectroscopic and molecular modeling study of sinomenine binding to transferrinDu, Hongyan / Xiang, Junfeng / Zhang, Yazhou / Tang, Yalin et al. | 2006
- 1705
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Structure–activity relationship studies on quorum sensing ComXRO-E-2 pheromoneOkada, Masahiro / Yamaguchi, Hisao / Sato, Isao / Cho, Soo Jeong / Dubnau, David / Sakagami, Youji et al. | 2006
- 1708
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Synthesis and QSAR studies on hypotensive 1-[3-(4-substituted phenylthio) propyl]-4-(substituted phenyl) piperazinesSaxena, Anil K. / Rao, Jyoti / Chakrabarty, Ruchika / Saxena, Mridula / Srimal, R.C. et al. | 2006
- 1713
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Comparison of N,N′-diarylsquaramides and N,N′-diarylureas as antagonists of the CXCR2 chemokine receptorMcCleland, Brent W. / Davis, Roderick S. / Palovich, Michael R. / Widdowson, Katherine L. / Werner, Michelle L. / Burman, Miriam / Foley, James J. / Schmidt, Dulcie B. / Sarau, Henry M. / Rogers, Martin et al. | 2006
- 1713
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Comparison of N,Nprime-diarylsquaramides and N,Nprime-diarylureas as antagonists of the CXCR2 chemokine receptorMcCleland, B. W. / Davis, R. S. / Palovich, M. R. / Widdowson, K. L. / Werner, M. L. / Burman, M. / Foley, J. J. / Schmidt, D. B. / Sarau, H. M. / Rogers, M. et al. | 2007
- 1718
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Discovery of tetralin ureas as potent melanin concentrating hormone 1 receptor antagonistsGuo, Tao / Gu, Huizhong / Hobbs, Doug W. / Busler, Dennis E. / Rokosz, Laura L. et al. | 2006
- 1722
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Oxazolidinones as novel human CCR8 antagonistsJin, Jian / Wang, Yonghui / Wang, Feng / Kerns, Jeffery K. / Vinader, Victoria M. / Hancock, Ashley P. / Lindon, Matthew J. / Stevenson, Graeme I. / Morrow, Dwight M. / Rao, Parvathi et al. | 2006
- 1726
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Carbonic anhydrase inhibitors: Binding of an antiglaucoma glycosyl-sulfanilamide derivative to human isoform II and its consequences for the drug design of enzyme inhibitors incorporating sugar moietiesFiore, Anna Di / Scozzafava, Andrea / Winum, Jean-Yves / Montero, Jean-Louis / Pedone, Carlo / Supuran, Claudiu T. / De Simone, Giuseppina et al. | 2006
- 1732
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Design, synthesis, and biological evaluation of novel analogues of archazolid: A highly potent simplified V-ATPase inhibitorMenche, Dirk / Hassfeld, Jorma / Sasse, Florenz / Huss, Markus / Wieczorek, Helmut et al. | 2006
- 1736
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New thiopyrazolo[3,4-d]pyrimidine derivatives as anti-mycobacterial agentsBallell, Lluis / Field, Robert A. / Chung, Gavin A.C. / Young, Robert J. et al. | 2006
- 1741
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1,3-Diaminopropan-2-ol Sulfonamides as potent and selective inhibitors of the glycine transporter type 1Rahman, Shahzad S. / Coulton, Steven / Herdon, Hugh J. / Joiner, Graham F. / Jin, Jian / Porter, Roderick A. et al. | 2006
- 1746
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Butyl 2-(4-[1.1′-biphenyl]-4-yl-1H-imidazol-2-yl)ethylcarbamate, a potent sodium channel blocker for the treatment of neuropathic painLiberatore, Anne-Marie / Schulz, Jocelyne / Favre-Guilmard, Christine / Pommier, Jacques / Lannoy, Jacques / Pawlowski, Emilia / Barthelemy, Marie-Anne / Huchet, Marion / Auguet, Michel / Chabrier, Pierre-Etienne et al. | 2006
- 1746
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Butyl 2-(4-[1.1prime-biphenyl]-4-yl-1H-imidazol-2-yl)ethylcarbamate, a potent sodium channel blocker for the treatment of neuropathic painLiberatore, A. M. / Schulz, J. / Favre-Guilmard, C. / Pommier, J. / Lannoy, J. / Pawlowski, E. / Barthelemy, M. A. / Huchet, M. / Auguet, M. / Chabrier, P. E. et al. | 2007
- 1750
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Identification of novel glycine sulfonamide antagonists for the EP1 receptorMcKeown, Stephen C. / Hall, Adrian / Blunt, Richard / Brown, Susan H. / Chessell, Iain P. / Chowdhury, Anita / Giblin, Gerard M.P. / Healy, Mark P. / Johnson, Matthew R. / Lorthioir, Olivier et al. | 2006
- 1755
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N-Caffeoylphenalkylamide derivatives as bacterial efflux pump inhibitorsMichalet, Serge / Cartier, Gilbert / David, Bruno / Mariotte, Anne-Marie / Dijoux-franca, Marie-Geneviève / Kaatz, Glenn W. / Stavri, Michael / Gibbons, Simon et al. | 2006
- 1759
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A quantitative assessment of hERG liability as a function of lipophilicityWaring, Michael J. / Johnstone, Craig et al. | 2006
- 1765
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Discovery of non-covalent dipeptidyl peptidase IV inhibitors which induce a conformational change in the active siteSheehan, Scott M. / Mest, Hans-Juergen / Watson, Brian M. / Klimkowski, Valentine J. / Timm, David E. / Cauvin, Annick / Parsons, Stephen H. / Shi, Qing / Canada, Emily J. / Wiley, Michael R. et al. | 2006
- 1769
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Specific stabilization of DNA triple helices by indolo[2,1-b]quinazolin-6,12-dione derivativesChen, Grace Shiahuy / Bhagwat, Bhalchandra V. / Liao, Pei-Yin / Chen, Hui-Ting / Lin, Shwu-Bin / Chern, Ji-Wang et al. | 2006
- 1773
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Orally active 4-amino-5-diarylurea-furo[2,3-d]pyrimidine derivatives as anti-angiogenic agent inhibiting VEGFR2 and Tie-2Miyazaki, Yasushi / Tang, Jun / Maeda, Yutaka / Nakano, Masato / Wang, Liping / Nolte, Robert T. / Sato, Hideyuki / Sugai, Masaki / Okamoto, Yuji / Truesdale, Anne T. et al. | 2006
- 1779
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Potential synergism and inhibitors to multiple target enzymes of Xuefu Zhuyu Decoction in cardiac disease therapeutics: A computational approachHuang, Qin / Qiao, Xuebin / Xu, Xiaojie et al. | 2006
- 1784
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Synthesis of potent and tissue-selective androgen receptor modulators (SARMs): 2-(2,2,2)-Trifluoroethyl-benzimidazole scaffoldNg, Raymond A. / Lanter, James C. / Alford, Vernon C. / Allan, George F. / Sbriscia, Tifanie / Lundeen, Scott G. / Sui, Zhihua et al. | 2006
- 1788
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Discovery and SAR of isonicotinamide BACE-1 inhibitors that bind b-secretase in a N-terminal 10s-loop down conformationStauffer, S. R. / Stanton, M. G. / Gregro, A. R. / Steinbeiser, M. A. / Shaffer, J. R. / Nantermet, P. G. / Barrow, J. C. / Rittle, K. E. / Collusi, D. / Espeseth, A. S. et al. | 2007
- 1788
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Discovery and SAR of isonicotinamide BACE-1 inhibitors that bind β-secretase in a N-terminal 10s-loop down conformationStauffer, Shaun R. / Stanton, Matthew G. / Gregro, Alison R. / Steinbeiser, Melissa A. / Shaffer, Jennifer R. / Nantermet, Philippe G. / Barrow, James C. / Rittle, Kenneth E. / Collusi, Dennis / Espeseth, Amy S. et al. | 2006
- 1793
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1,2,3-Thiadiazole substituted pyrazolones as potent KDR/VEGFR-2 kinase inhibitorsTripathy, Rabindranath / Ghose, Arup / Singh, Jasbir / Bacon, Edward R. / Angeles, Thelma S. / Yang, Shi X. / Albom, Mark S. / Aimone, Lisa D. / Herman, Joseph L. / Mallamo, John P. et al. | 2006
- 1799
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Synthesis of novel diaryl ethers and their evaluation as antimitotic agentsIn, Jin-Kyung / Lee, Mi-Sung / Yang, Jung-Eun / Kwak, Jae-Hwan / Lee, Heesoon / Boovanahalli, Shanthaveerappa K. / Lee, Kyeong / Kim, Soo Jin / Moon, Seung Kee / Lee, Sungsook et al. | 2006
- 1803
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The synthesis and structure–activity relationship studies of selective acetyl-CoA carboxylase inhibitors containing 4-(thiazol-5-yl)but-3-yn-2-amino motif: Polar region modificationsXu, Xiangdong / Weitzberg, Moshe / Keyes, Robert F. / Li, Qun / Wang, Rongqi / Wang, Xiaojun / Zhang, Xiaolin / Frevert, Ernst U. / Camp, Heidi S. / Beutel, Bruce A. et al. | 2006
- 1808
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Antihyperglycemic and antidyslipidemic agent from Aegle marmelosNarender, T. / Shweta, S. / Tiwari, P. / Papi Reddy, K. / Khaliq, T. / Prathipati, P. / Puri, A. / Srivastava, A.K. / Chander, R. / Agarwal, S.C. et al. | 2006
- 1812
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The evaluation and structure–activity relationships of 2-benzoylaminobenzoic esters and their analogues as anti-inflammatory and anti-platelet aggregation agentsHsieh, Pei-Wen / Hwang, Tsong-Long / Wu, Chin-Chung / Chiang, Shin-Zan / Wu, Chung-I / Wu, Yang-Chang et al. | 2006
- 1818
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HeLa cells apoptosis induced by 1,7-dimethyl-1,4,7,10-tetraazacyclododecaneYang, Li / Liang, Feng / Liu, Min / Zheng, Congyi / Wan, Shuhui / Xiong, Xiaoqin / Zhang, Xiaolian / Shen, Chao / Zhou, Xiang et al. | 2006
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Instructions to contributors| 2007
- IFC
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Editorial board| 2007