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
- 4283
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Graphical contents list| 2010
- 4308
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Allosteric and ATP-competitive kinase inhibitors of mTOR for cancer treatmentGarcía-Echeverría, Carlos et al. | 2010
- 4313
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5-Nitro-2-furoic acid hydrazones: Design, synthesis and in vitro antimycobacterial evaluation against log and starved phase culturesSriram, Dharmarajan / Yogeeswari, Perumal / Vyas, Devambatla Ravi Kumar et al. | 2010
- 4317
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Peptide deformylase inhibitors with retro-amide scaffold: Synthesis and structure–activity relationshipsLee, Seung Kyu / Choi, Kwang Hyun / Lee, Sang Jae et al. | 2010
- 4320
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Development of enzyme-activated photosensitizer based on intramolecular electron transferYogo, Takatoshi / Urano, Yasuteru / Kamiya, Mako et al. | 2010
- 4324
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The discovery of potent inhibitors of aldosterone synthase that exhibit selectivity over 11-β-hydroxylaseAdams, Christopher M. / Hu, Chii-Whei / Jeng, Arco Y. et al. | 2010
- 4324
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The discovery of potent inhibitors of aldosterone synthase that exhibit selectivity over 11-b-hydroxylaseAdams, C. M. / Hu, C. W. / Jeng, A. Y. et al. | 2010
- 4328
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Biaryl ethers as potent allosteric inhibitors of reverse transcriptase and its key mutant viruses: Aryl substituted pyrazole as a surrogate for the pyrazolopyridine motifSu, Dai-Shi / Lim, John J. / Tinney, Elizabeth et al. | 2010
- 4333
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Glucose uptake enhancing activity of puerarin and the role of C-glucoside suggested from activity of related compoundsKato, Eisuke / Kawabata, Jun et al. | 2010
- 4337
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Absolute configuration determination of isoflavan-4-ol stereoisomersKim, Mihyang / Won, Dongho / Han, Jaehong et al. | 2010
- 4342
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Synthesis and binding ability of 1,2,3-triazole-based triterpenoid receptors for recognition of Hg2+ ionHu, Jun / Zhang, Meng / Yu, Li B. et al. | 2010
- 4346
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Furan based cyclic homo-oligopeptides bind G-quadruplex selectively and repress c-MYC transcriptionAgarwal, Tani / Roy, Saumya / Chakraborty, Tushar Kanti et al. | 2010
- 4350
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6-Phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitorsCai, Jiaqiang / Baugh, Mark / Black, Darcey et al. | 2010
- 4355
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LuxR-dependent quorum sensing: Computer aided discovery of new inhibitors structurally unrelated to N-acylhomoserine lactonesSoulère, Laurent / Sabbah, Mohamad / Fontaine, Fanny et al. | 2010
- 4359
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Pyrido[2,3-b]pyrazines, discovery of TRPV1 antagonists with reduced potential for the formation of reactive metabolitesHodgetts, Kevin J. / Blum, Charles A. / Caldwell, Timothy et al. | 2010
- 4364
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Selective delivery of 2-hydroxy APA to Trypanosoma brucei using the melamine motifKlee, Nina / Wong, Pui Ee / Baragaña, Beatriz et al. | 2010
- 4367
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10-23 DNAzyme modified with (2′R)- and (2′S)-2′-deoxy-2′-C-methyluridine in the catalytic coreRobaldo, Laura / Montserrat, Javier M. / Iribarren, Adolfo M. et al. | 2010
- 4367
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10-23 DNAzyme modified with (2primeR)- and (2primeS)-2prime-deoxy-2prime-C-methyluridine in the catalytic coreRobaldo, L. / Montserrat, J. M. / Iribarren, A. M. et al. | 2010
- 4371
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Carbamoyloximes as novel non-competitive mGlu5 receptor antagonistsGalambos, János / Wágner, Gábor / Nógrádi, Katalin et al. | 2010
- 4376
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Carbonic anhydrase inhibitors. The X-ray crystal structure of human isoform II in adduct with an adamantyl analogue of acetazolamide resides in a less utilized binding pocket than most hydrophobic inhibitorsAvvaru, Balendu Sankara / Wagner, Jason M. / Maresca, Alfonso et al. | 2010
- 4382
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Synthesis of a d-Ala-d-Ala peptide isostere via olefin cross-metathesis and evaluation of vancomycin bindingQuinn, Ryan K. / Cianci, Amelia L. / Beaudoin, Jennifer A. et al. | 2010
- 4386
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A novel, broad-spectrum anticancer compound containing the imidazo[4,5-e][1,3]diazepine ring systemXie, Min / Ujjinamatada, Ravi K. / Sadowska, Mariola et al. | 2010
- 4390
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3-Cyano-5-fluoro-N-arylbenzamides as negative allosteric modulators of mGlu5: Identification of easily prepared tool compounds with CNS exposure in ratsFelts, Andrew S. / Lindsley, Stacey R. / Lamb, Jeffrey P. et al. | 2010
- 4395
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Synthesis and SAR of azolopyrimidines as potent and selective dipeptidyl peptidase-4 (DPP4) inhibitors for type 2 diabetesBrigance, Robert P. / Meng, Wei / Fura, Aberra et al. | 2010
- 4399
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Spiroindane based amides as potent and selective MC4R agonists for the treatment of obesityHe, Shuwen / Ye, Zhixiong / Dobbelaar, Peter H. et al. | 2010
- 4406
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A new group of oxime carbamates as reversible inhibitors of fatty acid amide hydrolaseGattinoni, Sonia / Simone, Chiara De / Dallavalle, Sabrina et al. | 2010
- 4412
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Enhancement of transcriptional activity of mutant p53 tumor suppressor protein through stabilization of tetramer formation by calix[6]arene derivativesKamada, Rui / Yoshino, Wataru / Nomura, Takao et al. | 2010
- 4416
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Synthesis and evaluation of b-carboline derivatives as inhibitors of human immunodeficiency virusBrahmbhatt, K. G. / Ahmed, N. / Sabde, S. et al. | 2010
- 4416
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Synthesis and evaluation of β-carboline derivatives as inhibitors of human immunodeficiency virusBrahmbhatt, Keyur G. / Ahmed, Nafees / Sabde, Sudeep et al. | 2010
- 4420
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Docking and SAR studies of salacinol derivatives as α-glucosidase inhibitorsNakamura, Shinya / Takahira, Kazunori / Tanabe, Genzoh et al. | 2010
- 4420
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Docking and SAR studies of salacinol derivatives as a-glucosidase inhibitorsNakamura, S. / Takahira, K. / Tanabe, G. et al. | 2010
- 4424
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Synthesis and anti-inflammatory activity of some 3-(4,6-disubtituted-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl) propanoic acid derivativesMokale, Santosh N. / Shinde, Sandeep S. / Elgire, Rupali D. et al. | 2010
- 4427
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Active site binding modes of dimeric phloroglucinols for HIV-1 reverse transcriptase, protease and integraseGupta, Pawan / Kumar, Rajender / Garg, Prabha et al. | 2010
- 4432
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Synthesis of highly functionalized 2,4-diaminoquinazolines as anticancer and anti-HIV agentsYan, Sheng-Jiao / Zheng, Han / Huang, Chao et al. | 2010
- 4436
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In silico studies on the substrate specificity of an l-arabinose isomerase from Bacillus licheniformisPrabhu, Ponnandy / Jeya, Marimuthu / Lee, Jung-Kul et al. | 2010
- 4440
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Synthesis and pharmacological evaluation of aryl aminosulfonamide derivatives as potent 5-HT6 receptor antagonistsNirogi, Ramakrishna V.S. / Daulatabad, Anand V. / Parandhama, G. et al. | 2010
- 4444
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Derivatives of tetrahydroisoquinoline: Synthesis and initial evaluation of novel non-peptide antagonists of the αIIbβ3-integrinKrysko, Andrei A. / Krysko, Olga L. / Kabanova, Tatyana A. et al. | 2010
- 4444
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Derivatives of tetrahydroisoquinoline: Synthesis and initial evaluation of novel non-peptide antagonists of the aIIbb3-integrinKrysko, A. A. / Krysko, O. L. / Kabanova, T. A. et al. | 2010
- 4447
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2-Phenyl-9H-purine-6-carbonitrile derivatives as selective cathepsin S inhibitorsCai, Jiaqiang / Bennett, D. Jonathan / Rankovic, Zoran et al. | 2010
- 4451
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Petiolins J–M, prenylated acylphloroglucinols from Hypericum pseudopetiolatum var. kiusianumTanaka, Naonobu / Otani, Mio / Kashiwada, Yoshiki et al. | 2010
- 4456
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Prostaglandin phospholipid conjugates with unusual biophysical and cytotoxic propertiesPedersen, Palle J. / Adolph, Sidsel K. / Andresen, Thomas L. et al. | 2010
- 4459
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6-(4′-Aryloxy-phenyl)vinyl-1,2,4-trioxanes: A new series of orally active peroxides effective against multidrug-resistant Plasmodium yoelii in Swiss miceSingh, Chandan / Verma, Ved Prakash / Naikade, Niraj Krishna et al. | 2010
- 4459
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6-(4prime-Aryloxy-phenyl)vinyl-1,2,4-trioxanes: A new series of orally active peroxides effective against multidrug-resistant Plasmodium yoelii in Swiss miceSingh, C. / Verma, V. P. / Naikade, N. K. et al. | 2010
- 4464
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Synthesis of 2-(4-substituted benzyl-1,4-diazepan-1-yl)-N-(3,4-dihydro-3-oxo-2H-benzo[b][1,4]oxazin-7-yl)acetamides and their positive inotropic evaluationYang, Kun / Sun, Liang-Peng / Liu, Ji-Yong et al. | 2010
- 4468
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Synthesis and in vitro evaluation of N-alkyl-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one analogs as potential anticancer agentsPenthala, Narsimha Reddy / Yerramreddy, Thirupathi Reddy / Madadi, Nikhil Reddy et al. | 2010
- 4472
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GPR109a agonists. Part 2: Pyrazole-acids as agonists of the human orphan G-protein coupled receptor GPR109aImbriglio, Jason E. / Chang, Sookhee / Liang, Rui et al. | 2010
- 4475
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Aryl boronic acid inhibition of synthetic melanin polymerizationBelitsky, Jason M. et al. | 2010
- 4479
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Synthesis and pharmacological evaluation of 1,1,3-substituted urea derivatives as potent TNF-α production inhibitorsEnomoto, Hiroshi / Sawa, Ayako / Suhara, Hiroshi et al. | 2010
- 4479
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Synthesis and pharmacological evaluation of 1,1,3-substituted urea derivatives as potent TNF-a production inhibitorsEnomoto, H. / Sawa, A. / Suhara, H. et al. | 2010
- 4483
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Optimization of privileged structures for selective and potent melanocortin subtype-4 receptor ligandsHong, Qingmei / Bakshi, Raman K. / Dellureficio, James et al. | 2010
- 4487
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Benzylisoquinoline alkaloids from the tubers of Corydalis ternata and their cytotoxicityKim, Ki Hyun / Lee, Il Kyun / Piao, Cheng Jie et al. | 2010
- 4491
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Design and synthesis of 4-[3,5-dioxo-11-oxa-4,9-diazatricyclo[5.3.1.02,6]undec-4-yl]-2-trifluoromethyl-benzonitriles as androgen receptor antagonistsXiao, Hai-Yun / Balog, Aaron / Attar, Ricardo M. et al. | 2010
- 4496
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Antimalarial 3-arylamino-6-benzylamino-1,2,4,5-tetrazinesNhu, Duong / Duffy, Sandra / Avery, Vicky M. et al. | 2010
- 4499
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N-Demethylation of N-methyl alkaloids with ferroceneKok, Gaik B. / Scammells, Peter J. et al. | 2010
- 4503
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Natural products-based insecticidal agents 6. Design, semisynthesis, and insecticidal activity of novel monomethyl phthalate derivatives of podophyllotoxin against Mythimna separata Walker in vivoXu, Hui / He, Xiao-Qiang et al. | 2010
- 4507
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4-(3-Trifluoromethylphenyl)-pyrimidine-2-carbonitrile as cathepsin S inhibitors: N3, not N1 is critically importantCai, Jiaqiang / Fradera, Xavier / van Zeeland, Mario et al. | 2010
- 4511
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Coumarins incorporating hydroxy- and chloro-moieties selectively inhibit the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII over the cytosolic ones I and IIMaresca, Alfonso / Supuran, Claudiu T. et al. | 2010
- 4515
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NF-kB inducing kinase (NIK) inhibitors: Identification of new scaffolds using virtual screeningMortier, J. / Masereel, B. / Remouchamps, C. et al. | 2010
- 4515
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NF-κB inducing kinase (NIK) inhibitors: Identification of new scaffolds using virtual screeningMortier, Jérémie / Masereel, Bernard / Remouchamps, Caroline et al. | 2010
- 4521
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Piperidinyl-nicotinamides as potent and selective somatostatin receptor subtype 5 antagonistsAlker, André / Binggeli, Alfred / Christ, Andreas D. et al. | 2010
- 4526
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Discovery of 3-(2-aminoethyl)-5-(3-phenyl-propylidene)-thiazolidine-2,4-dione as a dual inhibitor of the Raf/MEK/ERK and the PI3K/Akt signaling pathwaysLi, Qianbin / Wu, Jingde / Zheng, Hui et al. | 2010
- 4531
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Small molecule functional analogs of peptides that inhibit l site-specific recombination and bind Holliday junctionsRanjit, D. K. / Rideout, M. C. / Nefzi, A. et al. | 2010
- 4531
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Small molecule functional analogs of peptides that inhibit λ site-specific recombination and bind Holliday junctionsRanjit, Dev K. / Rideout, Marc C. / Nefzi, Adel et al. | 2010
- 4535
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N-Benzylsalicylthioamides as novel compounds with promising antimycotic activityPetrlíková, Eva / Waisser, Karel / Buchta, Vladimír et al. | 2010
- 4539
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Synthesis and anti-HCV activity of 3′,4′-oxetane nucleosidesChang, Wonsuk / Du, Jinfa / Rachakonda, Suguna et al. | 2010
- 4539
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Synthesis and anti-HCV activity of 3prime,4prime-oxetane nucleosidesChang, W. / Du, J. / Rachakonda, S. et al. | 2010
- 4544
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Celecoxib prodrugs possessing a diazen-1-ium-1,2-diolate nitric oxide donor moiety: Synthesis, biological evaluation and nitric oxide release studiesAbdellatif, Khaled R.A. / Chowdhury, Morshed A. / Velázquez, Carlos A. et al. | 2010
- 4550
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Discovery of novel sphingosine kinase-1 inhibitors. Part 2Xiang, Yibin / Hirth, Bradford / Kane, John L. Jr. et al. | 2010
- 4555
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Synthesis and activity of polyacetylene substituted 2-hydroxy acids, esters, and amides against microbes of clinical importanceKyi, Stella / Wongkattiya, Nalin / Warden, Andrew C. et al. | 2010
- 4558
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β-Secretase (BACE-1) inhibitory effect of biflavonoidsSasaki, Hiroaki / Miki, Kazuhiko / Kinoshita, Kaoru et al. | 2010
- 4558
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b-Secretase (BACE-1) inhibitory effect of biflavonoidsSasaki, H. / Miki, K. / Kinoshita, K. et al. | 2010
- 4561
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Identification of novel α7 nAChR positive allosteric modulators with the use of pharmacophore in silico screening methodsCapelli, Anna Maria / Castelletti, Laura / Salvagno, Cristian et al. | 2010
- 4561
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Identification of novel a7 nAChR positive allosteric modulators with the use of pharmacophore in silico screening methodsCapelli, A. M. / Castelletti, L. / Salvagno, C. et al. | 2010
- 4566
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A specific and direct comparison of the trifluoromethyl and pentafluoro sulfanyl groups on the selective dopamine D3 antagonist 3-(3-{[4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-4H-1,2,4-triazol-3-yl]thio}propyl)-1-phenyl-3-azabicyclo[3.1.0]hexane templateMicheli, Fabrizio / Andreotti, Daniele / Braggio, Simone et al. | 2010
- 4569
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Ceratinadins A–C, new bromotyrosine alkaloids from an Okinawan marine sponge Pseudoceratina sp.Kon, Yuji / Kubota, Takaaki / Shibazaki, Azusa et al. | 2010
- 4573
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Rational design of a novel peripherally-restricted, orally active CB1 cannabinoid antagonist containing a 2,3-diarylpyrrole motifHortala, Laurent / Rinaldi-Carmona, Murielle / Congy, Christian et al. | 2010
- 4578
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Regioselective synthesis of folate receptor-targeted agents derived from epothilone analogs and folic acidVlahov, Iontcho R. / Vite, Gregory D. / Kleindl, Paul J. et al. | 2010
- 4582
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A novel aryl-hydrazide from the marine lichen Lichina pygmaea: Isolation, synthesis of derivatives, and cytotoxicity assaysRoullier, Catherine / Chollet-Krugler, Marylène / Weghe, Pierre van de et al. | 2010
- 4587
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Heteroaryl-linked 5-(1H-benzimidazol-1-yl)-2-thiophenecarboxamides: Potent inhibitors of polo-like kinase 1 (PLK1) with improved drug-like propertiesRheault, Tara R. / Donaldson, Kelly H. / Badiang-Alberti, Jennifer G. et al. | 2010
- 4593
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Aryl sulfonamides containing tetralin allylic amines as potent and selective bradykinin B1 receptor antagonistsLiu, Qingyian / Qian, Wenyuan / Li, Aiwen et al. | 2010
- 4598
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5-Lipoxygenase-activating protein inhibitors. Part 3: 3-{3-tert-Butylsulfanyl-1-[4-(5-methoxy-pyrimidin-2-yl)-benzyl]-5-(5-methyl-pyridin-2-ylmethoxy)-1H-indol-2-yl]-2,2-dimethyl-propionic acid (AM643)—A potent FLAP inhibitor suitable for topical administrationStock, Nicholas / Baccei, Christopher / Bain, Gretchen et al. | 2010
- 4602
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T-type calcium channel blockers: spiro-piperidine azetidines and azetidinones—optimization, design and synthesisSmith, Elizabeth M. / Sorota, Steve / Kim, Hyunjin M. et al. | 2010
- 4607
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Addressing PXR liabilities of phthalazine-based hedgehog/smoothened antagonists using novel pyridopyridazinesKaizerman, Jacob A. / Aaron, Wade / An, Songzhu et al. | 2010
- 4611
-
Dimeric cyclohexane-1,3-dione oximes inhibit wheat acetyl-CoA carboxylase and show anti-malarial activityLouie, Theola / Goodman, C. Dean / Holloway, Georgina A. et al. | 2010
- 4614
-
Cyclic amide bioisosterism: Strategic application to the design and synthesis of HCV NS5B polymerase inhibitorsYang, Hanbiao / Hendricks, Robert T. / Arora, Nidhi et al. | 2010
- 4620
-
Structure–activity relationship of indoline-2-carboxylic acid N-(substituted)phenylamide derivativesKwak, Jae-Hwan / Kim, Yoseob / Park, Hyunjeong et al. | 2010
- 4624
-
Synthesis and evaluation of novel antifungal agents-quinoline and pyridine amide derivativesNakamoto, Kazutaka / Tsukada, Itaru / Tanaka, Keigo et al. | 2010
- 4627
-
Anibamine, a natural product CCR5 antagonist, as a novel lead for the development of anti-prostate cancer agentsZhang, Xueping / Haney, Kendra M. / Richardson, Amanda C. et al. | 2010
- 4631
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Identification of glycosylated exendin-4 analogue with prolonged blood glucose-lowering activity through glycosylation scanning substitutionUeda, Taichi / Ito, Takaomi / Tomita, Kazuyoshi et al. | 2010
- 4635
-
Propenylamide and propenylsulfonamide cephalosporins as a novel class of anti-MRSA β-lactamsPohlmann, Jens / Vasilevich, Natalya I. / Glushkov, Andrei I. et al. | 2010
- 4635
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Propenylamide and propenylsulfonamide cephalosporins as a novel class of anti-MRSA b-lactamsPohlmann, J. / Vasilevich, N. I. / Glushkov, A. I. et al. | 2010
- 4639
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BACE-1 hydroxyethylamine inhibitors using novel edge-to-face interaction with Arg-296Clarke, Brian / Cutler, Leanne / Demont, Emmanuel et al. | 2010
- 4645
-
Deoxynojirimycin and its hexosaminyl derivatives bind to natural killer cell receptors rNKR-P1A and hCD69Catelani, Giorgio / D’Andrea, Felicia / Griselli, Alessio et al. | 2010
- 4649
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Use of 2-[18F]fluoroethylazide for the Staudinger ligation – Preparation and characterisation of GABAA receptor binding 4-quinolonesGaeta, Alessandra / Woodcraft, John / Plant, Stuart et al. | 2010
- 4653
-
Structure–activity relationships and in vivo activity of (1H-pyrazol-4-yl)acetamide antagonists of the P2X7 receptorBeswick, Paul J. / Billinton, Andy / Chambers, Laura J. et al. | 2010
- 4657
-
Design, synthesis, and structure–activity relationships of pyrazole derivatives as potential FabH inhibitorsLv, Peng-Cheng / Sun, Juan / Luo, Yin et al. | 2010
- 4661
-
Synthesis, antidepressant evaluation and QSAR studies of novel 2-(5H-[1,2,4]triazino[5,6-b]indol-3-ylthio)-N-(substituted phenyl)acetamidesShelke, Suhas M. / Bhosale, Sharad H. et al. | 2010
- 4665
-
Synthesis of polyhalo acridones as pH-sensitive fluorescence probesHuang, Chao / Yan, Sheng-Jiao / Li, Yan-Mei et al. | 2010
- 4670
-
Synthesis and biological evaluation of novel benzodioxinocarbazoles (BDCZs) as potential anticancer agentsAyerbe, Nathalie / Routier, Sylvain / Gillaizeau, Isabelle et al. | 2010
- 4675
-
Synthesis of novel a-pyranochalcones and pyrazoline derivatives as Plasmodium falciparum growth inhibitorsWanare, G. / Aher, R. / Kawathekar, N. et al. | 2010
- 4675
-
Synthesis of novel α-pyranochalcones and pyrazoline derivatives as Plasmodium falciparum growth inhibitorsWanare, Gajanan / Aher, Rahul / Kawathekar, Neha et al. | 2010
- 4679
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Enantioselective biocatalytic synthesis of (S)-monastrolBlasco, Maria Alfaro / Thumann, Silvia / Wittmann, Jürgen et al. | 2010
- 4683
-
Pyrazolopyridazine alpha-2-delta-1 ligands for the treatment of neuropathic painMyatt, James W. / Healy, Mark P. / Bravi, Gianpaolo S. et al. | 2010
- 4689
-
Conformational organizations of G-quadruplexes composed of d(G4Tn)3G4Wong, Wan Chi / Zhuang, Jinyi / Ng, Selina Ling Ling et al. | 2010
- 4693
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Synthesis, larvicidal activity, and SAR studies of new benzoylphenylureas containing oxime ether and oxime ester groupSun, Ranfeng / Li, Yongqiang / Lü, Maoyun et al. | 2010
- 4700
-
Synthesis and evaluation of a new series of Neuropeptide S receptor antagonistsMelamed, Jeffrey Y. / Zartman, Amy E. / Kett, Nathan R. et al. | 2010
- 4704
-
Tricyclic imidazole antagonists of the Neuropeptide S ReceptorTrotter, B. Wesley / Nanda, Kausik K. / Manley, Peter J. et al. | 2010
- 4709
-
3-Cyano-6-(5-methyl-3-pyrazoloamino)pyridines: Selective Aurora A kinase inhibitorsAndo, Ryoichi / Ikegami, Hiroshi / Sakiyama, Makoto et al. | 2010
- 4712
-
Cancer cell specific gene delivery by laminin-derived peptide AG73-labeled liposomesIijima, Hiroshi / Negishi, Yoichi / Omata, Daiki et al. | 2010
- 4715
-
In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part IRevesz, Laszlo / Schlapbach, Achim / Aichholz, Reiner et al. | 2010
- 4719
-
In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part IIRevesz, Laszlo / Schlapbach, Achim / Aichholz, Reiner et al. | 2010
- IFC
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Editorial board| 2010