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| 1 | Design, synthesis, and characterization of 6 beta-nahrexol analogs, and their selectivity for in vitro opioid receptor subtypes 显示文摘 | Pelotte A L Smith R M Ayestas M | 2009 | Bioorg Med Chem Left2009，19，10： | 1 |
| 2 | Bone-targeted 2,6,9-trisubstituted purines:novel inhibitors of Src tyrosine kinase for the treatment of bone diseases显示文摘 | Wang Y Metcalf CA Shakespeare WC | 2003 | Bioorg Med Chem Left2003，13，： | 1 |
| 3 | Synthesis and e- valuation of vancomycin and vancomycin aglycon ana- logues that bear modifications in the residue 3 aspargine 显示文摘 | Jeffrey M Steven L C Boger D L | 2002 | Bioorg&Med Chem Left2002，12，9： | 1 |
| 4 | Benzoxazole benzenesulfonaniides are novel allosterie inhlbitors of fructose-1, 6-hisphosphatase with a distinct billding mode 显示文摘 | VONGELDERN T W LAI C Q GUM R J | 2006 | Bioorg Med Chem Left2006，16，7： | 1 |
| 5 | Investigating the antiproliferative activity of quinoline-5,8-diones and styrylquinolinecarboxylic acids on tumor cell lines 显示文摘 | Podeszwa B Niedbala H Polanski J | 2007 | Bioorg Med Chem Left2007，17，22： | 1 |
| 6 | Discovery of 1 I~-hydroxysteroid dchydrogenase type I inhibitor显示文摘 | Hong S P Nam K Y Shin Y J | 2015 | Bioorg Med Chem Left2015，25，17： | 1 |
| 7 | Structure-based design of a thiazolidinedione which targets the mitochondrial protein mitoNEET显示文摘 | Geldenhuys WJ Funk MO Barnes KF | 2010 | Bioorg Med Chem Left2010，20，3： | 1 |
| 8 | Synthesis and biological evaluation of novel 1-O- and 14-O-derivatives of oridonin as potential anticancer drug candidates 显示文摘 | Xu J Yang J Ran Q | 2008 | Bioorg Med Chem Left2008，18，16： | 1 |
| 9 | Anti-inflammatory property of the urinary metabolites of nobiletin in mouse 显示文摘 | Li SM Sang SM Pan MH | 2007 | Bioorg Med Chem Left2007，17，18： | 1 |
| 10 | Synthesis and evaluation of 1-( quinoliloxypropyl )-4-aryl piperazines for atypical antipsychotie effect 显示文摘 | Bali A Malhotra S Dhir H | 2009 | Bioorg Med Left2009，19，： | 1 |
| 11 | Synthesis and activity of folate peptide camptothecin prodrug 显示文摘 | Henne WA Doorneweerd DD Hilgenbrink AR | 2006 | Bioorg Med Chem Left2006，16，20： | 1 |
| 12 | Synthesis and in vitro antibacterial activity of 7-(3-alkoxyimino-5-amino/meth-ylaminopiperidin-l-yl ) fluoroquinolone derivatives 显示文摘 | Zhang Y B Li G Q Liu M L | 2011 | Bioorg Med Chem Left2011，21，3： | 1 |
| 13 | Synthesis, characterization, and direct aqueous superoxide anion scavenging of a highly water-dispersible astaxanthinamino acid conjugate显示文摘 | Jackson H L Cardounel A J Zweier J L | 2004 | Bioorg Med Chem Left2004，14，： | 1 |
| 14 | Synthesis and evaluation of cytotoxic effects of novel a-methylenelactone tetracyclic diterpenoids 显示文摘 | Zeng Y F Wu J Q Shi L Y | 2012 | Bioorg Med Chem Left2012，22，5： | 1 |
| 15 | Novel, water-soluble phosphate derivatives of 2'-ethoxy carbonylpaclitaxel as potential prodmgs of paclitaxel: synthesis and antitumor evaluation显示文摘 | Ueda Y Matiskella JD Mikkilineni AB | 1995 | Bioorg Med Chem Left1995，5，3： | 1 |
| 16 | Discovery ofDA-1229: a potent, long acting dipeptidyl peptidase-4 inhibitor for the treatment of type 2 diabetes显示文摘 | Kim HJ Kwak WY Min JP | 2011 | Bioorg Med Chem Left2011，21，12： | 1 |
| 17 | 3-cyanoindole-based inhibitors of inosine monophosphate dehydrogenase: synthesis and initial structure-activity relationships 显示文摘 | DHAR T G SHEN Z GU H H | 2003 | Bioorg Med Chem Left2003，13，20： | 1 |
| 18 | Quinoline-carbox- rlie acids are potent inhibitors that inhibit the binding of insulin-like growth factor(IGF) to IGF-binding proteins 显示文摘 | Zhu Y F Wang X C Connors P et o2 | 2003 | Bioorg Med Chem Left2003，13，11： | 1 |
| 19 | Synthesis of the optical isomers of new anticholinergic drug, penehyclidine hydrochloride(8018) 显示文摘 | Han XY Liu H Liu CH | 2005 | Bioorg Med Chem Left2005，15，8： | 1 |
| 20 | 3-Pyridyl-ethanolamines: potent and selective human β3 adrenergic receptor agonists 显示文摘 | Naylor EM Colandrea VJ Candelore MR | 1998 | Bioorg Med Chem Left1998，8，21： | 1 |
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