|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Methyloxime-substituted aminopyrrolidine: A new surrogate for 7-basic group of quinolone 显示文摘 | Hong C Y Kim Y K Lee Y H | 1998 | Bioorg Med Chem Lett1998，，8： | 2 |
| 2 | Triarylimidazole inhibitors of IL- 1 biosynthesis 显示文摘 | Gallageher TG Fier-Thompson SM Garigipati etal | 1995 | Bioorg Med Chem Lett1995，5，8： | 2 |
| 3 | Modelisation, synthesis and anti-HIV activities of N, N, N',N'', N-pentakistetraazamacrocycles salts derivatives显示文摘 | Trabaud C Dessolin J Vileghe P | 1997 | Bioorg Med Chem Lett1997，7，： | 2 |
| 4 | Potent non- steroidal progesterone receptor agonists: synthesis and SAR study of 6-aryl benzoxazines 显示文摘 | ZHANG P TEREFENKO EA FENSOME A | 2002 | Bioorg Med Chem Lett2002，12，5： | 1 |
| 5 | Aplysamine-1 and related analogs as histamine H3 receptor antagonists显示文摘 | SWANSON D M WILSON S J BOGGS J D | 2006 | Bioorg Med Chem Lett2006，16，4： | 1 |
| 6 | Antioxidant activity and xanthine oxidase inhibition activity of reductic acid: ascorbic acid analogue显示文摘 | Mashino T Takigawa Y Saito N | 2000 | Bioorg Med Chem Lett2000，10，24： | 1 |
| 7 | Cyclin-dependent kinase 4 inhibitors as a treatment for cancer, part 1 : identification and optimisation of substituted 4,6-bis anilino pyrimidines 显示文摘 | Beattie J F Breault G A Green S | 2003 | Bioorg Med Chem Lett2003，13，18： | 1 |
| 8 | Synthesis and cytotoxicity of water soluble quaternary salt derivatives of camptothecin显示文摘 | Zu Yuangang Li Qingyong Fu Yujie | 2004 | Bioorg Med Chem Lett2004，14，15： | 1 |
| 9 | Synthesis and antiHIV activities of 2'-deoxy-2',2'-difluorofl-L -ribofuranosyl-pyrimidine and -purine nucleosides显示文摘 | Xiang YJ Lakshmi P Kotra CK | 1995 | Bioorg Med Chem Lett1995，5，7： | 1 |
| 10 | First identification of xanthone sulfonamides as potent acyl-CoA:cholesterol acyltransferase (ACAT) inhibitors显示文摘 | Hu HongGang Liao HongLi Zhang Jun | 2010 | Bioorg Med Chem Lett2010，20，10： | 1 |
| 11 | Inhibition of Mast Cell Leukotriene Release by Thiourea Derivatives显示文摘 | Venkatachalam T K Qazi S Samuel P | 2003 | Bioorg Med Chem Lett2003，13，： | 1 |
| 12 | 7-Substituted 2-phenyl-benzofurans as ERβ selective ligands显示文摘 | COLLINI M D KAUFMAN D H MANAS E S | 2004 | Bioorg Med Chem Lett2004，14，19： | 1 |
| 13 | Synthesis and antibacterial activity of novel neamine derivatives显示文摘 | Minowa N Akiyama Y Hiraiwa Y | 2006 | Bioorg Med Chem Lett2006，16，24： | 1 |
| 14 | DNA gyrase inhibitory and antibacterial activity of some flavones ( I ) 显示文摘 | Chemeng K A Schwender C F Fu K P | 1993 | Vioorg Med Chem Lett1993，3，2： | 1 |
| 15 | Synthesis and anti-HIV-1 activities of novel podo- phyllotoxin derivatives显示文摘 | CHEN Shi-wu WANG Yun-hua JIN Yan | 2007 | Bioorg Med Chem Lett2007，17，7： | 1 |
| 16 | Radical scavenging activites ofα-alanine C60ad-duct显示文摘 | Sun T Xu Z | 2006 | Bioorg Med Chem Lett2006，16，14： | 1 |
| 17 | Synthesis and pharma- cological validation of a novel series of non-steroidal FXR agonists 显示文摘 | Abel U Schluter T Schulz A | 2010 | Bioorg Med Chem Lett2010，20，： | 1 |
| 18 | Valsartan, a potent, orally active angiotensin II antagonist developed from the structurally new amino acid series 显示文摘 | Buhlmayer P Furet P Criscione L | 1994 | Bioorg Med Chem Lett1994，4，1： | 1 |
| 19 | 2, 4-Diaminopyrim- idine inhibitors of c-Met kinase bearing benzoxazepine anilines 显示文摘 | Zificsak CA Theroff JP Aimone LD | 2011 | Bioorg Med Chem Lett2011，21，2： | 1 |
| 20 | Discovery of diarylpyridine deriva- tives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors 显示文摘 | Tian XT Qin B J Lu H | 2009 | Bioorg Med Chem Lett2009，19，18： | 1 |
您所在的机构暂未开通此部分的功能，请联系管理员