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10107篇 您的检索式:期刊名="Bioorg"
    题名 作者 年代 出处 被引量
1Methyloxime-substituted aminopyrrolidine: A new surrogate for 7-basic group of quinolone 显示文摘Hong C Y Kim Y K Lee Y H 1998Bioorg Med Chem Lett1998,,8:2
2Structure determination of metabolites isolated from urine and bile after administration of AY4166, a novel D-phenylalanine-derivative hypoglycemic agent 显示文摘Takesada H Matsuda K Ohtake R 1996Bioorg Med Chem1996,4,10:2
3Triarylimidazole inhibitors of IL- 1 biosynthesis 显示文摘Gallageher TG Fier-Thompson SM Garigipati etal 1995Bioorg Med Chem Lett1995,5,8:2
4Modelisation, synthesis and anti-HIV activities of N, N, N',N'', N-pentakistetraazamacrocycles salts derivatives显示文摘Trabaud C Dessolin J Vileghe P 1997Bioorg Med Chem Lett1997,7,:2
5Potent non- steroidal progesterone receptor agonists: synthesis and SAR study of 6-aryl benzoxazines 显示文摘ZHANG P TEREFENKO EA FENSOME A 2002Bioorg Med Chem Lett2002,12,5:1
6显示文摘Schneider R Sehmitt F 2005Bioorg Med Chem2005,13,:1
7Synthesis and Preliminary Biological Evaluation of the ^99Tc^m Labeled Nitrobenzoimidazole and Nitrotriazole as Tumor Hypoxia Markers 显示文摘Zhang Y Chu T Gao X 2006Bioorg Med Chem Let2006,16,:1
8Aplysamine-1 and related analogs as histamine H3 receptor antagonists显示文摘SWANSON D M WILSON S J BOGGS J D 2006Bioorg Med Chem Lett2006,16,4:1
9Discovery and structure-activity relationships of 4-aminoquinazoline derivatives,a novel class of opioid receptor like-1 (ORL1) antagonists显示文摘Okano M Mito J Maruyama Y 2009Bioorg Med ChemLett2009,17,:1
10Antioxidant activity and xanthine oxidase inhibition activity of reductic acid: ascorbic acid analogue显示文摘Mashino T Takigawa Y Saito N 2000Bioorg Med Chem Lett2000,10,24:1
11Synthesis and biological evaluation of new derivatives of emodin 显示文摘Lars Teich Katja Scarlett Daub Vera Krugel 2004Bioorg Med Chem2004,12,22:1
12Synthesis and biological evaluation of 4-morpholino-2- phenylquinazolines and related derivatives as novel PI3 kinase p110alpha inhibitors 显示文摘Hayakawa M Kaizawa H Moritomo H 2006Bioorg Med Chem2006,14,20:1
13Cyclin-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 2003Bioorg Med Chem Lett2003,13,18:1
14Synthesis and cytotoxicity of water soluble quaternary salt derivatives of camptothecin显示文摘Zu Yuangang Li Qingyong Fu Yujie 2004Bioorg Med Chem Lett2004,14,15:1
15The design,sy-nthesis,and anti-tumor mechanism study of N-phosphoryl amino acid modified resveratrol analogues显示文摘LIU H C DONG A GAO C 2008Bioorg Med Chem2008,16,10:1
16Thalassiolins A-C: new marine-derived inhibitors of HIV eDNA integrase显示文摘Rowley D C Hansen M S T Rhodes D 2002Bioorg Med Chen2002,10,:1
17Amidine derived inhibitors of acidsensing ion channel-3(ASIC3)显示文摘Knduk S D Chang R K Wai J M 2009Bioorg Mad Chem Lett2009,19,15:1
18Synthesis and evaluation of 2' ,4',6'-trihydroxychalcones as a new class of tyrosinase inhibitors 显示文摘Jun N Hong G Jun K 2007Bioorg Med Chem2007,15,6:1
19Structural requirements of flavonoids for nitric oxide pro- duction inhibitory activity and mechanism of action 显示文摘Matsuda H 2003Bioorg Med Chem2003,9,:1
20Haemolytic ac tivity,cytotoxicity and membrane cell permeabilization of semi synthetic and natural lupane-and oleanane-type saponins显示文摘Gauthier C Legault J Girard-Lalancette IC 2009Bioorg med chem2009,17,5:1
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