维普中文期刊产品整合服务
11篇 您的检索式:作者名="BOYER SH"
    题名 作者 年代 出处 被引量
1Design,synthesis,and characterization of a series of cytochrome P 450 3A-activated prodrugs useful for targeting phosph(on)ate-based drugs to the liver显示文摘Erion MD Reddy KR Boyer SH 2004J Am Chem Soc2004,126,16:1
2Design, synthesis, and characterization of a series of cytochrome P(450) 3A-activated prodrugs ( HepDirect prodrugs) useful for targeting phosph (on)ate-based drugs to the liver显示文摘ERION MD REDDY KR BOYER SH 2004J Am Chem Soc2004,126,16:1
3Design, synthesis, and characterization of a series of cytochrome P4503A-activated prodmgs(HepDirect prodrugs)useful for targeting phosph(on)atebased drugs to the liver显示文摘ERION MD REDDY KR BOYER SH 2004J Am Chem Soc2004,126,16:1
4Stereoselective synthesis of nucleoside monophosphate HepDirect prodrugs 显示文摘REDDY KR BOYER SH ERION MD 2005Tetrahedron Lett2005,46,25:1
5Synthesis and characterization of a novel liver-targeted prodrug of cytosine-1-β-D-arabinofaranoside monophosphate for the treatment of hepatocellular carcinoma显示文摘BOYER SH SUN Z JIANG HJ 2006J Med Chem2006,49,26:1
6Design, synthesis,and characterization of a series of cytochrome P(450) 3A-activated prodrugs (HepDirect prodrugs) usefulfor targeting phosph(on)ate-based drugs to the liver显示文摘Erion MD Reddy KR Boyer SH 2004JAm Chem Soc2004,126,16:1
7Fetal hemo- globin restriction to a few erythrocytes (F cells) in nor- mal humanadults显示文摘Boyer SH Belding TK Margolet L 1975Science1975,188,4186:1
8Mechanism of negative regula-tion of rat glutathione S-transferase A2 by the cytokine inter-leukin 6 显示文摘Voss SH Whalen R Boyer TD 2002Biochem J2002,365,1:1
9Decreased expression levels of rat liver glutathione S-transferase A2 and albumin during the acute phase response are mediated by HNF1 (hepatic nuclear factor 1) and IL6DEX-NP 显示文摘Whalen R Voss SH Boyer TD 2004Biochem J2004,377,3:1
10Design,synthesis,and characterization of a series of cytochrome P (450) 3A-activated prodrugs(HepDirect prodrugs)useful for targeting phosph(on)ate-based drugs to the liver显示文摘Erion MD Reddy KR Boyer SH 2004J Am Chem Soc2004,126,16:1
11Structures of HIV-1 RT-DNA complexes before and after incorporation of the anti-AIDS drug tenofovir显示文摘Tenofovir, also known as PMPA, R-9-(2-(phosphonomethoxypropyl)adenine, is a nucleotide reverse transcriptas e(RT) inhibitor. We have determined the crystal structures of two related complexes ofHIV-1 RT with template primer and tenofovir: (i) a ternary complex at a resolution of 3.0 Angstrom of RT crosslinked to a dideoxy-terminated DNA with tenofovir-diphosphate bound as the incoming substrate; and (ii) a RT DNA complex at a resolution of 3,1 Angstrom with tenofovir at the 3 primer terminus. The tenofovir nucleotide in the tenofovir-terminated structure seems to adopt multiple conformations. Some nucleoside reverse transcriptase inhibitors, including 3TC and AZT, have dements (handles) that project beyond the corresponding elements on normal dNTPs (the substrate envelope). HIV-1 RT resistance mechanisms to AZT and 3TC take advantage of these handles; tenofovir's structure lacks handles that could protrude through the substrate envelope to cause resistance.Tuske,S Sarafianos,SG Clark,AD Ding,JP Naeger,LK White,KL Miller,MD Gibbs,CS Boyer,PL Clark,P Wang,G Gaffney,BL Jones,RA Jerina,DM Hughes,SH Arnold,E 2005中国生物学文摘2005,19,2:0
返回顶部 每页显示:
共1页 首页 上一页 第1页 下一页 末页 /1 跳转

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费