synthesis and anti-human immunodeficiency virus type 1 activity of (e)-n-phenylstyryl-n-alkylacetamide derivatives合成和反人类免疫缺陷病毒1型(e)活动-n-phenylstyryl-n-alkylacetamide衍生品.pdfVIP
- 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
- 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载。
- 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
- 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
- 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们。
- 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
- 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
synthesis and anti-human immunodeficiency virus type 1 activity of (e)-n-phenylstyryl-n-alkylacetamide derivatives合成和反人类免疫缺陷病毒1型(e)活动-n-phenylstyryl-n-alkylacetamide衍生品
Molecules 2009, 14, 3176-3186; doi:10.3390/molecule
OPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Article
Synthesis and Anti-Human Immunodeficiency Virus Type 1
Activity of (E)-N-Phenylstyryl-N-alkylacetamide Derivatives
1, 2 3 3 3
Pi Cheng *, Ji-Jun Chen , Ning Huang , Rui-Rui Wang , Yong-Tang Zheng and
1
Yi-Zeng Liang
1 School of Chemistry and Chemical Engineering, Central South University, Changsha 410083,
China
2 State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of
Botany, the Chinese Academy of Sciences, Kunming 650204, China
3 Laboratory of Molecular Immunopharmacology, Key Laboratory of Animal Models and Human
Diseases Mechanisms, Kunming Institute of Zoology, the Chinese Academy of Sciences, Kunming
650223, China
* Author to whom correspondence should be addressed; E-mail: picheng55@126.com;
Tel.: +86-731-8836376.
Received: 1 July 2009; in revised form: 30 July 2009 / Accepted: 26 August 2009 /
Published: 26 August 2009
Abstract: A series of (E)-N-phenylstyryl-N-alkylacetamides, 5, were synthesized by direct
reduction-acetylation of β-arylnitroolefins, followed by N-alkylation. The title compounds
were characterized by 1H-NMR, EIMS and IR analysis. All the synthesized compounds
were assayed as HIV-1 non-nucleoside reverse transcriptase inhibitors. A SAR study
您可能关注的文档
- substernal epicardial echocardiography in a patient undergoing left ventricular assist device a case report胸骨下的心外膜超声心动图在病人接受左心室辅助装置一个案例报告.pdf
- substitution treatment for opioid addicts in germany替代治疗阿片成瘾者在德国.pdf
- substitution of the α-lactalbumin transcription unit by a cat cdna within a bac clone silenced the locus in transgenic mice without affecting the physically linked cyclin t1 gene替换α-lactalbumin转录单位的一只猫cdna bac克隆中沉默的轨迹转基因老鼠而不影响身体的细胞周期蛋白t1基因有关.pdf
- substitution of exudative trace element losses in burned children替换在烧伤儿童渗出性微量元素的损失.pdf
- substrate binding mode and its implication on drug design for botulinum neurotoxin a衬底绑定模式及其对药物设计的含义为肉毒神经毒素.pdf
- substrate cooperativity in marine luciferases在海洋荧光素酶底物协同.pdf
- substrate temperature dependent surface morphology and photoluminescence of germanium quantum dots grown by radio frequency magnetron sputtering衬底温度依赖的表面形态和锗量子点的光致发光增长了射频磁控溅射.pdf
- sub-threshold depression and antidepressants use in a community sample searching anxiety and finding bipolar disorder亚阈值焦虑抑郁和抗抑郁药在社区样本中使用搜索,发现双相情感障碍.pdf
- substrate promiscuity of n-acetylhexosamine 1-kinases衬底的滥交n-acetylhexosamine 1-kinases.pdf
- subtitle synchronization across multiple screens and devices跨多个屏幕和字幕同步设备.pdf
文档评论(0)