维普中文期刊产品整合服务
15篇 您的检索式:作者名="Natero"
    题名 作者 年代 出处 被引量
1Ascaleable synthesis of BAY 43-9006 : a potent Raf ki-nase inhibitor for the treatment of cancer 显示文摘BANKSTON D DUMAS J NATERO R 2002OrgProc Res Dev2002,6,6:1
2A scaleable synthesis of Bay 43-9006:a potent raf kinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 2002Org Process Res Dev2002,6,6:1
3A scalable synthesis of BAY 43-9006:A potent Rafkinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 0,,06:1
4A scaleable synthesis of BAY 43-9006: a potent Raf kinase inhibitor for the treatment of cancer 显示文摘Bankston D Dumas J Natero R 2002Org Proc Res Dev2002,6,:1
5A scaleable synthesis of BAY 43-9006: a potent Raf kinase inhibitor for the treatment of cancer 显示文摘BANKSTON D DUMAS J NATERO R 2002Org Process Res Dev2002,6,6:1
6A scalable synthesis of BAY 43-9006:A potent Raf kinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 0,,06:1
7查看详情显示文摘Bankston D Dumas J Natero R Riedl B. Monahan M. Sibley R 0,,:1
8A scaleable synthesis of BAY 43-9006: A potent raf kinase inhibitor for the treatment of cancer显示文摘BANKSTON D DUMAS J NATERO R 2002Org Proc Res Dev2002,6,6:1
9A scalable synthesis of bay 43-9006: a potent rafkinase inhibitor for the treatment of cancer 显示文摘Monahan MK Sibley R Natero R 2002Org Process Res Dev2002,6,6:1
10Ascaleable synthesis of bay 43-9006 : a potential Raf ki-nase inhibitor for the treatment of cancer 显示文摘BANKSON D DUMAS J NATERO R 2002OrgProcess Res Dev2002,6,6:1
11Novel pyrrolidine melanin-concentrating hormone receptor 1 antagonists with reduced hERG inhibition显示文摘Fox BM Natero R Richard K Connors R Roveto PM Beckmann H 2011Bioorg Med Chem Lett2011,21,8:1
12A scaleable synthesis of BAY 43-9006:a potent raf kinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 2002Org Process Res Dev2002,6,6:1
13A scaleable synthesis of BAY43-9006:A potent raf kinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 0,,06:1
14A scaleable syn- thesis of BAY 43-9006: a potent raf kinase Inhibitor for the treat- ment of cancer 显示文摘BANKSTON D DUMAS J NATERO R 2002Org Process Res Dev2002,6,6:1
15A scaleable synthesis of BAY 43-9006: A potent raf kinase inhibitor for the treatment of cancer显示文摘Bankston D Dumas J Natero R 2002Org Process Res Deve2002,6,6:1
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