Novel Pyran and Polyhydroquinoline Derivatives: Inhibiting Human Osteosarcoma Activity


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

A series of pyran 1–6 and polyhydroquinoline derivatives 7–9 are synthesized targeting anticancer agents for clinical trials. Their structures are characterized by IR, 1H NMR, and HRMS spectra, and single crystal X-ray crystallography. Their anticancer activity against four human osteosarcoma cells (Saos-2, MG-63, 143B, and U2-OS) is evaluated in vitro using the MTT assay. The compounds 7–9 demonstrate high anticancer activity against the four cancer cells.

作者简介

X.-X. Fan

Department of Orthopaedics

Email: xinhua_zhou666@yeah.net
中国, Huzhou, Zhejiang, 313003

P. Shen

Department of Orthopaedics

Email: xinhua_zhou666@yeah.net
中国, Huzhou, Zhejiang, 313003

X.-H. Zhou

Department of Orthopaedics

编辑信件的主要联系方式.
Email: xinhua_zhou666@yeah.net
中国, Huzhou, Zhejiang, 313003


版权所有 © Pleiades Publishing, Ltd., 2018
##common.cookie##