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Synthesis and anti-hepatocellular carcinoma evaluation of salicylic acid-modified indole trimethoxy flavonoid derivatives

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成果类型:
期刊论文
作者:
Zou, Yang;Lu, Na;Yang, Xiaoyan;Xie, Zhizhong;Lei, Xiaoyong;...
通讯作者:
Wang, Z;Tang, GT
作者机构:
[Wang, Zhe; Zou, Yang; Wang, Z] Univ South China, Affiliated Hosp 2, Hengyang Med Sch, Dept Pharm, Hengyang 421001, Hunan, Peoples R China.
[Yang, Xiaoyan; Xie, Zhizhong; Lei, Xiaoyong; Zou, Yang; Tang, Guotao] Univ South China, Inst Pharm & Pharmacol, Hengyang Med Sch, Hunan Prov Key Lab Tumor Microenvironm Respons Dru, Hengyang 421001, Hunan, Peoples R China.
[Lu, Na] Univ South China, Sch Nursing, Hengyang Med Sch, Hengyang 421001, Hunan, Peoples R China.
[Li, Yong; Liu, Xingyun] Univ South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Hengyang 421001, Hunan, Peoples R China.
[Huang, Sheng] Jiuzhitang Co Ltd, Changsha 410007, Hunan, Peoples R China.
通讯机构:
[Wang, Z ; Tang, GT ] U
Univ South China, Affiliated Hosp 2, Hengyang Med Sch, Dept Pharm, Hengyang 421001, Hunan, Peoples R China.
Univ South China, Inst Pharm & Pharmacol, Hengyang Med Sch, Hunan Prov Key Lab Tumor Microenvironm Respons Dru, Hengyang 421001, Hunan, Peoples R China.
语种:
英文
期刊:
RSC Medicinal Chemistry
ISSN:
2632-8682
年:
2023
卷:
14
期:
6
页码:
1172-1185
基金类别:
Hunan Provincial Key Laboratory of Tumor Microenvironment Responsive Drug Research [2019-56]; Natural Science Foundation of Hunan Province [2020JJ4534]; Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study
机构署名:
本校为第一且通讯机构
院系归属:
药学与生物科学学院
护理学院
摘要:
Simultaneous inhibition of tumor vasculature and the glycolysis pathway may be a targeted anti-tumor strategy to inhibit tumor nutrient supply. Flavonoids are natural products with strong biological activity, which inhibit hypoxia induction factor 1α (HIF-1α) regulating glycolysis and tumor angiogenesis, while salicylic acid can reduce the glycolysis level of tumor cells by inhibiting related rate-limiting enzymes. A series of salicylic acid-modified indole trimethoxy-flavone derivatives were designed and synthesized by introducing benzotrime...

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