中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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上海药物研究所 [22]
上海生物化学与细胞生... [3]
西北高原生物研究所 [2]
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期刊论文 [32]
会议论文 [2]
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2022 [1]
2020 [1]
2018 [2]
2017 [3]
2016 [5]
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Biochemist... [3]
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Design and semisynthesis of oleanolic acid derivatives as VEGF in- hibitors: Inhibition of VEGF-induced proliferation, angiogenesis, and VEGFR2 activation in HUVECs
期刊论文
OAI收割
CHINESE JOURNAL OF NATURAL MEDICINES, 2022, 卷号: 20, 期号: 3, 页码: 229-240
作者:
Meng Ning
;
Xie Hong-Xu
;
Hou Jia-Rong
;
Chen Yon-Bin
;
Wu Meng-Jun
  |  
收藏
  |  
浏览/下载:36/0
  |  
提交时间:2022/06/15
Oleanolic acid
Structural modification
VEGF inhibitor
VEGFR2
Angiogenesis
Discovery of a highly selective VEGFR2 kinase inhibitor CHMFL-VEGFR2-002 as a novel anti-angiogenesis agent
期刊论文
OAI收割
ACTA PHARMACEUTICA SINICA B, 2020, 卷号: 10
作者:
Jiang, Zongru
;
Wang, Li
;
Liu, Xuesong
;
Chen, Cheng
;
Wang, Beilei
  |  
收藏
  |  
浏览/下载:55/0
  |  
提交时间:2020/11/26
Cancer
VEGFR2 kinase
Kinase inhibitor
Angiogenesis
Inhibitor selectivity
PBA2 exhibits potent anti-tumor activity via suppression of VEGFR2 mediated-cell proliferation and angiogenesis
期刊论文
OAI收割
BIOCHEMICAL PHARMACOLOGY, 2018, 卷号: 150, 页码: 131-140
作者:
Fang, Xiaona
;
Xie, Hua
;
Luo, Min
;
Chen, Zhen
;
Wang, Fang
  |  
收藏
  |  
浏览/下载:44/0
  |  
提交时间:2019/01/08
Angiogenesis
And-tumor activity
Multi-tyrosine kinases inhibitor
PBA2
VEGFR2
Preclinical characterization of anlotinib, a highly potent and selective vascular endothelial growth factor receptor-2 inhibitor
期刊论文
OAI收割
CANCER SCIENCE, 2018, 卷号: 109, 期号: 4, 页码: 1207-1219
作者:
Xie, Chengying
;
Wan, Xiaozhe
;
Quan, Haitian
;
Zheng, Mingyue
;
Fu, Li
  |  
收藏
  |  
浏览/下载:55/0
  |  
提交时间:2019/01/08
angiogenesis
anlotinib
tyrosine kinase inhibitor
VEGF
VEGFR2
Evaluation of in vitro and in vivo activity of a multityrosine kinase inhibitor, AL3810, against human thyroid cancer
期刊论文
OAI收割
ACTA PHARMACOLOGICA SINICA, 2017, 卷号: 38, 期号: 11, 页码: 1533-1542
作者:
Xie, Qin
;
Chen, Hui
;
Ai, Jing
;
Gao, Ying-lei
;
Geng, Mei-yu
  |  
收藏
  |  
浏览/下载:27/0
  |  
提交时间:2019/01/08
thyroid cancer
AL3810
multi-tyrosine kinases inhibitor
angiogenesis
RET
Anti-angiogenesis through noninvasive to minimally invasive intraocular delivery of the peptide CC12 identified by in vivo-directed evolution
期刊论文
OAI收割
BIOMATERIALS, 2017, 卷号: 112, 页码: 218-233
作者:
Chen, Chong
;
Liu, Kun
;
Xu, Yupeng
;
Zhang, Pengwei
;
Suo, Yan
  |  
收藏
  |  
浏览/下载:36/0
  |  
提交时间:2019/01/08
Angiogenesis inhibitor
Cell-penetrating peptides
Intraocular drug delivery
In vivo-direction evolution
Neovascularization
Phage display
evaluationofinvitroandinvivoactivityofamultityrosinekinaseinhibitoral3810againsthumanthyroidcancer
期刊论文
OAI收割
actapharmacologicasinica, 2017, 卷号: 38, 期号: 11, 页码: 1533
作者:
Xie Qin
;
Chen Hui
;
Al Jing
;
Gao Yinglei
;
Geng Meiyu
  |  
收藏
  |  
浏览/下载:20/0
  |  
提交时间:2020/07/01
TARGETED THERAPIES
RET
CARCINOMA
MODELS
GROWTH
TUMORS
CELLS
thyroid cancer
AL3810
multi-tyrosine kinases inhibitor
angiogenesis
RET
DW10075, a novel selective and small-molecule inhibitor of VEGFR, exhibits antitumor activities both in vitro and in vivo
期刊论文
OAI收割
acta pharmacologica sinica, 2016, 卷号: 37, 期号: 3, 页码: 398-407
作者:
Li, Meng-yuan
;
Lv, Yong-cong
;
Tong, Lin-jiang
;
Peng, Ting
;
Qu, Rong
收藏
  |  
浏览/下载:27/0
  |  
提交时间:2016/07/19
DW10075
VEGF/VEGF receptor inhibitor
antitumor
angiogenesis
U87-MG human glioblastoma
DW10075, a novel selective and small-molecule inhibitor of VEGFR, exhibits antitumor activities both in vitro and in vivo
期刊论文
OAI收割
ACTA PHARMACOLOGICA SINICA, 2016, 卷号: 37, 期号: 3, 页码: 398-407
作者:
Li, Meng-yuan
;
Lv, Yong-cong
;
Tong, Lin-jiang
;
Peng, Ting
;
Qu, Rong
  |  
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2019/01/08
DW10075
VEGF/VEGF receptor inhibitor
antitumor
angiogenesis
U87-MG human glioblastoma
Design, synthesis and biological evaluation of biphenylurea derivatives as VEGFR-2 kinase inhibitors (II)
期刊论文
OAI收割
CHINESE CHEMICAL LETTERS, 2016, 卷号: 27, 期号: 2, 页码: 200-204
作者:
Gao, Guo-Rui
;
Li, Meng-Yuan
;
Lv, Yong-Cong
;
Cao, Su-Fen
;
Tong, Lin-Jiang
  |  
收藏
  |  
浏览/下载:18/0
  |  
提交时间:2019/01/08
Angiogenesis
Kinase
Inhibitor
VEGFR-2