Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Bixia Weng"'
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 1, Pp o63-o63 (2013)
The title compound, C22H21Cl2NO, is a derivative of mono-carbonyl analogues of curcumin (MACs). The molecule has an E conformation for each of the olefinic bonds. The 1-propylpiperidin-4-one ring has a distorted chair conformation with the ring N and
Externí odkaz:
https://doaj.org/article/fb06ee5e8d3c4c378e2b7bba8f6bde97
Publikováno v:
Acta Microscopica. 2019, Vol. 28 Issue 4, p791-795. 5p.
Autor:
Bixia Weng, Chengxi Jiang, Jianzhang Wu, Qian Li, Huimin Li, Sicen Wang, Renyu Lin, Hui Deng, Xiaoyan Wei, Liping Chen, Haonan Wang
Publikováno v:
Apoptosis. 24:74-82
Pyroptosis is a novel manner of cell death that can be mediated by chemotherapy drugs. The awareness of pyroptosis is significantly increasing in the fields of anti-tumor research and chemotherapy drugs. Invoking the occurrence of pyroptosis is an at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66f387ab931199bded201b81fd246d57
https://doi.org/10.1007/s10495-018-1499-y
https://doi.org/10.1007/s10495-018-1499-y
Autor:
Liping, Chen, Bixia, Weng, Huimin, Li, Haonan, Wang, Qian, Li, Xiaoyan, Wei, Hui, Deng, Sicen, Wang, Chengxi, Jiang, Renyu, Lin, Jianzhang, Wu
Publikováno v:
Apoptosis : an international journal on programmed cell death. 24(1-2)
Pyroptosis is a novel manner of cell death that can be mediated by chemotherapy drugs. The awareness of pyroptosis is significantly increasing in the fields of anti-tumor research and chemotherapy drugs. Invoking the occurrence of pyroptosis is an at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e12fd48a4172de5fcbb9af3b45e3ebb6
https://pubmed.ncbi.nlm.nih.gov/30519834
https://pubmed.ncbi.nlm.nih.gov/30519834
Autor:
Guang Liang, Lingyi Shi, Guanqun Huang, Shilong Ying, Bixia Weng, Yanting Kang, Xiaojing Du, Zhankun Wang, Qiuxiang Chen, Jianzhang Wu, Rong Jin, Yiqun Xia
Publikováno v:
Tumor Biology. 37:4791-4801
The therapeutic agent selectively killing cancer cells is urgently needed for gastric cancer treatment. Curcumin has been investigated for its effect on the cancer treatment because of its significant therapeutic potential and safety profile. A synth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb83decda4dee93bd92ecf9c49c38c14
https://doi.org/10.1007/s13277-015-4277-2
https://doi.org/10.1007/s13277-015-4277-2
Autor:
Peihong Qiu, Thanchanok Sirirak, Jiabing Wang, Yangyang Zhou, Dezhi Cheng, Jianzhang Wu, Qian Li, Liping Chen, Bixia Weng
Publikováno v:
European journal of medicinal chemistry. 151
EF24 and F35 both were effective monocarbonyl curcumin analogues (MCACs) with excellent anti-tumor activity, however, drug defect such as toxicity may limit their further development. To get anti-lung cancer drugs with high efficiency, low toxicity a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87009531389a5aa538aafb16f4ef69a5
https://pubmed.ncbi.nlm.nih.gov/29655083
https://pubmed.ncbi.nlm.nih.gov/29655083
Autor:
Karvannan Kanchana, Xiaokun Li, Jiansong Ji, Bixia Weng, Yuepiao Cai, Peihong Qiu, Guang Liang, Yi Wang, Jianzhang Wu, Tao Wei
Publikováno v:
Oncotarget
Accumulating evidence suggests that high expression of FGFR1 is closely related to the development of lung cancer especially in non-small cell lung cancers (NSCLC), to which non-ATP competitive inhibitors represent an effective therapeutical approach
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ca0fcf8a5fafeace34dd132e84cc297
https://doi.org/10.18632/oncotarget.2122
https://doi.org/10.18632/oncotarget.2122
Autor:
Xiaokun Li, Kesong Peng, Bixia Weng, Yi Wang, Jie Hu, Shanmei Xu, Guang Liang, Tao Wei, Xiaoyan Wei, Yuepiao Cai, Huiping Zhou
Publikováno v:
Journal of Medicinal Chemistry. 56:9601-9611
Current precious-metal-containing anticancer agents are mostly chelated with N-containing ligands and function by interacting with DNA. In the present study, Pd(acac)2, a Pd(II) complex containing four O-donor ligands, has been evaluated as an active
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cde9f1df7d3dccf0f0f05b84e322e33c
https://doi.org/10.1021/jm4016312
https://doi.org/10.1021/jm4016312
Autor:
Bixia Weng, Xiangjian Chen, Jian Wang, Jianzhang Wu, Zheer Pan, Qinqin Tang, Guang Liang, Yuepiao Cai, Shulin Yang, Yali Zhang
Publikováno v:
Bioorganic & Medicinal Chemistry. 21:3058-3065
We previously reported the design and discovery of three series of 5-carbon linker-containing mono-carbonyl analogs of curcumin (MCACs) as excellent anti-inflammatory agents. In continuation of our ongoing research, we designed and synthesized the fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::902616437f7b1c18abf0c9268b2c0301
https://doi.org/10.1016/j.bmc.2013.03.057
https://doi.org/10.1016/j.bmc.2013.03.057
Publikováno v:
Acta Crystallographica Section E: Structure Reports
Acta Crystallographica Section E, Vol 69, Iss 1, Pp o63-o63 (2013)
Acta Crystallographica Section E, Vol 69, Iss 1, Pp o63-o63 (2013)
The title compound, C22H21Cl2NO, is a derivative of mono-carbonyl analogues of curcumin (MACs). The molecule has an E conformation for each of the olefinic bonds. The 1-propylpiperidin-4-one ring has a distorted chair conformation with the ring N and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aede98bbd5e72ec8871475777487f79
https://pubmed.ncbi.nlm.nih.gov/23476444
https://pubmed.ncbi.nlm.nih.gov/23476444