Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Wen-Fang Xu"'
Publikováno v:
Frontiers in Neuroscience, Vol 4 (2010)
Bestatin, a small molecular weight dipeptide, is a potent inhibitor of various aminopeptidases as well as LTA4 hydrolase. Various physiological functions of Bestatin have been identified, viz.: (1) an immunomodifier for enhancing the proliferation of
Externí odkaz:
https://doaj.org/article/aa92a7a7a90a4d7f8c6e45c9209e7070
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 1, Pp o148-o148 (2010)
In the title compound, C7H6O4S, a monoester derivative of 2,5-thiophenedicarboxylic acid, the carboxylic acid and the carboxylic acid ester groups are approximately coplanar with thiophene ring, making a dihedral angle of 3.1 (4) and 3.6 (4)°, respe
Externí odkaz:
https://doaj.org/article/890699398b6940ce87f9f1748aaf0948
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 12, Pp o2447-o2447 (2008)
The structure of the title compound, C15H21N3O6·H2O, is of interest with respect to assumed anticancer activity. The title molecules are linked through intermolecular O—H...O hydrogen-bonded chains along the a axis. These chains are connected by i
Externí odkaz:
https://doaj.org/article/fb3a1f78639f4757a710e17dfe1a2f8c
Publikováno v:
Journal of Coordination Chemistry. 70:1617-1631
Eight substituted bidentate Schiff base ligands HOC6H4CH=N-R (HL) (HL1: R = 4-ClC6H4, HL2: R = 2-ClC6H4, HL3: R = 4-NO2C6H4, HL4: R = 4-MeC6H4, HL5: R = 2,6-Me2C6H3, HL6: R = 2,46-Me3C6H2, HL7: R = CH2C6H5, and HL8: R = n-Pr) were synthesized by the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad86d09a800568105947a824a0aa95cf
https://doi.org/10.1080/00958972.2017.1317346
https://doi.org/10.1080/00958972.2017.1317346
Autor:
Hui Shao, Jie Li, Jian-Ping Zhong, Wen-fang Xu, Heping Rao, Yong Wu, Qiu-qiong Lv, Jian-kang Zhou
Publikováno v:
Laboratory Medicine. 48:57-64
Objective: To evaluate cluster of differentiation (CD)127 expression in T cells of patients with HIV-1 and the relationship of CD127 expression with disease progression. Methods: We divided 139 patients infected with human immunodeficiency virus type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ba1f93b9ca98a4189fff59dfe9b2e78
https://doi.org/10.1093/labmed/lmw053
https://doi.org/10.1093/labmed/lmw053
Publikováno v:
Chinese Journal of Chemistry. 30:2423-2430
Two new series of diaryl thiourea containing sorafenib derivatives 9a–9t were designed and synthesized, and their antiproliferative activities against PC-3, HCT116 and MDA-MB-231 cell lines were evaluated. All compounds generally showed antiprolife
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aaad2297e2db036109b950432c4477a3
https://doi.org/10.1002/cjoc.201200708
https://doi.org/10.1002/cjoc.201200708
Autor:
Wen Fang Xu, Xing Po Wang
Publikováno v:
Applied Mechanics and Materials. 108:294-296
A series of novel Hydroxylated 9,10-anthraquinone derivatives were designed and synthesized as potential antitumor agents starting from the natural product Emodin. The structures of the compounds were identified by NMR, ESI-MS and elemental analysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::414359fa4e3fe74fff328d12da6154d6
https://doi.org/10.4028/www.scientific.net/amm.108.294
https://doi.org/10.4028/www.scientific.net/amm.108.294
Autor:
Wen-Fang, Xu, Yong, Wu, Guo-Shao, Pan, Jian-Ping, Zhong, Shao-Bo, Lan, Xue-Fang, Chen, Qiu-Qiong, Lu
Publikováno v:
Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine. 34(2)
To explore the effect of Qiling Decoction (QD) combined highly active antiretroviral treatment (HAART) on expression levels of peripheral blood Th17 and Treg cells in HIV/AIDS patients.Totally 55 HIV/AIDS patients were randomly assigned to the treatm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0a5332b55a31d01c2b825616d897055e
https://pubmed.ncbi.nlm.nih.gov/24672938
https://pubmed.ncbi.nlm.nih.gov/24672938
Publikováno v:
Acta Crystallographica: Section E. Feb2005, Vol. 61 Issue 2, po349-o351. 3p. 3 Diagrams, 1 Chart, 1 Graph.
Publikováno v:
Yao xue xue bao = Acta pharmaceutica Sinica. 47(9)
Sorafenib, the first oral multikinase inhibitor, can inhibit several kinases involved in tumor proliferation and angiogenesis including Raf, VEGFR, PDGFR, kit and so on. Due to the advantages of multi-mechanisms, broad-spectrum anticancer potency, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac607c15f7b24954aafb13e7a1d1d035
https://pubmed.ncbi.nlm.nih.gov/23227538
https://pubmed.ncbi.nlm.nih.gov/23227538