Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Shiow Yunn Sheu"'
Autor:
Lin-Wen Lee, Mei-Hsiang Lin, Keng-Liang Ou, Shiow-Yunn Sheu, Tiffany Chen, Chien-Ling Su, Pen-Yuan Lin, Kuang-Sheng Yeh
Publikováno v:
Molecules, Vol 17, Iss 9, Pp 10846-10863 (2012)
Coumarin derivatives are used as fluorescent dyes and medicines. They also have some notable physiological effects, including the acute hepatoxicity and carcinogenicity of certain aflatoxins, the anticoagulant action of dicoumarol, and the antibiotic
Externí odkaz:
https://doaj.org/article/1b5606cb269e46609fd92a2cfa6d8b0d
Autor:
Ling-Ling Chiang, Ing-Jy Tseng, Pen-Yuan Lin, Shiow-Yunn Sheu, Ching-Tung Lin, Yun-Han Hsieh, Yi-Jing Lin, Hsiao-Ling Chen, Mei-Hsiang Lin
Publikováno v:
Molecules, Vol 21, Iss 1, p 100 (2016)
The cantharidinimide derivatives, 5a–h, including sulfanilamides containing pyrimidyl, pyrazinyl, hydrogen, thiazolyl, and oxazolyl groups were synthesized. Modification of cantharidinimide by means of the reaction of activated aziridine ring openi
Externí odkaz:
https://doaj.org/article/e85550060b4641b9b72a43b21ddb8161
Autor:
Rey Yue Yuan, Hsin Chien Lee, Shin Chia Tsai, Shiow Yunn Sheu, Li Nien Chien, Eunice Jia Shiow Yuan
Publikováno v:
British Journal of Clinical Pharmacology. 84:2000-2009
Aims We conducted a cohort study utilizing a nationwide health insurance database to assess the European Medicines Agency's restrictions on using metoclopramide and its association with the risk of parkinsonism. Methods New oral metoclopramide users
Publikováno v:
Educational Research and Reviews. 11:1424-1431
In this research, we aim to understand the effectiveness of adopting educational technologies in a computer literacy course to students in a medical university. The course was organized with three core components: Open Education Resources (OER) readi
Publikováno v:
Journal of the Chinese Chemical Society. 62:59-63
Various acidic anhydrides including cantharidin were converted into corresponding aminobenzylcantharidinimide 3a and analogous imides 3b∼k (at the ortho, meta, and para positions) with 35%∼87% yields by reacting with aminobenzylamines and triethy
Autor:
Tsurng Juhn Huang, Li Ming Yang, Shwu Jiuan Lin, Pan Chun Liu, Chin Yang Chen, Shwu Fen Chang, Shiow Yunn Sheu
Publikováno v:
Phytochemistry. 95:268-276
The biotransformation of dihydroisosteviol with Absidia pseudocylindrospora ATCC 24169, Streptomyces griseus ATCC 10137, Mucor recurvatus MR36, and Aspergillus niger BCRC 31130 yielded 15 metabolites, eight of which were previously unknown. Structure
Autor:
Ahmed E. Fazary, Chia Ching Liaw, Shun Ying Chen, Ching Te Chien, Ju Liang Hsieh, Ya-Ching Shen, Bor-Luen Chiang, Shiow Yunn Sheu, Yao-Haur Kuo, Yu-Chen Chen
Publikováno v:
Phytochemistry Letters. 6:397-402
A novel C 6 –C 3 prenylated compound, illicarborene A ( 1 ), together with illioliganfunone D ( 2 ), 1-allyl-3,5-dimethoxy-4-(3-methylbut-2-enyloxy)benzene ( 3 ), (−)-illicinone A ( 4 ), (−)-illicinone B ( 5 ) and (−)-illicinone A derivative
Publikováno v:
Journal of Biomedical Materials Research Part A. 101:3457-3466
Osteoarthritis is a type of arthritis that is caused by breakdown of cartilage, with eventual loss of the cartilage of the joints. The ability of self-repair in damaged cartilage tissue is limited; the aim of this work is to fabricate and characteriz
Publikováno v:
Journal of Experimental & Clinical Medicine. 4:280-283
Background Cantharidin isolated from the blister beetle is used as a traditional Chinese medicine. The anticancer activity of thiadizolyl and some known N-substituted thiazolyl of cantharidin has been reported. We obtained a novel type of cantharidin
Autor:
Pen-Yuan Lin, Yi-Jing Lin, Mei-Hsiang Lin, Ching Tung Lin, Shiow-Yunn Sheu, Yun-Han Hsieh, Ling Ling Chiang, Hsiao-Ling Chen, Ing Jy Tseng
Publikováno v:
Molecules; Volume 21; Issue 1; Pages: 100
Molecules, Vol 21, Iss 1, p 100 (2016)
Molecules
Molecules, Vol 21, Iss 1, p 100 (2016)
Molecules
The cantharidinimide derivatives, 5a-h, including sulfanilamides containing pyrimidyl, pyrazinyl, hydrogen, thiazolyl, and oxazolyl groups were synthesized. Modification of cantharidinimide by means of the reaction of activated aziridine ring opening