Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Kai-Wei Tang"'
Autor:
Kai-Wei Tang, Ching-Yun Hsu, Ibrahim A. Aljuffali, Ahmed Alalaiwe, Wang-Ni Lai, Pei-Yu Gu, Chih-Hua Tseng, Jia-You Fang
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 170, Iss , Pp 116073- (2024)
Atopic dermatitis (AD) is one of the most common skin autoimmune diseases needing continuous anti-inflammatory management. Pterostilbene is reported to exhibit anti-inflammatory activity with higher bioavailability and stability than its parent compo
Externí odkaz:
https://doaj.org/article/bdba88d4f6e54ad3bb8b20bf19f71fd3
Autor:
Jia-You Fang, Kai-Wei Tang, Sien-Hung Yang, Ahmed Alalaiwe, Yu-Ching Yang, Chih-Hua Tseng, Shih-Chun Yang
Publikováno v:
Frontiers in Microbiology, Vol 11 (2020)
Candida albicans is the most common cause of fungal infection. The emergence of drug resistance leads to the need for novel antifungal agents. We aimed to design naphthofuranquinone analogs to treat drug-resistant C. albicans for topical application
Externí odkaz:
https://doaj.org/article/ff7553bf3e1f4c41a0f52b49c9722314
Autor:
Kai-Wei Tang, Chien-Chih Ke, Chih-Hua Tseng, Yeh-Long Chen, Cherng-Chyi Tzeng, Yi-Jin Chen, Chia-Chi Hsu, Hsiao-Ting Tai, Ya-Ju Hsieh
Publikováno v:
Molecules, Vol 26, Iss 16, p 4840 (2021)
Pterostilbene, a natural metabolite of resveratrol, has been indicated as a potent anticancer molecule. Recently, several pterostilbene derivatives have been reported to exhibit better anticancer activities than that of the parent pterostilbene molec
Externí odkaz:
https://doaj.org/article/38f056ec54a34972a3f0cd793a114205
Publikováno v:
Frontiers in Microbiology, Vol 10 (2019)
Methicillin-resistant Staphylococcus aureus (MRSA) is the primary microbe responsible for skin infections that are particularly difficult to eradicate. This study sought to inhibit planktonic and biofilm MRSA using furanoquinone-derived compounds con
Externí odkaz:
https://doaj.org/article/cbb65c69ff97420794571dcfa5b49315
Autor:
Yu-Tse Kao, Yi-Siao Chen, Kai-Wei Tang, Jin-Ching Lee, Chih-Hua Tseng, Cherng-Chyi Tzeng, Chia-Hung Yen, Yeh-Long Chen
Publikováno v:
Molecules, Vol 25, Iss 14, p 3133 (2020)
Activation of nuclear factor erythroid-2-related factor 2 (NRF2) has been proven to be an effective means to prevent the development of cancer, and natural curcumin stands out as a potent NRF2 activator and cancer chemopreventive agent. In this study
Externí odkaz:
https://doaj.org/article/6d65ded367e04782813145cf68477211
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 19, p 4786 (2019)
We designed and synthesized a series of novel 3-arylquinoxaline derivatives and evaluated their biological activities as potential dengue virus (DENV) replication inhibitors. Among them, [3-(4-methoxyphenyl)quinoxalin-2-yl](phenyl)methanol (19a), [6,
Externí odkaz:
https://doaj.org/article/4f0169f6531545c983370fd6f0a8dbd3
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 18, p 4564 (2019)
Staphylococcus aureus resistance to current antibiotics has become the greatest global challenge facing public health. The development of new antimicrobial agents is urgent and important and is needed to provide additional therapeutic options. In our
Externí odkaz:
https://doaj.org/article/0046ae1e1ceb421fa7e6b189acd62bc3
Autor:
Cheng-Yao Yang, Yung-Li Hung, Kai-Wei Tang, Shu-Chi Wang, Chih-Hua Tseng, Cherng-Chyi Tzeng, Po-Len Liu, Chia-Yang Li, Yeh-Long Chen
Publikováno v:
Molecules, Vol 24, Iss 6, p 1162 (2019)
We describe herein the preparation of certain 2-substituted 3-arylquinoline derivatives and the evaluation of their anti-inflammatory effects in LPS-activated murine J774A.1 macrophage cells. Among these newly synthesized 2-substituted 3-arylquinolin
Externí odkaz:
https://doaj.org/article/158dad5f18e648f1b6c04a8f4b642fbe
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 10, p 3061 (2018)
Several thalidomide derivatives were synthesized and evaluated for their anti-inflammatory activity. Introduction of the benzyl group to the parent thalidomide is unfavorable in which 2-(1-benzyl-2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione (4a) was
Externí odkaz:
https://doaj.org/article/f4f6e6f0eae54b24b15f6ae2d88c9fc6
Autor:
Kai-Wei Tang, 湯凱崴
99
During software testing, the sets of requirements (e.g. the code coverage) that are satisfied by different test cases may not be mutually exclusive because the test suites are often generated automatically. Thus, to reduce the cost of softwar
During software testing, the sets of requirements (e.g. the code coverage) that are satisfied by different test cases may not be mutually exclusive because the test suites are often generated automatically. Thus, to reduce the cost of softwar
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/28180401886140776611