Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Ming Fu Cheng"'
Publikováno v:
Applied Sciences, Vol 11, Iss 4, p 1715 (2021)
Storage devices in the computer industry have gradually transformed from the hard disk drive (HDD) to the solid-state drive (SSD), of which the key component is error correction in not-and (NAND) flash memory. While NAND flash memory is under develop
Externí odkaz:
https://doaj.org/article/a5dad116d435471798cae36fdccd0e69
Autor:
Ming-fu cheng, 鄭名甫
107
In NB industry, the marketing trend about storage device, from HDD transformation to SSD, the most important key component of SSD is called NAND flash memory, SSD industry keep research and development for more higher density SSD, but they d
In NB industry, the marketing trend about storage device, from HDD transformation to SSD, the most important key component of SSD is called NAND flash memory, SSD industry keep research and development for more higher density SSD, but they d
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/d559mq
Autor:
Jen Shin Song, An Shiou Li, Yu-Sheng Chao, Su Ying Wu, Shu Yu Lin, Chuan Shih, Shiow Lin Pan, Chun Hsien Chiu, Ya Chu Tang, Shau-Hua Ueng, Ching Chuan Kuo, Teng Kuang Yeh, Shu Ying Cheng, Yi Jyun Lin, Wen-Chi Hsiao, Hsin Huei Chang, Ming Fu Cheng, Manwu Sun, Chin Hsiang Huang, Li Mei Lin, Zih Ting Huang, Fang Yu Liao, Mine Hsine Wu, Ming Shiu Hung, Yi Hsin Wang
Publikováno v:
Bioorganic chemistry. 77
Indoleamine 2,3-dioxygenase is a heme-containing enzyme implicated in the down regulation of the anti-tumor immune response, and considered a promising anti-cancer drug target. Several pharmaceutical companies, including Pfizer, Merck, and Bristol-My
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::012b417f4b305b7f1f5151ff6af47287
https://pubmed.ncbi.nlm.nih.gov/29494816
https://pubmed.ncbi.nlm.nih.gov/29494816
Autor:
Po-Kuan, Chao, Shau-Hua, Ueng, Li-Chin, Ou, Teng-Kuang, Yeh, Wan-Ting, Chang, Hsiao-Fu, Chang, Shu-Chun, Chen, Pao-Luh, Tao, Ping-Yee, Law, Horace H, Loh, Ming-Fu, Cheng, Jian-Ying, Chuang, Chiung-Tong, Chen, Chuan, Shih, Shiu-Hwa, Yeh
Publikováno v:
Anesthesiology. 126(5)
The authors investigated the pharmacology and signaling pathways of the opioid receptors modulated by compound 1, 1-(2,4-dibromophenyl)-3,6,6-trimethyl-1,5,6,7-tetrahydro-4H-indazol-4-one.In vitro studies of compound 1 were assessed by using a radiol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0af117db86bd07337b78bde1a2ef53cb
https://pubmed.ncbi.nlm.nih.gov/28212204
https://pubmed.ncbi.nlm.nih.gov/28212204
Autor:
Horace H. Loh, Ping-Yee Law, Shau-Hua Ueng, Li Chin Ou, Wan Ting Chang, Ming Fu Cheng, Shu Chun Chen, Chuan Shih, Shiu Hwa Yeh, Yu-Sheng Chao
Publikováno v:
Bioorganic & Medicinal Chemistry. 22:4694-4703
The μ-opioid receptor (MOR) is the major opioid receptor targeted by most analgesics in clinical use. However, the use of all known MOR agonists is associated with severe adverse effects. We reported that the 1-phenyl-3,6,6-trimethyl-1,5,6,7-tetrahy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1d44659fc49c1daefa5b893122130cc
https://doi.org/10.1016/j.bmc.2014.07.012
https://doi.org/10.1016/j.bmc.2014.07.012
Autor:
Fang Yu Liao, Yi Hui Peng, Chia-Ling Hsieh, Han Li Huang, Wen-Chi Hsiao, Shau-Hua Ueng, Shu Yu Lin, Ming Fu Cheng, Chun Yu Yang, Jian Sung Wu, Ming Shiu Hung, Manwu Sun, Su Ying Wu, Chuan Shih, Jen Shin Song, Shiow Lin Pan, Teng Kuang Yeh, Li Mei Lin, Ching Chuan Kuo, Min Wu Chao, Mine Hsine Wu, Yi Lin Chen, Yu-Sheng Chao
Publikováno v:
Journal of medicinal chemistry. 59(1)
Tryptophan metabolism has been recognized as an important mechanism in immune tolerance. Indoleamine 2,3-dioxygenase plays a key role in local tryptophan metabolism via the kynurenine pathway and has emerged as a therapeutic target for cancer immunot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::574ce1bb194f18e4a4b093cc5fdc5c1f
https://pubmed.ncbi.nlm.nih.gov/26653033
https://pubmed.ncbi.nlm.nih.gov/26653033
Autor:
Mine-Hsine Wu, Chuan Shih, Chih-Hsiang Tu, Ming-Shiu Hung, Shau-Hua Ueng, Chen-Tso Tseng, Wen-Chi Hsiao, Lung-Chun Lee, Kak-Shan Shia, Yu-Shiou Fan, Jen-Shin Song, Jian-Sung Wu, Ming-Fu Cheng, Shu Yu Lin, Yi-Hui Peng, Fang-Yu Liao, Ching-Cheng Hsueh, Chia-Yi Cheng, Su-Ying Wu
Publikováno v:
Journal of medicinal chemistry. 59(1)
Indoleamine 2,3-dioxygenase 1 (IDO1), promoting immune escape of tumors, is a therapeutic target for the cancer immunotherapy. A number of IDO1 inhibitors have been identified, but only limited structural biology studies of IDO1 inhibitors are availa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::349ebb46530487cd97e38d92e2c9a3c7
https://pubmed.ncbi.nlm.nih.gov/26642377
https://pubmed.ncbi.nlm.nih.gov/26642377
Autor:
Ming-Fu Cheng, Jim-Min Fang
Publikováno v:
Journal of Combinatorial Chemistry. 6:99-104
A library of 1,4-benzodiazepine-2,5-dione dicarboxylate derivatives containing aryl substituents at N(1)- and N(4)-positions to mimic the amino acid residues of Try-13, Phe-14, and Asp-18 in endothelin-1 is established by using the starting materials
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1718f3284db5ce845ace66f6b2833fb
https://doi.org/10.1021/cc030034d
https://doi.org/10.1021/cc030034d
Autor:
Tong-Ing Ho, Jim-Min Fang, Bor-Wen Ko, Hui-Ming Yu, Ming-Yi Chen, Yu Chang, Ming-Fu Cheng, Yeun-Min Tsai
Publikováno v:
Organicbiomolecular chemistry. 4(3)
The expedient synthesis of various 1,4-benzodiazepine-2,5-dione compounds, particularly those having substituents at the C3-, N1- and N4-positions is achieved. The important features in these synthetic strategies include: (i) using the coupling react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9952046d7501f816ef80968d537273c6
https://pubmed.ncbi.nlm.nih.gov/16446809
https://pubmed.ncbi.nlm.nih.gov/16446809
Autor:
Ming-Fu Cheng, 鄭名富
93
Part I: Liquid-Phase Combinatorial Synthesis of 1,4-Benzodiazepine-2,5-diones as Endothelin Receptor Antagonists A series of 1,4-benzodiazepine-2,5-diones are prepared by using 2-nitrobenzoyl chloride as a synthetic equivalent of anthranilic
Part I: Liquid-Phase Combinatorial Synthesis of 1,4-Benzodiazepine-2,5-diones as Endothelin Receptor Antagonists A series of 1,4-benzodiazepine-2,5-diones are prepared by using 2-nitrobenzoyl chloride as a synthetic equivalent of anthranilic
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/17163598195047816342