Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yong-fu Qiu"'
Publikováno v:
Pharmaceutical Fronts, Vol 04, Iss 04, Pp e223-e236 (2022)
Abstract Anaplastic lymphoma kinase (ALK) is one of the most popular targets for anticancer therapies. In the past decade, the use of anaplastic lymphoma tyrosine kinase inhibitors (ALK-TKIs), including crizotinib and ceritinib, has been a reliable
Externí odkaz:
https://doaj.org/article/d12e9a1b096a48b08f93869c905d3e63
Publikováno v:
Pharmaceutical Fronts, Vol 04, Iss 03, Pp e136-e150 (2022)
Anaplastic lymphoma kinase (ALK) is a promising target for the treatment of non-small cell lung cancer. Under crizotinib treatment, drug resistance and progressive disease appeared after the point mutations arising in the kinase domain of ALK. Second
Externí odkaz:
https://doaj.org/article/ca6dc60993134d31a8dce22aa21614d8
Autor:
Xin Wang, Yue Han, Xuan Feng, Yun-Zhen Li, Bao-Xiang Qin, Ji-Jing Luo, Zheng Wei, Yong-Fu Qiu, Fang Liu, Rong-Bai Li
Publikováno v:
Czech Journal of Genetics and Plant Breeding, Vol 55, Iss 3, Pp 93-100 (2019)
Glutinous cytoplasmic male sterile (CMS) line is necessary to select hybrid glutinous rice combination with high yield and quality. To develop glutinous CMS with low amylose content, in this study, we firstly knocked out the granule-bound starch synt
Externí odkaz:
https://doaj.org/article/5805f2d8f03340498d1156efd7ff2331
Autor:
Wen-ai HE, Da-hui HUANG, Rong-bai LI, Yong-fu QIU, Jian-dong SONG, Hai-ning YANG, Jia-xing ZHENG, Yue-yue HUANG, Xiao-qiong LI, Chi LIU, Yue-xiong ZHANG, Zeng-feng MA, Yong YANG
Publikováno v:
Journal of Integrative Agriculture, Vol 11, Iss 6, Pp 962-969 (2012)
Bacterial leaf streak (BLS) of rice, caused by Xanthomonas oryzae pv. oryzicola (Xoc) is a worldwide destructive disease. Development of resistant varieties is considered to be one of the most effective and eco-friendly ways to control the disease. H
Externí odkaz:
https://doaj.org/article/8f9306c9eb3c40cf9cf8d3ff49ea80de
Publikováno v:
New Journal of Chemistry. 47:515-515
Correction for ‘AgNO3-catalyzed decarboxylative cross-coupling reaction: an approach to coenzyme Q’ by Wan-Yue Luo et al., New J. Chem., 2020, 44, 8702–8704, https://doi.org/10.1039/D0NJ01497D.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f73f1c44a689347c4577a919b6b229d2
https://doi.org/10.1039/d2nj90168d
https://doi.org/10.1039/d2nj90168d
Publikováno v:
New Journal of Chemistry. 44:8702-8704
An efficient and general method for the synthesis of coenzyme Q compounds through the activation of the 1,4-benzoquinone Csp2–H bond has been developed. This C–C bond formation reaction proceeds readily in an open flask by the direct cross-coupli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::552ef63e43d3fa17794b5de3bcdb536a
https://doi.org/10.1039/d0nj01497d
https://doi.org/10.1039/d0nj01497d
Publikováno v:
Organic Preparations and Procedures International. 51:602-605
Coenzyme Qs (CoQn), also known as the ubiquinones, act as mobile mediators for electron transfer and protein translocation between redox enzymes in the electron transport chain of mitochondria.1 Co...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a768c450088e6c3b9e58380494c44fd1
https://doi.org/10.1080/00304948.2019.1673616
https://doi.org/10.1080/00304948.2019.1673616
Publikováno v:
Journal of Chemical Research. 43:553-556
A convenient method for the preparation of Coenzyme Q1 from cheap and readily available 3,4,5-trimethoxytoluene is developed. Coenzyme Q1 is synthesized in a moderate yield by a two-step procedure involving the key reaction of an allyl bromide with C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75e6e753ab102ce330741ceb1ca415e9
https://doi.org/10.1177/1747519819876524
https://doi.org/10.1177/1747519819876524
Publikováno v:
Chemical Papers. 73:2745-2748
The title compound, a key intermediate for preparing Coenzyme Qn family, was prepared in an excellent yield by a reaction sequence starting from the commercially available 3,4,5-trimethoxytoluene 1 via bromination, methoxylation and oxidation reactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::330b8b64ba0cf3bed8ea5de485e3e430
https://doi.org/10.1007/s11696-019-00826-6
https://doi.org/10.1007/s11696-019-00826-6
Autor:
Yi-Yu Yan, Jian-Hua Tian, Bin Lu, Wan-Yue Luo, Yong-Fu Qiu, Tian-Li Zhang, Xiao Hu, Jin Wang, Shi Qi
Publikováno v:
Asian Journal of Applied Chemistry Research. :1-5
1-amino anthraquinone (2) is the most important intermediate in the synthesis of acid dyes. This paper presents a new method for the preparation of title compound (2) in a highly chemo- and regioselective reduction of 1-nitro anthraquinone (1) by NaH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e23293fca6b4c5cc2e37bd6f992248cf
https://doi.org/10.9734/ajacr/2019/v3i130081
https://doi.org/10.9734/ajacr/2019/v3i130081