Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Hui-Ding Xie"'
Autor:
Ting‐Ting Cao, Ruo‐Yue Huang, Xu Li, Teng‐Yun Yang, Hui‐Ding Xie, Yun‐Heng Shen, Fei Li, Xian Li
Publikováno v:
Chemistry & Biodiversity. 19
Three new xanthone compounds, 1,3,5-trihydroxy-2-(2-hydroxy-3-methylbut-3-enyl)-4-(3-methylbut-2-enyl)xanthone (1), toxyloxanthone E (2), dehydrocycloguanandin B (3) along with 15 known xanthones (4-18) were isolated from the aerial parts of Calophyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27d031d207ea23bffc311a157ba92192
https://doi.org/10.1002/cbdv.202200268
https://doi.org/10.1002/cbdv.202200268
Publikováno v:
Organic & Biomolecular Chemistry. 19:8607-8612
The chiral keto-substituted propargylamines are an essential class of multifunctional compounds in the field of organic and pharmaceutical synthesis and have attracted considerable attention, but the related synthetic approaches remain limited. There
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44af4f9641c10dec4f3edd5f88bdceaa
https://doi.org/10.1039/d1ob01555a
https://doi.org/10.1039/d1ob01555a
Autor:
Yuan-Yi Li, Ya-Ting Shao, Zhong-Wen Sun, Yu-Lu Ma, Tianpeng Yin, Bao-Chun Shen, Hui-Ding Xie, Wei Li, Hui Yan
Publikováno v:
Journal of Natural Products. 83:3471-3475
Penisarins A (1) and B (2), sesquiterpene coumarins with an unusual tricyclic sesquiterpene system, were isolated from endophytic Penicillium sp. KMU18029. Their structures were elucidated on the b...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ca3fe1b39c21b1f873f2df2a840c2a5
https://doi.org/10.1021/acs.jnatprod.0c00393
https://doi.org/10.1021/acs.jnatprod.0c00393
Autor:
Wei Li, Wen Zhang, Fang Yu, Zhong-Wen Sun, Kaixiong Qiu, Shu-Qun Zhang, Ya-Juan Chen, Hui-Ding Xie
Publikováno v:
Current Computer-Aided Drug Design. 16:222-230
Background: B-RafV600E kinase was identified as an important target in current cancer treatment, and the type II B inhibitors show good qualities in preclinical studies. Therefore, it is very important to discover novel II B inhibitors of B-RafV600E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43e73437562e0cdba8f9064b0d3f00c8
https://doi.org/10.2174/1573409915666190130162821
https://doi.org/10.2174/1573409915666190130162821
Publikováno v:
Organicbiomolecular chemistry. 19(39)
The chiral keto-substituted propargylamines are an essential class of multifunctional compounds in the field of organic and pharmaceutical synthesis and have attracted considerable attention, but the related synthetic approaches remain limited. There
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::62aff15822c1e64e10ff48b28908b832
https://pubmed.ncbi.nlm.nih.gov/34569587
https://pubmed.ncbi.nlm.nih.gov/34569587
Autor:
Wei, Li, Ya-Ting, Shao, Tian-Peng, Yin, Hui, Yan, Bao-Chun, Shen, Yuan-Yi, Li, Hui-Ding, Xie, Zhong-Wen, Sun, Yu-Lu, Ma
Publikováno v:
Journal of natural products. 83(11)
Penisarins A (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a2a0f560f2b0d75ec91d8bf304c3036
https://pubmed.ncbi.nlm.nih.gov/33180498
https://pubmed.ncbi.nlm.nih.gov/33180498
Publikováno v:
Computational Biology and Chemistry. 70:186-190
B-Raf kinase has been identified as an important target in recent cancer treatment. In order to discover structurally diverse and novel B-Raf inhibitors (BRIs), a virtual screening of BRIs against ZINC database was performed by using a combination of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f79b8f9f3780098e5b9a3da12ce12ac
https://doi.org/10.1016/j.compbiolchem.2017.08.017
https://doi.org/10.1016/j.compbiolchem.2017.08.017
Autor:
Cui-Ping Miao, Xue-Qiong Yang, Li-Xing Zhao, Wei Li, Zhong-Tao Ding, Ya-Bin Yang, Zhi-Hui Shao, Hao Zhou, Hui-Ding Xie
Publikováno v:
Planta Medica. 83:654-660
The rare anishidiol and five new isochromans, including three novel dimers with unprecedented skeletons, were isolated from Stachybotrys sp. PH30583. Their structures were determined by spectral analyses. The bioactivities of these compounds were als
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f796a571f4a2629beb82a4baa7ff854
https://doi.org/10.1055/s-0042-119650
https://doi.org/10.1055/s-0042-119650
Autor:
Kai-Xiong, Qiu, Wen, Zhang, Fang, Yu, Wei, Li, Zhong-Wen, Sun, Shu-Qun, Zhang, Ya-Juan, Chen, Hui-Ding, Xie
Publikováno v:
Current computer-aided drug design. 16(3)
B-RafV600E kinase was identified as an important target in current cancer treatment, and the type II B inhibitors show good qualities in preclinical studies. Therefore, it is very important to discover novel II B inhibitors of B-RafV600E kinase.In or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0ee8bbae7a8b5e7138dfde8b333b465
https://pubmed.ncbi.nlm.nih.gov/30706826
https://pubmed.ncbi.nlm.nih.gov/30706826
Publikováno v:
Journal of Fluorescence. 20:1077-1085
In this paper we describe a semi-empirical quantum method for predicting the wavelength of maximum fluorescence excitation and emission for several known and new maleimide derivatives. All new maleimides, containing a N-Benzyl attachment, were succes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1feddc15a5f6bd26eba4d866d9de9fe
https://doi.org/10.1007/s10895-010-0660-y
https://doi.org/10.1007/s10895-010-0660-y