Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hui-Juan Liang"'
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 12, Pp o3355-o3355 (2011)
In the title compound, C46H80O3, a natural ursane-type triperpenoid, four of the five six-membered rings adopt chair conformations; the fifth, which has a C=C double bond, adopts an approximate half-boat conformation. In the crystal, molecules are li
Externí odkaz:
https://doaj.org/article/e9abcda0b18945b8b85a7b5768d91149
Autor:
Wen-Rui Cao, Qiu-Ru Huang, Nan Zhang, Hui-Juan Liang, Ben-Song Xian, Xiao-Fang Gan, Dong Roman Xu, Ying-Si Lai
Publikováno v:
Journal of Transport Geography. 102:103381
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e572f069936b77b75eb5445468e3efa8
https://doi.org/10.1016/j.jtrangeo.2022.103381
https://doi.org/10.1016/j.jtrangeo.2022.103381
Autor:
Li-ming, Yang, Hui-juan, Liang, Cheng-hai, Peng, Jia-li, Cheng, Huan, Wang, Ld-qing, Weng, Zhi-tao, Li, Ye, Tian
Publikováno v:
Zhongguo ying yong sheng li xue za zhi = Zhongguo yingyong shenglixue zazhi = Chinese journal of applied physiology. 31(2)
We aim to investigate the sonodynamic effect induced by hydroxyl acetylated curcumin (HAC) on THP-1 macrophages.THP-1 derived macrophages (1 x 10(5) per milliliter) were cultured with HAC at a concentration of 5 µg/mL for 4 h and then exposed to pul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4abf014d3a39df32a1b06b82aa805f98
https://pubmed.ncbi.nlm.nih.gov/26248410
https://pubmed.ncbi.nlm.nih.gov/26248410
Publikováno v:
Journal of Chemical Research. 37:563-565
A new guaianolide named 8-α-acetoxy-15β- O-β-D-glucopyranosyl-guaia-1(10),3(4)- diene-2-one-6,12-olide and 12 known compounds were isolated from the roots of Pterocypsela elata (Hemsl.) C. Shih, and eight of which were isolated from this genus for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52614b1e19d953751ed8da5514306280
https://doi.org/10.3184/174751913x13744984599621
https://doi.org/10.3184/174751913x13744984599621
Publikováno v:
Chemistry of Natural Compounds. 49:258-260
A novel eremophilane-type sesquiterpenoid, named isoligularonic acid (1), was isolated from the roots and rhizomes of Ligularia intermedia Nakai. Its structure was elucidated by extensive spectroscopic analysis including 1D, 2D NMR, and HR-MS spectra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f30a2751f89e01e65b69da15d5d9375
https://doi.org/10.1007/s10600-013-0575-3
https://doi.org/10.1007/s10600-013-0575-3
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6cf7947ff80f733effc68d31bfc25f4
https://doi.org/10.1002/chin.201413217
https://doi.org/10.1002/chin.201413217
Autor:
Hai Guangfan, Yun-Xiao Zhang, Dan-Dan Ye, Nan-Qian Zhou, Hui-Juan Liang, Su-Ping Bai, Yong-Liang Yuan
Publikováno v:
Planta medica. 78(6)
Three new ENT-kaurane diterpenoids, glaucocalyxin H ( 1), glaucocalyxin I ( 2), and glaucocalyxin J ( 3), together with four known diterpenoids ( 4- 7), were isolated from the leaves of Isodon japonica Hara var. glaucocalyx. Their structures were elu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee66e263d1a5416438d3e346ea66ae63
https://pubmed.ncbi.nlm.nih.gov/22322394
https://pubmed.ncbi.nlm.nih.gov/22322394
Publikováno v:
Acta Crystallographica Section E: Structure Reports
In the title compound, C(46)H(80)O(3), a natural ursane-type triperpenoid, four of the five six-membered rings adopt chair conformations; the fifth, which has a C=C double bond, adopts an approximate half-boat conformation. In the crystal, mol-ecules
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4066c8f0d718b990d37885d290229cee
https://doi.org/10.1107/s1600536811047106
https://doi.org/10.1107/s1600536811047106
Autor:
Hui-Juan Liang, Yun-Xiao Zhang, Guang-Fan Hai, Su-Ping Bai, Yong-Liang Yuan, Dan-Dan Ye, Nan-Qian Zhou
Publikováno v:
Planta Medica; May2012, Vol. 78 Issue 7, p589-596, 8p