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Cong-Luan Tran Thi-Bich-Ngoc Dao Thanh-Nha Tran Dinh-Tri Mai Thi-Minh-Dinh Tran Nguyen-Minh-An Tran Van-Son Dang Thi-Xuyen Vo Thuc-Huy Duong Jirapast Sichaem 《Molecules (Basel, Switzerland)》2021,26(8)
Bioactive-guided phytochemical investigation of Euphorbia antiquorum L. growing in Vietnam led to the isolation of five ent-atisanes, one seco-ent-atisane, and one lathyrane (ingol-type). The structures were elucidated as ent-1α,3α,16β,17-tetrahydroxyatisane (1), ethyl ent-3,4-seco-4,16β,17-trihydroxyatisane-3-carboxylate (2), ent-atisane-3-oxo-16β,17-acetonide (3), ent-3α-acetoxy-16β,17-dihydroxyatisane (4), ent-16β,17-dihydroxyatisane-3-one (5), calliterpenone (6), and ingol 12-acetate (7). Their chemical structures were unambiguously determined by analysis of one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance (NMR) and high resolution mass spectrometry, as well as by comparison with literature data. Among them, 1 is a new compound while 2 is an ethylated artifact of ent-3,4-seco-4,16β,17-trihydroxyatisane-3-carboxylic acid, a new compound. Isolates were evaluated for alpha-glucosidase inhibition. Compound 3 showed the most significant inhibitory activity against alpha-glucosidase with an IC50 value of 69.62 µM. Further study on mechanism underlying yeast alpha-glucosidase inhibition indicated that 3 could retard the enzyme function by noncompetitive. 相似文献
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Tran Thi-Minh-Dinh Duong Thuc-Huy Tran Thanh-Nha Nguyen Thi-Hang Nguyen Ngoc-Phuong Nguyen Ngoc-Hong Dinh Minh-Hiep Nguyen Thi-Anh-Tuyet 《Chemistry of Natural Compounds》2021,57(2):388-389
Chemistry of Natural Compounds - 相似文献
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Hung Banh Katharina Dilchert Christine Schulz Dr. Christian Gemel Dr. Rüdiger W. Seidel Dr. Régis Gautier Dr. Samia Kahlal Prof. Dr. Jean‐Yves Saillard Prof. Dr. Roland A. Fischer 《Angewandte Chemie (International ed. in English)》2016,55(10):3285-3289
The bottom‐up synthesis of organometallic zinc clusters is described. The cation {[Zn10](Cp*)6Me}+ ( 1 ) is obtained by reacting [Zn2Cp*2] with [FeCp2][BAr4F] in the presence of ZnMe2. In the presence of suitable ligands, the high reactivity of 1 enables the controlled abstraction of single Zn units, providing access to the lower‐nuclearity clusters {[Zn9](Cp*)6} ( 2 ) and {[Zn8](Cp*)5(tBuNC)3}+ ( 3 ). According to DFT calculations, 1 and 2 can be described as closed‐shell species that are electron‐deficient in terms of the Wade–Mingos rules because the apical ZnCp* units that constitute the cluster cage do not have three, but only one, frontier orbitals available for cluster bonding. Zinc behaves flexibly in building the skeletal metal–metal bonds, sometimes providing one major frontier orbital (like Group 11 metals) and sometimes providing three frontier orbitals (like Group 13 elements). 相似文献
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Dr. Kerstin Freitag Dr. Christian Gemel Dr. Paul Jerabek Prof. Dr. Iris M. Oppel Dr. Rüdiger W. Seidel Prof. Dr. Gernot Frenking Hung Banh Katharina Dilchert Prof. Dr. Roland A. Fischer 《Angewandte Chemie (International ed. in English)》2015,54(14):4370-4374
The triangular clusters [Zn3Cp*3]+ and [Zn2CuCp*3] were obtained by addition of the in situ generated, electrophilic, and isolobal species [ZnCp*]+ and [CuCp*] to Carmona’s compound, [Cp*Zn? ZnCp*], without splitting the Zn? Zn bond. The choice of non‐coordinating fluoroaromatic solvents was crucial. The bonding situations of the all‐hydrocarbon‐ligand‐protected clusters were investigated by quantum chemical calculations revealing a high degree of σ‐aromaticity similar to the triatomic hydrogen ion [H3]+. The new species serve as molecular building units of CunZnm nanobrass clusters as indicated by LIFDI mass spectrometry. 相似文献
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The induction of liquid crystal orientation through mechanical stretching was investigated for polymer dispersed liquid crystals (PDLCs) by means of infrared dichroism. Using a nematic liquid crystal BL006 and polyacrylic acid as the polymer matrix, it was possible to stretch the PDLC films with BL006 in either the isotropic or the nematic phase. After cooling the films under strain to room temperature, the molecular orientation of BL006 was found to be much higher for films that contained isotropic liquid droplets of BL006 at the time of stretching than for films that had nematic droplets. Stretching PDLC films with isotropic droplets results in no molecular orientation, but the orientation is induced during the subsequent cooling when BL006 goes through the isotropic-to-nematic phase transition. Interestingly for PAA/BL006, the nematic director orients along the long axes of the elongated droplets despite liquid crystal anchoring perpendicular to the polymer interface. 相似文献
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