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Triterpenoids and Flavonoids from the Leaves of Astragalus membranaceus and Their Inhibitory Effects on Nitric Oxide Production 下载免费PDF全文
Zhi‐Bin Wang Ya‐Dong Zhai Zhen‐Ping Ma Chun‐Juan Yang Rong Pan Jia‐Li Yu Qiu‐Hong Wang Bing‐You Yang Hai‐Xue Kuang 《化学与生物多样性》2015,12(10):1575-1584
Four new cycloartane triterpenes, named huangqiyegenins V and VI and huangqiyenins K and L ( 1 – 4 , resp.), together with nine known triterpenoids, 5 – 13 , and eight flavonoids, 14 – 21 , were isolated from a 70%‐EtOH extract of Astragalus membranaceus leaves. The structures of the new compounds were elucidated by detailed spectroscopic analyses, and the compounds were identified as (9β,11α,16β,20R,24S)‐11,16,25‐trihydroxy‐20,24‐epoxy‐9,19‐cyclolanostane‐3,6‐dione ( 1 ), (9β,16β,24S)‐16,24,25‐trihydroxy‐9,19‐cyclolanostane‐3,6‐dione ( 2 ), (3β,6α,9β,16β,20R,24R)‐16,25‐dihydroxy‐3‐(β‐D ‐xylopyranosyloxy)‐20,24‐epoxy‐9,19‐cyclolanostan‐6‐yl acetate ( 3 ), and (3β,6α,9β,16β,24E)‐26‐(β‐D ‐glucopyranosyloxy)‐16‐hydroxy‐3‐(β‐D ‐xylopyranosyloxy)‐9,19‐cyclolanost‐24‐en‐6‐yl acetate ( 4 ). All isolated compounds were evaluated for their inhibitory activities against LPS‐induced NO production in RAW264.7 macrophage cells. Compounds 1 – 3, 14, 15 , and 18 exhibited strong inhibition on LPS‐induced NO release by macrophages with IC50 values of 14.4–27.1 μM . 相似文献
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You‐Min Ying Cui‐Yu Li Yan Chen Jia‐Gui Xiang Ling Fang Jian‐Biao Yao Fa‐Song Wang Ru‐Wei Wang Wei‐Guang Shan Zha‐Jun Zhan 《化学与生物多样性》2015,12(8):1222-1228
Two new triterpenoids, 30‐hydroxylup‐20(29)‐ene 3β‐caffeate ( 1 ) and 24‐nor‐friedelan‐6α,10‐dihydroxy‐1,2‐dioxo‐4,7‐dien‐29‐oic acid ( 2 ), together with eight known compounds 3 – 10 , were isolated from the roots of Celastrus stylosus. The structures of these compounds were elucidated on the basis of spectroscopic analyses. To the best of our knowledge, this represents the first study on the chemical constituents of C. stylosus. The antiproliferative activities of the triterpenoids against six human cancer cell lines (PANC‐1, A549, PC‐3, HepG2, SGC‐7901, and HCCLM3) were evaluated. Compounds 3, 4 , and 10 exhibited comparable activities against PC‐3 and HCCLM3 cell lines as the positive control taxol. 相似文献
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从元谋栽培印楝Azadirachta indica的枝叶中分离得到15个化合物,结构类型有三萜、倍半萜、甾体等。经波谱解析鉴定为nimbin(1),6-deacetylnimbin(2),6-deacetylnimbinene(3),nimbinene(4),azadiradi-one(5),7-acetoxy-elema-1,3-dien-8-ol(6),1-naphthalenone(7),acarusnol(8),colvane-2β,9α-diol(9),乌苏酸(10),马斯里酸(11),2α-羟基乌苏酸(12),猕猴桃酸B(13),2α,3α,4β-trihydroxypregnan-16-one(14),2β,3β,4β-trihydroxypregnan-16-one(15)。化合物6~15为首次从该植物中分离得到。 相似文献
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Sambucus adnata Wall. belongs to Caprifoliaceae family. Phytochemical investigation on the aerial parts of S. adnata led to the isolation and identification of 17 known compounds (1–17) including triterpenoids and sterols. Compounds 1 and 8 are isolated from Sambucus adnata for the first time, and it is the first report that compounds 2, 5–6, 9–10, 12–15, and 17 are isolated from the plants of genus Sambucus. Importantly, three types of abundant components: (3β)-urs-12-en-3-yl stearate (0.33 g/kg, ursane type), (3β)-olean-12-en-3-yl stearate (0.17 g/kg, oleanane type), and lupenyl palmitate (0.52 g/kg, lupinane type) could be used as potential chemotaxonomic markers to distinguish among species of Sambucus. 相似文献
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Novel semisynthetic derivatives of betulin and betulinic acid with cytotoxic activity 总被引:1,自引:0,他引:1
Rita C. Santos Jorge A.R. Salvador Silvia Marín Marta Cascante 《Bioorganic & medicinal chemistry》2009,17(17):6241-6250
A series of new imidazole carboxylic esters (carbamates) and N-acylimidazole derivatives of betulin and betulinic acid (14–29) have been synthesized. The new compounds were screened for in vitro cytotoxicity activity against human cancer cell lines HepG2, Jurkat and HeLa. A number of compounds have shown IC50 values lower than 2 μM against the cancer cell lines tested and the vast majority has shown a better cytotoxicity profile than betulinic acid, including the betulin derivatives. N-Acylimidazole derivatives 26 and 27 (IC50 0.8 and 1.7 μM in HepG2 cells) and the C-3 carbamate derivative 16 (IC50 2.0 μM in HepG2 cells) were the most promising compounds. Based on the observed cytotoxicity, structure–activity relationships have been established. 相似文献
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Xue‐Feng Zhou Peng Zhang Hui‐Fang Pi Yong‐Hui Zhang Han‐Li Ruan Hui Wang Ji‐Zhou Wu 《化学与生物多样性》2009,6(8):1202-1207
Two new triterpenoids, 1 and 2 , were isolated from the hepatoprotective AcOEt fraction of the roots of Actinidia chinensis, together with eight known 12‐en‐28‐oic acids of oleanane or ursane type, 3 – 10 . The two new compounds were elucidated as 2α,3β‐dihydroxyurs‐12‐en‐28,30‐olide ( 1 ) and 2α,3β,24‐trihydroxyurs‐12‐en‐28,30‐olide ( 2 ), on the basis of spectroscopic (IR, NMR, and MS) analyses. The chemotaxonomic significances of some triterpenoids were also discussed. 相似文献
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Six new triterpenoids, meliasenins S–X ( 1 – 6 , resp.), were isolated from the stem bark of Melia toosendan. Their structures were elucidated by mass spectrometry, NMR experiments, and comparison with the known compounds. Particularly, the absolute configuration at C(24) in new compounds was determined through their CD spectra of the [Pr(FOD)3] complex (fod=1,1,1,2,2,3,3,7,7,7‐decafluoroheptane‐4,6‐dione) in CCl4, as well as by using Mosher's method. 相似文献
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