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He ZD Ma CY Zhang HJ Tan GT Tamez P Sydara K Bouamanivong S Southavong B Soejarto DD Pezzuto JM Fong HH 《化学与生物多样性》2005,2(10):1378-1386
Bioassay-guided fractionation of the antimalarial-active CHCl3 extract of the dried stem of Nauclea orientalis (L.) L. (Rubiaceae) has resulted in the isolation of two novel tetrahydro-beta-carboline monoterpene alkaloid glucosides, naucleaorine (= (16alpha,17beta)-3,14:15,20-tetradehydro-16-ethenyl-17-(beta-D-glucopyranosyloxy)-19alpha-methoxyoxayohimban-21-one; 1) and epimethoxynaucleaorine (2), as well as the known compounds, strictosidine lactam (= (15beta,16alpha,17beta)-19,20-didehydro-16-ethenyl-17-(beta-D-glucopyranosyloxy)oxayohimban-21-one; 3), 3,4,5-trimethoxyphenol (4), 3alpha-hydroxyurs-12-en-28-oic acid methyl ester (5), 3alpha,23-dihydroxyurs-12-en-28-oic acid (6), 3alpha,19alpha,23-trihydroxyurs-12-en-28-oic acid methyl ester (7), and oleanolic acid (8). Compounds 1, 2, 6, and 8 showed moderate in vitro activities against Plasmodium falciparum. Their structures and configurations were elucidated by spectroscopic methods including 1D- and 2D-NMR analyses. 相似文献
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He ZD Ma CY Tan GT Sydara K Tamez P Southavong B Bouamanivong S Soejarto DD Pezzuto JM Fong HH Zhang HJ 《Phytochemistry》2006,67(13):1378-1384
Bioassay-directed fractionation of the antimalarial active CHCl(3) extract of the dried stems of Rourea minor (Gaertn.) Aubl. (Connaraceae) liana led to isolation of two glycosides, rourinoside (1) and rouremin (2), as well as five known compounds, 1-(26-hydroxyhexacosanoyl)-glycerol (3), 1-O-beta-D-glucopyranosyl-(2S,3R,4E-8Z)-2-N-(2'-hydroxypalmitoyl)-octadecasphinga-4,8-dienine, 9S,12S,13S-trihydroxy-10E-octadecenoic acid, dihydrovomifoliol-9-beta-D-glucopyranoside, and beta-sitosterol glucoside. Compounds 1-3 showed weak in vitro activities against Plasmodium falciparum. Their structures and stereochemistry were elucidated by spectroscopic methods and selected enzyme hydrolysis. 相似文献
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Cui‐Ying Ma Sebisubi Fred Musoke Ghee Teng Tan Kongmany Sydara Somsanith Bouamanivong Bounhoong Southavong D. Doel Soejarto Harry H. S. Fong Hong‐Jie Zhang 《化学与生物多样性》2008,5(11):2442-2448
Bioassay‐directed fractionation led to the isolation of seven compounds from a sample of the dried leaves, twigs, and branches of Diospyros quaesita Thw . (Ebenaceae). One of the isolates, betulinic acid 3‐caffeate ( 1 ), showed in vitro antimalarial activity against Plasmodium falciparum clones D6 (chloroquine‐sensitive) and W2 (chloroquine‐resistant) with IC50 values of 1.40 and 0.98 μM , respectively. Evaluation of compound 1 in the human oral epidermoid (KB) cancer cell line revealed cytotoxicity at ED50 of 4.0 μM . In an attempt to reduce the cytotoxicity of 1 , the acetylated derivative 1a and betulinic acid ( 1b ) were prepared. Of the seven isolates, diospyrosin ( 2 ) was determined to be a new neolignan. In addition to 1 , other known compounds isolated in this study were pinoresinol, lariciresinol, N‐benzoyl‐L ‐phenylalaninol, scopoletin, and poriferast‐5‐en‐3β,7α‐diol. The structure of 2 was elucidated based on spectroscopic data analysis including 1D‐ and 2D‐NMR, and HR‐ESI‐MS. 相似文献
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