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Previously, we had characterized several structurally interesting brominated phenols from the marine red alga Symphyocladia latiuscula collected from various sites. However, Phytochemical investigations on this species collected from the Weihai coastline of Shandong Province remains blank. Therefore, we characterized the chemical constituents of individuals of this species collected from the region. Eight bromophenols were isolated and identified. Using detailed spectroscopic techniques and comparisons with published data, these compounds were identified as 2,3-dibromo-4,5-dihydroxybenzyl methyl ether (1), 3,5-dibromo-4-hydroxybenzoic acid (2), 2,3,6-tribromo-4,5-dihydroxymethylbenzene (3), 2,3,6-tribromo-4,5-dihydroxybenzaldehyde (4), 2,3,6-tribromo-4,5-dihydroxybenzyl methyl ether (5), bis(2,3,6-tribromo-4,5-dihydroxyphenyl)methane (6), 1,2-bis(2,3,6-tribromo-4,5-dihydroxyphenyl)-ethane (7), and 1-(2,3,6-tribromo-4,5-dihydroxybenzyl)-pyrrolidin-2-one (8). Among these compounds, 1 and 2 were isolated for the first time from S. latiuscula. Each compound was evaluated on the ability to inhibit protein tyrosine phosphatase 1B (PTP1B), which is a potential therapeutic target in the treatment of type 2 diabetes. Bromophenols 5, 6, and 7 showed strong activities with IC50 values of 3.9, 4.3, and 3.5 μmol/L, respectively. This study provides further evidence that bromophenols are predominant among the chemical constituents of Symphyocladia, and that some of these compounds may be candidates for the development of anti-diabetes drugs. 相似文献
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对采自海南东寨港的海洋红树林植物黄瑾(Hibiscus tiliaceus)叶中分离到的一株内生真菌Aspergillus sydowii EN-198的次生代谢产物进行了研究.利用正相与反相硅胶柱层析、葡聚糖凝胶Sephadex LH-20柱层析以及制备薄层层析(PTLC)等分离手段从其发酵液中分离得到14个化合物,通过一维、二维核磁共振技术、质谱技术等鉴定了所有化合物的结构,分别为:环-(S-脯氨酸-S-苯丙氨酸)(1),环-(S-脯氨酸-S-亮氨酸)(2),环-(S-苯丙氨酸-S-色氨酸)(3),(1S)-1-(4 '-间羟基苯甲酸)-1,1,5,5-二甲基己二醇(4),曲酸(5),N-[2-(4-吲哚)乙基]乙酰胺(6),N-[2-(4-对羟基苯酚)乙基]乙酰胺(7),胸腺嘧啶脱氧核苷(8),尿嘧啶脱氧核苷(9),尿嘧啶核苷(10),过氧化麦角甾醇(11),麦角甾醇(12),(2S,2'R,3R,3 'E,4E,8E)-N-(2’-羟基-3’-十六烯酰基)-9-甲基-4,8-二十碳二烯-1,3-二醇(13)以及1-O-β-D-葡萄糖基-(2S,2'R,3R,3'E,4E,8E)-N-(2’-羟基-3’-十六烯酰基)-9-甲基-4,8-二十碳二烯-1,3-二醇(14)；其中化合物1和2为首次从Aspergillus sydowii中分离得到.对所有化合物测试其抑菌活性,发现化合物5与7对金黄色葡萄球菌有较好抑制活性. 相似文献
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从采自青岛近海的红藻多管藻(Polysiphonia urceolata)中分离到一株毛壳霉属真菌球毛壳菌(Chaetomium globosum.),对其发酵代谢产物的化学成分进行了研究。采用溶剂提取、分配,硅胶柱层析、葡聚糖凝胶柱层析以及制备薄层层析等技术已分离获得6个单体化合物,通过一维、二维超导核磁共振技术、质谱技术等鉴定了其中4个化合物的结构,均为苯甲醛类衍生物,分别为2-(1-庚烯基)-3、6-二羟基-5-(3-甲基-2-丁烯基)苯甲醛(Ⅰ)、2-庚基-3、6-二羟基-5-(3-甲基-2-丁烯基)苯甲醛(Ⅱ)、2-(3、5-庚二烯基)-3、6-二羟基-5-(3-甲基-2-丁烯基)苯甲醛(Ⅲ)、2-(1、3、5-庚三烯基)-3、6-二羟基-5-(3-甲基-2-丁烯基)苯甲醛(Ⅳ)。 相似文献
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Bioassay-guided fractionation of the crude extract from Penicillium commune SD-118, a fungus obtained from a deep-sea sediment sample, resulted in the isolation of a known antibacterial compound, xanthocillin X (1), and 14 other known compounds comprising three steroids (2-4), two ceramides (5 and 6), six aromatic compounds (7-12), and three alkaloids (13-15). Xanthocillin X (1) was isolated for the first time from a marine fungus. In the bioassay, xanthocillin X (1) displayed remarkable antimicrobial activity against Staphylococcus aureus and Escherichia coli, and significant cytotoxicity against MCF-7, HepG2, H460, Hela, Du145, and MDA-MB-231 cell lines. Meleagrin (15) exhibited cytotoxicity against HepG2, Hela, Du145, and MDA-MB-231 cell lines. This is the first report of the cytotoxicity of xanthocillin X (1). 相似文献
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焦曲霉(Aspergillusustus)TK-5是分离自土耳其海域海鞘(Pyuramomus)新鲜组织中的一株内生真菌,利用正相与反相硅胶柱层析、葡聚糖凝胶Sephadex LH-20柱层析以及高效液相制备等色谱方法从其发酵产物中分离得到17个化合物,通过一维、二维核磁共振、质谱等技术鉴定了所有化合物的结构,分别为血苋烷型倍半萜类化合物strobilactone A(1), ustusolate E(2), ustusolate C(3), ustusolate D(4),11-hydroustusolate E(5), 11, 6’-hydroustusolate E(6),(2’E, 4’E, 6’E)-6-(1’-carboxyocta-2’, 4’, 6’-triene)-11,12-epoxy-9, 11-dihydroxydrim-7-ene(7), 12-hydroxy-6-epi-albrassitriol (8), ustusolate A (9), deoxyuvidin B(10)和二倍半萜类化合物6-epi-ophiobolinG(11),(6α)-21,21-O-dihydroophiobolinG(12),6-epi-ophiobolin K(13), ophiobolin P(14) ophiobolin H(15), ophiobolin Q(16)及ophiobolin R(17)。活性筛选表明化合物2、6、7、9、11和13对神经氨酸酶具有一定的抑制活性,其半数抑制浓度(IC50)分别为31.8、37.3、28.4、36.8、46.6和37.6μmol/L。 相似文献
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对采自海南文昌红树林根际土壤样品中分离到的真菌Penicillium sp. MA-37的次生代谢产物的化学成分进行了研究.利用硅胶柱层析、葡聚糖凝胶Sephadex LH-20柱层析、制备薄层层析以及重结晶等分离方法并通过现代波谱技术共分离、鉴定了8个天然产物,分别为:氮-(2-甲氧基-4-羟基苯)-丙酰胺酸(1),氮-(2,4-二甲氧基苯)-丙酰胺酸(2),氮-(2,4-二甲氧基苯)-丙酰胺酸甲酯(3),(22E,24R)-麦角甾-5,7,22-三烯-3β-醇(4),(22E,24R)-麦角甾-4,6,8(14),22-四烯-3-酮(5),(22E,24R)-5α,8α-环二氧麦角甾-6,22-双烯-3β-醇(6), asperamide B (7), cis-4-hydroxy-6-deoxyscytalone (8);其中化合物1为新化合物,化合物2和3为新天然产物. 相似文献
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对海鞘内生真菌棒曲霉Aspergillus clavatus AS-107的次级代谢产物进行了化学研究。利用反相和正相硅胶柱层析、制备薄层层析(pTLC)以及葡聚糖凝胶柱层析等色谱方法从其发酵产物中分离得到7个喹唑啉酮生物碱类单体化合物,并综合其理化性质和波谱数据鉴定了它们的化学结构,分别是norquinadoline A (1)、quinadoline A (2)、epi-fiscalin D (3)、fiscalin B (4)、quinadoline B (5)、prelapatin B (6)和tryptoquivalines L (7)。对所有化合物进行了抗水产致病菌实验,测试结果表明化合物2对嗜水气单胞菌(Aeromonas hydrophilia)具有一定的抑制作用,其MIC值为16μg/mL;化合物6对副溶血性弧菌(Vibrioparahaemolyticus)、哈氏弧菌(V.harveyi)和嗜水气单胞菌(Aeromonashydrophilia)有一定的抑制活性,其MIC值分别为16、32和32μg/mL。 相似文献
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A chemical investigation of the ethyl acetate extract of the fermentation broth of Alternaria tenuissima EN-192,an endophytic fungus obtained from the stems of the marine mangrove plant Rhizophora stylosa,resulted in the isolation of nine known secondary metabolites,including four indole-diterpenoids:penijanthine A(1),paspaline(2),paspalinine(3),and penitrem A(4);three tricycloalternarene derivatives:tricycloalternarene 3a(5),tricycloalternarene 1b(6),and tricycloalternarene 2b(7);and two alternariol congeners:djalonensone(8) and alternariol(9).The chemical structures of these metabolites were characterized through a combination of detailed spectroscopic analyses and their comparison with reports from the literature.The inhibitory activities of each isolated compound against four bacteria were evaluated and compounds 5 and 8 displayed moderate activity against the aquaculture pathogenic bacterium Vibrio anguillarum,with inhibition zone diameters of 8 and 9 mm,respectively,at 100 μg/disk.To the best of our knowledge,this is the first report on the secondary metabolites of mangrove-derived Alternaria tenuissima and also the first report of the isolation of indole-diterpenoids from fungal genus Alternaria. 相似文献
10.
药用红树林植物黄槿的化学成分研究 总被引：1，自引：0，他引：1
利用正相硅胶柱色谱、反相硅胶柱色谱、凝胶Sephadex LH-20柱色谱、制备薄层色谱（PTLC）及重结晶等分离手段，从海洋红树林植物黄槿（Hibiscus tilisceus）中分离得到11个化合物，通过MS、1D和2D NMR等波谱技术鉴定了所有化合物的结构，分别为coniferaldehyde（1），3,4-二羟基苯甲酸甲酯（2），松脂醇（3），丁香脂素（4），格榄酮（5），黄芪苷（6），植醇（7），胆甾-5-烯-3β，7α-二醇（8），胆甾-5-烯-3β，7β-二醇（9），胆甾醇（10）和声-胡萝卜苷（11）。这些化合物均为首次从该植物中分离获得。 相似文献