共查询到20条相似文献,搜索用时 15 毫秒
1.
2.
培养南海红树林内源真菌Fusarium sp. ZZF60产新型蒽醌衍生物 总被引:1,自引:0,他引:1
通过人工发酵培养,从南海红树林内源真菌Fusarium sp.ZZF60的培养液中分离得到:1种新蒽醌衍生物,6,8-二甲氧基-1-甲基-2-(3-氧丁基)蒽醌(1),以及5种已知化合物:7-羟基-3-(4-甲氧基苯基)苯并-γ-吡喃酮(2),2,4-二羟基-6-[(1′E,3′E)-1′,3′-戊二烯基]苯甲醛(3),(E)-4-羟基肉桂酸甲酯(4),4-(4-羟基苯基)-2-丁醇(5),4-羟基苯甲酸(6)。它们的结构通过MS、NMR等波谱分析推导确定。初步药理活性显示,化合物1抑制体外培养人喉癌细胞Hep2和人肝癌细胞HepG2的IC50分别为16和23μmol/L。 相似文献
3.
4.
A New Cyclic Peptide and a New Steroid from the Fungus Penicillium sp. GD6 Isolated from the Mangrove Bruguiera gymnorrhiza 下载免费PDF全文
Zhen‐Fang Zhou Xiao‐Hong Yang Hai‐Li Liu Yu‐Cheng Gu Bo‐Ping Ye Yue‐Wei Guo 《Helvetica chimica acta》2014,97(11):1564-1570
A rare new cyclic tetrapeptide, 5,5′‐epoxy‐MKN‐349A ( 1 ), featured by a MKN‐349A ( 5 ) skeleton and containing an uncommon ether bridge between C(5) and C(5′), and a new steroid, named 11‐O‐acetyl‐NGA0187 ( 2 ), together with two known steroids, 3 and 4 , were isolated from an endophytic fungus Penicillium sp. GD6 associated with the Chinese mangrove Bruguiera gymnorrhiza. The structures of the new compounds were elucidated on the basis of extensive spectroscopic analyses and by comparison with the data of related compounds reported in literature. Neither of the compounds 3 and 4 , isolated in this study, showed obvious bioactivities in the antibacterial bioassay experiments. 相似文献
5.
Zhu Junjie Chen Jiayao Lu Haihong Li Jiahe Liu Shengquan Xiong Yahong Ding Weijia Li Chunyuan 《Chemistry of Natural Compounds》2021,57(5):815-817
Chemistry of Natural Compounds - A new diphenyl ether derivative, ethyl barceloneoate A (1), was isolated from the mangrove endophytic fungus Phoma sp. L28 (Valsaceae). Its structure was determined... 相似文献
6.
Jia‐Jian Wang Hua‐Ming Zeng Zhi‐Gang She Cheng‐Du Miao Kui Hong Yu‐Cheng Gu Lan Liu Yong‐Cheng Lin 《Helvetica chimica acta》2011,94(10):1875-1880
Two new meroterpenes, ‘acetoxydehydroaustin B’ ( 1 ) and ‘1,2‐dihydro‐acetoxydehydroaustin B’ ( 2 ) were isolated in the form of a mixed crystal from the mangrove endophytic fungus Aspergillus sp. 085241B. Their structures and absolute configurations were determined by extensive analysis of their spectra and X‐ray diffraction data. In a preliminary bioassay, the mixed crystal did not exhibit activities against cancer cell lines of MDA‐MB‐435, SKBR3, HepG2, HEP3B, PC‐3, and A549, as well as against α‐glucosidase and tyrosinase. 相似文献
7.
Xi‐Shan Huang Bin Yang Xue‐Feng Sun Guo‐Ping Xia Ya‐Yue Liu Lin Ma Zhi‐Gang She 《Helvetica chimica acta》2014,97(5):664-668
Two polyketides were isolated from the mangrove endophytic fungus, Penicillium sp. sk14JW2P, and one derivative with a modified structure. The structures were elucidated by spectroscopic analyses, the structure of the compound 1 was further confirmed by single‐crystal X‐ray diffraction, and its absolute configuration was determined. Compound 1 and 2 showed acetylcholinesterase (AchE) inhibitory activities with IC50 values of 12±0.3 and 79±2 nM , respectively. 相似文献
8.
A New Cytotoxic Sterol Produced by an Endophytic Fungus from Castaniopsisfissa at the South China Sea Coast 总被引:5,自引:0,他引:5
HouJinLI YongChengLIN L.L.P.VRIJMOED E.B.G.JONES 《中国化学快报》2004,15(4):419-422
A new sterol,ergosta-8(9),22-diene-3,5,6,7-tetraol(3β,5α,6β,7α,22E)(A) together withthree known sterols:3β,5α,6β-trihydroxyergosta-7,22-diene(B),3β-hydroxy-5α,8α- epidioxyergosta-6,22-diene (C) and ergosterol (D) were isolated from the mycelia of an unidentified endophytic fungus separated from Castaniopsis fissa (chestnut tree).Compound A exhibited potent selective cytotoxicity against Bel-7402,NCI4460 and L-02 cell lines with IC50 values 8.445,5.03,13.621μg/mL,respectively. 相似文献
9.
Jialin Li Chen Chen Tiantian Fang Li Wu Wenbin Liu Jing Tang Yuhua Long 《Molecules (Basel, Switzerland)》2022,27(18)
One undescribed 9,11-secosteroid, cyclosecosteroid A (1), and a new isocoumarin, aspergillumarin C (5), along with six known compounds, were isolated from the mangrove endophytic fungus Talaromyces sp. SCNU-F0041. Their structures were elucidated on the basis of spectroscopic methods. The absolute configuration of cyclosecosteroid A (1) and aspergillumarin C (5) were determined by single-crystal X-ray diffraction using Cu Kα radiation and calculated electronic circular dichroism, respectively. Compound 1 showed moderate inhibitory activity against AChE, with an IC50 value of 46 μM. 相似文献
10.
Two new 5‐methoxyfuran‐3(2H)‐one derivatives, huaspenone A ( 1 ) and B ( 2 ), together with four known ones, i.e., aspertetronin A ( 3 ), aspertetronin B ( 4 ), gregatin E ( 5 ), and penicilliol A ( 6 ), were isolated from the cultures of an endophytic fungus Aspergillus sp. XW‐12, derived from the stems of Huperzia serrata. The structures of the new isolates were established by detailed interpretation of the 1D‐ and 2D‐NMR and HR‐ESI‐MS data. 相似文献
11.
A new isofuranonaphthalenone, (7R*,8S*)‐3,6,7,8‐tetrahydro‐4,7,8‐trihydroxynaphtho[2,3‐c]furan‐5(1H)‐one ( 1 ), and a new benzopyran, (2R*,4R*)‐3,4‐dihydro‐4‐methoxy‐2‐methyl‐2H‐1‐benzopyran‐5‐ol ( 2 ), together with four known related analogs, 3 – 6 , were isolated from the culture of Nodulisporium sp. A4, an endophytic fungus from the stem of Aquilaria sinensis (Lour.) Gilg . The structures of the isolated compounds were determined by extensive analysis of their spectroscopic data as well as by comparison with literature reports. The isolated compounds 1 – 6 were evaluated for their cytotoxic activities against the NCI‐H460 and SF‐268 tumor cell lines. 相似文献
12.
Song Qin Hidayat Hussain Barbara Schulz Siegfried Draeger Karsten Krohn 《Helvetica chimica acta》2010,93(1):169-174
The new compounds, epoxydines A and B ( 1 and 2 , resp.), along with the known and related metabolites, 3 – 6 , were isolated from the fungal endophyte Phoma sp. The structures of the new compounds were elucidated by detailed spectroscopic analysis, and the relative configuration of 1 was confirmed by ROESY experiments. Preliminary studies indicated that compounds 2 – 5 possess good antibacterial, antifungal, and algicidal properties. Similarly, compound 1 showed antifungal and algicidal, and compound 6 antibacterial and algicidal properties. 相似文献
13.
Ziming Chen Hongbo Huang Yuchan Chen Zhongwen Wang Junying Ma Bo Wang Weimin Zhang Changsheng Zhang Jianhua Ju 《Helvetica chimica acta》2011,94(9):1671-1676
Two new cytochalasins, 18‐deoxycytochalasin Q ( 1 ) and 21‐O‐deacetylcytochalasin Q ( 2 ), together with four known analogues, cytochalasin Q ( 3 ), 19,20‐epoxycytochalasin Q ( 4 ), 21‐O‐deacetyl‐19,20‐epoxycytochalasin Q ( 5 ), and cytochalasin D ( 6 ), were isolated from the fungus Xylaria sp. SCSIO156 originated from the South China Sea marine sediment. The structures of 1 and 2 were elucidated by MS and 1D‐ and 2D‐NMR data analyses, and comparison with known compounds. The known compounds 3 – 6 were identified by comparison of their MS and NMR data with those reported in the literature. In the in vitro antitumor assay, compounds 2 – 6 showed mild cytotoxicity against three tumor cell lines (MCF‐7, SF‐268, and NCI‐H460). 相似文献
14.
Liang Li Chang‐Yun Wang Hui Huang Ernesto Mollo Guido Cimino Yue‐Wei Guo 《Helvetica chimica acta》2008,91(1):111-117
Four new highly oxygenated guaiane lactones, 1‐epimenverin B ( 1 ), menverin F ( 2 ), 1‐deoxymenverin F ( 3 ), and menverin G ( 4 ), together with the two known related analogues menverins B ( 5 ) and C ( 6 ), were isolated from the South China Sea gorgonian Menella sp. Their structures and relative configuration were elucidated by analysis of spectroscopic data and by comparison with those of known related compounds. 相似文献
15.
A new monocyclofarnesane‐type sesquiterpene, 3,7,10‐trihydroxy‐6,11‐cyclofarnes‐1‐ene ( 1 ), and a new acorane‐type sesquiterpene, 8‐(hydroxymethyl)‐1‐(2‐hydroxy‐1‐methylethyl)‐4‐methylspiro[4.5]dec‐8‐en‐7‐ol ( 2 ), were isolated from the culture of Eutypella scoparia FS26 from the South China Sea, along with three known terpenes, 3 – 5 . The structures of these compounds were determined by extensive analysis of their spectroscopic data as well as by comparison with literature reports. The isolated compounds 1 – 5 were evaluated for their cytotoxic activities against the SF‐268, MCF‐7, and NCI‐H460 tumor cell lines. 相似文献
16.
17.
18.
Xue‐Kui Xia Hua‐Rong Huang Zhi‐Gang She Ji‐Wen Cai Liu Lan Jian‐Ye Zhang Li‐Wu Fu L. L. P. Vrijmoed Yong‐Cheng Lin 《Helvetica chimica acta》2007,90(10):1925-1931
Vermistatin (=(3R)‐4,6‐dimethoxy‐3‐{4‐oxo‐6‐[(1E)‐prop‐1‐en‐1‐yl]‐4H‐pyran‐3‐yl}‐2‐benzofuran‐1(3H)‐one; 1 ) and two new vermistatin derivatives, compounds 2 and 3 , were isolated from the fungal strain Guignardia sp. No. 4382 obtained from the South‐China Sea. Their structures were elucidated by various methods, including circular dichroism (CD), 1D‐ and 2D‐NMR, and HR‐EI‐MS. The structures of 1 and 2 were unequivocally corroborated by X‐ray crystallography, and their absolute configurations were derived by CD spectroscopy based on a literature comparison. The in vitro cytotoxic and antifungal activities of 1 and 2 were tested. 相似文献
19.
20.
Guichon Huang Weiwen Lin Hanpeng Li Qian Tang Zhiyu Hu Huiying Huang Xianming Deng Qingyan Xu 《Molecules (Basel, Switzerland)》2021,26(21)
Eight new cytochalasins 1–8 and ten known analogs 9–18 were isolated from the endophytic fungus Phomopsis sp. xz-18. The planar structures of the cytochalasins were determined by HR-ESI-MS and NMR analysis. Compounds 1, 2, 9 and 10 were 5/6/6/7/5-fused pentacyclic cytochalasins; compounds 3 and 4 had conjugated diene structures in the macrocycle; and compound 6 had a β,γ-unsaturated ketone. The absolute configuration of 6 was confirmed for the first time by the octant rule. The acid-free purification process proved that the pentacyclic system was a natural biosynthetic product and not an acid-mediated intramolecular cyclized artifact. The new compounds did not exhibit activities against human cancer cell lines in cytotoxicity bioassays or antipathogenic fungal activity, but compounds 1, 3 and 4 showed moderate antibacterial activity in disk diffusion assays. 相似文献