共查询到20条相似文献,搜索用时 15 毫秒
1.
Lijun Liu Wei Xu Shumin Li Mengying Chen Yongjun Cheng Wangjun Yuan 《Natural product research》2019,33(20):2988-2994
A new indole diterpene, named penicindopene A (1), together with seven known compounds (2?–?8), was isolated from the deep-sea fungus Penicillium sp. YPCMAC1. The structure of penicindopene A was elucidated by extensive spectroscopic analyses (1?D and 2?D NMR, and HRESIMS data), in addition to the ECD calculations for the assignments of its absolute configuration. Penicindopene A represented the first example of indole diterpenes possessing a 3-hydroxyl-2-indolone moiety, and it exhibited moderate cytotoxicities against A549 and HeLa cell lines with IC50 values of 15.2 and 20.5?µM, respectively. 相似文献
2.
3.
Xiqing Bian Meili Shao Huaqi Pan Kaibo Wang Shengdong Huang Xin Wu 《Natural product research》2016,30(2):125-130
A new 2(1H)-pyrazinone ring-containing natural product, paenibacillin A (1), together with five known diketopiperazine derivatives 2–6 and two known isoflavones 7–8, was isolated from the culture of an endophytic bacterium Paenibacillus sp. Xy-2. The structure of compound 1 was elucidated by extensive spectral methods, including UV, IR, HR-ESI-MS, 1D and 2D NMR and ECD experiments. Compound 1 exhibited moderate cytotoxicity against HL-60 cell line with IC50 value of 50.48 μM. 相似文献
4.
Priyanka Michael Espen Hansen Johan Isaksson Jeanette H. Andersen 《Natural product research》2020,34(14):2059-2064
AbstractThe new guanidine alkaloid Dendrobeaniamine A (1) was isolated from the organic extract of the Arctic marine bryozoan Dendrobeania murrayana. The chemical structure of 1 was elucidated by spectroscopic experiments, including 1D and 2D NMR and HRESIMS analysis. Compound 1 is a lipoamino acid, consisting of a C12 fatty acid anchored to the amino acid arginine. The bioactivity of 1 was evaluated using cellular and biochemical assays, but the compound did not show cytotoxic, antimicrobial, anti-inflammatory or antioxidant activities 相似文献
5.
Zhiyong Guo Xueshuang Li Liang Zhang Ziwei Feng Haibo He 《Natural product research》2016,30(22):2582-2589
Two new tremulanes and two new 5,6-secotremulanes, davotremulanes A-D 1–4, along with four known compounds 5–8, were isolated from the culture extract of X1-2, an unidentified plant-associated fungus, which was isolated from the endangered plant, Davidia involucrate Baill. in Shennongjia District. The structures of new compounds 1–4 were established on the basis of extensive spectroscopic analysis. Compounds 1–8 were evaluated for cytotoxic activity to four cancer cell lines, and compounds 1, 2 and 5 displayed selectively moderate activities to A549 cell line with IC50 at 15.3, 25.2, 35.2 μg/mL. 相似文献
6.
The isolation and structure elucidation of belamide A from the marine cyanobacterium Symploca sp. is described. Belamide A is a highly methylated linear tetrapeptide with structural analogy to the important linear peptides dolastatins 10 and 15. Disruption of the microtubule network in A-10 cells was observed at 20 μM and displayed classic tubulin destabilizing antimitotic characteristics. The moderate cytotoxicity of belamide A (IC50 0.74 μM vs HCT-116 colon cancer line) provides new insights into structure-activity relationships for this drug class. 相似文献
7.
A new cyclic peptide, prepatellamide A (1), along with three known cyclic peptides (2)— (4), was isolated from the ascidianLissoclinum patella. The structure of prepatellamide A was determined from one- and two-dimensional1H and13C NMR spectra. The known cyclic peptides were identified as patellamides A (2), B (3) and C (4). 相似文献
8.
A new cyclic peptide, prepatellamide A (1), along with three known cyclic peptides (2)-(4), was isolated from the ascidian Lissodinum patella. The structure of prepatellamide A was determined from one- and two-dimensional H and 13C NMR spectra. The known cyclic peptides were identified as patellamides A (2), B (3) and C (4). 相似文献
9.
Three new isomeric furanocoumarins named feroniellic acids A-C (1-3) were isolated from the BuOH extract of Feroniella lucida roots. They are diastereomerically different to each other in configuration at C-2″ and C-3″. The structures were elucidated on the basis of spectroscopic data while their configurations were established by synthesis of model compounds together with application of Mosher’s method. 相似文献
10.
Sasiphimol Sawadsitang Nuttika Suwannasai Wiyada Mongkolthanaruk Peni Ahmadi 《Natural product research》2018,32(19):2260-2267
The secondary metabolites of Xylaria cf. cubensis SWUF08-86 fungus were investigated, and the chromatographic separation of the crude extracts yielded seventeen compounds. The structure elucidation by spectroscopic analysis including 1D and 2D NMR and the comparison of these data with literature, along with HREIMS spectrometry, revealed one new amino amidine derivative (1), together with five known simple cyclic dipeptide analogs, diketopiperazines (2–6) and eleven other known compounds, including one hemi-cycline (10), three aromatic derivatives (11–13), one sesquiterpene (14) and three sterols (15–17). The isolated compounds were screened for anticancer and anti-pathogenic bacterial and fungal activities. Based on this work, Xylaria cf. cubensis SWUF08-86 has proven to be a diverse secondary metabolites producer. 相似文献
11.
The reactions of dialkylurethanes R1
2NCOOR (RO is the residue of a secondary but not a primary alcohol) with nitrating reagents leads to the formation of the corresponding
sccondaryN-nitroamines R1
2NNO2.
Translated fromIzvestiya Akademii Nauk Seriya Khimicheskaya, No. 6, pp. 1162–1164, June, 1998. 相似文献
12.
Cai-Juan Zheng Guo-Lei Huang Yan Xu Xin-Ming Song Jun Yao Hui Liu 《Natural product research》2016,30(7):821-825
One new benzopyran derivative (2R*,4R*)-3,4-dihydro-5-methoxy-2-methyl-2H-1-benzopyran-4-ol (1), together with five known compounds (2?6), were obtained from the EtOAc extract of the endophytic fungus Penicillium citrinum HL-5126 isolated from the mangrove Brguiera sexangula var. rhynchopetala collected in the South China Sea. Their structures were elucidated by the detailed analysis of comprehensive spectroscopic data. All compounds were evaluated for their antibacterial activities. Compound 6 exhibited potent inhibitory activity against Bacillus subtilis, Bacillus cereus and Micrococcus tetragenus with the same MIC values of 6.94 μM. 相似文献
13.
A new cyclic peptide, prepatellamide A (1), along with three known cyclic peptides (2)— (4), was isolated from the ascidianLissoclinum patella. The structure of prepatellamide A was determined from one- and two-dimensional1H and13C NMR spectra. The known cyclic peptides were identified as patellamides A (2), B (3) and C (4). 相似文献
14.
(+)-Xyloketal D was prepared in a one-pot multistep domino reaction by heating optically active 5-hydroxy-4-methyl-3-methylenepentan-2-one (R) in toluene with 2,4-dihydroxyacetophenone. The absolute configuration of the natural product was confirmed by preparation of the starting enone from a lactone of established absolute configuration. 相似文献
15.
《Tetrahedron: Asymmetry》1999,10(7):1219-1222
A new chiral iminophosphine ligand derived from (1S,4S)-fenchone has been developed, and its usefulness as a chiral ligand in asymmetric synthesis was demonstrated in palladium-catalyzed allylic alkylations. 相似文献
16.
Sheila Marie Pimentel-Elardo Tobias A.M. Gulder Ute Hentschel Gerhard Bringmann 《Tetrahedron letters》2008,49(48):6889-6892
The new macrolactams cebulactams A1 and A2 were isolated from an extract of the first obligate marine strain of the genus Saccharopolyspora. Their constitutionally identical structures, each bearing a six-membered cyclic ether as part of the macrocycle, and their relative configurations were elucidated by MS methods and by 1D and 2D NMR techniques. 相似文献
17.
Francesco Vinale Judyta Strakowska Pierluigi Mazzei Alessandro Piccolo Roberta Marra Nadia Lombardi 《Natural product research》2016,30(22):2575-2581
Trichoderma based products are considered an alternative to synthetic pesticides and fertilizers. These Trichoderma spp. are among the most studied and applied fungal BCAs in industry and agriculture and are known to secrete several secondary metabolites with different biological activities. The analysis of metabolic profiles (the ‘metabolome’) of Trichoderma species is complex because of the wide range of compounds produced and the molecular activities identified, including the recently determined role in the activation of plant resistance to biotic and abiotic stresses and growth promotion. A new 10-member lactone, but-2-enoic acid 7-acetoxy-6-hydroxy-2-methyl-10-oxo-5,6,7,8,9,10-hexahydro-2H-oxecin-5-yl ester, named cremenolide (1), has been isolated from culture filtrates of Trichoderma cremeum. The structure of cremenolide was determined by spectroscopic methods, including UV, MS, and 1D and 2D NMR analyses. In vitro tests showed that the purified compound inhibited the radial mycelium growth of Fusarium oxysporum, Botrytis cinerea and Rhizoctonia solani, and exerted a significant promotion of growth of tomato seedlings. 相似文献
18.
Roman Labuda Markus Bacher Hannes Gratzl Maria Doppler Alexandra Parich Mohammed Aufy Rosa Lemmens-Gruber Rainer Schuhmacher Kathrin Rychli Martin Wagner Thomas Rosenau Joseph Strauss Christoph Schüller 《Molecules (Basel, Switzerland)》2021,26(21)
In the process of screening for new bioactive microbial metabolites we found a novel ƴ-pyrone derivative for which we propose the trivial name luteapyrone, in a recently described microscopic filamentous fungus, Metapochonia lutea BiMM-F96/DF4. The compound was isolated from the culture extract of the fungus grown on modified yeast extract sucrose medium by means of flash chromatography followed by preparative HPLC. The chemical structure was elucidated by NMR and LC-MS. The new compound was found to be non-cytotoxic against three mammalian cell lines (HEK 263, KB-3.1 and Caco-2). Similarly, no antimicrobial activity was observed in tested microorganisms (gram positive and negative bacteria, yeast and fungi). 相似文献
19.
The syntheses of new chiral cyclic 1,2-diacetals from (2R, 3R)-( )-tartaric acid are described. C(2)-symmetrical diamines were prepared via direct amidation of the tartrate or from the corresponding bismesylate via reaction with sodium azide. For C1-symmetrical compounds, the Appel reaction was used to form the key intermediate, a monochlorocarbinol, from the diol. Some of the new chiral compounds, produced in good to high yields, may be potentially useful as asymmetric organocatalysts or as nitrogen and sulfur chelating ligands for asymmetric metal catalyzed reactions. Thus, a bis-N-methyl-methanamine derivative, used in substoichiometric amounts, was found to catalyze the enantioselective addition of cyclohexanone to (E)-beta-nitrostyrene with high diastereoselectivity (syn / anti = 92:8), albeit giving moderate optical purity (syn: 30 %). 相似文献
20.
Shengxin Cai Xianglan Kong Wei Wang Huinan Zhou Tianjiao Zhu Dehai Li Qianqun Gu 《Tetrahedron letters》2012,53(21):2615-2617
A novel diketopiperazine (DKP) dimer, aspergilazine A (1), dimerized by two DKP units via a rare N-1 to C-6 linkage, was isolated from the marine-derived fungus Aspergillus taichungensis ZHN-7-07. The structure was determined by the combination of spectroscopic and Marfey’s methods. Biological evaluation indicated that aspergilazine A (1) had a weak activity against influenza A (H1N1) virus. 相似文献