Qing-Fang Wang , Jing-Rong Ou-Yang , Ting-Ting Guo , Ming-Ming Li , Hong-Ping He
{"title":"Chemical constituents from Albatrellus confluence and their chemotaxonomic significance","authors":"Qing-Fang Wang , Jing-Rong Ou-Yang , Ting-Ting Guo , Ming-Ming Li , Hong-Ping He","doi":"10.1016/j.bse.2024.104831","DOIUrl":null,"url":null,"abstract":"<div><p>The phytochemical study of the fruiting bodies of <em>Albatrellus confluens</em> afforded a new natural product methyl 2-hydroxyimino-3- phenylpropionate (<strong>1</strong>), as well as 14 known compounds: phenylalanine (<strong>2</strong>), zarzissine (<strong>3</strong>), uridine (<strong>4</strong>), emeheterone (<strong>5</strong>), uracil (<strong>6</strong>), nicotinamide (<strong>7</strong>), adenosine (<strong>8</strong>)), methyl 4-hydroxyphenylacetate (<strong>9</strong>), grifolin (<strong>10</strong>), neogrifolin (<strong>11</strong>), grifolin methyl ether (<strong>12</strong>), 4-O-methyl grifolin acid (<strong>13</strong>), confluentin (<strong>14</strong>), albatrelin G (<strong>15</strong>). The structures of these compounds were deduced using spectroscopic methods, including IR, MS, 1D and 2D NMR, as well as by comparisons with data reported in the literature. Furthermore, the chemotaxonomic significance of the isolates was also discussed.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"114 ","pages":"Article 104831"},"PeriodicalIF":1.4000,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical Systematics and Ecology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0305197824000498","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The phytochemical study of the fruiting bodies of Albatrellus confluens afforded a new natural product methyl 2-hydroxyimino-3- phenylpropionate (1), as well as 14 known compounds: phenylalanine (2), zarzissine (3), uridine (4), emeheterone (5), uracil (6), nicotinamide (7), adenosine (8)), methyl 4-hydroxyphenylacetate (9), grifolin (10), neogrifolin (11), grifolin methyl ether (12), 4-O-methyl grifolin acid (13), confluentin (14), albatrelin G (15). The structures of these compounds were deduced using spectroscopic methods, including IR, MS, 1D and 2D NMR, as well as by comparisons with data reported in the literature. Furthermore, the chemotaxonomic significance of the isolates was also discussed.
期刊介绍:
Biochemical Systematics and Ecology is devoted to the publication of original papers and reviews, both submitted and invited, in two subject areas: I) the application of biochemistry to problems relating to systematic biology of organisms (biochemical systematics); II) the role of biochemistry in interactions between organisms or between an organism and its environment (biochemical ecology).
In the Biochemical Systematics subject area, comparative studies of the distribution of (secondary) metabolites within a wider taxon (e.g. genus or family) are welcome. Comparative studies, encompassing multiple accessions of each of the taxa within their distribution are particularly encouraged. Welcome are also studies combining classical chemosystematic studies (such as comparative HPLC-MS or GC-MS investigations) with (macro-) molecular phylogenetic studies. Studies that involve the comparative use of compounds to help differentiate among species such as adulterants or substitutes that illustrate the applied use of chemosystematics are welcome. In contrast, studies solely employing macromolecular phylogenetic techniques (gene sequences, RAPD studies etc.) will be considered out of scope. Discouraged are manuscripts that report known or new compounds from a single source taxon without addressing a systematic hypothesis. Also considered out of scope are studies using outdated and hard to reproduce macromolecular techniques such as RAPDs in combination with standard chemosystematic techniques such as GC-FID and GC-MS.