Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Ten cytochalasin derivatives, including six new methylthioether-containing chaetoglobosins (thiochaetoglobosins A-F, ), a new related congener (18-nor-prochaetoglobosin II, ), and three known unsulfured counterparts (), were isolated and identified from AS-506, an endozoic fungus isolated from a deep-sea sponge, which was collected from Magellan Seamounts in the Western Pacific Ocean. Their structures were determined by extensive interpretation of the spectroscopic and X-ray crystallographic data, as well as by ECD calculations. Structurally, thiochaetoglobosins A-F () represent the first examples of chaetoglobosin derivatives containing a methylthioether group in the molecules, while 18-nor-prochaetoglobosin II () is the first 18-nor-chaetoglobosin derivative. Precursor incubation experiments with [C-CH]-l-methionine confirmed that the thio-linked methyl was derived from methionine, and a new isotope-labeled thiochaetoglobosin () was also isolated and identified. Compound exhibited activity against the aquatic pathogenic bacterium (MIC = 0.5 μg/mL), comparable to that of the positive control chloramphenicol. The cell morphology of was studied by using growth curves and scanning electron microscopy (SEM) data. The results showed that compound could affect the integrity of the membrane to induce bacteriolysis and death of . Additionally, compounds , , , , and showed cytotoxic activities against several tumor cell lines with IC values ranging from 0.72 to 17.66 μM.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acs.jafc.4c09395 | DOI Listing |
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