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
The CHCl-MeOH (1:1) extract of roots of (Polygonaceae) displayed significant antibacterial activity against five bacterial strains with MICs (62.5-31.2 μg.mL). The EtOAc soluble fraction displayed a significant activity against the same strains with MICs (31.2-3.9 μg.mL). The purification of the EtOAc fraction yielded one new phenylisobenzofuranone derivative, berquaertiide (), along with 19 known compounds (-). Their structures were elucidated based on the analysis of their NMR and MS data. All the isolated compounds were assessed for their antibacterial activity. Compound was the most active against all the tested strains (15.7 to 1.9 μg.mL), while compounds - displayed good activities on at least one of the tested strains. In addition, seven analogues (-) of compound were prepared and further assessed for their antibacterial activity. Compounds and were most active than against with MIC (125 and 15.6 μg.mL, respectively).
Download full-text PDF |
Source |
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http://dx.doi.org/10.1080/14786419.2022.2162894 | DOI Listing |
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