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
Forty-two Amaryllidaceae alkaloids, including eleven previously undescribed alkaloids, crinasiaticines C-M, and three undescribed naturally occurring alkaloids, (+)-dihydroepivittatine, (+)-dihydrovittatine and (+)-dihydrohamayne, were isolated from the leaves of Crinum asiaticum L. var. asiaticum. Their structures and configurations were elucidated using NMR and MS spectroscopic techniques, along with the comparison of experimental electronic circular dichroism spectra to calculated data. The anti-inflammatory activity against nitric oxide (NO) production in lipopolysaccharide-stimulated RAW264.7 cells was evaluated for most of the isolated alkaloids. Compounds 39, 21, 22, and 35 exhibited considerable NO inhibitory activity, with IC values of 2.5-2.6 μM, compared to positive control dexamethasone (IC 2.7 μM). However, these compounds demonstrated cytotoxic effects on cells. Compound 15 also possessed the highest selectivity index of 22.5 with minimal cytotoxicity.
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Source |
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http://dx.doi.org/10.1016/j.phytochem.2025.114383 | DOI Listing |
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