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: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
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
Drug repurposing is an important approach to the assignment of already approved drugs for new indications. This technique bypasses some steps in the traditional drug approval system, which saves time and lives in the case of pandemics. Direct acting antivirals (DAAs) have repeatedly repurposed from treating one virus to another. In this study, 16 FDA-approved hepatitis C virus (HCV) DAA drugs were studied to explore their activities against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) human and viral targets. Among the 16 HCV DAA drugs, telaprevir has shown the best evidence to work on both indirect human targets (cathepsin L [CTSL] and human angiotensin-converting enzyme 2 [ACE2] receptor) and direct viral targets (main protease [M]). Moreover, the docked poses of telaprevir inside both ACE2 and M were subjected to additional molecular dynamics simulations monitored by calculating the binding free energy using MM-GBSA. analysis of telaprevir showed inhibition of SARS-CoV-2 replication in cell culture (IC = 11.552 μM, CC = 60.865 μM, and selectivity index = 5.27). Accordingly, based on the studies and supported by the presented analysis, we suggest that telaprevir may be considered for therapeutic development against SARS-CoV-2.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8426143 | PMC |
http://dx.doi.org/10.1016/j.heliyon.2021.e07962 | DOI Listing |
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