Author: Poochi, Saravana Prabha; Easwaran, Murugesh; Balasubramanian, Balamuralikrishnan; Anbuselvam, Mohan; Meyyazhagan, Arun; Park, Sungkwon; Bhotla, Haripriya Kuchi; Anbuselvam, Jeeva; Arumugam, Vijaya Anand; Keshavarao, Sasikala; Kanniyappan, Gopalakrishnan Velliyur; Pappusamy, Manikantan; Kaul, Tanushri
Title: Employing bioactive compounds derived from Ipomoea obscura (L.) to evaluate potential inhibitor for SARSâ€CoVâ€2 main protease and ACE2 protein Cord-id: 4ad8ubrt Document date: 2020_7_6
ID: 4ad8ubrt
Snippet: Angiotensin converting enzyme 2 (ACE2) and main protease (M(Pro)) are significant target proteins, mainly involved in the attachment of viral genome to host cells and aid in replication of severe acute respiratory syndromeâ€coronaviruses or SARSâ€CoV genome. In the present study, we identified 11 potent bioactive compounds from ethanolic leaf extract of Ipomoea obscura (L.) by using GCâ€MS analysis. These potential bioactive compounds were considered for molecular docking studies against ACE2
Document: Angiotensin converting enzyme 2 (ACE2) and main protease (M(Pro)) are significant target proteins, mainly involved in the attachment of viral genome to host cells and aid in replication of severe acute respiratory syndromeâ€coronaviruses or SARSâ€CoV genome. In the present study, we identified 11 potent bioactive compounds from ethanolic leaf extract of Ipomoea obscura (L.) by using GCâ€MS analysis. These potential bioactive compounds were considered for molecular docking studies against ACE2 and M(Pro) target proteins to determine the antiviral effects against SARSâ€COV. Results exhibits that among 11 compounds from I. obscura (L.), ursoâ€deoxycholic acid, demeclocycline, tetracycline, chlorotetracycline, and ethyl isoâ€allocholate had potential viral inhibitory activity. Hence, the present findings suggested that chemical constitution present in I. obscura (L.) will address inhibition of corona viral replication in host cells.
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