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Peptidomimetics Inhibition against SARS CoV-2 Growth: A Tethering Approach

Implementing Organization

Maulana Abul Kalam Azad University of Technology
Principal Investigator
Dr. Krishnendu Maji
Maulana Abul Kalam Azad University of Technology

About

Recent outbreak and spreading of SARS-CoV-2 is a real threat to human health. Presently 756,581,850 people are infected globally and 6,844,267 people died because of COVID-19 infection. Till today not a single drug molecule is available which can cure COVID-19 infection completely. Scientists are continuously trying to develop new molecules which can effectively inhibit the growth SARS-CoV-2 and stop the COVID-19 infection. Peoples have targeted the receptor Binding Domain (RBD), using which viral attachment to ACE2 receptors present in humans takes place. But due to rapid mutation in protein present in RBD, targeting RBD domain is not so affected. Then Mpro protease, which is essential for viral replication, is a fantastic targeting protein. A few molecules have been reported, which effectively bind with Mpro protease and stop its activities. So development of new kinds of peptidomimetic compounds which will bind with the active sites of Mpro protease by different chemistry is highly desirable. Herein, a series of peptidomimetic molecules have been proposed which will attach to the active sites of Mpro protease through the formation of disulphide bonds and thus the peptidomimetic molecules having minimal cell toxicity will have a significant inhibitory effect on the growth of SARS-CoV-2.

Source

Source
Anusandhan National Research Foundation/Science and Engineering Research Board (SERB), DST 2023-24
Funding Organization
Funding Organization
Science and Engineering Research Board (SERB), New Delhi
Anusandhan National Research Foundation (ANRF)
Quick Information
Area of Research
Chemical Sciences
Start Year
2023
End Year
2025
Sanction Amount
₹ 32.97 L
Status
Completed
Contact
maji.krishnendu@gmail.com
Output
No. of Research Paper
00
Technologies (If Any)
00
No. of PhD Produced
00
No. of Patents
Filed : 00
Grant : 00
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