The study of binding modes by molecular docking simulations
suggested that these ligands may act by interacting with the predictive
allosteric active site of the soybean lipoxygenase (PDB: 1RRH) instead of the
metal binding site. An In Silico study was carried out on a series of chalcone
ligands to understand their binding pattern with various molecular targets and
to evaluate the possible pharmacological potency with relevance to their
literature reports. In order for this, molecular docking was carried out on the
active molecules against IMPDH and PARP1 enzymes to find out their binding
pattern. The analysis was done by testing ligands against various molecular
targets like 1PAX, 4OQA, 3WIL, 1FCZ, 2ZBH, 1YQT, 1SRE and 1ME7 for various
cancers, HIV, Immunotherapy, Viral infection, inflammation, etc. The
synthesised compounds were screened for possible anti-cancer activity on the
A549 cell line (lung adenocarcinoma cell line) and anti-tuberculosis activity
on the Mycobacterium tuberculosis strain. Further, molecular docking was also
carried out on the active molecules against IMPDHand PARP1 enzymes to find out
their binding pattern.
Author(s)
Details
Rambabu
Anandam
Department of Chemistry, Acharya Nagarjuna University, Guntur-522
510, AP, India.
Vasu
Babu Ala
Department of Chemistry, QIS College of Engineering and
Technology, Ongole, AP, India.
Bala
Murali Krishna K
Department of Chemistry, Acharya Nagarjuna University, Guntur-522
510, AP, India.
Jyothi
K Kasturi
Department of Chemistry, Acharya Nagarjuna University, Guntur-522
510, AP, India.
Vijaya
Durga Trripuram
Department of Chemistry, Acharya Nagarjuna University, Guntur-522
510, AP, India.
Parvathi
Thota
Department of Chemistry, Acharya Nagarjuna University, Guntur-522
510, AP, India.
Anitha
Uppuluri
Department of Chemistry, Acharya Nagarjuna University, Guntur-522
510, AP, India.
Ravi
Varala
Scrips Pharma, Mallapur, Hyderab
Hari
Babu Bollikolla
Department of Chemistry, Acharya Nagarjuna University, Guntur-522
510, AP, India.
Please see the book
here:- https://doi.org/10.9734/bpi/psnid/v6/4434
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