Copper(ii) complexes supported by modified azo-based ligands: Nucleic acid binding and molecular docking studies

Two new copper(ii) complexes [CuL1] (1) and [CuL2] (2) derived from azo-based ligands 2-hydroxy-5-p-tolylazo-benzaldehyde (HL1) and 1-(2-hydroxy-5-p-tolylazo-phenyl)-ethan-one (HL2) were synthesized. These two ligands and their metal complexes were characterized by elemental analysis, nuclear magnet...

Full description

Bibliographic Details
Main Authors: Tripathi Mamta, Asatkar Ashish Kumar, Antony Stalin, Dash Mrinal Kanti, Roymahapatra Gourisankar, Pande Rama, Sarkar Avijit, Aldakheel Fahad M., Binshaya Abdulkarim S., Alharthi Nahed S., Alaofi Ahmed L., Alqahtani Mohammed S., Syed Rabbani
Format: Article
Language:English
Published: De Gruyter 2022-06-01
Series:Open Chemistry
Subjects:
Online Access:https://doi.org/10.1515/chem-2022-0164
_version_ 1811194142784487424
author Tripathi Mamta
Asatkar Ashish Kumar
Antony Stalin
Dash Mrinal Kanti
Roymahapatra Gourisankar
Pande Rama
Sarkar Avijit
Aldakheel Fahad M.
Binshaya Abdulkarim S.
Alharthi Nahed S.
Alaofi Ahmed L.
Alqahtani Mohammed S.
Syed Rabbani
author_facet Tripathi Mamta
Asatkar Ashish Kumar
Antony Stalin
Dash Mrinal Kanti
Roymahapatra Gourisankar
Pande Rama
Sarkar Avijit
Aldakheel Fahad M.
Binshaya Abdulkarim S.
Alharthi Nahed S.
Alaofi Ahmed L.
Alqahtani Mohammed S.
Syed Rabbani
author_sort Tripathi Mamta
collection DOAJ
description Two new copper(ii) complexes [CuL1] (1) and [CuL2] (2) derived from azo-based ligands 2-hydroxy-5-p-tolylazo-benzaldehyde (HL1) and 1-(2-hydroxy-5-p-tolylazo-phenyl)-ethan-one (HL2) were synthesized. These two ligands and their metal complexes were characterized by elemental analysis, nuclear magnetic resonance (1H and 13C), infrared, and UV/Vis spectroscopic techniques. Spectroscopy and other theoretical studies reveal the geometry of copper complexes, and their binding affinity towards nucleic acids are major groove binding.
first_indexed 2024-04-12T00:20:57Z
format Article
id doaj.art-3300bde14d7548399c672cc732aa54e5
institution Directory Open Access Journal
issn 2391-5420
language English
last_indexed 2024-04-12T00:20:57Z
publishDate 2022-06-01
publisher De Gruyter
record_format Article
series Open Chemistry
spelling doaj.art-3300bde14d7548399c672cc732aa54e52022-12-22T03:55:43ZengDe GruyterOpen Chemistry2391-54202022-06-0120150551610.1515/chem-2022-0164Copper(ii) complexes supported by modified azo-based ligands: Nucleic acid binding and molecular docking studiesTripathi Mamta0Asatkar Ashish Kumar1Antony Stalin2Dash Mrinal Kanti3Roymahapatra Gourisankar4Pande Rama5Sarkar Avijit6Aldakheel Fahad M.7Binshaya Abdulkarim S.8Alharthi Nahed S.9Alaofi Ahmed L.10Alqahtani Mohammed S.11Syed Rabbani12School of Studies in Chemistry, Pt. Ravishankar Shukla University, Raipur, 492010, Chhattisgarh, IndiaDepartment of Chemistry, Government Gundadhur P. G. College, Kondagaon, 494226, Chhattisgarh, IndiaDepartment of Traditional Chinese Medicine, State Key Laboratory of Subtropical Silviculture, Zhejiang A&F University, Hangzhou, 311300, ChinaDepartment of Applied Sciences, Haldia Institute of Technology, Haldia, 721657, IndiaDepartment of Applied Sciences, Haldia Institute of Technology, Haldia, 721657, IndiaSchool of Studies in Chemistry, Pt. Ravishankar Shukla University, Raipur, 492010, Chhattisgarh, IndiaDepartment of Chemistry, Bhairab Ganguly College, Belghoria, Kolkata, 700056, IndiaDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, Riyadh, 11433, Saudi ArabiaDepartment of Medical Laboratory Sciences, College of Medical Sciences, Prince Sattam bin Abdulaziz University (PSAU), Alkharz, Saudi ArabiaDepartment of Medical Laboratory Sciences, College of Applied Medical Sciences, Prince Sattam bin Abdulaziz University (PSAU), Alkharj, Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, P.O Box. 2457, Riyadh, 11451, Kingdom of Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, P.O Box. 2457, Riyadh, 11451, Kingdom of Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, P.O Box. 2457, Riyadh, 11451, Kingdom of Saudi ArabiaTwo new copper(ii) complexes [CuL1] (1) and [CuL2] (2) derived from azo-based ligands 2-hydroxy-5-p-tolylazo-benzaldehyde (HL1) and 1-(2-hydroxy-5-p-tolylazo-phenyl)-ethan-one (HL2) were synthesized. These two ligands and their metal complexes were characterized by elemental analysis, nuclear magnetic resonance (1H and 13C), infrared, and UV/Vis spectroscopic techniques. Spectroscopy and other theoretical studies reveal the geometry of copper complexes, and their binding affinity towards nucleic acids are major groove binding.https://doi.org/10.1515/chem-2022-0164azocopper(ii) complexesdftct-dnat-rnamolecular docking
spellingShingle Tripathi Mamta
Asatkar Ashish Kumar
Antony Stalin
Dash Mrinal Kanti
Roymahapatra Gourisankar
Pande Rama
Sarkar Avijit
Aldakheel Fahad M.
Binshaya Abdulkarim S.
Alharthi Nahed S.
Alaofi Ahmed L.
Alqahtani Mohammed S.
Syed Rabbani
Copper(ii) complexes supported by modified azo-based ligands: Nucleic acid binding and molecular docking studies
Open Chemistry
azo
copper(ii) complexes
dft
ct-dna
t-rna
molecular docking
title Copper(ii) complexes supported by modified azo-based ligands: Nucleic acid binding and molecular docking studies
title_full Copper(ii) complexes supported by modified azo-based ligands: Nucleic acid binding and molecular docking studies
title_fullStr Copper(ii) complexes supported by modified azo-based ligands: Nucleic acid binding and molecular docking studies
title_full_unstemmed Copper(ii) complexes supported by modified azo-based ligands: Nucleic acid binding and molecular docking studies
title_short Copper(ii) complexes supported by modified azo-based ligands: Nucleic acid binding and molecular docking studies
title_sort copper ii complexes supported by modified azo based ligands nucleic acid binding and molecular docking studies
topic azo
copper(ii) complexes
dft
ct-dna
t-rna
molecular docking
url https://doi.org/10.1515/chem-2022-0164
work_keys_str_mv AT tripathimamta copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT asatkarashishkumar copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT antonystalin copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT dashmrinalkanti copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT roymahapatragourisankar copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT panderama copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT sarkaravijit copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT aldakheelfahadm copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT binshayaabdulkarims copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT alharthinaheds copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT alaofiahmedl copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT alqahtanimohammeds copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies
AT syedrabbani copperiicomplexessupportedbymodifiedazobasedligandsnucleicacidbindingandmoleculardockingstudies