Synthesis, characterization and biological docking simulation of new thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 and its Cu(II) complex

New thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 (PS) and its corresponding Cu(II) complex were synthesized and characterized using CHN elemental analysis, UV–Visible and FT-IR spectroscopies. The structure of PS was experimentally investigated by single crystal X-ray diffraction. PS crystallizes...

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Main Authors: Atekeh Tarahhomi, Zeinab Albobaledi
Format: Article
Language:English
Published: Elsevier 2025-07-01
Series:Results in Chemistry
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Online Access:http://www.sciencedirect.com/science/article/pii/S2211715625004941
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author Atekeh Tarahhomi
Zeinab Albobaledi
author_facet Atekeh Tarahhomi
Zeinab Albobaledi
author_sort Atekeh Tarahhomi
collection DOAJ
description New thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 (PS) and its corresponding Cu(II) complex were synthesized and characterized using CHN elemental analysis, UV–Visible and FT-IR spectroscopies. The structure of PS was experimentally investigated by single crystal X-ray diffraction. PS crystallizes in the triclinic crystal system, space group P1¯, with one independent molecule in the asymmetric unit. The hydrogen bonding pattern in the PS structure involves a centrosymmetric dimer formed through classical NH…N hydrogen bond interactions. For the Cu(II) complex, the proposed structure consists of two tridentate O,N,N-donor amidothiophosphate ligands (S)P[O−][NH-2Py-(5-CH3)]2. The Cu(II) center adopts an octahedral geometry with a six-coordinate Cu(N)4(O)2 environment. For a biological evaluation, molecular docking simulations were conducted on both PS and its Cu(II) complex against target proteins of DNA, SARS-CoV-2 and Monkeypox (Mpox) providing maximum binding energies of −8.2, −7.5 and − 7.2 kcal/mol, respectively, for PS. These results suggest that the compounds studied, particularly PS, possess considerable potential as inhibitors of DNA and viral targets, with docking affinities comparable to those of established anticancer and antiviral drugs. This makes them promising candidates for further therapeutic investigation.
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spelling doaj-art-458ea42a24e04ea6a891aebb58bf27b82025-08-20T03:02:27ZengElsevierResults in Chemistry2211-71562025-07-011610251110.1016/j.rechem.2025.102511Synthesis, characterization and biological docking simulation of new thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 and its Cu(II) complexAtekeh Tarahhomi0Zeinab Albobaledi1Corresponding author.; Department of Chemistry, Semnan University, Semnan 35131-19111, IranDepartment of Chemistry, Semnan University, Semnan 35131-19111, IranNew thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 (PS) and its corresponding Cu(II) complex were synthesized and characterized using CHN elemental analysis, UV–Visible and FT-IR spectroscopies. The structure of PS was experimentally investigated by single crystal X-ray diffraction. PS crystallizes in the triclinic crystal system, space group P1¯, with one independent molecule in the asymmetric unit. The hydrogen bonding pattern in the PS structure involves a centrosymmetric dimer formed through classical NH…N hydrogen bond interactions. For the Cu(II) complex, the proposed structure consists of two tridentate O,N,N-donor amidothiophosphate ligands (S)P[O−][NH-2Py-(5-CH3)]2. The Cu(II) center adopts an octahedral geometry with a six-coordinate Cu(N)4(O)2 environment. For a biological evaluation, molecular docking simulations were conducted on both PS and its Cu(II) complex against target proteins of DNA, SARS-CoV-2 and Monkeypox (Mpox) providing maximum binding energies of −8.2, −7.5 and − 7.2 kcal/mol, respectively, for PS. These results suggest that the compounds studied, particularly PS, possess considerable potential as inhibitors of DNA and viral targets, with docking affinities comparable to those of established anticancer and antiviral drugs. This makes them promising candidates for further therapeutic investigation.http://www.sciencedirect.com/science/article/pii/S2211715625004941ThiophosphoramideX-ray crystallographyMolecular dockingDNASARS-CoV-2Monkeypox
spellingShingle Atekeh Tarahhomi
Zeinab Albobaledi
Synthesis, characterization and biological docking simulation of new thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 and its Cu(II) complex
Results in Chemistry
Thiophosphoramide
X-ray crystallography
Molecular docking
DNA
SARS-CoV-2
Monkeypox
title Synthesis, characterization and biological docking simulation of new thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 and its Cu(II) complex
title_full Synthesis, characterization and biological docking simulation of new thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 and its Cu(II) complex
title_fullStr Synthesis, characterization and biological docking simulation of new thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 and its Cu(II) complex
title_full_unstemmed Synthesis, characterization and biological docking simulation of new thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 and its Cu(II) complex
title_short Synthesis, characterization and biological docking simulation of new thiophosphoric triamide (S)P[NH-2Py-(5-CH3)]3 and its Cu(II) complex
title_sort synthesis characterization and biological docking simulation of new thiophosphoric triamide s p nh 2py 5 ch3 3 and its cu ii complex
topic Thiophosphoramide
X-ray crystallography
Molecular docking
DNA
SARS-CoV-2
Monkeypox
url http://www.sciencedirect.com/science/article/pii/S2211715625004941
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