Synthesis, Antibacterial and Antileishmanial Activity, Cytotoxicity, and Molecular Docking of New Heteroleptic Copper(I) Complexes with Thiourea Ligands and Triphenylphosphine

Larik, F. A. (author): Quaid I Azam Univ, Dept Chem, Islamabad 45320, Pakistan

Jabeen, F. (author): Laurentian Univ, Cardiovasc & Metab Res Unit, 935 Ramsey Lake Rd, Sudbury, ON P3E 2C6, Canada

Mehfooz, H. (author): Quaid I Azam Univ, Dept Chem, Islamabad 45320, Pakistan

Ghumro, S. A. (author): Univ Karachi, HEJ Res Inst Chem, Int Ctr Chem & Biol Sci, Karachi 75270, Pakistan

Ali, M. (author): Quaid I Azam Univ, Dept Biol Sci, Islamabad 45320, Pakistan

Channar, P. A. (author): Quaid I Azam Univ, Dept Chem, Islamabad 45320, Pakistan

Ashraf, H. (author): Quaid I Azam Univ, Dept Chem, Islamabad 45320, Pakistan

(creator_code:org_t)

MAIK NAUKA/INTERPERIODICA/SPRINGER, 2018
2018
English.
In: Russian journal of general chemistry. - : MAIK NAUKA/INTERPERIODICA/SPRINGER. - 1070-3632 .- 1608-3350. ; 88:3, s. 541-550

Related links:: https://urn.kb.se/re...; show more...; https://doi.org/10.1...; show less...

Abstract Subject headings

A series of copper(I) complexes with triphenylphosphine and N-acyl-N'-arylthioureas were synthesized and characterized by elemental analysis and IR and NMR (H-1, C-13, P-31) spectroscopy. The thiourea ligands and their copper(I) triphenylphosphine complexes were screened for antibacterial and antileishmanial activities and cytotoxicity. The synthesized compounds showed much better activity as compared to glucantime and Kanamycin used as reference drugs. The thiourea ligands showed better activity than their Cu(I) complexes. The molecular docking technique was utilized to ascertain the mechanism of action toward molecular targets (GP63 and 16S-rRNA A-site). It was found that the ligands and complexes were stabilized at the active site by electrostatic and hydrophobic forces, consistent with the corresponding experimental results. The in silico study of the binding pattern predicted that one of the synthesized ligands, N-(5-chloro-2-nitrophenyl)-N'-pentanoylthiourea, can serve as a potential surrogate for hit-to-lead generation and design of novel antibacterial and antileishmanial agents.

By the author/editor: Saeed, A.; Larik, F. A.; Jabeen, F.; Mehfooz, H.; Ghumro, S. A.; El-Seedi, Hesham ...; show more...; Ali, M.; Channar, P. A.; Ashraf, H.; show less...

About the subject

NATURAL SCIENCES: NATURAL SCIENCES; and Chemical Science ...; and Organic Chemistr ...

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.