Synthesis, Characterization and Biological Activity Evaluation of Some 1,N-bis-(4-amino-5-mercapto-1,2,4-triazol-3-yl) Alkanes
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Published:2024-07-16
Issue:14
Volume:14
Page:6180
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ISSN:2076-3417
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Container-title:Applied Sciences
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language:en
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Short-container-title:Applied Sciences
Author:
Alexa Andreea-Anda1, Bercean Vasile-Nicolae2ORCID, Boncea Sabina Elena3, Ledeţi Adriana4ORCID, Badea Valentin2ORCID, Ridichie Amalia4ORCID, Motoc Marilena1, Ledeţi Ionuţ4ORCID
Affiliation:
1. Discipline of Biochemistry, Department of Biochemistry and Pharmacology, Faculty of Medicine, Victor Babeş University of Medicine and Pharmacy, 2 Eftimie Murgu Square, 300041 Timisoara, Romania 2. Department of Applied Chemistry and Organic and Natural Compounds Engineering, Politehnica, University Timisoara, Vasile Pârvan 6, 300223 Timisoara, Romania 3. Biology and Geology Faculty, Babes-Bolyai University, 5–7 Clinicilor Str., 400015 Cluj-Napoca, Romania 4. Advanced Instrumental Screening Center, Faculty of Pharmacy, Victor Babeş University of Medicine and Pharmacy, 2 Eftimie Murgu Square, 300041 Timisoara, Romania
Abstract
In this paper, we present the synthesis, characterization and evaluation of antiproliferative activity for four compounds carrying the 4-amino-5-mercapto-1,2,4-triazol-3-yl scaffold. The synthesis of 1,n-bis-(4-amino-5-mercapto-1,2,4-triazol-3-yl) alkanes was carried out using as starting reagents the dihydrazides of oxalic, malonic, succinic and adipic acids, using mercaptoacetic acid dianion as a leaving group, by a one-pot synthesis method implemented in our research group for the synthesis of 3-substituted-5-mercapto-1,2,4-triazoles. The compounds were obtained with modest yields (12–60%) but with good purity and were characterized by elemental analysis, FTIR, 1H-NMR and 13C-NMR spectroscopy. Also, the stability of the synthesized bis-triazoles was investigated under controlled thermal stress in a dynamic oxidative atmosphere. The last part of the study consisted of biological activity evaluation, by evaluating the antiproliferative activity against the A375 line (human malignant melanoma), as well as on viability of the BJ fibroblast cell line, using MTT and LDH assays.
Funder
University of Medicine and Pharmacy Timisoara
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