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Amino acids and amide bonds (-C(O)-NH-) are the essential components of proteins, which serve as the foundation of life on Earth. As a result, molecules containing peptide bonds are of great interest in studies related to the origin of life and are central to both terrestrial and prebiotic chemistry. Despite this, our understanding of how nitrogen-containing compounds like formamide and urea, along with their sulfur analogs thioformamide and thiourea, form in the cold interstellar medium (ISM) remains incomplete. The chemistry underlying their formation is largely elusive, making the elucidation of their mechanism in the ISM and EA a topic of ongoing interest. This study employs //density functional theory (DFT) calculations to predict the possible formation routes of amides and thioamides. The rate constants () for barrierless reactions were determined using statistical rate theory, such as microcanonical variational transition state theory (µVTST) and Rice-Ramsperger-Kassel-Marcus (RRKM)/master equation (ME) simulations, to understand their kinetic behavior. Using basic interstellar precursors-CO, CS, NH, H, and NH-we assessed gas-phase formation routes for amides and thioamides. The data reveal that thioamides (HCSNH, NHCSNH) may form under ISM conditions, while amides (HCONH, NHCONH) are less likely due to their relatively high energy barriers (>5 kcal/mol). In this work, we suggest the potential detection of four new molecules in ISM environments based on enthalpy and rate constant calculations: (i) ·CSNH, (ii) HCSN·H, (iii) HCSNH, and (iv) NHCSNH. Furthermore, organosulfur-bearing molecules are identified as potential precursors to iron-sulfide grains and astrobiologically significant compounds, such as the amino acids methionine and cysteine. Understanding these mechanisms is crucial for linking the chemistries of carbon, nitrogen, oxygen, and sulfur in deep space, thereby expanding our knowledge of the sulfur cycle within the Galaxy.
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http://dx.doi.org/10.3389/fchem.2025.1615586 | DOI Listing |
Metab Brain Dis
September 2025
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Acute or chronic liver damage can result in Hepatic Encephalopathy (HE), a potentially fatal neuropsychiatric condition that leads to cerebral and neurological alterations. Dapagliflozin (DAPA), an orally active Sodium/Glucose cotransporter 2 inhibitor with long duration of action. The study aim was to evaluate the potential protective impact of DAPA against HE caused by Thioacetamide (TAA) in rats.
View Article and Find Full Text PDFPLoS One
September 2025
Plant Production Department, College of Food & Agriculture Sciences, King Saud University, Riyadh, Saudi Arabia.
Background: Hepatic fibrosis unfolds as a pathological buildup of extracellular matrix triggered by liver injury. Thioacetamide (TAA) plays a versatile role across various fields-from industrial processes and laboratory research to chemical stabilization. Teucrium plants, widely traditional plants, owing to its myriads of pharmacological activities.
View Article and Find Full Text PDFSci Rep
August 2025
Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yildirim University, Erzincan, 24100, Turkey.
The objective of this study was to elucidate the impact of D-(-)-Quinic acid (D-(-)-QA), a natural phenolic acid, on the molecular mechanisms of inflammation and oxidative stress in brain and liver damage in thioacetamide (TAA)-induced hepatic encephalopathy (HE) in rats. To establish an experimental HE model, rats were injected with three doses (200 mg/kg, intraperitoneally) of TAA every other day, followed by the administration of D-(-)- QA (200 or 400 mg/kg, orally) for fourteen days. Serum ammonia, alanine transaminase (ALT), and aspartate transaminase (AST) levels were detected.
View Article and Find Full Text PDFChemistry
August 2025
Institute of Organic Chemistry, Polish Academy of Science, Kasprzaka 44/52, Warsaw, 01-224, Poland.
Pursuing innovative and environmentally friendly synthetic strategies is always a desirable goal in organic synthesis, and thus, we have developed green and sustainable electrochemical (EC) and photoelectrochemical (iPEC) transformations of thioamides into amides. The established EC protocol is inexpensive, mild, and metal- and catalyst-free. iPEC cells are extensively studied for solar energy conversion, but their application in synthesizing high-value organic molecules has been limited.
View Article and Find Full Text PDFBiomolecules
July 2025
Department of Physiology, "Iuliu Hatieganu" University of Medicine and Pharmacy, 1-3 Clinicilor Street, 400006 Cluj-Napoca, Romania.
The present study aimed to evaluate the therapeutic benefits of a hybrid material based on gold nanoparticles and natural extracts on an experimental model of thioacetamide-induced (TAA) liver injury in rats. The nanomaterials were synthesized using a green method, with L. extract as a reducing and capping agent (NPCS), and were then mixed with L.
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