Items 221 to 230 of 289 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Tiagabine-d9 4-Carboxy Hydrochloride | sc-475014 | 1 mg | $380.00 | |||
Tiagabine-d9 4-Carboxy Hydrochloride is an isotopically labeled compound that facilitates advanced studies in metabolic pathways and molecular interactions. The presence of deuterium enhances the sensitivity of spectroscopic techniques, allowing for precise tracking of molecular dynamics. Its unique isotopic labeling can alter reaction kinetics, providing insights into enzyme-substrate interactions and the behavior of carboxylic acids in biochemical systems. This compound serves as a valuable resource for understanding complex metabolic networks. | ||||||
Tiagabine-d9 4-Carboxy-O-ethyl | sc-475017 | 2.5 mg | $380.00 | |||
Tiagabine-d9 4-Carboxy-O-ethyl is an isotopically labeled biochemical that offers unique insights into molecular behavior and reaction mechanisms. The incorporation of deuterium allows for enhanced resolution in NMR and mass spectrometry, enabling detailed analysis of molecular conformations and interactions. Its distinct isotopic signature can influence hydrogen bonding patterns and solvation dynamics, providing a deeper understanding of carboxylic acid reactivity and its role in biochemical processes. | ||||||
7,8,9,10-Tetrahydro-benzo[a]pyren-7-ol-13C4 | sc-475112 | 1 mg | $430.00 | |||
7,8,9,10-Tetrahydro-benzo[a]pyren-7-ol-13C4 is an isotopically labeled biochemical that serves as a valuable tool for studying metabolic pathways and environmental interactions. The incorporation of carbon-13 enhances the sensitivity of spectroscopic techniques, allowing for precise tracking of molecular transformations. Its unique isotopic labeling can alter reaction kinetics and facilitate the investigation of carbon-centered radical mechanisms, shedding light on complex biochemical processes. | ||||||
Terizidone-13N2,d6 | 25683-71-0 (unlabeled) | sc-475130 | 0.5 mg | $583.00 | ||
Terizidone-13N2,d6 is an isotopically labeled biochemical that provides insights into nitrogen metabolism and isotopic fractionation. The incorporation of deuterium and nitrogen-13 allows for enhanced nuclear magnetic resonance (NMR) sensitivity, enabling detailed analysis of molecular dynamics and interactions. This labeling can influence reaction pathways, offering a unique perspective on enzyme catalysis and substrate specificity, thus enriching our understanding of biochemical mechanisms. | ||||||
Xamoterol-d5 | sc-475136 | 1 mg | $380.00 | |||
Xamoterol-d5 is an isotopically labeled biochemical that serves as a valuable tool for studying metabolic pathways and molecular interactions. The incorporation of deuterium enhances mass spectrometry detection, allowing for precise tracking of molecular transformations. Its unique isotopic signature can alter reaction kinetics, providing insights into enzyme mechanisms and substrate behavior. This labeling facilitates a deeper understanding of molecular dynamics and the influence of isotopic effects on biochemical processes. | ||||||
(Z)-2-(2-Tritylaminothiazol-4-yl)-2-methoxyiminoacetic Acid-d3 Methyl Ester | sc-475138 | 5 mg | $330.00 | |||
(Z)-2-(2-Tritylaminothiazol-4-yl)-2-methoxyiminoacetic Acid-d3 Methyl Ester is an isotopically labeled compound that offers unique insights into biochemical interactions and reaction mechanisms. The presence of deuterium allows for enhanced resolution in NMR spectroscopy, enabling detailed analysis of conformational changes and molecular dynamics. Its distinct isotopic labeling can influence hydrogen bonding patterns and solvation effects, providing a deeper understanding of reaction pathways and enzyme specificity. | ||||||
N-Trityl Losartan-d4 Carboxaldehyde | sc-475141 | 5 mg | $380.00 | |||
N-Trityl Losartan-d4 Carboxaldehyde is an isotopically labeled compound that facilitates advanced studies in metabolic pathways and enzymatic reactions. The incorporation of deuterium enhances mass spectrometry sensitivity, allowing for precise tracking of molecular transformations. Its unique structure promotes specific interactions with biomolecules, influencing reaction kinetics and stability. This compound serves as a valuable tool for elucidating complex biochemical processes and understanding isotopic effects on molecular behavior. | ||||||
1,2,4-Trioctyl Ester 1,2,4-Benzenetricarboxylic Acid-d51 | sc-475142 | 1 mg | $380.00 | |||
1,2,4-Trioctyl Ester 1,2,4-Benzenetricarboxylic Acid-d51 is an isotopically labeled compound that plays a significant role in studying molecular dynamics and interactions. The presence of deuterium allows for enhanced resolution in spectroscopic analyses, aiding in the investigation of reaction mechanisms. Its unique ester functional groups facilitate specific binding affinities, influencing solubility and reactivity in various environments, thus providing insights into complex biochemical systems. | ||||||
3,6,9,12,15,18,21-Tetracosaheptaynoic Acid Methyl-d3 Ester | sc-475182 | 1 mg | $595.00 | |||
3,6,9,12,15,18,21-Tetracosaheptaynoic Acid Methyl-d3 Ester is an isotopically labeled biochemical that serves as a valuable tool for tracing metabolic pathways. The incorporation of deuterium enhances NMR and mass spectrometry techniques, allowing for precise tracking of molecular transformations. Its long-chain structure influences lipid interactions and membrane dynamics, providing insights into fatty acid metabolism and the behavior of complex lipid systems in biological contexts. | ||||||
2,4,5,6-Tetrachlorophenol-13C6 | 1246820-81-4 | sc-475162 | 1 mg | $540.00 | ||
2,4,5,6-Tetrachlorophenol-13C6 is an isotopically labeled compound that facilitates the study of chlorinated phenolic compounds in environmental and biochemical research. The incorporation of carbon-13 allows for enhanced detection in NMR spectroscopy, aiding in the analysis of metabolic pathways and degradation processes. Its unique chlorinated structure influences electron distribution and reactivity, impacting interactions with enzymes and microbial communities, thus providing insights into bioremediation and environmental fate studies. |