Items 141 to 150 of 289 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Sulindac Sulfide-d6 (Major) | sc-474103 | 1 mg | $380.00 | |||
Sulindac Sulfide-d6 is an isotopically labeled compound that facilitates advanced studies in biochemical pathways. The presence of deuterium enhances its mass spectrometric properties, enabling precise tracking of metabolic transformations. This isotopic labeling can modify reaction kinetics, influencing enzyme interactions and substrate specificity. Additionally, its unique isotopic signature aids in elucidating molecular conformations and dynamics, providing deeper insights into biochemical processes. | ||||||
Tazarotene-d8 | 1246815-76-8 | sc-474153 sc-474153A | 1 mg 10 mg | $367.00 $2336.00 | ||
Tazarotene-d8 is an isotopically labeled compound that serves as a valuable tool for probing molecular interactions and reaction mechanisms. The incorporation of deuterium alters the vibrational frequencies of the molecule, which can affect its reactivity and stability in various environments. This isotopic labeling allows for enhanced resolution in spectroscopic analyses, facilitating the study of conformational changes and dynamic behavior in complex biochemical systems. | ||||||
Sodium Colistin B-d7 Methanesulfonate | 8068-28-8 (unlabeled) | sc-474155 | 0.5 mg | $430.00 | ||
Sodium Colistin B-d7 Methanesulfonate is an isotopically labeled biochemical that provides insights into metabolic pathways and molecular dynamics. The presence of deuterium modifies the kinetic isotope effects, influencing reaction rates and mechanisms. This compound enhances the precision of NMR and mass spectrometry analyses, allowing researchers to track molecular interactions and conformational shifts in biological systems with greater accuracy. Its unique isotopic signature aids in elucidating complex biochemical processes. | ||||||
Sodium Dichloroacetate-13C2 | 1173022-90-6 | sc-474166 | 1 mg | $430.00 | ||
Sodium Dichloroacetate-13C2 is an isotopically labeled biochemical that serves as a valuable tool for tracing carbon metabolism and studying metabolic flux. The incorporation of carbon-13 alters the vibrational frequencies of molecular bonds, enhancing the sensitivity of spectroscopic techniques. This compound facilitates the investigation of enzymatic pathways and metabolic regulation, providing a clearer understanding of carbon dynamics in various biological contexts. Its distinct isotopic labeling allows for precise tracking of metabolic intermediates. | ||||||
(3β,20S)-21-O-Tosyl-4,4,20-trimethyl-pregna-5,7-diene-3,21-diol-d6 3-Benzoate | sc-474172 | 0.5 mg | $540.00 | |||
(3β,20S)-21-O-Tosyl-4,4,20-trimethyl-pregna-5,7-diene-3,21-diol-d6 3-Benzoate is an isotopically labeled compound that enables detailed studies of steroid metabolism and biosynthetic pathways. The deuterium labeling enhances NMR spectroscopy resolution, allowing for the observation of subtle conformational changes and reaction kinetics. This compound's unique structure facilitates the exploration of molecular interactions and the dynamics of enzymatic transformations, providing insights into metabolic processes. | ||||||
Sodium D-Gluconate-13C6 | 527-07-1 unlabeled | sc-474183 | 5 mg | $300.00 | ||
Sodium D-Gluconate-13C6 is an isotopically labeled compound that serves as a valuable tool in metabolic research. The incorporation of carbon-13 isotopes allows for enhanced tracking of metabolic pathways through techniques like mass spectrometry. Its unique labeling aids in elucidating reaction mechanisms and substrate interactions, providing insights into enzymatic activity and the dynamics of biochemical transformations. This compound's distinct isotopic signature enables precise quantification and analysis of metabolic flux. | ||||||
Sodium Oxo-De(aminodimethyl) Bedoradrine-13C, d2 | sc-474185 | 1 mg | $540.00 | |||
Sodium Oxo-De(aminodimethyl) Bedoradrine-13C, d2 is an isotopically labeled biochemical that facilitates advanced studies in metabolic flux and reaction dynamics. The incorporation of deuterium enhances NMR spectroscopy sensitivity, allowing for detailed observation of molecular interactions and conformational changes. Its unique isotopic composition aids in distinguishing reaction pathways, providing insights into kinetic behaviors and the influence of isotopic effects on enzymatic processes. | ||||||
Sodium β-Hydroxyethoxyacetate-d4 | 142047-97-0 unlabeled | sc-474190 sc-474190A | 1 mg 10 mg | $340.00 $2400.00 | ||
Sodium β-Hydroxyethoxyacetate-d4 is an isotopically labeled biochemical that serves as a powerful tool for tracing metabolic pathways and studying reaction mechanisms. The presence of deuterium allows for enhanced mass spectrometry resolution, enabling precise tracking of molecular transformations. Its unique isotopic labeling can influence hydrogen bonding and solvation dynamics, offering insights into molecular interactions and the role of isotopic substitution in enzymatic activity. | ||||||
Solifenacin-13C6 Succinate | sc-474215 | 0.5 mg | $540.00 | |||
Solifenacin-13C6 Succinate is an isotopically labeled compound that facilitates advanced studies in metabolic flux analysis and kinetic modeling. The incorporation of carbon-13 isotopes enhances NMR spectroscopy sensitivity, allowing for detailed observation of molecular conformations and dynamics. This labeling can alter reaction rates and equilibria, providing insights into substrate specificity and enzyme interactions, while also revealing the effects of isotopic labeling on molecular stability and reactivity. | ||||||
(1S,3S-)Solifenacin Hydrochloride-d5 | sc-474216 | 1 mg | $480.00 | |||
(1S,3S-)Solifenacin Hydrochloride-d5 is an isotopically labeled compound that serves as a valuable tool for tracing metabolic pathways and studying molecular interactions. The deuterium labeling enhances mass spectrometry resolution, enabling precise tracking of reaction kinetics and pathways. This compound can influence hydrogen bonding patterns and isotopic effects, providing insights into molecular behavior, stability, and the dynamics of enzyme-substrate interactions in biochemical systems. |