Items 51 to 60 of 289 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Paclitaxel-d5 | 1129540-33-5 | sc-219546 sc-219546A | 1 mg 10 mg | $557.00 $4086.00 | 11 | |
Paclitaxel-d5 is an isotopically labeled derivative of paclitaxel, featuring deuterium substitutions that modify its molecular vibrations and enhance analytical techniques like NMR and mass spectrometry. The deuterium labeling affects the compound's hydrophobic interactions and solubility characteristics, potentially altering its binding affinity to microtubules. This unique isotopic signature can also facilitate studies on metabolic pathways and reaction mechanisms, providing deeper insights into its biochemical interactions. | ||||||
Simvastatin-d6 Hydroxy Acid, Ammonium Salt | 139893-43-9 (unlabeled) | sc-220105 sc-220105A | 1 mg 10 mg | $403.00 $2249.00 | 1 | |
Simvastatin-d6 Hydroxy Acid, Ammonium Salt is an isotopically labeled compound that incorporates deuterium, influencing its kinetic behavior and molecular dynamics. The presence of deuterium alters the vibrational frequencies, enhancing the sensitivity of spectroscopic analyses. This modification can impact the compound's interaction with enzymes and substrates, providing a unique perspective on metabolic pathways. Its isotopic labeling allows for precise tracking in biochemical studies, revealing intricate details of reaction mechanisms. | ||||||
5-Methyl-N-phenyl-2-1H-pyridone-d5 | 1020719-62-3 | sc-217219 | 1 mg | $290.00 | 1 | |
5-Methyl-N-phenyl-2-1H-pyridone-d5 is an isotopically labeled compound featuring deuterium, which modifies its electronic properties and enhances NMR spectral resolution. The incorporation of deuterium affects hydrogen bonding interactions, potentially altering solubility and reactivity in various environments. This unique isotopic signature facilitates advanced studies in reaction kinetics and mechanistic pathways, allowing researchers to dissect complex biochemical processes with greater precision. | ||||||
Trazodone-d6 Hydrochloride | 1181578-71-1 | sc-220319 | 1 mg | $380.00 | ||
Trazodone-d6 Hydrochloride is an isotopically labeled compound that incorporates deuterium, influencing its vibrational spectra and enhancing mass spectrometry analysis. The presence of deuterium alters the dynamics of molecular interactions, particularly in hydrogen bonding, which can lead to distinct solvation behaviors. This unique isotopic labeling aids in tracing metabolic pathways and elucidating reaction mechanisms, providing insights into molecular behavior in complex biochemical systems. | ||||||
Raloxifene-d4 | 1185076-44-1 | sc-219925 | 1 mg | $380.00 | ||
Raloxifene-d4 is an isotopically labeled compound featuring deuterium, which modifies its nuclear magnetic resonance (NMR) properties, allowing for enhanced resolution in structural analysis. The incorporation of deuterium affects the compound's rotational dynamics and can influence its interaction with biomolecules, leading to altered binding affinities. This isotopic labeling facilitates the study of reaction kinetics and provides a deeper understanding of molecular interactions in various biochemical contexts. | ||||||
Mirtazapine-d3 | 1216678-68-0 | sc-218855 | 1 mg | $380.00 | ||
Mirtazapine-d3 is an isotopically labeled compound that incorporates tritium, enhancing its mass spectrometry profiles and enabling precise tracking in metabolic studies. The presence of tritium alters the compound's vibrational modes, which can affect its reactivity and interaction with enzymes. This isotopic labeling aids in elucidating metabolic pathways and provides insights into the kinetics of biochemical reactions, offering a unique perspective on molecular behavior in complex systems. | ||||||
Loxapine-d8 Hydrochloride | 1246820-19-8 | sc-280940 | 1 mg | $305.00 | ||
Loxapine-d8 Hydrochloride is an isotopically labeled compound featuring deuterium, which modifies its spectral characteristics and enhances analytical precision in various biochemical investigations. The incorporation of deuterium influences hydrogen bonding dynamics and alters reaction kinetics, providing a distinct advantage in studying molecular interactions. This labeling facilitates the exploration of metabolic pathways and offers insights into the stability and reactivity of related compounds in complex biological systems. | ||||||
5-Hydroxy Dantrolene-d4 | 1217225-15-4 | sc-217194 sc-217194A | 1 mg 10 mg | $326.00 $2086.00 | ||
5-Hydroxy Dantrolene-d4 is an isotopically labeled compound that incorporates deuterium, enhancing its mass spectrometric properties and enabling precise tracking in biochemical studies. The presence of deuterium alters vibrational frequencies, allowing for improved resolution in spectroscopic analyses. This modification can influence the compound's solubility and reactivity, providing unique insights into its interactions within metabolic networks and facilitating the investigation of reaction mechanisms in various biochemical contexts. | ||||||
Benazepril-d5 | 1279200-03-1 | sc-217708 | 1 mg | $367.00 | ||
Benazepril-d5 is an isotopically labeled derivative that features five deuterium atoms, enhancing its analytical capabilities in research. The incorporation of deuterium modifies the compound's kinetic isotope effects, which can influence reaction rates and pathways in enzymatic processes. This labeling allows for detailed studies of molecular interactions and dynamics, providing insights into the compound's behavior in complex biological systems and aiding in the elucidation of metabolic pathways. | ||||||
(+)cis,trans-Abscisic Acid-d6 | 721948-65-8 | sc-217922 sc-217922A | 1 mg 10 mg | $554.00 $3723.00 | 37 | |
(+)cis,trans-Abscisic Acid-d6 is an isotopically labeled variant that incorporates six deuterium atoms, facilitating advanced studies in plant physiology and biochemistry. The presence of deuterium alters the vibrational frequencies of the molecule, enabling precise tracking in metabolic pathways. This labeling enhances the understanding of its role in stress responses and signaling mechanisms, allowing researchers to investigate its interactions with receptors and other biomolecules in greater detail. |