Metabolites
Items 151 to 160 of 253 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ciclopirox beta-D-Glucuronide | 79419-54-8 | sc-207433 | 1 mg | $415.00 | ||
Ciclopirox beta-D-Glucuronide, a metabolite, is characterized by its glucuronidation, which significantly increases its hydrophilicity, promoting renal clearance. This compound exhibits unique interactions with cellular membranes, influencing permeability and transport mechanisms. Its metabolic pathway involves phase II reactions, where it undergoes conjugation, altering its reactivity and stability. The compound's distinct stereochemical configuration may also impact its interactions with various biomolecules, affecting its overall metabolic fate. | ||||||
Norfluoxetine Hydrochloride | 57226-68-3 | sc-208105 sc-208105A sc-208105B | 10 mg 100 mg 500 mg | $332.00 $2062.00 $9533.00 | 5 | |
Norfluoxetine Hydrochloride, a notable metabolite, is primarily formed through the demethylation of fluoxetine. This compound exhibits unique binding affinity to serotonin transporters, influencing neurotransmitter dynamics. Its metabolic pathway involves oxidative processes, leading to the formation of reactive intermediates that can interact with various biomolecules. Additionally, its solubility characteristics facilitate its distribution in biological systems, impacting its kinetic behavior during metabolism. | ||||||
Pyriproxyfen | 95737-68-1 | sc-205827 sc-205827A | 5 g 25 g | $89.00 $321.00 | ||
Pyriproxyfen, a significant metabolite, is characterized by its unique interactions with juvenile hormone receptors in insects, mimicking natural hormones. Its metabolic pathways involve hydrolysis and oxidation, leading to the formation of active metabolites that can modulate developmental processes. The compound's lipophilicity enhances its permeability across biological membranes, influencing its distribution and persistence in various environments. Its reaction kinetics are shaped by enzymatic activity, affecting its overall metabolic stability. | ||||||
Rosuvastatin Lactone | 503610-43-3 | sc-219993 | 10 mg | $353.00 | ||
Rosuvastatin Lactone is a notable metabolite formed through the lactonization of rosuvastatin, characterized by its unique structural conformation that influences its reactivity. This compound engages in specific interactions with various enzymes, impacting its metabolic pathways. Its lipophilic nature enhances membrane permeability, allowing for efficient cellular uptake. Additionally, the compound exhibits distinct kinetic properties, influencing its stability and degradation in biological systems. | ||||||
Acetoacetyl coenzyme A sodium salt | 102029-52-7 | sc-252348 sc-252348B | 5 mg 10 mg | $469.00 $826.00 | ||
Acetoacetyl coenzyme A sodium salt serves as a crucial metabolite in various biochemical pathways, particularly in fatty acid synthesis and degradation. It participates in acyl transfer reactions, facilitating the formation of acetoacetyl-CoA, which is pivotal for energy metabolism. The compound exhibits unique interactions with enzymes involved in the citric acid cycle, influencing reaction rates and substrate availability. Its solubility in aqueous environments enhances its bioavailability, promoting efficient metabolic processes. | ||||||
4-(Methylsulfonyl)-2-nitrobenzoic acid | 110964-79-9 | sc-284071 sc-284071A | 1 g 5 g | $40.00 $120.00 | 3 | |
4-(Methylsulfonyl)-2-nitrobenzoic acid acts as a significant metabolite, engaging in diverse biochemical interactions. Its unique nitro and methylsulfonyl groups enable specific hydrogen bonding and electrostatic interactions, influencing enzyme activity and substrate specificity. This compound participates in metabolic pathways by modulating the activity of key enzymes, thereby affecting reaction kinetics. Its distinct solubility characteristics facilitate its role in cellular processes, enhancing metabolic efficiency. | ||||||
6-Hydroxy buspirone | 125481-61-0 | sc-210515 sc-210515-CW | 1 mg 1 mg | $299.00 $459.00 | 1 | |
6-Hydroxy buspirone serves as a notable metabolite, characterized by its hydroxyl group that enhances hydrogen bonding capabilities. This feature allows for unique interactions with biomolecules, potentially influencing protein conformation and stability. It participates in metabolic pathways by altering the kinetics of enzymatic reactions, while its solubility profile aids in cellular transport and distribution. The compound's distinct structural attributes contribute to its role in metabolic regulation. | ||||||
6α-Hydroxy Paclitaxel | 153212-75-0 | sc-210577 | 1 mg | $580.00 | 19 | |
6α-Hydroxy Paclitaxel is a significant metabolite distinguished by its hydroxyl functional group, which facilitates enhanced molecular interactions through hydrogen bonding. This compound engages in metabolic pathways, influencing the activity of cytochrome P450 enzymes, thereby affecting the kinetics of drug metabolism. Its unique structural characteristics also impact solubility and permeability, allowing for efficient cellular uptake and distribution, ultimately shaping its metabolic fate. | ||||||
Telmisartan Acyl-β-D-glucuronide | 250780-40-6 | sc-222341 | 2.5 mg | $445.00 | 2 | |
Telmisartan Acyl-β-D-glucuronide is a notable metabolite characterized by its glucuronidation, which enhances its solubility and facilitates renal excretion. This conjugation alters its interaction with transport proteins, influencing its pharmacokinetic profile. The compound exhibits distinct reaction kinetics, as it undergoes hydrolysis in biological systems, impacting its stability and bioavailability. Its unique structural features contribute to its behavior in metabolic pathways, affecting overall metabolic dynamics. | ||||||
Desvenlafaxine succinate monohydrate | 386750-22-7 | sc-358117 sc-358117A | 25 mg 100 mg | $150.00 $450.00 | ||
Desvenlafaxine succinate monohydrate is a significant metabolite that undergoes extensive biotransformation, primarily through phase I and phase II metabolic pathways. Its unique structure allows for specific interactions with cytochrome P450 enzymes, influencing its metabolic rate and clearance. The compound's solubility is enhanced by its ionic nature, promoting efficient distribution in biological systems. Additionally, its stability in various pH environments affects its reactivity and interaction with biomolecules, shaping its overall metabolic behavior. | ||||||