Items 101 to 110 of 253 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Ethoxyquin Dimer | 74681-77-9 | sc-214978A sc-214978 | 1 mg 2.5 mg | $265.00 $398.00 | ||
Ethoxyquin Dimer serves as a notable metabolite characterized by its ability to form stable complexes with reactive oxygen species, thereby influencing oxidative stress pathways. Its unique dimeric structure facilitates specific interactions with cellular membranes, enhancing permeability and altering lipid dynamics. The compound's kinetic behavior in redox reactions showcases its role in modulating enzymatic processes, contributing to metabolic regulation and cellular homeostasis. | ||||||
Oxybutynin N-Oxide | 80976-68-7 | sc-212490 | 1 mg | $330.00 | ||
Oxybutynin N-Oxide is a significant metabolite distinguished by its unique interaction with neurotransmitter receptors, influencing synaptic transmission dynamics. Its structural conformation allows for selective binding, impacting signal transduction pathways. The compound exhibits distinct solubility characteristics, which affect its distribution in biological systems. Additionally, its metabolic pathway involves enzymatic oxidation, highlighting its role in biotransformation processes within the body. | ||||||
4′-Hydroxy Tamoxifen | 82413-23-8 | sc-210192 sc-210192A | 2.5 mg 25 mg | $390.00 $2800.00 | 1 | |
4'-Hydroxy Tamoxifen is a notable metabolite characterized by its ability to form stable complexes with estrogen receptors, modulating gene expression. Its unique hydroxyl group enhances hydrogen bonding, influencing receptor affinity and selectivity. The compound undergoes phase II metabolism, primarily through conjugation, which alters its pharmacokinetic profile. Additionally, its lipophilic nature affects membrane permeability, impacting its distribution and interaction within cellular environments. | ||||||
1-Oleoyl-2-acetyl-sn-glycerol (OAG) | 86390-77-4 | sc-200417 sc-200417A | 10 mg 50 mg | $117.00 $444.00 | 1 | |
1-Oleoyl-2-acetyl-sn-glycerol (OAG) is a significant metabolite known for its role in lipid signaling pathways. It acts as a potent activator of protein kinase C, influencing various cellular processes. The compound's unique acyl chain structure facilitates membrane integration, enhancing its interaction with lipid bilayers. OAG's reactivity is characterized by its ability to undergo hydrolysis, generating bioactive lipids that participate in cellular signaling cascades, thereby modulating metabolic responses. | ||||||
Galiellalactone | 133613-71-5 | sc-202165 | 1 mg | $410.00 | 9 | |
Galiellalactone is a notable metabolite recognized for its role in modulating cellular signaling pathways. This compound exhibits unique interactions with specific receptors, influencing gene expression and cellular responses. Its structural features allow for effective binding to target proteins, facilitating distinct biochemical pathways. Galiellalactone's stability and reactivity enable it to participate in various metabolic processes, contributing to the regulation of cellular homeostasis and metabolic balance. | ||||||
Varenicline Carbamoyl β-D-Glucuronide | 535920-98-0 | sc-213148 | 1 mg | $430.00 | ||
Varenicline Carbamoyl β-D-Glucuronide serves as a significant metabolite characterized by its unique conjugation with glucuronic acid, enhancing solubility and facilitating excretion. This compound undergoes specific enzymatic transformations, primarily through UDP-glucuronosyltransferases, which influence its pharmacokinetic profile. Its interactions with various biological matrices can alter the bioavailability of parent compounds, impacting metabolic pathways and influencing systemic distribution. | ||||||
Varenicline Lactam | 873302-30-8 | sc-213149 | 1 mg | $360.00 | ||
Varenicline Lactam is a notable metabolite that arises from the oxidative transformation of its parent compound. This lactam form exhibits distinct stability and reactivity due to its cyclic structure, which can influence its interaction with biomolecules. The compound participates in unique metabolic pathways, often involving cytochrome P450 enzymes, leading to varied reaction kinetics. Its presence can modulate the pharmacodynamics of related substances, affecting their overall metabolic fate. | ||||||
Theobromine | 83-67-0 | sc-203296 sc-203296A | 25 g 100 g | $41.00 $87.00 | ||
Theobromine is a methylxanthine metabolite that plays a significant role in various biochemical pathways. It exhibits unique interactions with adenosine receptors, influencing neurotransmitter release and cellular signaling. The compound undergoes extensive hepatic metabolism, primarily via cytochrome P450 enzymes, resulting in distinct kinetic profiles. Its solubility and stability in biological systems facilitate diverse metabolic fates, impacting energy regulation and vascular function. | ||||||
5-Methyltetrahydrofolic Acid Calcium Salt Hydrate | sc-207045 | 10 mg | $360.00 | |||
5-Methyltetrahydrofolic Acid Calcium Salt Hydrate is a key metabolite involved in one-carbon metabolism, crucial for nucleotide synthesis and amino acid interconversion. It participates in methylation reactions, influencing gene expression and cellular function. The compound exhibits strong binding affinity to enzymes like methylene tetrahydrofolate reductase, enhancing its role in folate metabolism. Its stability in aqueous environments supports efficient transport and bioavailability in various biological systems. | ||||||
Glycidamide | 5694-00-8 | sc-394244 | 100 mg | $371.00 | ||
Glycidamide is a notable metabolite that arises from the epoxidation of acrylamide, showcasing unique reactivity through its electrophilic nature. It readily interacts with nucleophiles, leading to the formation of adducts with proteins and DNA, which can influence cellular processes. Glycidamide's metabolic pathways involve enzymatic conversion, highlighting its role in oxidative stress responses. Its distinct kinetic properties facilitate rapid transformation in biological systems, impacting cellular integrity and function. |