Items 221 to 230 of 253 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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α-Apo-oxytetracycline | 18695-01-7 | sc-213198 | 2.5 mg | $360.00 | ||
α-Apo-oxytetracycline is a notable metabolite characterized by its ability to interact with various biological macromolecules, influencing metabolic pathways. It exhibits unique binding affinities to ribosomal RNA, affecting protein synthesis and cellular function. This compound also participates in redox reactions, contributing to oxidative stress responses. Its amphipathic nature allows it to traverse lipid membranes, enhancing its role in cellular signaling and metabolic modulation. | ||||||
N-Desmethyl Dextrorphan β-D-O-Glucuronide | 19153-89-0 | sc-212185 | 1 mg | $388.00 | ||
N-Desmethyl Dextrorphan β-D-O-Glucuronide is a significant metabolite known for its role in the glucuronidation pathway, where it undergoes conjugation to enhance solubility and facilitate excretion. This compound exhibits distinct interactions with UDP-glucuronosyltransferases, influencing its metabolic stability and clearance. Its hydrophilic properties enable efficient transport across biological membranes, impacting its distribution and bioavailability within various tissues. | ||||||
Propionyl L-carnitine hydrochloride | 119793-66-7 | sc-344979 | 1 g | $51.00 | ||
Propionyl L-carnitine hydrochloride serves as a key metabolite involved in energy metabolism, particularly in fatty acid transport across mitochondrial membranes. Its unique structure allows for specific interactions with carnitine acyltransferases, enhancing the efficiency of fatty acid oxidation. This compound also participates in the modulation of cellular energy dynamics, influencing metabolic pathways and contributing to the regulation of oxidative stress within cells. | ||||||
rac trans-4-Hydroxy Glyburide | 23155-00-2 | sc-208281 sc-208281A sc-208281B sc-208281C | 2.5 mg 5 mg 10 mg 25 mg | $439.00 $704.00 $1336.00 $1510.00 | ||
Rac trans-4-Hydroxy Glyburide acts as a significant metabolite, exhibiting unique interactions with various enzymes involved in glucose metabolism. Its structural characteristics facilitate specific binding to sulfonylurea receptors, influencing insulin secretion dynamics. Additionally, it plays a role in modulating cellular signaling pathways, impacting the regulation of ion channels and contributing to the overall metabolic balance within cells. Its kinetic profile suggests distinct reaction rates in metabolic pathways, highlighting its role in energy homeostasis. | ||||||
3′-Azido-3′-deoxythymidine 5′-Monophosphate Sodium Salt | 128506-29-6 | sc-220901 | 10 mg | $343.00 | ||
3'-Azido-3'-deoxythymidine 5'-Monophosphate Sodium Salt serves as a notable metabolite, characterized by its ability to engage in specific interactions with nucleic acid polymerases. This compound influences nucleotide incorporation during DNA synthesis, affecting replication fidelity. Its unique structural features allow for distinct binding affinities, altering reaction kinetics in metabolic pathways. Additionally, it may impact cellular signaling by modulating the activity of various kinases, thereby influencing metabolic regulation. | ||||||
Dapsone Hydroxylamine | 32695-27-5 | sc-211209D sc-211209 sc-211209A sc-211209B sc-211209C | 5 mg 10 mg 25 mg 50 mg 100 mg | $285.00 $377.00 $805.00 $1489.00 $2346.00 | 3 | |
Dapsone Hydroxylamine acts as a significant metabolite, exhibiting unique reactivity through its ability to form stable adducts with various biomolecules. This compound participates in redox reactions, influencing oxidative stress pathways and cellular defense mechanisms. Its distinct electron-donating properties facilitate interactions with reactive oxygen species, potentially altering cellular redox states. Furthermore, it may modulate enzyme activity through covalent modifications, impacting metabolic flux. | ||||||
4-Keto Retinal | 33532-44-4 | sc-210098 | 5 mg | $300.00 | ||
4-Keto Retinal serves as a notable metabolite, characterized by its role in visual processes and its interaction with proteins involved in phototransduction. This compound undergoes isomerization, influencing the dynamics of retinal binding proteins. Its unique structural features allow for specific hydrogen bonding and hydrophobic interactions, which can affect the stability of protein complexes. Additionally, it participates in metabolic pathways that regulate visual pigment regeneration, showcasing its importance in cellular signaling. | ||||||
Stercobilin hydrochloride | 34217-90-8 free base | sc-264326 sc-264326A | 5 mg 10 mg | $196.00 $342.00 | 3 | |
Stercobilin hydrochloride is a significant metabolite derived from the breakdown of bilirubin, primarily in the intestines. It exhibits unique chromatic properties, contributing to the coloration of feces. This compound engages in specific interactions with gut microbiota, influencing microbial metabolism and the overall gut environment. Its formation involves enzymatic reduction processes, highlighting its role in the enterohepatic circulation and the regulation of bile pigment levels. | ||||||
Tetrahydro Curcumin | 36062-04-1 | sc-391609 | 1 g | $291.00 | 1 | |
Tetrahydro Curcumin is a notable metabolite formed from curcumin through reduction processes. It exhibits enhanced solubility and stability compared to its parent compound, facilitating distinct interactions with cellular components. This metabolite participates in various biochemical pathways, influencing oxidative stress responses and cellular signaling. Its unique structural features allow for effective scavenging of free radicals, contributing to its role in modulating metabolic processes within the body. | ||||||
Benzydamine N-Oxide | 36504-71-9 | sc-207328B sc-207328 sc-207328A sc-207328C sc-207328D | 2 mg 5 mg 10 mg 25 mg 50 mg | $220.00 $353.00 $633.00 $1475.00 $2454.00 | 3 | |
Benzydamine N-Oxide is a significant metabolite derived from benzydamine, characterized by its unique oxidation state. This compound engages in specific electron transfer reactions, influencing redox balance within biological systems. Its distinct molecular structure enhances its interaction with membrane lipids, potentially altering membrane fluidity and permeability. Additionally, Benzydamine N-Oxide exhibits varied reaction kinetics, impacting its stability and reactivity in metabolic pathways. |