Amino Acids
Items 101 to 110 of 115 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
L-Glutamic acid γ-(7-amido-4-methylcoumarin) | 72669-53-5 | sc-281542 sc-281542A | 50 mg 100 mg | $154.00 $217.00 | ||
L-Glutamic acid γ-(7-amido-4-methylcoumarin) features a distinctive coumarin moiety that enhances its fluorescence properties, making it a valuable tool for studying protein interactions. The presence of the amido group facilitates specific hydrogen bonding, influencing its solubility and reactivity in aqueous environments. This compound can participate in unique molecular interactions, potentially altering reaction kinetics and pathways in biochemical systems, thereby impacting metabolic dynamics. | ||||||
LTC4 (Leukotriene C4) | 72025-60-6 | sc-201046 sc-201046A | 50 µg 300 µg | $300.00 $2850.00 | ||
Leukotriene C4 is a potent lipid mediator that plays a crucial role in inflammatory responses. Its unique structure allows for specific interactions with cysteinyl leukotriene receptors, triggering signaling cascades that influence cellular behavior. As an acid halide, it exhibits reactivity with nucleophiles, facilitating the formation of conjugates that can modulate various biological processes. Its hydrophobic nature affects membrane permeability, impacting its distribution and activity in tissues. | ||||||
SLIGRL-NH2 | 171436-38-7 | sc-359903 | 1 mg | $82.00 | ||
SLIGRL-NH2 is a distinctive amino acid characterized by its unique side chain that enhances its ability to form hydrogen bonds, influencing protein folding and stability. This compound participates in specific enzymatic pathways, acting as a substrate or modulator in metabolic processes. Its zwitterionic nature contributes to solubility in aqueous environments, while its reactivity with electrophiles allows for diverse interactions in biochemical systems, impacting cellular signaling and function. | ||||||
γ-Secretase Inhibitor III | sc-302013 sc-302013A | 1 mg 5 mg | $102.00 $510.00 | |||
γ-Secretase Inhibitor III is a notable compound that exhibits unique interactions with membrane proteins, influencing the dynamics of cellular signaling pathways. Its structure allows for specific binding to active sites, modulating enzymatic activity and altering substrate processing. The compound's hydrophobic regions facilitate membrane penetration, while its polar functionalities enhance solubility in biological systems, promoting diverse biochemical interactions and regulatory mechanisms within cells. | ||||||
Cdk5 substrate | sc-3066 | 500 µg | $89.00 | 2 | ||
Cdk5 Substrate is a critical protein involved in neuronal signaling, characterized by its phosphorylation by cyclin-dependent kinase 5 (Cdk5). This substrate exhibits unique interactions with specific amino acid residues, facilitating the modulation of various signaling pathways. Its phosphorylation alters protein conformation and stability, influencing downstream effects on neuronal function and development. The substrate's role in synaptic plasticity highlights its importance in cellular communication and neural network dynamics. | ||||||
NG-Monoethyl-L-arginine TFA | sc-391814 sc-391814A | 10 mg 100 mg | $127.00 $209.00 | |||
NG-Monoethyl-L-arginine TFA is a modified amino acid that plays a pivotal role in nitric oxide synthesis pathways. Its unique ethyl substitution enhances solubility and alters interaction dynamics with nitric oxide synthase, potentially affecting enzyme kinetics. This compound exhibits distinct binding affinities, influencing the regulation of vascular tone and cellular signaling. Its structural properties allow for specific interactions with receptor sites, impacting downstream signaling cascades. | ||||||
Oxytocin acetate salt | 50-56-6 | sc-279938 sc-279938A sc-279938B sc-279938C sc-279938D sc-279938E | 1 mg 5 mg 25 mg 100 mg 250 mg 1 g | $59.00 $176.00 $330.00 $650.00 $950.00 $1800.00 | 4 | |
Oxytocin acetate salt is a peptide derivative characterized by its unique cyclic structure, which facilitates specific receptor binding and modulates intercellular communication. Its acetate form enhances solubility and stability, promoting efficient transport across membranes. The compound exhibits distinct conformational flexibility, allowing it to engage in diverse molecular interactions. This behavior influences various signaling pathways, contributing to its role in cellular processes and physiological responses. | ||||||
Melphalan | 148-82-3 | sc-204799 sc-204799A | 100 mg 250 mg | $136.00 $237.00 | 5 | |
Melphalan is an alkylating agent that features a unique bifunctional structure, enabling it to form covalent bonds with nucleophilic sites on DNA. This interaction leads to cross-linking, which disrupts replication and transcription processes. The compound's hydrophobic characteristics enhance its membrane permeability, facilitating cellular uptake. Additionally, its reactivity is influenced by pH and temperature, affecting its stability and interaction kinetics in various environments. | ||||||
6-Diazo-5-oxo-L-norleucine | 157-03-9 | sc-227078 sc-227078A sc-227078B sc-227078C | 5 mg 25 mg 100 mg 250 mg | $82.00 $285.00 $908.00 $2152.00 | ||
6-Diazo-5-oxo-L-norleucine is a potent inhibitor of specific enzymatic pathways, particularly those involving amino acid metabolism. Its unique structure allows for competitive binding to active sites, disrupting normal enzymatic function. The compound exhibits distinct solubility properties, influencing its distribution in biological systems. Additionally, its reactivity is modulated by the presence of metal ions, which can alter its interaction dynamics and stability in various biochemical contexts. | ||||||
Glycocholic acid | 475-31-0 | sc-218574 sc-218574A sc-218574B sc-218574C sc-218574D sc-218574E | 100 mg 1 g 5 g 10 g 50 g 100 g | $72.00 $184.00 $637.00 $1234.00 $1642.00 $3070.00 | 4 | |
Glycocholic acid is a bile acid derivative that exhibits unique amphipathic properties, allowing it to interact effectively with lipid membranes. Its hydroxyl groups facilitate hydrogen bonding, enhancing solubility in aqueous environments. This compound plays a crucial role in emulsifying dietary fats, promoting their absorption. Additionally, its structural conformation enables it to modulate the activity of membrane-bound proteins, influencing various cellular signaling pathways. | ||||||