Items 111 to 115 of 115 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Enniatin B | 917-13-5 | sc-202150 | 1 mg | $300.00 | 4 | |
Enniatin B is a cyclic peptide that exhibits remarkable ionophoric properties, enabling it to form complexes with cations, particularly potassium and sodium ions. This interaction facilitates the transport of these ions across lipid membranes, impacting cellular ion homeostasis. Its unique structure allows for specific binding interactions, influencing membrane potential and cellular excitability. Additionally, Enniatin B's hydrophobic regions contribute to its ability to integrate into lipid bilayers, altering membrane fluidity and permeability. | ||||||
3-Guanidinopropionic acid | 353-09-3 | sc-254485 sc-254485A | 1 g 5 g | $55.00 $193.00 | ||
3-Guanidinopropionic acid is characterized by its guanidine group, which enhances its ability to form hydrogen bonds and engage in ionic interactions. This compound plays a role in modulating cellular energy metabolism by influencing the activity of key enzymes involved in the urea cycle. Its zwitterionic nature contributes to its solubility in aqueous environments, facilitating its participation in various biochemical reactions. The compound's unique structural features also allow it to act as a competitive inhibitor in specific metabolic pathways. | ||||||
4-Amino-phenylalanine | 943-80-6 | sc-299377 sc-299377A | 5 g 50 g | $153.00 $454.00 | ||
4-Amino-phenylalanine is a non-standard amino acid characterized by its unique side chain that enhances its ability to participate in hydrogen bonding and π-π stacking interactions. This structural feature allows it to stabilize protein conformations and influence enzyme kinetics through specific molecular interactions. Its presence can modulate the folding and stability of peptides, impacting their overall functionality and reactivity in biochemical pathways. | ||||||
Carbobenzyloxy-L-valine | 1149-26-4 | sc-239478 | 5 g | $10.00 | ||
Carbobenzyloxy-L-valine is a modified amino acid distinguished by its carbobenzyloxy protecting group, which enhances its hydrophobic character and steric bulk. This modification influences peptide synthesis by providing stability against premature hydrolysis and facilitating selective coupling reactions. Its unique structure allows for specific interactions with other amino acids, potentially altering the conformational dynamics of peptides and influencing their reactivity in various biochemical environments. | ||||||
3,3′,5′-Triiodo-L-thyronine | 5817-39-0 | sc-209692 | 10 mg | $199.00 | ||
3,3',5'-Triiodo-L-thyronine, a potent thyroid hormone, exhibits unique molecular interactions due to its tri-iodinated structure, which enhances its lipophilicity and influences receptor binding affinity. This compound participates in distinct metabolic pathways, modulating gene expression and energy metabolism. Its kinetic behavior is characterized by rapid cellular uptake and specific enzymatic conversion, impacting physiological processes at the cellular level. The presence of iodine atoms also contributes to its stability and reactivity in biochemical systems. |