Items 161 to 168 of 168 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Furosemide-d5 | 1189482-35-6 | sc-218550 sc-218550A | 1 mg 10 mg | $520.00 $2305.00 | 1 | |
Furosemide-d5 is a distinctive compound characterized by its ability to modulate ion transport mechanisms, particularly in renal systems. Its deuterated form enhances stability and alters isotopic labeling, providing insights into metabolic pathways. The compound's unique binding affinity to the Na-K-2Cl cotransporter influences electrolyte balance, while its solubility properties facilitate interactions with various biological matrices. This behavior underscores its role in influencing cellular ion homeostasis. | ||||||
Ivermectin-d2 | 70288-86-7 unlabeled | sc-495570 sc-495570A sc-495570B | 1 mg 10 mg 50 mg | $357.00 $2458.00 $9868.00 | ||
Ivermectin-d2 is a complex molecule known for its unique interactions with specific ion channels in parasites, leading to increased permeability and subsequent paralysis. Its structural features allow for selective binding, which enhances its efficacy in disrupting neurotransmission. The compound exhibits distinct reaction kinetics, influenced by its stereochemistry, which plays a crucial role in its biological activity. Additionally, its lipophilic characteristics facilitate membrane penetration, impacting its distribution in biological systems. | ||||||
Ornidazole | 16773-42-5 | sc-205779 sc-205779A | 5 g 50 g | $51.00 $460.00 | ||
Ornidazole is a nitroimidazole compound characterized by its ability to undergo reduction in anaerobic conditions, leading to the formation of reactive intermediates that interact with microbial DNA. This interaction results in the disruption of DNA synthesis and function. Its lipophilic nature enhances cellular uptake, while its unique structural features allow for specific binding to target sites, influencing its reactivity and overall biological behavior. | ||||||
Secnidazole | 3366-95-8 | sc-212917 | 10 mg | $134.00 | ||
Secnidazole is a nitroimidazole derivative known for its selective reduction in anaerobic environments, generating reactive species that can form covalent bonds with nucleophilic sites in biomolecules. This compound exhibits a unique affinity for electron-rich environments, facilitating its interaction with various cellular components. Its hydrophobic characteristics promote membrane permeability, enhancing its distribution within biological systems and influencing its kinetic behavior in diverse chemical reactions. | ||||||
2′-Deoxy-L-uridine-13C,15N2 | 31501-19-6 (unlabeled) | sc-214050 | 1 mg | $360.00 | ||
2'-Deoxy-L-uridine-13C,15N2 is a stable nucleoside analog that incorporates isotopic labels, allowing for detailed metabolic tracing in biological systems. Its structural similarity to natural nucleosides enables it to engage in specific hydrogen bonding interactions with nucleic acids, influencing polymerase activity. The presence of carbon and nitrogen isotopes enhances its detection in mass spectrometry, providing insights into metabolic pathways and cellular dynamics. Its unique isotopic composition allows for the study of nucleic acid metabolism and turnover in various biological contexts. | ||||||
Dichlorvos | 62-73-7 | sc-207557 | 250 mg | $41.00 | 1 | |
Dichlorvos is an organophosphate compound known for its ability to inhibit acetylcholinesterase, leading to the accumulation of acetylcholine at synaptic junctions. This mechanism disrupts neurotransmission, showcasing its potent reactivity with serine residues in the enzyme's active site. Its lipophilic nature facilitates rapid penetration through biological membranes, enhancing its efficacy. Additionally, the compound's stability under various conditions allows for prolonged activity, making it a subject of interest in studies of neurochemical pathways. | ||||||
Isothiazole-5-carboxylic acid | 10271-85-9 | sc-396325 sc-396325A | 250 mg 1 g | $260.00 $670.00 | ||
Isothiazole-5-carboxylic acid exhibits unique reactivity due to its heterocyclic structure, which allows for specific interactions with biological macromolecules. Its carboxylic acid group can engage in hydrogen bonding, enhancing solubility in polar environments. The compound's ability to form stable complexes with metal ions may influence enzymatic activity, while its distinct electronic properties can modulate redox reactions. This versatility makes it a subject of interest in various chemical studies. | ||||||
Crystal Violet | 548-62-9 | sc-207460 sc-207460A | 100 g 500 g | $98.00 $246.00 | 34 | |
Crystal Violet is a synthetic dye characterized by its cationic nature, which facilitates strong electrostatic interactions with negatively charged surfaces, such as bacterial membranes. Its planar structure allows for effective stacking interactions, enhancing its binding affinity. The compound's unique photophysical properties, including fluorescence, enable it to act as a visual marker in various assays. Additionally, its ability to form aggregates can influence reaction kinetics, making it a fascinating subject for studies in molecular interactions and dynamics. |