Items 1 to 10 of 12 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(±)-S-Nitroso-N-acetylpenicillamine | 79032-48-7 | sc-200319B sc-200319 sc-200319A | 10 mg 20 mg 100 mg | $74.00 $114.00 $374.00 | 18 | |
(±)-S-Nitroso-N-acetylpenicillamine is a versatile compound known for its ability to release nitric oxide, facilitating unique redox reactions. Its structure allows for specific interactions with thiol groups, influencing cellular signaling pathways. The compound exhibits distinct reaction kinetics, characterized by rapid formation and decomposition of nitrosothiol species, which can modulate protein function. Additionally, its solubility in various solvents enhances its reactivity in diverse biochemical environments. | ||||||
3-Morpholinosydnonimine | 16142-27-1 | sc-200339 sc-200339A | 20 mg 100 mg | $89.00 $369.00 | 10 | |
3-Morpholinosydnonimine is a notable compound recognized for its ability to generate reactive nitrogen species, which can engage in diverse chemical transformations. Its unique morpholino group enhances solubility and facilitates interactions with biological macromolecules, influencing electron transfer processes. The compound exhibits distinct reactivity patterns, particularly in redox cycling, which can affect various biochemical pathways. Its stability under specific conditions allows for controlled release of active intermediates, making it a subject of interest in chemical research. | ||||||
YC-1 | 170632-47-0 | sc-202856 sc-202856A sc-202856B sc-202856C | 1 mg 5 mg 10 mg 50 mg | $33.00 $124.00 $218.00 $947.00 | 9 | |
YC-1 is a distinctive compound characterized by its ability to modulate nitric oxide signaling pathways through specific interactions with heme-containing proteins. Its unique structural features enable it to act as a potent ligand, influencing the conformational dynamics of target proteins. The compound exhibits selective reactivity, facilitating the formation of stable adducts that can alter enzymatic activity. Additionally, its solubility properties enhance its accessibility in various environments, promoting diverse chemical interactions. | ||||||
Protoporphyrin IX disodium salt | 50865-01-5 | sc-258048 sc-258048A sc-258048B | 250 mg 1 g 5 g | $58.00 $177.00 $747.00 | 1 | |
Protoporphyrin IX disodium salt is a unique chelating agent that exhibits strong affinity for metal ions, particularly iron, facilitating the formation of metalloporphyrins. Its distinct planar structure allows for effective π-π stacking interactions, enhancing its stability in solution. The compound's zwitterionic nature contributes to its solubility in aqueous environments, promoting dynamic equilibria in complexation reactions. This behavior enables it to participate in various electron transfer processes, influencing redox chemistry. | ||||||
Guanylin (human) | 183200-12-6 | sc-203066 sc-203066B | 100 µg 500 µg | $136.00 $582.00 | 1 | |
Guanylin is a peptide that plays a crucial role in regulating electrolyte balance and fluid homeostasis. It interacts specifically with guanylate cyclase receptors, leading to the conversion of GTP to cGMP, a secondary messenger that modulates various physiological processes. The unique structure of Guanylin allows for selective binding, triggering distinct signaling pathways that influence ion transport and cellular responses. Its rapid kinetics in receptor activation underscores its importance in gastrointestinal function. | ||||||
12(S)-HPETE | 71774-10-2 | sc-200961A sc-200961 | 25 µg 50 µg | $156.00 $265.00 | ||
12(S)-HPETE is a hydroperoxy fatty acid that serves as a key signaling molecule in various biological processes. It is involved in the regulation of lipid peroxidation and can influence cellular responses through its interaction with specific receptors. The compound participates in distinct metabolic pathways, particularly in the formation of eicosanoids, which are crucial for mediating inflammatory responses. Its reactivity and ability to form adducts with proteins highlight its role in modulating cellular functions. | ||||||
4-Phenyl-3-furoxancarbonitrile | 125520-62-9 | sc-206935 | 10 mg | $96.00 | ||
4-Phenyl-3-furoxancarbonitrile is a unique compound characterized by its furoxan ring, which enhances its reactivity through the presence of both nitrile and furoxan functionalities. This structure facilitates specific molecular interactions, allowing it to engage in diverse reaction pathways, including cycloaddition and nucleophilic attack. Its kinetic properties are influenced by the electron-withdrawing nature of the nitrile group, promoting rapid reactions under certain conditions. The compound's distinct physical properties, such as solubility and stability, further contribute to its behavior in various chemical environments. | ||||||
Guanylin (rat, mouse) | 144940-98-7 | sc-203067 sc-203067A | 100 µg 500 µg | $150.00 $900.00 | ||
Guanylin, a peptide hormone found in rats and mice, plays a crucial role in regulating electrolyte balance and fluid homeostasis. It interacts specifically with guanylate cyclase receptors, leading to the production of cyclic GMP, a secondary messenger that modulates various signaling pathways. This interaction influences smooth muscle relaxation and ion transport, showcasing its unique ability to affect cellular responses. The peptide's stability and conformational flexibility enhance its biological activity, allowing for precise modulation of physiological processes. | ||||||
Molsidomine | 25717-80-0 | sc-200337 sc-200337A | 50 mg 250 mg | $20.00 $33.00 | ||
Molsidomine is a unique compound that acts as a nitric oxide donor, facilitating vasodilation through its conversion to the active metabolite, linsidomine. This transformation involves specific enzymatic pathways that enhance the release of nitric oxide, promoting smooth muscle relaxation. The compound exhibits distinct reaction kinetics, characterized by rapid activation and a prolonged effect on vascular tone. Its lipophilic nature allows for efficient membrane permeability, influencing its bioavailability and interaction with cellular targets. | ||||||
A 350619 hydrochloride | 538368-27-3 | sc-203787 sc-203787A | 10 mg 50 mg | $179.00 $756.00 | 1 | |
A 350619 hydrochloride is a distinctive compound that functions as a GCS, engaging in selective interactions with specific receptors to modulate intracellular signaling pathways. Its unique structure allows for enhanced binding affinity, leading to altered reaction kinetics that favor rapid cellular uptake. The compound's solubility profile facilitates effective distribution in various environments, while its stability under physiological conditions ensures sustained activity, impacting downstream molecular processes. | ||||||