Nitric Oxide Donors
Items 1 to 10 of 56 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Streptozotocin (U-9889) | 18883-66-4 | sc-200719 sc-200719A | 1 g 5 g | $110.00 $510.00 | 152 | |
Streptozotocin (U-9889) acts as a nitric oxide donor through its ability to release nitric oxide upon enzymatic or chemical activation. This compound engages in specific redox reactions, facilitating the generation of reactive nitrogen species. Its unique structure allows for selective interactions with cellular targets, influencing various signaling pathways. The kinetics of its release are influenced by environmental factors, leading to distinct biological responses that underscore its role in modulating cellular functions. | ||||||
S-Nitrosoglutathione (GSNO) | 57564-91-7 | sc-200349 sc-200349B sc-200349A sc-200349C | 10 mg 25 mg 50 mg 100 mg | $85.00 $206.00 $339.00 $449.00 | 15 | |
S-Nitrosoglutathione (GSNO) serves as a nitric oxide donor by undergoing a unique S-nitrosation reaction, which allows for the controlled release of nitric oxide in biological systems. This compound exhibits distinct reactivity with thiol groups, enabling it to participate in redox signaling and modulate protein function. Its stability and reaction kinetics are influenced by pH and temperature, leading to diverse interactions that can affect cellular signaling pathways and oxidative stress responses. | ||||||
(±)-S-Nitroso-N-acetylpenicillamine | 79032-48-7 | sc-200319B sc-200319 sc-200319A | 10 mg 20 mg 100 mg | $73.00 $112.00 $367.00 | 18 | |
(±)-S-Nitroso-N-acetylpenicillamine acts as a nitric oxide donor through a distinctive mechanism involving S-nitrosation, facilitating the release of nitric oxide in a regulated manner. This compound demonstrates notable interactions with metal ions, enhancing its reactivity and influencing coordination chemistry. Its unique structural features allow for selective targeting of biological macromolecules, potentially altering their functional states and contributing to intricate cellular signaling networks. | ||||||
NOC-12 | 146724-89-2 | sc-202246 | 10 mg | $225.00 | 3 | |
NOC-12 serves as a nitric oxide donor by engaging in a unique redox reaction that promotes the release of nitric oxide in a controlled fashion. Its molecular structure features a highly reactive nitroso group, which interacts favorably with thiol-containing compounds, leading to the formation of S-nitrosothiols. This interaction not only enhances its stability but also influences electron transfer processes, making it a key player in various biochemical pathways. | ||||||
NOC-18 | 146724-94-9 | sc-202247 sc-202247A sc-202247B sc-202247C | 10 mg 50 mg 100 mg 500 mg | $50.00 $180.00 $299.00 $1100.00 | 18 | |
NOC-18 functions as a nitric oxide donor through a distinctive mechanism involving the cleavage of its nitroso moiety, facilitating the rapid release of nitric oxide. Its structural configuration allows for effective interaction with metal ions, enhancing its reactivity and influencing coordination chemistry. The compound exhibits unique reaction kinetics, characterized by a swift release profile, which can be modulated by environmental factors, thereby impacting its behavior in diverse chemical contexts. | ||||||
MAHMA NONOate | 146724-86-9 | sc-202250 | 10 mg | $51.00 | 4 | |
MAHMA NONOate acts as a nitric oxide donor by undergoing hydrolysis, leading to the generation of nitric oxide and other byproducts. Its unique ester linkage promotes selective reactivity, allowing for controlled release in various environments. The compound's ability to form stable complexes with transition metals enhances its reactivity, while its solubility in polar solvents facilitates efficient diffusion. This behavior underscores its potential for diverse applications in chemical research and development. | ||||||
3-Morpholinosydnonimine | 16142-27-1 | sc-200339 sc-200339A | 20 mg 100 mg | $97.00 $362.00 | 10 | |
3-Morpholinosydnonimine serves as a nitric oxide donor through a distinct mechanism involving the cleavage of its morpholino ring, which facilitates the release of nitric oxide. This compound exhibits unique reactivity due to its electron-rich structure, promoting rapid interactions with biological targets. Its stability in aqueous environments and ability to participate in redox reactions further enhance its kinetic profile, making it a subject of interest in various chemical studies. | ||||||
Angeli′s salt | 13826-64-7 | sc-202464 | 10 mg | $90.00 | 5 | |
Angeli's salt acts as a nitric oxide donor by undergoing hydrolysis, leading to the release of nitric oxide in a controlled manner. Its unique structure allows for specific interactions with metal ions, influencing reaction pathways and enhancing its reactivity. The compound's stability in various pH conditions and its ability to form complexes with biomolecules contribute to its distinctive kinetic behavior, making it a fascinating subject for exploring nitric oxide dynamics in chemical research. | ||||||
NOR-1 | 163032-70-0 | sc-202736 | 10 mg | $285.00 | 1 | |
NOR-1 functions as a nitric oxide donor through a distinctive mechanism that involves the cleavage of its nitroso group, facilitating the release of nitric oxide. Its unique electronic configuration allows for selective interactions with reactive species, influencing the rate of NO release. The compound exhibits notable stability under varying environmental conditions, and its ability to engage in redox reactions enhances its reactivity, making it an intriguing candidate for studying nitric oxide's role in various chemical processes. | ||||||
DPTA NONOate | 146724-95-0 | sc-202144 sc-202144B sc-202144A sc-202144C sc-202144D | 5 mg 10 mg 25 mg 50 mg 100 mg | $53.00 $56.00 $135.00 $200.00 $360.00 | 11 | |
DPTA NONOate serves as a nitric oxide donor by undergoing hydrolysis, which triggers the release of nitric oxide in a controlled manner. Its structural design promotes specific interactions with biological targets, enhancing its reactivity. The compound's stability in diverse pH environments allows for sustained NO release, while its unique electron-donating properties facilitate rapid reaction kinetics. This behavior makes it a compelling subject for exploring nitric oxide's dynamics in various chemical contexts. | ||||||