Nitric Oxide Donors
Items 11 to 20 of 56 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Diethylamine NONOate | 372965-00-9 | sc-202575 sc-202575A sc-202575B sc-202575C | 10 mg 50 mg 100 mg 500 mg | $37.00 $111.00 $199.00 $882.00 | 1 | |
Diethylamine NONOate acts as a nitric oxide donor through a unique mechanism involving the cleavage of its N-O bond, leading to the release of nitric oxide. Its molecular structure allows for selective interactions with various nucleophiles, enhancing its reactivity profile. The compound exhibits notable stability under varying conditions, which influences its release kinetics. Additionally, its electron-rich environment contributes to its ability to participate in diverse redox reactions, making it an intriguing candidate for studying nitric oxide's role in chemical processes. | ||||||
NOC-5 | 146724-82-5 | sc-202248A sc-202248B sc-202248 sc-202248C | 1 mg 5 mg 10 mg 25 mg | $59.00 $156.00 $216.00 $410.00 | 5 | |
NOC-5 functions as a nitric oxide donor by facilitating the generation of nitric oxide through a distinctive pathway involving the activation of its nitroso group. This compound showcases a high degree of reactivity due to its unique electronic configuration, which promotes rapid interactions with biological and chemical substrates. Its stability in diverse environments allows for controlled release, while its ability to engage in complex coordination chemistry enhances its potential for exploring nitric oxide's multifaceted roles in various reactions. | ||||||
Spermine NONOate | 136587-13-8 | sc-202816 sc-202816A | 5 mg 25 mg | $52.00 $192.00 | 5 | |
Spermine NONOate acts as a nitric oxide donor by undergoing hydrolysis, leading to the release of nitric oxide in a controlled manner. Its unique polyamine structure allows for specific interactions with cellular components, influencing signaling pathways. The compound exhibits notable reaction kinetics, characterized by a rapid initial release followed by a sustained output, making it an intriguing subject for studying nitric oxide's diverse biological effects and mechanisms. | ||||||
NOC-7 | 146724-84-7 | sc-202249 | 10 mg | $210.00 | 5 | |
NOC-7 functions as a nitric oxide donor through a distinct mechanism involving the cleavage of its nitro group, facilitating the release of nitric oxide. Its unique structural features enable selective interactions with metal ions, enhancing its reactivity. The compound demonstrates a biphasic release profile, with an initial burst followed by a gradual release, allowing for nuanced modulation of nitric oxide levels. This behavior makes it a compelling candidate for exploring the dynamics of nitric oxide in various chemical environments. | ||||||
Sodium nitroprusside dihydrate | 13755-38-9 | sc-203395 sc-203395A sc-203395B | 1 g 5 g 100 g | $42.00 $83.00 $155.00 | 7 | |
Sodium nitroprusside dihydrate acts as a nitric oxide donor by undergoing photolytic decomposition, which liberates nitric oxide in a controlled manner. Its coordination with transition metals enhances its stability and reactivity, allowing for specific interactions that influence reaction kinetics. The compound exhibits a unique solubility profile, facilitating its dispersion in various media, and its ability to form complexes with ligands can modulate its release characteristics, making it an intriguing subject for studying nitric oxide dynamics. | ||||||
JS-K | 205432-12-8 | sc-211683 sc-211683A | 5 mg 25 mg | $153.00 $530.00 | 14 | |
JS-K functions as a nitric oxide donor through a unique mechanism involving the release of nitric oxide via a reductive pathway. Its structure allows for selective interactions with biological thiols, leading to the formation of stable adducts that influence its reactivity. The compound's distinct electron-donating properties enhance its ability to participate in redox reactions, while its solubility in organic solvents facilitates diverse experimental applications, making it a compelling candidate for exploring nitric oxide signaling. | ||||||
Piloty′s Acid | 599-71-3 | sc-205436 sc-205436A | 500 mg 1 g | $20.00 $32.00 | ||
Piloty's Acid acts as a nitric oxide donor by undergoing hydrolysis, which generates nitric oxide in a controlled manner. Its unique structure promotes interactions with metal ions, enhancing its reactivity and stability in various environments. The compound exhibits distinct kinetic properties, allowing for a gradual release of nitric oxide, which can be fine-tuned by altering reaction conditions. This behavior makes it an intriguing subject for studying nitric oxide dynamics in complex systems. | ||||||
GEA 5583 | sc-205946 sc-205946A | 10 mg 50 mg | $41.00 $164.00 | |||
GEA 5583 functions as a nitric oxide donor through a distinctive mechanism involving the cleavage of specific bonds, leading to the release of nitric oxide. Its molecular architecture facilitates unique interactions with biological substrates, influencing reaction pathways and enhancing its efficacy. The compound's reactivity is characterized by rapid kinetics under certain conditions, allowing for precise modulation of nitric oxide release, making it a compelling candidate for exploring redox processes in various chemical environments. | ||||||
PROLI NONOate | 178948-42-0 | sc-222190 sc-222190A sc-222190B | 10 mg 50 mg 100 mg | $45.00 $206.00 $360.00 | ||
PROLI NONOate acts as a nitric oxide donor by undergoing hydrolysis, which generates nitric oxide through a controlled release mechanism. Its structural features promote selective interactions with target molecules, influencing downstream signaling pathways. The compound exhibits notable stability in aqueous environments, allowing for sustained nitric oxide production. Its reaction kinetics are finely tuned, enabling it to participate in diverse biochemical processes while maintaining a balance between reactivity and stability. | ||||||
Fructose-SNAP-1 | sc-221631 | 5 mg | $76.00 | |||
Fructose-SNAP-1 functions as a nitric oxide donor through a unique mechanism that involves the cleavage of its ester bonds, facilitating the release of nitric oxide in a regulated manner. Its molecular structure enhances solubility and promotes specific interactions with biological targets, influencing various signaling cascades. The compound's reaction kinetics are characterized by a rapid onset of activity, while its stability in physiological conditions allows for prolonged nitric oxide availability, making it a versatile agent in biochemical contexts. | ||||||