Nitric Oxide Donors
Items 51 to 56 of 56 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
N,N-Dicarboxymethyl-N,N-dinitroso-p-phenylenediamine, Disodium Salt | 1042969-16-3 | sc-219273 sc-219273A | 1 mg 5 mg | $320.00 $1300.00 | ||
N,N-Dicarboxymethyl-N,N-dinitroso-p-phenylenediamine, Disodium Salt, acts as a potent nitric oxide donor, characterized by its dual nitroso groups that enhance reactivity. The compound's unique carboxymethyl substituents facilitate solubility in aqueous environments, promoting efficient release of nitric oxide. Its distinct electron distribution allows for controlled reaction kinetics, enabling selective interactions with biological targets. This compound's structural features contribute to its dynamic behavior in various chemical contexts. | ||||||
NO-Aspirin 1 | 175033-36-0 | sc-212401A sc-212401 sc-212401B | 5 mg 25 mg 100 mg | $190.00 $320.00 $1030.00 | 1 | |
NO-Aspirin 1 is a specialized nitric oxide donor distinguished by its unique structural framework that promotes rapid NO release. The presence of specific functional groups enhances its reactivity, allowing for efficient interaction with cellular components. Its ability to modulate electron density facilitates diverse reaction pathways, leading to selective activation of signaling mechanisms. This compound's innovative design supports its role in dynamic chemical environments, showcasing its versatility in nitric oxide delivery. | ||||||
Glyco-SNAP-2 | 188849-82-3 | sc-218911 sc-218911A | 10 mg 50 mg | $153.00 $765.00 | ||
Glyco-SNAP-2 is a distinctive nitric oxide donor characterized by its innovative molecular architecture, which enables controlled NO release through specific enzymatic pathways. Its unique functional groups enhance solubility and reactivity, allowing for targeted interactions with biological substrates. The compound exhibits remarkable stability under physiological conditions, while its kinetic profile supports rapid NO generation, making it an intriguing candidate for exploring diverse biochemical processes. | ||||||
Tricarbonyldichlororuthenium(II) dimer | 22594-69-0 | sc-229558 | 500 mg | $143.00 | 1 | |
Tricarbonyldichlororuthenium(II) dimer stands out as a nitric oxide donor due to its unique coordination chemistry and metal-ligand interactions. The ruthenium center facilitates the release of nitric oxide through a series of ligand exchange reactions, promoting efficient NO liberation. Its distinct electronic properties enhance reactivity, while the dimeric structure contributes to stability and controlled release kinetics, making it a fascinating subject for studying metal-mediated NO dynamics. | ||||||
N-Ethyl-N-nitroso-1-propanamine-d4 | 25413-61-0 (unlabeled) | sc-496784 sc-496784A | 2.5 mg 25 mg | $340.00 $2400.00 | ||
N-Ethyl-N-nitroso-1-propanamine-d4 is a distinctive nitroso compound characterized by its ability to release nitric oxide, a crucial signaling molecule. Its deuterated structure enhances stability and allows for precise tracking in kinetic studies. The compound engages in specific interactions with metal ions, influencing redox reactions and cellular signaling pathways. Its unique reactivity profile facilitates the exploration of nitric oxide's role in various biochemical processes, shedding light on its complex behavior in biological systems. | ||||||
N-Acetyl-D,L-penicillamine disulfide | sc-205957 sc-205957A | 1 mg 5 mg | $36.00 $91.00 | 1 | ||
N-Acetyl-D,L-penicillamine disulfide acts as a nitric oxide donor, showcasing unique redox properties that facilitate the release of nitric oxide in biological systems. Its disulfide bond plays a crucial role in electron transfer processes, promoting reactive nitrogen species formation. The compound's ability to undergo thiol-disulfide exchange reactions enhances its reactivity, allowing for specific interactions with cellular targets. This dynamic behavior influences signaling pathways and modulates oxidative stress responses. | ||||||