Nitric Oxide Donors
Items 41 to 50 of 56 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
BNN3 | 6947-38-2 | sc-202977 | 1 mg | $330.00 | ||
BNN3 is a novel nitric oxide donor featuring a unique bicyclic structure that promotes efficient NO release through a distinct mechanism involving electron transfer. Its design incorporates specific functional groups that stabilize reactive intermediates, leading to accelerated reaction kinetics. The compound's ability to engage in selective interactions with biological targets is influenced by its conformational flexibility, allowing for precise modulation of nitric oxide levels in diverse environments. | ||||||
3-(Methylnitrosamino)propionitrile | 60153-49-3 | sc-391794 | 250 mg | $300.00 | ||
3-(Methylnitrosamino)propionitrile is a distinctive nitric oxide donor known for its intricate molecular structure that promotes efficient NO release through specific catalytic pathways. Its reactivity is influenced by the presence of electron-withdrawing groups, which modulate the kinetics of nitric oxide generation. The compound's ability to engage in selective interactions with biological macromolecules highlights its potential for nuanced modulation of redox signaling, making it a subject of interest in chemical research. | ||||||
S-Nitrosocaptopril | 122130-63-6 | sc-222277 sc-222277A | 10 mg 50 mg | $67.00 $253.00 | ||
S-Nitrosocaptopril is a notable nitric oxide donor characterized by its unique S-nitrosothiol structure, which facilitates the release of nitric oxide via thiol-disulfide exchange reactions. This compound exhibits distinct reactivity patterns influenced by steric and electronic factors, allowing for controlled NO delivery. Its interactions with metal ions can enhance its stability and reactivity, making it a fascinating subject for studies on redox biology and signaling pathways. | ||||||
NOR-2 | 163032-71-1 | sc-202737 sc-202737A | 5 mg 10 mg | $200.00 $400.00 | ||
NOR-2 is a distinctive nitric oxide donor that operates through a unique mechanism involving the cleavage of N-O bonds, leading to the release of nitric oxide. Its reactivity is influenced by the presence of electron-withdrawing groups, which modulate its kinetics and stability. The compound's ability to engage in specific molecular interactions with biological targets enhances its potential for selective NO release, making it an intriguing candidate for exploring cellular signaling dynamics. | ||||||
V-PYRRO/NO | 179344-98-0 | sc-205538 sc-205538A | 5 mg 10 mg | $34.00 $60.00 | 1 | |
V-PYRRO/NO is a specialized nitric oxide donor characterized by its ability to release nitric oxide via a controlled decomposition pathway. This compound exhibits unique reactivity due to its structural features, which facilitate interactions with reactive species in its environment. The presence of specific functional groups influences its stability and reaction kinetics, allowing for tailored release profiles. Its distinct molecular interactions contribute to its role in modulating redox states and influencing various biochemical processes. | ||||||
SE 175 | 258278-64-7 | sc-205506 sc-205506A | 5 mg 10 mg | $60.00 $114.00 | ||
SE 175 is a distinctive nitric oxide donor that operates through a unique mechanism of action, enabling the selective release of nitric oxide under specific conditions. Its molecular architecture promotes interactions with cellular components, enhancing its reactivity. The compound's kinetic profile is influenced by its electronic structure, allowing for precise modulation of nitric oxide release rates. This behavior facilitates intricate signaling pathways, impacting various biological systems through its dynamic interactions. | ||||||
L-NMMA (citrate) | sc-364686 sc-364686A sc-364686B | 10 mg 50 mg 100 mg | $57.00 $257.00 $459.00 | 1 | ||
L-NMMA (citrate) is a specialized nitric oxide donor characterized by its ability to modulate nitric oxide synthesis through competitive inhibition of nitric oxide synthase. Its structural features enable it to engage in specific hydrogen bonding interactions, influencing its solubility and reactivity in biological environments. The compound exhibits unique reaction kinetics, allowing for controlled release of nitric oxide, which can affect cellular signaling and regulatory mechanisms in diverse contexts. | ||||||
NO-Indomethacin | 301838-28-8 | sc-205414 sc-205414A sc-205414B sc-205414C | 1 mg 5 mg 10 mg 50 mg | $25.00 $108.00 $192.00 $849.00 | ||
NO-Indomethacin functions as a specialized nitric oxide donor, characterized by its unique structural features that influence its reactivity. The presence of an indole moiety enhances its ability to engage in electron transfer processes, facilitating the release of nitric oxide. This compound exhibits distinct reaction kinetics, with a propensity for rapid decomposition under certain conditions, leading to a controlled release of nitric oxide. Its interactions with biological membranes can also alter permeability, impacting cellular signaling pathways. | ||||||
Lansoprazole Sulfone N-Oxide | 953787-54-7 | sc-211719 | 1 mg | $430.00 | ||
Lansoprazole Sulfone N-Oxide serves as a distinctive nitric oxide donor, exhibiting unique molecular interactions that enhance its reactivity. Its sulfone group facilitates electron delocalization, promoting efficient nitric oxide release through specific pathways. The compound's stability under varying pH conditions allows for tailored release profiles, influencing its kinetics. Additionally, its ability to form transient complexes with metal ions can modulate redox reactions, further diversifying its biochemical impact. | ||||||
N-Nitrosodiethylamine | 55-18-5 | sc-257861 sc-257861A | 5 ml 25 ml | $136.00 $362.00 | 1 | |
N-Nitrosodiethylamine serves as a notable nitric oxide donor, distinguished by its unique nitrosamine structure that promotes selective reactivity. Its electron-rich nitrogen atoms facilitate the generation of nitric oxide through specific cleavage pathways. The compound exhibits intriguing reaction kinetics, often undergoing rapid transformations in various environments. Additionally, its hydrophobic characteristics influence membrane interactions, potentially modulating cellular responses and signaling cascades. | ||||||