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Home  > Inhibitors/Agonists  > Immunology/Inflammation  > NADPH Oxidase  > 2-(2-Chlorophenyl)-4-(3-(dimethylamino)phenyl)-5-methyl-1h-pyrazolo[4,3-c]pyridine-3,6(2h,5h)-dione

AA54663

1218942-37-0 | 2-(2-Chlorophenyl)-4-(3-(dimethylamino)phenyl)-5-methyl-1h-pyrazolo[4,3-c]pyridine-3,6(2h,5h)-dione

Packsize Purity Availability Price Discounted Price    Quantity
1mg 95% in stock $42.00 $29.00 -   +
5mg 95% in stock $78.00 $55.00 -   +
100mg 95% in stock $114.00 $80.00 -   +
250mg 95% in stock $187.00 $131.00 -   +
1g 95% in stock $488.00 $342.00 -   +
5g 95% in stock $2,384.00 $1,669.00 -   +

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*All prices are in USD.

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Description
Catalog Number: AA54663
Chemical Name: 2-(2-Chlorophenyl)-4-(3-(dimethylamino)phenyl)-5-methyl-1h-pyrazolo[4,3-c]pyridine-3,6(2h,5h)-dione
CAS Number: 1218942-37-0
Molecular Formula: C21H19ClN4O2
Molecular Weight: 394.8542
MDL Number: MFCD27923122
SMILES: Clc1ccccc1n1[nH]c2c(c1=O)c(c1cccc(c1)N(C)C)n(c(=O)c2)C

 

Computed Properties
Complexity: 732  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 28  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 3.2  

 

 

Upstream Synthesis Route 
  • GKT-137831 is a potent and selective inhibitor of NADPH oxidase and nitric oxide synthases. In chemical synthesis, this compound can be utilized as a powerful tool for studying oxidative stress-related pathways and mechanisms. Its ability to specifically target and inhibit key enzymes involved in the production of reactive oxygen species and nitric oxide makes it valuable in investigating redox signaling pathways and their implications in various chemical processes. Researchers can use GKT-137831 to explore the role of oxidative stress in chemical reactions, elucidate signaling cascades affected by reactive oxygen species, and develop strategies for modulating these pathways in synthetic applications. With its targeted action and high potency, GKT-137831 offers a promising avenue for advancing the understanding and manipulation of oxidative stress in chemical synthesis.
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