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N-(3-PYRIDYL)-INDOMETHACIN AMIDE

Product Name
N-(3-PYRIDYL)-INDOMETHACIN AMIDE
CAS No.
261766-29-4
Chemical Name
N-(3-PYRIDYL)-INDOMETHACIN AMIDE
Synonyms
N-3PYIA;Indomethacin N-Pyridyl Impurity;N-(3-PYRIDYL)-INDOMETHACIN AMIDE;N-(3-PYRIDYL)-1-P-CHLOROBENZOYL-5-METHOXY-2-METHYLINDOLE-3-ACETAMIDE;N-(3-PYRIDYL)-1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOLE-3-ACETAMIDE;1-(4-Chlorobenzoyl)-5-Methoxy-2-Methyl-N-3-pyridinyl-1H-indole-3-acetaMide;1H-Indole-3-acetamide, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-N-3-pyridinyl-;2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]-N-pyridin-3-ylacetamide;N-3PyIA, N-(3-Pyridyl)-1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetamide
CBNumber
CB7244320
Molecular Formula
C24H20ClN3O3
Formula Weight
433.89
MOL File
Mol file
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N-(3-PYRIDYL)-INDOMETHACIN AMIDE Property

storage temp. 
−20°C
solubility 
≤3mg/ml in ethanol;3mg/ml in DMSO;3mg/ml in dimethyl formamide
form 
crystalline solid
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Safety

WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
P0865
Product name
N-(3-Pyridyl)indomethacinamide
Purity
≥98%
Packaging
5MG
Price
$280
Updated
2023/01/07
Cayman Chemical
Product number
70274
Product name
N-(3-pyridyl)-Indomethacin amide
Purity
≥98%
Packaging
1mg
Price
$18
Updated
2024/03/01
Cayman Chemical
Product number
70274
Product name
N-(3-pyridyl)-Indomethacin amide
Purity
≥98%
Packaging
5mg
Price
$73
Updated
2024/03/01
Cayman Chemical
Product number
70274
Product name
N-(3-pyridyl)-Indomethacin amide
Purity
≥98%
Packaging
10mg
Price
$129
Updated
2024/03/01
Cayman Chemical
Product number
70274
Product name
N-(3-pyridyl)-Indomethacin amide
Purity
≥98%
Packaging
50mg
Price
$553
Updated
2024/03/01
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N-(3-PYRIDYL)-INDOMETHACIN AMIDE Chemical Properties,Usage,Production

Uses

An aromatic amide of indomethacin recently reported to be a potent and selective reversible inhibitor of COX-2. Inhibits human recombinant COX-2 with IC50 of 0.1 uM.

Biological Activity

n-(3-pyridyl)-indomethacin amide is a reversible, potent and selective cox-2 inhibitor [1].cyclooxygenase (cox) is an enzyme responsible for formation of prostanoids, including thromboxane and prostaglandins such as prostacyclin. cox-1 is the constitutive isoform and is mainly responsible for the synthesis of cytoprotective prostaglandins in the gastrointestinal tract (gi) and of the proaggregatory thromboxane in blood platelets. cox-2 is inducible and short-lived that is stimulated by endotoxin, cytokines, and mitogens. cox-2 plays important roles in prostaglandin biosynthesis in inflammatory cells the central nervous system [1].n-(3-pyridyl)-indomethacin amide (n-3pyia) is a reversible, potent and selective cox-2 inhibitor that inhibits human recombinant cox-2 and ovine cox-1 with ic50 values of 0.052 and >66 μm, respectively. it is over 1300 times less potent as an inhibitor of ovine cox-1. n-(3-pyridyl)-indomethacin amide is the 3-pyridyl amide derivative of indomethacin that shows selective against cox-2 [1].

References

[1]. kalgutkar as, marnett ab, crews bc, et al. ester and amide derivatives of the nonsteroidal antiinflammatory drug, indomethacin, as selective cyclooxygenase-2 inhibitors. j med chem. 2000 jul 27;43(15):2860-70.

N-(3-PYRIDYL)-INDOMETHACIN AMIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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N-(3-PYRIDYL)-INDOMETHACIN AMIDE Suppliers

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261766-29-4, N-(3-PYRIDYL)-INDOMETHACIN AMIDERelated Search:


  • N-(3-PYRIDYL)-1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOLE-3-ACETAMIDE
  • N-(3-PYRIDYL)-1-P-CHLOROBENZOYL-5-METHOXY-2-METHYLINDOLE-3-ACETAMIDE
  • N-(3-PYRIDYL)-INDOMETHACIN AMIDE
  • N-3PYIA
  • N-3PyIA, N-(3-Pyridyl)-1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetamide
  • 1-(4-Chlorobenzoyl)-5-Methoxy-2-Methyl-N-3-pyridinyl-1H-indole-3-acetaMide
  • 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]-N-pyridin-3-ylacetamide
  • Indomethacin N-Pyridyl Impurity
  • 1H-Indole-3-acetamide, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-N-3-pyridinyl-
  • 261766-29-4
  • 261755-29-4
  • C24H20N3O3Cl
  • C24H20ClN3O3
  • Inhibitors