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Merck

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SML2014

Deracoxib

≥98% (HPLC)

Sinônimo(s):

4-[3-(Difluoromethyl)-5-(3-fluoro-4-methoxyphenyl)-1H-pyrazol-1-yl]benzenesulfonamide, 4-[5-(3-Fluoro-4-methoxyphenyl)-3-(difluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide, SC-046, SC-46, SC-59046

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Sobre este item

Fórmula empírica (Notação de Hill):
C17H14F3N3O3S
Número CAS:
Peso molecular:
397.37
UNSPSC Code:
12352200
NACRES:
NA.77
Assay:
≥98% (HPLC)
Form:
powder
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assay

≥98% (HPLC)

form

powder

color

white to brown

solubility

DMSO: 2 mg/mL, clear

storage temp.

room temp

SMILES string

FC(F)c1n[n](c(c1)c3cc(c(cc3)OC)F)c2ccc(cc2)[S](=O)(=O)N

InChI

1S/C17H14F3N3O3S/c1-26-16-7-2-10(8-13(16)18)15-9-14(17(19)20)22-23(15)11-3-5-12(6-4-11)27(21,24)25/h2-9,17H,1H3,(H2,21,24,25)

InChI key

WAZQAZKAZLXFMK-UHFFFAOYSA-N

Biochem/physiol Actions

Deracoxib is an orally active cyclooxygenase-2 (COX-2) inhibitor with >48-fold selectivity over COX-1 (IC50 of 203-189 nM against COX-2-dependent PGE2 production vs. IC50 of 9.85-9.96 μM against COX-1-dependent TxB2 production in dog whole blood). Deracoxib is also reported to exhibit inhibitory activity against phosphodiesterase (Ki = 3.6 μM against human PDE4D3) as well as positive modulatory effiacy toward 2-APB-stimulated transient receptor potential vanilloid 3 channel (TRPV3) activity.
Orally active COX-2 inhibitor with >48-fold selectivity over COX-1. Also inhibits PDE4D3 and enhances 2-APB-stimulated TRPV3 activity.


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Warning

Códigos de risco

Declarações de precaução

Hazard Classifications

Acute Tox. 4 Oral

Classe de armazenamento

11 - Combustible Solids

WGK

WGK 3

Ponto de inflamação (°F)

Not applicable

Ponto de inflamação (°C)

Not applicable



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Questions

  1. SML- portfolio recommended for which segments? Can we offer this to customer as INNs (International Nonproprietary Names) standards. Please also share with us the complete brochure of SML- products.

    1 answer
    1. This product is suitable for research use only. There are a number of products that are identified as 'generic' compounds, including those with the SML prefix. However, none of these compounds would be suitable for use as Active Pharmaceutical Ingredients. Unfortunately, these products have not been listed in a single brochure.

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