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1285750

USP

Flurbiprofen

United States Pharmacopeia (USP) Reference Standard

Sinonimo/i:

(±)-2-Fluoro-α-methyl-4-biphenylacetic acid, L-790,330

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200 MG
CHF 391.00

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200 MG
CHF 391.00

About This Item

Formula condensata:
C6H5C6H3(F)CH(CH3)CO2H
Numero CAS:
Peso molecolare:
244.26
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

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Grado

pharmaceutical primary standard

Famiglia di API

flurbiprofen

Produttore/marchio commerciale

USP

Punto di fusione

110-112 °C (lit.)

applicazioni

pharmaceutical (small molecule)

Formato

neat

Stringa SMILE

CC(C(O)=O)c1ccc(c(F)c1)-c2ccccc2

InChI

1S/C15H13FO2/c1-10(15(17)18)12-7-8-13(14(16)9-12)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)
SYTBZMRGLBWNTM-UHFFFAOYSA-N

Informazioni sul gene

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Descrizione generale

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.
For further information and support please go to the website of the issuing Pharmacopoeia.

Applicazioni

Flurbiprofen USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia. Also, for use with USP monographs such as:
  • Flurbiprofen Tablets
  • Flurbiprofen Sodium
  • Flurbiprofen Sodium Ophthalmic Solution

Azioni biochim/fisiol

Cyclooxygenase (COX) inhibitor; non-steroidal anti-inflammatory agent with antifungal activity. The S enantiomer inhibits prostaglandin synthesis and has both anti-inflammatory and analgesic activity, while the R enantiomer does not inhibit prostaglandin synthesis and displays only analgesic activity.
Fluibiprofen is a cyclooxygenase (COX) inhibitor, which is an enzyme responsible for the conversion of arachidonic acid to prostaglandin G2 (PGG2) and PGG2 to prostaglandin H2 (PGH2) in the prostaglandin synthesis pathway. This decreases the prostaglandins which cause inflammation, pain, swelling and fever. Flurbiprofen inhibits the activity of both COX-1 and -2. The S enantiomer inhibits prostaglandin synthesis and has both anti-inflammatory and analgesic activity, while the R enantiomer does not inhibit prostaglandin synthesis and displays only analgesic activity.

Risultati analitici

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

Altre note

Sales restrictions may apply.

Pittogrammi

Skull and crossbones

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Oral

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Flurbiprofen Sodium
USP43-NF38: United States Pharmacopeia and National Formulary
United States Pharmacopeia, 48(3), 1981-1981 (2020)
Flurbiprofen Tablets
USP43-NF38: United States Pharmacopeia and National Formulary
United States Pharmacopeia, 48(3), 1980-1980 (2015)
Flurbiprofen Sodium Ophthalmic Solution
USP43-NF38: United States Pharmacopeia and National Formulary
United States Pharmacopeia, 48(3), 1982-1982 (2013)

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