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Merck

K1751

Sigma-Aldrich

Ketoprofen

Ketoprofen

≥98% (TLC), powder, non-steroidal anti-inflammatory compound

Synonym(e):

2-(3-Benzoylphenyl)-propionsäure

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1 G
€ 54,00
5 G
€ 150,00
25 G
€ 425,00
100 G
€ 943,00

About This Item

Empirische Formel (Hill-System):
C16H14O3
CAS-Nummer:
Molekulargewicht:
254.28
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:
NACRES:
NA.77

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Produktbezeichnung

Ketoprofen, ≥98% (TLC)

Biologische Quelle

synthetic

Assay

≥98% (TLC)

Form

powder

Löslichkeit

ethanol: 50 mg/mL, clear, colorless to yellow

Ersteller

Bayer

SMILES String

CC(C(O)=O)c1cccc(c1)C(=O)c2ccccc2

InChI

1S/C16H14O3/c1-11(16(18)19)13-8-5-9-14(10-13)15(17)12-6-3-2-4-7-12/h2-11H,1H3,(H,18,19)

InChIKey

DKYWVDODHFEZIM-UHFFFAOYSA-N

Angaben zum Gen

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Allgemeine Beschreibung

Ketoprofen belongs to the class of 2-arylpropionic acid.[1]

Anwendung

Ketoprofen has been used:
  • as sample to analyse the effects of long storage period by chromatographic and microscopic techniques[2]
  • as a nonselective COX inhibitor to inject subcutaneously in rats to study its effect on stress/methamphetamine hydrochloride-induced changes in occludin, claudin-5 and COX-2 protein immunoreactivity, truncation of β-dystroglycan, brain water content and fluorescein isothiocyanate-dextran extravasation[3]
  • in phosphate buffer to study its ability to inhibit heat-induced denaturation of albumin[4]

Biochem./physiol. Wirkung

Nicht-steroidaler Entzündungshemmer, selektiv für COX-1.
It serves as an efficient drug to treat ankylosing spondylitis, rheumatoid arthritis and osteoarthritis.[1] It also has antipyretic and analgesic effects. Ketoprofen prevents the action of prostaglandin synthetase.[5]

Leistungsmerkmale und Vorteile

This compound was developed by Bayer. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Piktogramme

Skull and crossbonesEnvironment

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2

Lagerklassenschlüssel

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

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Die Dokumentenbibliothek aufrufen

In vitro chiral conversion, phase separation, and wave propagation in aged profen solutions
Sajewicz M, et al.
Journal of Liquid Chromatography and Related Technologies, 32(9), 1359-1372 (2009)
Polyamidoamine dendrimers used as solubility enhancers of ketoprofen
Yiyun C, et al.
European Journal of Medicinal Chemistry, 40(12), 1390-1393 (2005)
Ekaterina Blinova et al.
Biomolecules, 11(6) (2021-07-03)
The main goal of our study was to explore the wound-healing property of a novel cerium-containing N-acethyl-6-aminohexanoate acid compound and determine key molecular targets of the compound mode of action in diabetic animals. Cerium N-acetyl-6-aminohexanoate (laboratory name LHT-8-17) as a
Ekaterina Blinova et al.
International journal of molecular sciences, 22(18) (2021-09-29)
The possible involvement of p53 signaling, FGFR3 expression, and FGFR3 mutation rates in the prediction of the NMIBC anti-PD-L1 treatment response needs to be clarified. The main aim of our study was to explore predictive value of p53 expression, FGFR3
Elisabeth Christiansen et al.
Journal of medicinal chemistry, 54(19), 6691-6703 (2011-08-23)
The free fatty acid receptor 1 (FFA1, also known as GPR40) enhances glucose-stimulated insulin secretion from pancreatic β-cells and is recognized as an interesting new target for treatment of type 2 diabetes. Several series of selective FFA1 agonists are already

Artikel

Human epithelial intestinal colonic organoids can be used as an alternative to Caco-2 drug permeability assays for drug screening and compound toxicity testing.

Discover Bioactive Small Molecules for Lipid Signaling Research

Chromatograms

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