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Mofezolac

Mofezolac Struktur
78967-07-4
CAS-Nr.
78967-07-4
Englisch Name:
Mofezolac
Synonyma:
N-22;Disopain;Mofezolac;3,4-Bis(4-methoxyphenyl)isoxazole-5-acetic acid;3,4-Bis(4-methoxyphenyl)-5-isoxazoleacetic acid;5-Isoxazoleacetic acid, 3,4-bis(4-methoxyphenyl)-;2-(3,4-bis(4-Methoxyphenyl)isoxazol-5-yl)acetic acid;α-[3,4-Bis(4-methoxyphenyl)-5-isoxazolyl]acetic acid;2-[3,4-bis(4-methoxyphenyl)-1,2-oxazol-5-yl]acetic acid;Mofezolac,inhibit,platelet,COX,Inhibitor,aggregation,NSAID,Cyclooxygenase,pain,anti-inflammatory,COX-1,analgesic
CBNumber:
CB7875698
Summenformel:
C19H17NO5
Molgewicht:
339.34
MOL-Datei:
78967-07-4.mol

Mofezolac Eigenschaften

Schmelzpunkt:
147.5℃
Siedepunkt:
527.2±50.0 °C(Predicted)
Dichte
1.250±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
L?slichkeit
DMSO: soluble
Aggregatzustand
A solid
pka
pKa ~3.3(at 25℃)
Farbe
White to off-white
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Toxizit?t LD50 in male, female mice, male, female rats (mg/kg): 1528, 1740, 920, 887 orally; 275, 321, 378, 342 i.p.; 612, 545, 572, 510 s.c. (Satoh)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.

Mofezolac Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Mofezolac is a new non-steroidal analgesic antiinflammatory agent introduced in Japan for the treatment of post-operative and post-traumatic pain, acute upper respiratory tract pain, osteoarthritis, and lumbago. In in vfim studies, mofezolac inhibits prostaglandin biosynthesis and platelet aggregation, reportedly through the inhibition of cyclooxygenase. In animal studies, mofezolac showed more potent suppression in various writhing models than agents such as ibuprofen, mefenamic acid and aspirin. Mofezolac also has a potent inhibitory activity on the algesic responses induced by the mechanical stimulus of the inflamed tissue. The ulcerogenic effect of mofezolac on the gastric mucosa is far weaker than that of indomethacin and other agents.

Originator

Pasteur Merieux (France)

Trademarks

Disopain

Mofezolac Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Mofezolac Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 49)Lieferanten
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  • Mofezolac
  • 3,4-Bis(4-methoxyphenyl)isoxazole-5-acetic acid
  • Disopain
  • N-22
  • α-[3,4-Bis(4-methoxyphenyl)-5-isoxazolyl]acetic acid
  • 2-(3,4-bis(4-Methoxyphenyl)isoxazol-5-yl)acetic acid
  • 3,4-Bis(4-methoxyphenyl)-5-isoxazoleacetic acid
  • 5-Isoxazoleacetic acid, 3,4-bis(4-methoxyphenyl)-
  • Mofezolac,inhibit,platelet,COX,Inhibitor,aggregation,NSAID,Cyclooxygenase,pain,anti-inflammatory,COX-1,analgesic
  • 2-[3,4-bis(4-methoxyphenyl)-1,2-oxazol-5-yl]acetic acid
  • 78967-07-4
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