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F0429

Sigma-Aldrich

Flunixinmeglumin

≥98% (HPLC)

Synonym(e):

2-[[2-Methyl-3-(trifluormethyl)-phenyl]-amino]-3-pyridincarbonsäure Megluminsalz, Banamine

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About This Item

Empirische Formel (Hill-System):
C14H11F3N2O2·C7H17NO5
CAS-Nummer:
42461-84-7
Molekulargewicht:
491.46
EG-Nummer:
255-836-0
MDL-Nummer:
MFCD01725419
UNSPSC-Code:
12352200
PubChem Substanz-ID:
24724478
NACRES:
NA.77

Assay

≥98% (HPLC)

Form

powder

Farbe

white to beige

mp (Schmelzpunkt)

136.6-137.4 °C

Löslichkeit

H2O: freely soluble

Lagertemp.

room temp

SMILES String

CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.Cc1c(Nc2ncccc2C(O)=O)cccc1C(F)(F)F

InChI

1S/C14H11F3N2O2.C7H17NO5/c1-8-10(14(15,16)17)5-2-6-11(8)19-12-9(13(20)21)4-3-7-18-12;1-8-2-4(10)6(12)7(13)5(11)3-9/h2-7H,1H3,(H,18,19)(H,20,21);4-13H,2-3H2,1H3/t;4-,5+,6+,7+/m.0/s1

InChIKey

MGCCHNLNRBULBU-WZTVWXICSA-N

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Anwendung

Flunixin meglumine has been used as a nonsteroidal anti-inflammatory drug standard in electrospray ionization mass spectrometry (LC-ESI/MS).
Flunixin meglumine (IC50 = 1 nM) can be used as a drug for animals for the management of intestinal ischaemia, colic, and endotoxemia in horses.

Biochem./physiol. Wirkung

Flunixin meglumine is a nonsteroidal anti-inflammatory drug, which blocks prostaglandin synthesis.
COX1, COX2 und PLA2-Inhibitor, nicht-narkotisches Schmerzmittel, antipyretisch, entzündungshemmend.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

A0257

Atropin -sulfat (Salz) Monohydrat

Aspirin meets USP testing specifications

Sigma-Aldrich

A2093

Aspirin

A J Morton et al.
Equine veterinary journal. Supplement, (39)(39), 112-116 (2011-08-04)
The effects of prostaglandins and nonsteroidal anti-inflammatory drugs (NSAIDs) on repair of equine intestinal mucosa are important since most horses with gastrointestinal diseases are routinely treated with NSAIDs, such as flunixin meglumine (FM), and these drugs can be toxic to
J Cuervo-Arango et al.
Theriogenology, 77(3), 514-524 (2011-10-01)
The development of hemorrhagic anovulatory follicles (HAF) involves luteinization and hemorrhage of the follicle. This is observed on ultrasound as an increase in the echogenicity of the granulosa layer and formation of echoic particles in the antrum. The inhibition of
E E Yeiser et al.
Journal of dairy science, 95(9), 4939-4949 (2012-08-25)
The use of flunixin meglumine (FM), a nonsteroidal antiinflammatory drug, during experimentally induced Escherichia coli mastitis was evaluated. Twenty-four primiparous and multiparous lactating dairy cows were challenged with 1×10(2) cfu of E. coli 727 in 1 uninfected quarter. Of the
J Huber et al.
Journal of dairy science, 96(1), 132-140 (2012-11-28)
Dehorning (DH) of calves is a common procedure on commercial dairy farms. Pain management of calves has been investigated in several studies. It is generally accepted that the use of local anesthesia before DH is essential for pain management. Postoperative
F L V Pinaffi et al.
Theriogenology, 78(3), 678-687 (2012-05-26)
The relationships between PRL and PGF(2α) and their effect on luteolysis were studied. Heifers were treated with a dopamine-receptor agonist (bromocriptine; Bc) and a Cox-1 and -2 inhibitor (flunixin meglumine [FM]) to inhibit PRL and PGF(2α), respectively. The Bc was
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