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Merck

SML0289

Sigma-Aldrich

Bromfenac sodium

≥98% (HPLC)

Sinónimos:

2-Amino-3-(4-bromobenzoyl)benzeneacetic acid sodium salt

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About This Item

Fórmula empírica (notación de Hill):
C15H11BrNNaO3
Número de CAS:
Peso molecular:
356.15
Número MDL:
Código UNSPSC:
12352200
ID de la sustancia en PubChem:
NACRES:
NA.77
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Nivel de calidad

Ensayo

≥98% (HPLC)

Formulario

powder

condiciones de almacenamiento

desiccated

color

faintly yellow to dark yellow

solubilidad

H2O: ≥5 mg/mL

temp. de almacenamiento

2-8°C

cadena SMILES

[Na+].Nc1c(CC([O-])=O)cccc1C(=O)c2ccc(Br)cc2

InChI

1S/C15H12BrNO3.Na/c16-11-6-4-9(5-7-11)15(20)12-3-1-2-10(14(12)17)8-13(18)19;/h1-7H,8,17H2,(H,18,19);/q;+1/p-1

Clave InChI

HZFGMQJYAFHESD-UHFFFAOYSA-M

Información sobre el gen

Aplicación

Bromfenac sodium has been used:
  • to study its ability to bind to melanin[1]
  • in the synthesis of bromfenac indolinone standard[2]
  • to analyze its permeability in porcine conjunctiva[3]

Acciones bioquímicas o fisiológicas

Bromfenac exhibits antipyretic and prostaglandin synthetase inhibiting properties.[4] It has therapeutic properties against the reduction of ocular pain and inflammation in postoperative cataract patients.[5] Bromfenac acts as an effective agent against allergic conjunctivitis.[4] It has the potential to treat acute muscle pain, osteoarthritis, and rheumatoid arthritis.[2]
Bromfenac is a nonsteroidal anti inflammatory drug (NSAID) that inhibits both COX1 and COX2. It is used as an opthalmic analgesic.
Bromfenac is a nonsteroidal anti inflammatory drug (NSAID); COX1 and COX2 inhibitor; opthalmic analgesic.

Pictogramas

Skull and crossbones

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

Acute Tox. 3 Oral

Código de clase de almacenamiento

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

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Steven M Silverstein et al.
Current medical research and opinion, 27(9), 1693-1703 (2011-07-15)
To evaluate the efficacy and ocular safety of bromfenac ophthalmic solution 0.09% dosed once daily for the treatment of ocular inflammation and pain following cataract extraction with posterior chamber intraocular lens implantation. A total of 455 subjects (455 study eyes:
James P Driscoll et al.
Chemical research in toxicology, 31(4), 223-230 (2018-03-24)
Bromfenac is a nonsteroidal anti-inflammatory drug that was approved in the United States in 1997. It was withdrawn from clinical use less than one year later, in 1998, due to hepatotoxicity. We investigate the potential of bromfenac to be metabolized
Naoko Endo et al.
Acta ophthalmologica, 88(8), 896-900 (2009-09-04)
To compare the efficacy of bromfenac sodium ophthalmic solution (BF) and a steroidal solution (ST) administered prophylactically against cystoid macular oedema and anterior-chamber inflammation after phacoemulsification and intraocular lens implantation and to assess macular thickness changes using optical coherence tomography
Sandrine A Zweifel et al.
Retina (Philadelphia, Pa.), 29(10), 1527-1531 (2009-11-10)
The purpose of this study was to assess the efficacy of topical bromfenac (0.09%) as an adjunctive therapy for patients with neovascular age-related macular degeneration demonstrating persistent exudation despite monthly intravitreal antivascular endothelial growth factor therapy. Twenty-one patients (22 eyes)
Frank A Bucci et al.
Advances in therapy, 28(12), 1089-1095 (2011-11-23)
We compared the prostaglandin E(2) (PGE(2)) inhibition of three topical nonsteroidal antiinflammatory drugs (NSAIDs): ketorolac 0.45%, bromfenac 0.09%, and nepafenac 0.1% at peak dosing levels in patients previously scheduled to undergo phacoemulsification. This was a single-center, double-masked observational study of

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