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Details

Stereochemistry ACHIRAL
Molecular Formula C15H11BrNO3.Na
Molecular Weight 356.147
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BROMFENAC SODIUM ANHYDROUS

SMILES

[Na+].NC1=C(CC([O-])=O)C=CC=C1C(=O)C2=CC=C(Br)C=C2

InChI

InChIKey=HZFGMQJYAFHESD-UHFFFAOYSA-M
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

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C15H11BrNO3
Molecular Weight 333.157
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including: https://www.drugs.com/pro/bromfenac-ophthlamic-solution.html | http://www.rxlist.com/xibrom-drug.htm

Bromfenac is a topical, nonsteroidal anti-inflammatory drug (NSAID) for ophthalmic use. It is indicated for the treatment of postoperative inflammation and reduction of ocular pain in patients who have undergone cataract surgery. The mechanism of its action is thought to be due to its ability to block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2. The most commonly reported adverse reactions in 3 to 8% of patients were anterior chamber inflammation, foreign body sensation, eye pain, photophobia and vision blurred.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
5.56 nM [IC50]
7.45 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
PROLENSA

Approved Use

Bromfenac Ophthalmic Solution, 0.09% is indicated for the treatment of postoperative inflammation and reduction of ocular pain in patients who have undergone cataract surgery. Bromfenac Ophthalmic Solution is a nonsteroidal anti-inflammatory drug (NSAID) indicated for the treatment of postoperative inflammation and reduction of ocular pain in patients who have undergone cataract extraction (1).

Launch Date

2013
Primary
PROLENSA

Approved Use

Bromfenac ophthalmic solution (0.07%) is indicated for the treatment of postoperative inflammation and reduction of ocular pain in patients who have undergone cataract surgery.

Launch Date

2013
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
58.4 ng/mL
1 drop single, ocular
dose: 1 drop
route of administration: Ocular
experiment type: SINGLE
co-administered:
BROMFENAC aqueous humor
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
313.8 ng × h/mL
1 drop single, ocular
dose: 1 drop
route of administration: Ocular
experiment type: SINGLE
co-administered:
BROMFENAC aqueous humor
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
1.4 h
1 drop single, ocular
dose: 1 drop
route of administration: Ocular
experiment type: SINGLE
co-administered:
BROMFENAC aqueous humor
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
0.2%
unknown, unknown
BROMFENAC plasma
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
0.09 % 2 times / day steady, ophthalmic
Recommended
Dose: 0.09 %, 2 times / day
Route: ophthalmic
Route: steady
Dose: 0.09 %, 2 times / day
Sources:
unhealthy, 20 years
n = 1
Health Status: unhealthy
Age Group: 20 years
Sex: F
Population Size: 1
Sources:
Disc. AE: Corneal melt...
AEs leading to
discontinuation/dose reduction:
Corneal melt (1 patient)
Sources:
200 mg single, oral
Highest studied dose
Dose: 200 mg
Route: oral
Route: single
Dose: 200 mg
Sources:
unhealthy, 23.7 years
n = 21
Health Status: unhealthy
Age Group: 23.7 years
Sex: M+F
Population Size: 21
Sources:
Other AEs: Headache, Nausea...
Other AEs:
Headache (1 patient)
Nausea (1 patient)
Dizziness (2 patients)
Drowsiness (1 patient)
Vomiting (1 patient)
Hypotension (1 patient)
Sources:
25 mg 4 times / day steady, oral
Recommended
Dose: 25 mg, 4 times / day
Route: oral
Route: steady
Dose: 25 mg, 4 times / day
Sources:
unhealthy, 60 years
n = 1
Health Status: unhealthy
Age Group: 60 years
Sex: F
Population Size: 1
Sources:
Disc. AE: Hepatitis fulminant...
AEs leading to
discontinuation/dose reduction:
Hepatitis fulminant (grade 5, 1 patient)
Sources:
0.1 % single, ophthalmic
Highest studied dose
Dose: 0.1 %
Route: ophthalmic
Route: single
Dose: 0.1 %
Sources:
unhealthy, 72.2 years (range: 24–95 years)
n = 54
Health Status: unhealthy
Condition: cataract
Age Group: 72.2 years (range: 24–95 years)
Sex: M+F
Population Size: 54
Sources:
AEs

AEs

AESignificanceDosePopulation
Corneal melt 1 patient
Disc. AE
0.09 % 2 times / day steady, ophthalmic
Recommended
Dose: 0.09 %, 2 times / day
Route: ophthalmic
Route: steady
Dose: 0.09 %, 2 times / day
Sources:
unhealthy, 20 years
n = 1
Health Status: unhealthy
Age Group: 20 years
Sex: F
Population Size: 1
Sources:
Drowsiness 1 patient
200 mg single, oral
Highest studied dose
Dose: 200 mg
Route: oral
Route: single
Dose: 200 mg
Sources:
unhealthy, 23.7 years
n = 21
Health Status: unhealthy
Age Group: 23.7 years
Sex: M+F
Population Size: 21
Sources:
Headache 1 patient
200 mg single, oral
Highest studied dose
Dose: 200 mg
Route: oral
Route: single
Dose: 200 mg
Sources:
unhealthy, 23.7 years
n = 21
Health Status: unhealthy
Age Group: 23.7 years
Sex: M+F
Population Size: 21
Sources:
Hypotension 1 patient
200 mg single, oral
Highest studied dose
Dose: 200 mg
Route: oral
Route: single
Dose: 200 mg
Sources:
unhealthy, 23.7 years
n = 21
Health Status: unhealthy
Age Group: 23.7 years
Sex: M+F
Population Size: 21
Sources:
Nausea 1 patient
200 mg single, oral
Highest studied dose
Dose: 200 mg
Route: oral
Route: single
Dose: 200 mg
Sources:
unhealthy, 23.7 years
n = 21
Health Status: unhealthy
Age Group: 23.7 years
Sex: M+F
Population Size: 21
Sources:
Vomiting 1 patient
200 mg single, oral
Highest studied dose
Dose: 200 mg
Route: oral
Route: single
Dose: 200 mg
Sources:
unhealthy, 23.7 years
n = 21
Health Status: unhealthy
Age Group: 23.7 years
Sex: M+F
Population Size: 21
Sources:
Dizziness 2 patients
200 mg single, oral
Highest studied dose
Dose: 200 mg
Route: oral
Route: single
Dose: 200 mg
Sources:
unhealthy, 23.7 years
n = 21
Health Status: unhealthy
Age Group: 23.7 years
Sex: M+F
Population Size: 21
Sources:
Hepatitis fulminant grade 5, 1 patient
Disc. AE
25 mg 4 times / day steady, oral
Recommended
Dose: 25 mg, 4 times / day
Route: oral
Route: steady
Dose: 25 mg, 4 times / day
Sources:
unhealthy, 60 years
n = 1
Health Status: unhealthy
Age Group: 60 years
Sex: F
Population Size: 1
Sources:
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Effects of nonsteroidal anti-inflammatory drugs on experimental allergic conjunctivitis in Guinea pigs.
2003 Dec
Gateways to clinical trials.
2003 Jun
Effect of non-steroidal anti-inflammatory ophthalmic solution on intraocular pressure reduction by latanoprost.
2003 Mar
Drug-induced liver injury.
2004 Mar 1
Do preclinical testing strategies help predict human hepatotoxic potentials?
2005
Hepatic disorders in patients treated with COX-2 selective inhibitors or nonselective NSAIDs: a case/noncase analysis of spontaneous reports.
2006 Aug
Analgesic and anti-inflammatory effectiveness of nepafenac 0.1% for cataract surgery.
2007 Dec
A review of the use of ketorolac tromethamine 0.4% in the treatment of post-surgical inflammation following cataract and refractive surgery.
2007 Dec
Effects of topical anti-inflammatory agents in a botulinum toxin B-induced mouse model of keratoconjunctivitis sicca.
2007 Feb
Effects of nonsteroidal ophthalmic drops on epithelial healing and pain in patients undergoing bilateral photorefractive keratectomy (PRK).
2007 Nov-Dec
Cytotoxicity of ophthalmic solutions with and without preservatives to human corneal endothelial cells, epithelial cells and conjunctival epithelial cells.
2008 Aug
Ocular pharmacokinetics of a single dose of bromfenac sodium ophthalmic solution 0.1% in human aqueous humor.
2008 Dec
Development of an in vitro assay for the investigation of metabolism-induced drug hepatotoxicity.
2008 Jan
Topical ophthalmic NSAIDs: a discussion with focus on nepafenac ophthalmic suspension.
2008 Jun
Topical ocular delivery of NSAIDs.
2008 Jun
Comparison of ketorolac 0.4% and bromfenac 0.09% at trough dosing: aqueous drug absorption and prostaglandin E2 levels.
2008 Sep
Etiology and treatment of the inflammatory causes of cystoid macular edema.
2009
Randomized controlled trial design in rheumatoid arthritis: the past decade.
2009
Topical bromfenac 0.09% vs. ketorolac 0.4% for the control of pain, photophobia, and discomfort following PRK.
2009 Feb
Concentration and dosing of ketorolac versus bromfenac.
2009 Jul
Efficacy of ophthalmic nonsteroidal antiinflammatory drugs in suppressing anterior capsule contraction and secondary posterior capsule opacification.
2009 Sep
Efficacy of bromfenac sodium ophthalmic solution in preventing cystoid macular oedema after cataract surgery in patients with diabetes.
2010 Dec
In vitro approach to assess the potential for risk of idiosyncratic adverse reactions caused by candidate drugs.
2012 Aug 20
A correlation between the in vitro drug toxicity of drugs to cell lines that express human P450s and their propensity to cause liver injury in humans.
2014 Jan
Multiparametric assay using HepaRG cells for predicting drug-induced liver injury.
2015 Jul 2
Patents

Sample Use Guides

Instill one drop into the affected eye once daily beginning 1 day prior to surgery, continued on the day of surgery, and through the first 14 days postsurgery.
Route of Administration: Topical
ARPE-19 cells treated with 4X and 2X clinical doses of bromfenac ophthalmic solution (BOS) showed mean CV of 16.95±3.04% (p<0.001), and 28.45±2.33% (p0.05). The ΔΨM was decreased and the caspase 3 /7 activity increased in ARPE-19 cells treated with all BOS concentrations when compared to untreated ARPE 19 controls (15.15±1.05). The ΔΨM of ARPE-19 cells were 2.74±0.36 (p<0.001), 2.35±0.33 (p<0.001), 2.63±0.20 (p<0.001), 5.30±0.18 (p<0.001) and 5.22±0.15 (p<0.001) for 4X, 2X, X, X/2 and X/4 concentrations respectively. The ROS activity was significantly increased for all BOS concentrations when compared to untreated control. Caspase 3/7 activity was significantly increased for all BOS concentrations.
Substance Class Chemical
Created
by admin
on Sat Dec 16 07:10:46 GMT 2023
Edited
by admin
on Sat Dec 16 07:10:46 GMT 2023
Record UNII
9X8YF771OU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BROMFENAC SODIUM ANHYDROUS
Common Name English
Bromfenac sodium [WHO-DD]
Common Name English
BENZENEACETIC ACID, 2-AMINO-3-(4-BROMOBENZOYL)-, SODIUM SALT (1:1)
Common Name English
BROMFENAC MONOSODIUM SALT [MI]
Common Name English
BENZENEACETIC ACID, 2-AMINO-3-(4-BROMOBENZOYL)-, MONOSODIUM SALT
Common Name English
SODIUM (-AMINO-3-(P-BROMOBENZOYL)PHENYL)ACETATE
Common Name English
Code System Code Type Description
CAS
91714-93-1
Created by admin on Sat Dec 16 07:10:47 GMT 2023 , Edited by admin on Sat Dec 16 07:10:47 GMT 2023
PRIMARY
PUBCHEM
23693301
Created by admin on Sat Dec 16 07:10:47 GMT 2023 , Edited by admin on Sat Dec 16 07:10:47 GMT 2023
PRIMARY
EPA CompTox
DTXSID70273981
Created by admin on Sat Dec 16 07:10:47 GMT 2023 , Edited by admin on Sat Dec 16 07:10:47 GMT 2023
PRIMARY
FDA UNII
9X8YF771OU
Created by admin on Sat Dec 16 07:10:47 GMT 2023 , Edited by admin on Sat Dec 16 07:10:47 GMT 2023
PRIMARY
MERCK INDEX
m2667
Created by admin on Sat Dec 16 07:10:47 GMT 2023 , Edited by admin on Sat Dec 16 07:10:47 GMT 2023
PRIMARY
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