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Nepafenac

CAS No.
78281-72-8
Chemical Name:
Nepafenac
Synonyms
Nevanac;CS-328;AL 6515;AHR 9434;Nepafenac;Nepafanac;Nepafenac>Nepafenac API;NEPAFENAC STD;Nepafenac 98%
CBNumber:
CB01116872
Molecular Formula:
C15H14N2O2
Molecular Weight:
254.28
MDL Number:
MFCD08067732
MOL File:
78281-72-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-10 18:53:57

Nepafenac Properties

Melting point 177-181°C
Boiling point 562.5±50.0 °C(Predicted)
Density 1.249±0.06 g/cm3(Predicted)
storage temp. room temp
solubility DMSO: ≥5mg/mL
form powder
pka 16.09±0.40(Predicted)
color faint yellow to dark yellow
Water Solubility 0.014 mg/mL in water
Merck 14,6469
InChI InChI=1S/C15H14N2O2/c16-13(18)9-11-7-4-8-12(14(11)17)15(19)10-5-2-1-3-6-10/h1-8H,9,17H2,(H2,16,18)
InChIKey QEFAQIPZVLVERP-UHFFFAOYSA-N
SMILES C1(CC(N)=O)=CC=CC(C(=O)C2=CC=CC=C2)=C1N
CAS DataBase Reference 78281-72-8(CAS DataBase Reference)
FDA UNII 0J9L7J6V8C
ATC code S01BC10
UNSPSC Code 41116107
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Environment (GHS09)
GHS09
Signal word  Warning
Hazard statements  H400
Precautionary statements  P273-P391-P501
Hazard Codes  N
Risk Statements  50/53
Safety Statements  60-61
RIDADR  UN 3077 9 / PGIII
WGK Germany  3
RTECS  CY1480710
HS Code  2924.29.6250
Storage Class 11 - Combustible Solids
Hazard Classifications Aquatic Acute 1
Aquatic Chronic 1

Nepafenac price More Price(67)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML0288 Nepafenac ≥98% (HPLC) 78281-72-8 10mg $89.7 2026-04-30 Buy
Sigma-Aldrich SML0288 Nepafenac ≥98% (HPLC) 78281-72-8 50mg $348 2026-04-30 Buy
TCI Chemical N0932 Nepafenac >98.0%(HPLC)(T) 78281-72-8 200mg $122 2026-04-30 Buy
TCI Chemical N0932 Nepafenac >98.0%(HPLC)(T) 78281-72-8 1g $428 2026-04-30 Buy
Cayman Chemical 23700 Nepafenac ≥98% 78281-72-8 10mg $49 2026-04-30 Buy
Product number Packaging Price Buy
SML0288 10mg $89.7 Buy
SML0288 50mg $348 Buy
N0932 200mg $122 Buy
N0932 1g $428 Buy
23700 10mg $49 Buy

Nepafenac Chemical Properties, Uses, Production

Description

Nepafenac, launched by Alcon Laboratories, is a topical ophthalmic medication indicated for the treatment of ocular pain and inflammation associated with cataract surgery. Nepafenac is a prodrug of amfenac, which is an NSAID and a potent non-selective inhibitor of COX-1 (IC50=0.25 μM)) and COX-2 (IC50=0.15μM). Nepefenac itself exhibits only weak activity against COX-1 (IC50=64.3μM). Amfenac (Fenazox) has been marketed in Japan since 1986 for the treatment of rheumatoid arthritis, post-surgical pain, and inflammation. With most NSAIDs that are currently being used as topical ophthalmic agents, the maximum drug concentration is achieved on the ocular surface, with progressively lower concentrations in the cornea, aqueous humor, vitreous, and retina. Nepafenac has been found to have a penetration coefficient that is 4-28 times greater than that achieved with conventional NSAIDs such as diclofenac, bromofenac, and ketorolac. In addition, the bioconversion of nepefenac to amfenac is primarily mediated by ocular tissue hydrolases, specifically in the iris, ciliary body, retina, and choroid. The enhanced permeability of nepefenac combined with rapid bioactivation in the ocular tissue translates into superior anti-inflammatory efficacy at the target sites.

Chemical Properties

Nepafenac is a light Yellow Solid or powder. It is soluble in organic solvents such as ethanol, DMSO, and dimethyl formamide (DMF).

Originator

AH Robins (US)

Uses

Nepafenac is a non-steroidal anti-inflammatory drug (NSAID), usually sold as a prescription eye drop. It reduces pain and inflammation in the eyes. Nepafenac ophthalmic is used to reduce pain and swelling after cataract surgery.

Definition

ChEBI: Nepafenac is a monocarboxylic acid amide that is amfenac in which the carboxylic acid group has been converted into the corresponding carboxamide. It is a prodrug for amfenac, used in eye drops to treat pain and inflammation following cataract surgery. It has a role as a prodrug, a cyclooxygenase 2 inhibitor, a cyclooxygenase 1 inhibitor, a non-steroidal anti-inflammatory drug and a non-narcotic analgesic.

brand name

Nevanac (Alcon).

Biochem/physiol Actions

Nepafenac is a NSAID (nonsteroidal anti inflammatory drug) that is routinely used in opthamology to control pain following cataract surgery.

Clinical Use

Nepafenac is a novel ophthalmic non-steroidal anti-inflammatory drug (NSAID), for the treatment of eye pain and inflammation caused by cataract surgery, compared with traditional NSAIDs, chemical structure of Nepafenac is conducive to make it rapidly penetrate the cornea and distribute to its target site, which is helpful to reduce the accumulation of the drug in the corneal surface and to reduce the incidence of complications of the eye surface, it has many advantages such as infiltration, targeting strong, little toxic side effects and so on.
August 19, 2005 ,the US Food and Drug Administration (FDA) approved nepafenac ophthalmic suspension for the treatment of cataract surgery-related pain and inflammation, it is the first ophthalmic NSAID prodrug formulation approved for marketing.
Nepafenac after ocular administration, can rapidly pass through the cornea , and under the action of eye tissue hydrolytic enzymes,it can become into ammonia diclofenac (a kind of NSAID); and ammonia diclofenac by inhibiting prostaglandin H synthase ( cyclooxygenase), can block prostaglandin synthesis to play its role as an anti-inflammatory analgesic. As is known, prostaglandin is one of the media causing ocular inflammation it can lead to blood-aqueous barrier crash, vasodilatation, increased vascular permeability and leukocyte chemotaxis, etc. In addition, prostaglandins can also control contraction of the iris sphincter through non-cholinergic mechanism which can trigger the miosis reaction during eye surgery and after surgery. After ocular administration of NSAIDs, it can inhibit prostaglandins synthesis in the iris, ciliary body and conjunctiva, so people can prevent eye inflammation, and reduce the associated pain.
The above information is edited by the chemicalbook of Tian Ye.

Synthesis

The synthesis of nepafenac started with commercially available 2-amino-benzophenone (89). Compound 89 was reacted with t-butyl hypochrite at ¨C 65C in DCM to give a mono-N-chloroaniline (90) which was subsequently treated with methylthioacetamide in THF at ¨C65C in the same pot to give an aza-sulfonium salt 91 as a solid. Compound 91 was slurred in DCM and triethylamine was added to give sulfer ylide 92 intermediate which under-went a Sommelet-Hauser type rearrangement to give compound 93 after re-aromatization of the intermediate cyclohexadienone imine. Compound 93 was finally reduced with Raney nickel to give nepafenac (XIV) in 73% yield as yellow needles.

Synthesis_78281-72-8

Veterinary Drugs and Treatments

Nepafenac is a nonsteroidal anti-inflammatory and analgesic prodrug. After topical ocular dosing, nepafenac penetrates the cornea and is converted by ocular tissue hydrolases to amfenac, a nonsteroidal anti-inflammatory drug. Amfenac is thought to inhibit the action of prostaglandin H synthase (cyclooxygenase), an enzyme required for prostaglandin production. Nepafenac is indicated for the treatment of pain and inflammation associated with cataract surgery.

Clinical claims and research

In preclinical models, a single topical ocular dose of nepefenac (0.1%) inhibits prostaglandin synthesis in the iris/ciliary body by 85–95% for more than 6 h, and in the retina/choroid by 55% for up to at least 4 h. By comparison, diclofenac (0.1%) shows 100% inhibition of prostaglandin synthesis in the iris/ciliary body for only 20 min, with 75% recovery observed within 6 h. Diclofenac’s inhibition of prostaglandin synthesis in the retina/choroids is minimal. The recommended dose of nepafenac ophthalmic suspension is one drop in the affected eye(s) three times daily beginning one day prior to cataract surgery, continued on the day of surgery and through the first two weeks of the postoperative period. Although the drug is applied topically, low but quantifiable plasma concentrations of nepefenac and amfenac are observed in majority of the subjects following t.i.d. dosing of nepefenac ophthalmic solution. The clinical significance of the systemic absorption of nepefenac after ophthalmic administration is unknown. The efficacy of nepafenac was demonstrated in two placebo-controlled clinical studies involving over 680 patients. Nepafenac suspension was dosed three times daily, beginning one day prior to cataract surgery, continuing on the day of surgery, and for 14 days postoperatively.

Mode of action

Nepafenac is a non-steroidal anti-inflammatory and analgesic prodrug. After topical ocular dosing, nepafenac penetrates the cornea and is converted by ocular tissue hydrolases to amfenac, a nonsteroidal anti-inflammatory drug. Amfenac inhibits the action of prostaglandin H synthase (cyclooxygenase), an enzyme required for prostaglandin production.

References

[1] bucolo c1, marrazzo g, platania cb, romano gl, drago f, salomone s. effects of topical indomethacin, bromfenac and nepafenac on lipopolysaccharide-induced ocular inflammation. j pharm pharmacol. 2014 jul;66(7):954-60.
[2] marshall jc1, caissie al, cruess sr, cools-lartigue j, burnier mn jr. the effects of a cyclooxygenase-2 (cox-2) expression and inhibition on human uveal melanoma cell proliferation and macrophage nitric oxide production. j carcinog. 2007 nov 27;6:17.

78281-61-5
78281-72-8
Synthesis of Nepafenac from 2-Amino-3-benzoyl-alpha-(methylthio)benzeneacetamide

Nepafenac Preparation Products And Raw materials

Global Suppliers ( 405)
Supplier Tel Email Country ProdList Advantage
Shandong Kehui Pharmaceutical Co. LTD 0531-68651908; 13276409687 469553953@qq.com China 38 58
Jinan Hongkangda Chemical Co., Ltd 0531-88901705 18753193522 810353473@qq.com China 156 58
Hangzhou LinghepharmTechnology Co.,Ltd. +86-19521660860 18571465433 sales@linghepharm.com China 49 58
Jinan chenghui-shuangda chemical co.,ltd. 13256107535 mahaiyan1123@126.com China 118 58
TargetMol Chemicals Inc. 021-021-33632979 15002134094 marketing@targetmol.com China 7993 58
Shanghai Boyle Chemical Co., Ltd. sales@boylechem.com China 2915 55
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
ZHIWE CHEMTECH CO LTD 021-20221225 13917446399 zwchem@163.com China 524 61
Chembest Research Laboratories Limited 021-20908456 sales@BioChemBest.com China 5996 61

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View Latest Price from Nepafenac manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Nepafenac pictures 2026-09-18 Nepafenac
78281-72-8
10g 98%-101.5% 10kg WUHAN FORTUNA CHEMICAL CO., LTD
Nepafenac pictures 2026-09-17 Nepafenac
78281-72-8
0.99 RongNa Biotechnology Co.,Ltd
Nepafenac pictures 2026-09-14 Nepafenac
78281-72-8
2Kg/Bag 98.5% up / EP 20 tons Sinoway Industrial co., ltd.
  • Nepafenac pictures
  • Nepafenac
    78281-72-8
  • $0.00
  • 98%-101.5%
  • WUHAN FORTUNA CHEMICAL CO., LTD
  • Nepafenac pictures
  • Nepafenac
    78281-72-8
  • 0.99
  • RongNa Biotechnology Co.,Ltd
  • Nepafenac pictures
  • Nepafenac
    78281-72-8
  • $0.00
  • 98.5% up / EP
  • Sinoway Industrial co., ltd.

Nepafenac Spectrum

AHR 9434 AL 6515 Nevanac Nepafenac 2-(2-amino-3-benzoyl-phenyl)acetamide 2-Amino-3-benzoylbenzeneacetamide Nepafenac - WS nepafenac,Nevance Nepafanac (R)-(but-3-yn-2-yloxy)trimethylsilane Nepafenac, 99%, a selective COX-2 inhibitor CS-328 Nepafenac> Benzeneacetamide, 2-amino-3-benzoyl- Nepafenac USP/EP/BP Nepafenac API Nepafenac (AHR9434 NepafenacQ: What is Nepafenac Q: What is the CAS Number of Nepafenac Q: What is the storage condition of Nepafenac Q: What are the applications of Nepafenac Nepafenac/AHR9434/AL6515/Nevanac NEPAFENAC STD Nepafenac (200 mg) Nepafenac, 10 mM in DMSO Nepafenac 98% Napafemin Standard Sample 78281-72-8 8281-72-8 C15H9D5N2O2 Nevanac Other APIs Amines Aromatics Intermediates & Fine Chemicals Isotope Labelled Compounds Pharmaceutical intermediate Pharmaceuticals API