Nepafenac
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Nepafenac
structure -
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CAS No:
78281-72-8
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Formula:
C15H14N2O2
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Chemical Name:
Nepafenac
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Synonyms:
Benzeneacetamide,2-amino-3-benzoyl-;2-Amino-3-benzoylbenzeneacetamide;AL 6515;Nepafenac;AHR 9434;Nevanac;Ilevro;2-(2-Amino-3-benzoylphenyl)acetamide
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CAS No:
Description
Nepafenac(AHR 9434; AL 6515; Nevanac) is a selective COX-2 inhibitor; is prodrug of Amfenac.IC50 value:Target: COX-2Nepafenac is a NSAID (nonsteroidal anti inflammatory drug) that is routinely used in opthamology to control pain following cataract surgery.
Solid
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.|Nepafenac is a non-steroidal anti-inflammatory prodrug (NSAID) usually sold as a prescription eye drop. It is used to treat pain and inflammation associated with cataract surgery.|Nepafenac is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of nepafenac is as a Cyclooxygenase Inhibitor.|Nepafenac is a topical nonsteroidal anti-inflammatory drug that is used in eye drops for the treatment of eye pain and swelling.
Nepafenac Basic Attributes
254.28400
254.28
0J9L7J6V8C
DTXSID0048638
C66228
S01BC10|S - Sensory organs
2924299090
Characteristics
86.18000
1.9
Solid
1.249 g/cm3
178-180 °C @ Solvent: Isopropanol
562.5ºC at 760 mmHg
294ºC
1.641
Refrigerator
Safety Information
Ⅲ
3077
3
9
60-61
N
P273
H400
|Warning|H400 (92.68%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]|P273, P391, and P501|Aggregated GHS information provided by 41 companies from 4 notifications to the ECHA C&L Inventory.
Toxicity
Ocularly applied non-steroidal anti-inflammatory drugs may cause increased bleeding of ocular tissues (including hyphemas) in conjunction with ocular surgery.
Amfenac has high affinity toward serum albumin proteins. In vitro, the percent bound to human albumin and human serum was 95.4% and 99.1% respectively.
Drug Information
For the treatment of pain and inflammation associated with cataract surgery.|FDA Label|Nevanac is indicated for:prevention and treatment of postoperative pain and inflammation associated with cataract surgery;reduction in the risk of postoperative macular oedema associated with cataract surgery in diabetic patients.|Prevention of post operative pain and inflammation associated with cataract surgery
Low but quantifiable plasma concentrations of nepafenac and amfenac were observed in the majority of subjects 2 and 3 hours postdose, respectively, following bilateral topical ocular TID dosing of nepafenac ophthalmic suspension, 0.1%. The mean steady-state Cmax for nepafenac and for amfenac were 0.310 ± 0.104 ng/ml and 0.422 ± 0.121 ng/ml, respectively, following ocular administration.
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)
Nepafenac rapidly cross the cornea (6 times faster than diclofenac in vitro).|After oral administration of 14C-nepafenac to healthy volunteers, urinary excretion was found to be the major route of radioactivity elimination, accounting for approximately 85% of the dose, while fecal excretion represented approximately 6% of the dose. Nepafenac (prodrug) and amfenac (active compound) were not quantifiable in the urine.
Nepafenac (prodrug) is deaminated to amfenac (active compound) in the ciliary body epithelium, retina, and choroid by intraocular hydrolases. Subsequently, amfenac undergoes extensive metabolism to more polar metabolites involving hydroxylation of the aromatic ring leading to glucuronide conjugate formation.
Nepafenac is a prodrug. After penetrating the cornea, nepafenac undergoes rapid bioactivation to amfenac, which is a potent NSAID that uniformly inhibits the COX1 and COX2 activity.
2-amino-3-benzoylbenzeneacetamide
Nepafenac Use and Manufacturing
Preparation of 2-amino-3-benzoylbenzeneacetamide (i.e. nepafenac, compound of formula I).This example illustrates the use of the compound (IV) Form B obtained according to the process of the invention, for preparing nepafenac.100 g of wet Raney-Ni catalyst was loaded in the filter reactor and purged with nitrogen or argon. The catalyst was washed twice with water and once with THF (the washings were done opening the bottom valve and applying argon or nitrogen pressure in the reactor). Then 25.0 g of 2-amino-3-benzoyl-α-(methylthio)benzeneacetamide (83.2 mmol; obtained in Example 3) were dissolved in a mixture of 330 mL of THF and 80 mL of water and the resulting solution was added in one portion through the addition funnel. The reaction mixture was vigorously stirred at room temperature for 10 min. The yellow solution was unloaded from the vessel and the catalyst was washed twice with 250 mL of THF. The THF solutions were combined and distilled until a volume of 250 mL. Then, 200 mL of 2-propanol were charged twice and distilled until a remaining volume of 250 mL. The solution was allowed to cool crystallizing a yellow solid which was collected by filtration. The product was dried yielding 18.2 g of yellow crystals in needle-like shape (Yield: 86percent).Analytical data: HPLC purity: 99.6percent before the purification, 99.8percent after the purification; No chlorination by-products were observed by HPLC; XRD: See FIG. 5; IR: See FIG. 6.Take 20.02g of the solid obtained in the second step, add 800mL of THF, cool down to -5 ~ 5 °C, and add 200.06g of Raney Nickel after treatment (Raney Nickel treatment: wash first with 3 X 200ml water, Then wash with 3X 200ml THF). After 0.5h of reaction, add 200ml of saturated sodium chloride solution, stand for layering, pour the upper layer liquid, filter to remove Raney Nickel, divide the filtrate into water layer, and spin down the organic layer. The spin-dried product was recrystallized by adding 500 ml of isopropanol, decrystallized at -5 ~ 5 °C for 2 hours, filtered, and dried to give 13.38 g of yellow needles. The purity by HPLC was 99.84percent and the yield was 78.8 percent.To a solution of 2-amino-3-benzoyl-α-(methylthio)phenylacetamide (26 gm) in tetrahydrofuran (340 mL) and water (80 mL), Raney nickel (wet 208 g) was added at room temperature. The mixture was stirred for 15 min and filtered through a hydrflo bed. The filtrate was concentarted under reduced pressure and the obtained solid was dissolved in isopropyl alcohol (780 mL) at about 75°-80°C. The solution was allowed to cool to room remperature and the resultant precipitate was filtered was dried at about 50-55° C under reduced pressure to afford nepafenac as yellow solid (13 g).
1. 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. Its side effects may inclu
2. Labelled Nepafenac (N390080). A non-steroidal anti-inflammatory with analgesic activity; selective COX-2 inhibitor. Prodrug of Amfenac.
Human drugs -> Nevanac -> EMA Drug Category|Ophthalmologicals -> Human pharmacotherapeutic group|Human Drugs -> EU pediatric investigation plans|Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients
Computed Properties
Molecular Weight:254.28
XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:254.105527694
Monoisotopic Mass:254.105527694
Topological Polar Surface Area:86.2
Heavy Atom Count:19
Complexity:337
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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