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1. 2-((2,6-dichlorophenyl)amino)phenylacetoxyacetic Acid
2. Airtal
3. Airtal Difucrem
4. Aital
5. Beofenac
6. Biofenac
7. Bristaflam
8. Clanza Cr
9. Falcol
10. Falcol Difucrem
11. Gerbin
12. Gerbin Difucrem
13. Preservex
14. Sanein
1. 89796-99-6
2. Preservex
3. Aceclofenaco
4. Aceclofenacum
5. Aceclofenac Betadex
6. Chebi:31159
7. 2-[2-[2-(2,6-dichloroanilino)phenyl]acetyl]oxyacetic Acid
8. Mfcd00864296
9. Airtal
10. Rpk779r03h
11. 2-(2-(2-((2,6-dichlorophenyl)amino)phenyl)acetoxy)acetic Acid
12. Ncgc00016957-01
13. Glycolic Acid [o-(2,6-dichloroanilino)phenyl]acetate Ester
14. 2-(2-(2-(2,6-dichlorophenylamino)phenyl)acetoxy)acetic Acid
15. Glycolic Acid, (o-(2,6-dichloroanilino)phenyl)acetate (ester)
16. 2-((2,6-dichlorophenyl)amino)benzeneacetic Acid Carboxymethyl Ester
17. 2-[(2,6-dichlorophenyl)amino]benzeneacetic Acid Carboxymethyl Ester
18. Cas-89796-99-6
19. Dsstox_cid_25522
20. Dsstox_rid_80928
21. Dsstox_gsid_45522
22. 2-[(2',6'-dichlorophenyl)amino]phenylacetoxyacetic Acid
23. Aceclofenacum [latin]
24. Aceclofenaco [spanish]
25. Hifenac
26. 2-[(2-{2-[(2,6-dichlorophenyl)amino]phenyl}acetyl)oxy]acetic Acid
27. Benzeneacetic Acid, 2-((2,6-dichlorophenyl)amino)-, Carboxymethyl Ester
28. Smr000718629
29. Sr-01000802972
30. Aceclofenac [inn:ban]
31. Brn 4884476
32. Unii-rpk779r03h
33. Cincofen
34. [({2-[(2,6-dichlorophenyl)amino]phenyl}acetyl)oxy]acetic Acid
35. Clanza
36. Benzeneacetic Acid, 2-[(2,6-dichlorophenyl)amino]-, Carboxymethyl Ester
37. (2-{2-[(2,6-dichlorophenyl)amino]phenyl}acetoxy)acetic Acid
38. Aceclofenac (tn)
39. Prestwick_772
40. 2-(o-(2,6-dichloranilino)phenylacetoxy)essigsaeure
41. Pr-82/3
42. Aceclofenac (jan/inn)
43. Aceclofenac [mi]
44. Prestwick0_000175
45. Prestwick1_000175
46. Prestwick2_000175
47. Prestwick3_000175
48. Aceclofenac [inn]
49. Aceclofenac [jan]
50. Aceclofenac [mart.]
51. Schembl25734
52. Aceclofenac [who-dd]
53. Bspbio_000069
54. Mls001032069
55. Mls001304028
56. Mls002154226
57. Chembl93645
58. Spbio_001990
59. Bpbio1_000077
60. Dtxsid7045522
61. Aceclofenac, >=98% (hplc)
62. Aceclofenac [ep Monograph]
63. Aceclofenac For Peak Identification
64. Hms1568d11
65. Hms2090g07
66. Hms2095d11
67. Hms2231b03
68. Hms3371a10
69. Hms3712d11
70. Hms3873i03
71. Bcp11932
72. Hy-b0634
73. Zinc3805798
74. Tox21_110710
75. Aceclofenac Betadex [who-dd]
76. Bbl010788
77. Bdbm50109016
78. S4835
79. Stk594349
80. Akos005516194
81. Tox21_110710_1
82. Ab07468
83. Ac-5282
84. Aceclofenac 1.0 Mg/ml In Acetonitrile
85. Ccg-213835
86. Db06736
87. Ks-5033
88. Ncgc00016957-02
89. Ncgc00016957-03
90. Ncgc00016957-05
91. Ba164135
92. Aceclofenac 100 Microg/ml In Acetonitrile
93. Ft-0621715
94. D01545
95. 796a996
96. Q481757
97. 2-(2,6-dichlorophenylamine)phenylacetoxyacetic Acid
98. Sr-01000802972-2
99. Sr-01000802972-3
100. 2-[2-(2,6-dichloroanilino)phenylacetoxy]acetic Acid
101. Brd-k68538666-001-03-2
102. Aceclofenac For Peak Identification, European Pharmacopoeia (ep) Reference Standard
| Molecular Weight | 354.2 g/mol |
|---|---|
| Molecular Formula | C16H13Cl2NO4 |
| XLogP3 | 4.3 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Exact Mass | 353.0221633 g/mol |
| Monoisotopic Mass | 353.0221633 g/mol |
| Topological Polar Surface Area | 75.6 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 411 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Aceclofenac is indicated for the relief of pain and inflammation in osteoarthritis, rheumatoid arthritis and ankylosing spondylitis.
Aceclofenac is a NSAID that inhibits both isoforms of COX enzyme, a key enzyme involved in the inflammatory cascade. COX-1 enzyme is a constitutive enzyme involved in prostacyclin production and protective functions of gastric mucosa whereas COX-2 is an inducible enzyme involved in the production of inflammatory mediators in response to inflammatory stimuli. Aceclofenac displays more selectivity towards COX-2 (IC50 of 0.77uM) than COX-1 (IC50 of >100uM), which promotes its gastric tolerance compared to other NSAIDs. The primary metabolite, 4'-hydroxyaceclofenac, also minimally inhibits COX-2 with IC50 value of 36uM. Although the mode of action of aceclofenac is thought to mainly arise from the inhibition of synthesis of prostaglandins (PGE2), aceclofenac also inhibits the production of inflammatory cytokines, interleukins (IL-1, IL-6), and tumor necrosis factors (TNF). It is also reported that aceclofenac also affects the cell adhesion molecules from neutrophils. Aceclofenac also targets the synthesis of glycosaminoglycan and mediates chrondroprotective effects.
Anti-Inflammatory Agents, Non-Steroidal
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.)
M01AB16
S76 | LUXPHARMA | Pharmaceuticals Marketed in Luxembourg | Pharmaceuticals marketed in Luxembourg, as published by d'Gesondheetskeess (CNS, la caisse nationale de sante, www.cns.lu), mapped by name to structures using CompTox by R. Singh et al. (in prep.). List downloaded from https://cns.public.lu/en/legislations/textes-coordonnes/liste-med-comm.html. Dataset DOI:10.5281/zenodo.4587355
M - Musculo-skeletal system
M01 - Antiinflammatory and antirheumatic products
M01A - Antiinflammatory and antirheumatic products, non-steroids
M01AB - Acetic acid derivatives and related substances
M01AB16 - Aceclofenac
M - Musculo-skeletal system
M02 - Topical products for joint and muscular pain
M02A - Topical products for joint and muscular pain
M02AA - Antiinflammatory preparations, non-steroids for topical use
M02AA25 - Aceclofenac
Absorption
Aceclofenac is rapidly and completely absorbed from the gastrointestinal tract and circulates mainly as unchanged drug following oral administration. Peak plasma concentrations are reached around 1.25 to 3 hours post-ingestion, and the drug penetrates into the synovial fluid where the concentration may reach up to 60% of that in the plasma. There is no accumulation in regular dosing, with similar maximum plasma concentration (Cmax) and time to reach peak plasma concentration (Tmax) after single and multiple doses.
Route of Elimination
The main route of elimination is via the urine where the elimination accounts for 70-80% of clearance of the drug. Approximately two thirds of the administered dose is excreted via the urine, mainly as glucuronidated and hydroxylated forms of aceclofenac. About 20% of the dose is excreted into feces.
Volume of Distribution
The volume of distribution is approximately 25 L.
Clearance
The mean clearance rate is approximately 5 L/h.
4'-hydroxyaceclofenac is the main metabolite detected in plasma however other minor metabolites include diclofenac, 5-hydroxyaceclofenac, 5-hydroxydiclofenac, and 4'-hydroxydiclofenac. It is probable that the metabolism of aceclofenac is mediated by CYP2C9.
Aceclofenac has known human metabolites that include 4'-hydroxy-aceclofenac, 5-hydroxy-aceclofenac, and diclofenac.
S73 | METXBIODB | Metabolite Reaction Database from BioTransformer | DOI:10.5281/zenodo.4056560
The mean plasma elimination half-life is approximately 4 hours.
Through COX-2 inhibition, aceclofenac downregulates the production of various inflammatory mediators including prostaglandin E2 (PGE2), IL-1, and TNF from the arachidonic acid (AA) pathway. Inhibition of IL-6 is thought to be mediated by diclofenac converted from aceclofenac. Suppressed action of inflammatory cytokines decreases the production of reactive oxygen species. Aceclofenac is shown to decreased production of nitrous oxide in human articular chondrocytes. In addition, aceclofenac interferes with neutrophil adhesion to endothelium by decreasing the expression of L-selectin (CD62L), which is a cell adhesion molecule expressed on lymphocytes. Aceclofenac is proposed to stimulate the synthesis of glycosaminoglycan in human osteoarthritic cartilage which may be mediated through its inhibitory action on IL-1 production and activity. The chrondroprotective effects are generated by 4'-hydroxyaceclofenac which suppresses IL-1 mediated production of promatrix metalloproteinase-1 and metalloproteinase-3 and interferes with the release of proteoglycan from chrondrocytes.
API SUPPLIERS
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24210
Submission : 2010-09-24
Status : Inactive
Type : II
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Certificate Number : R0-CEP 2022-180 - Rev 00
Status : Valid
Issue Date : 2022-09-01
Type : Chemical
Substance Number : 1281
Certificate Number : R1-CEP 2008-129 - Rev 01
Status : Valid
Issue Date : 2020-05-07
Type : Chemical
Substance Number : 1281
Certificate Number : R0-CEP 2022-419 - Rev 00
Status : Valid
Issue Date : 2022-12-09
Type : Chemical
Substance Number : 1281
Certificate Number : R1-CEP 2014-100 - Rev 00
Status : Valid
Issue Date : 2021-02-10
Type : Chemical
Substance Number : 1281
Certificate Number : R0-CEP 2006-050 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2009-10-14
Type : Chemical
Substance Number : 1281
Certificate Number : R1-CEP 2006-133 - Rev 01
Status : Valid
Issue Date : 2014-04-15
Type : Chemical
Substance Number : 1281
Certificate Number : CEP 2023-072 - Rev 00
Status : Valid
Issue Date : 2024-07-25
Type : Chemical
Substance Number : 1281
Certificate Number : R1-CEP 2013-274 - Rev 01
Status : Valid
Issue Date : 2021-07-20
Type : Chemical
Substance Number : 1281
Certificate Number : R1-CEP 2004-006 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2010-04-23
Type : Chemical
Substance Number : 1281
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results] EU WC
Date of Issue : 2022-08-08
Valid Till : 2025-08-09
Written Confirmation Number : WC-0253
Address of the Firm : Plot No: W-60(B), W-61(B), W-62(B),W-71(B), W-72(B), W-73(B), MIDC,Tarapur, Tal:...
Date of Issue : 2022-07-23
Valid Till : 2025-02-07
Written Confirmation Number : WC-0134
Address of the Firm : Plot No. 322/4, 40 Shed Area, GIDC, VAPI-396195, DIST. -VALSAD, GUJARAT STATE, I...
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0112nA2
Address of the Firm : Plot No. 69/A-2, GIDC Industrial Estate, Vapi, Dist -Valsad 396 195, Gujarat Sat...
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
About the Company : Kreative Organics Private Limited is a manufacturer of Active Pharmaceutical Ingredients (APIs) for the world market. Kreative started operations in 1990. Kreative was established ...
About the Company : Lunan Pharmaceutical Group is an integrated pharmaceutical group setting production, scientific research and sale of traditional Chinese medicines, chemicals, biological products i...
About the Company : Public health is always an imperative that implies immense responsibility, not a mere re-adjustable option. As a company operating under world’s second largest industry of Pharma...
About the Company : OM Pharmaceutical Industries is one of the established pharmaceutical company in India, which is engaged in manufacturing of Active Pharmaceutical Ingredients (API) and intermediat...
About the Company : Pellsys Pharma drives a new era of Value based Pharmaceutical deliverables. It is well recognized that several explicit, transparent, and consistent Production Standards including ...
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PharmaCompass offers a list of Aceclofenac API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Aceclofenac manufacturer or Aceclofenac supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aceclofenac manufacturer or Aceclofenac supplier.
PharmaCompass also assists you with knowing the Aceclofenac API Price utilized in the formulation of products. Aceclofenac API Price is not always fixed or binding as the Aceclofenac Price is obtained through a variety of data sources. The Aceclofenac Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hifenac manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hifenac, including repackagers and relabelers. The FDA regulates Hifenac manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hifenac API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Hifenac manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hifenac supplier is an individual or a company that provides Hifenac active pharmaceutical ingredient (API) or Hifenac finished formulations upon request. The Hifenac suppliers may include Hifenac API manufacturers, exporters, distributors and traders.
click here to find a list of Hifenac suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hifenac DMF (Drug Master File) is a document detailing the whole manufacturing process of Hifenac active pharmaceutical ingredient (API) in detail. Different forms of Hifenac DMFs exist exist since differing nations have different regulations, such as Hifenac USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hifenac DMF submitted to regulatory agencies in the US is known as a USDMF. Hifenac USDMF includes data on Hifenac's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hifenac USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hifenac suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Hifenac Drug Master File in Korea (Hifenac KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Hifenac. The MFDS reviews the Hifenac KDMF as part of the drug registration process and uses the information provided in the Hifenac KDMF to evaluate the safety and efficacy of the drug.
After submitting a Hifenac KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Hifenac API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Hifenac suppliers with KDMF on PharmaCompass.
A Hifenac CEP of the European Pharmacopoeia monograph is often referred to as a Hifenac Certificate of Suitability (COS). The purpose of a Hifenac CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hifenac EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hifenac to their clients by showing that a Hifenac CEP has been issued for it. The manufacturer submits a Hifenac CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hifenac CEP holder for the record. Additionally, the data presented in the Hifenac CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hifenac DMF.
A Hifenac CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hifenac CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Hifenac suppliers with CEP (COS) on PharmaCompass.
A Hifenac written confirmation (Hifenac WC) is an official document issued by a regulatory agency to a Hifenac manufacturer, verifying that the manufacturing facility of a Hifenac active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Hifenac APIs or Hifenac finished pharmaceutical products to another nation, regulatory agencies frequently require a Hifenac WC (written confirmation) as part of the regulatory process.
click here to find a list of Hifenac suppliers with Written Confirmation (WC) on PharmaCompass.
Hifenac Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Hifenac GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Hifenac GMP manufacturer or Hifenac GMP API supplier for your needs.
A Hifenac CoA (Certificate of Analysis) is a formal document that attests to Hifenac's compliance with Hifenac specifications and serves as a tool for batch-level quality control.
Hifenac CoA mostly includes findings from lab analyses of a specific batch. For each Hifenac CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Hifenac may be tested according to a variety of international standards, such as European Pharmacopoeia (Hifenac EP), Hifenac JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Hifenac USP).
