X
API Suppliers
US DMFs Filed
0
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
0
USA (Orange Book)
0
Europe
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
0
U.S. Medicaid
0
Annual Reports
0
0
USFDA Orange Book Patents
0
USFDA Exclusivities
0
Blog #PharmaFlow
0
News
0
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
0
1. Beta-morpholinoethyl Niflumate
2. Niflumic Acid Beta-morpholinoethyl Ester
1. 65847-85-0
2. Up 164
3. Flomax;up 164
4. 2-morpholin-4-ylethyl 2-[3-(trifluoromethyl)anilino]pyridine-3-carboxylate
5. R133mwh7x1
6. 2-morpholinoethyl 2-((3-(trifluoromethyl)phenyl)amino)nicotinate
7. Up-164
8. Morniflumate (usan)
9. Morniflumatum
10. Morniflumate [usan]
11. Morniflumato
12. 2-(morpholin-4-yl)ethyl 2-{[3-(trifluoromethyl)phenyl]amino}pyridine-3-carboxylate
13. 3-pyridinecarboxylic Acid, 2-((3-(trifluoromethyl)phenyl)amino)-, 2-(4-morpholinylethyl) Ester
14. Morniflumate [usan:inn]
15. Morniflumatum [inn-latin]
16. Morniflumato [inn-spanish]
17. Unii-r133mwh7x1
18. Nifluminsaeure 2-morpholinoethylester
19. Niflumic Acid Beta-morpholinoethyl Ester
20. Morniflumate [inn]
21. Dsstox_cid_31587
22. Dsstox_rid_97471
23. Dsstox_gsid_57798
24. Schembl50683
25. Morniflumate [mart.]
26. Morniflumate [who-dd]
27. 2-morpholinoethyl 2-(3-trifluoromethylanilino)nicotinat
28. Chembl2105059
29. Dtxsid6057798
30. Chebi:136018
31. Tox21_113913
32. Zinc21999791
33. 2-morpholinoethyl 2-(alpha,alpha,alpha-trifluoro-m-toluidino)nicotinate
34. Akos015918126
35. Db09285
36. Ncgc00262915-01
37. As-15259
38. Hy-17488
39. Cas-65847-85-0
40. Db-054848
41. Cs-0009223
42. Ft-0628990
43. D05078
44. 847m850
45. A835248
46. Niflumic Acid .beta.-morpholinoethyl Ester
47. 2,4-dimethyl-thiazole-5-carboxylicacidamide
48. Q-201412
49. Q6912761
50. Niflumic Acid .beta.-morpholinoethyl Ester [mi]
51. 2-morpholinoethyl 2-(3-(trifluoromethyl)phenylamino)nicotinate
52. 2-morpholinoethyl2-((3-(trifluoromethyl)phenyl)amino)nicotinate
53. 2-morpholinoethyl 2-(a,a,a-trifluoro-m-toluidino)nicotinate
54. 2-[3-(trifluoromethyl)anilino]-3-pyridinecarboxylic Acid 2-(4-morpholinyl)ethyl Ester
55. 2-morpholin-4-ylethyl 2-[[3-(trifluoromethyl)phenyl]amino]pyridine-3-carboxylate
| Molecular Weight | 395.4 g/mol |
|---|---|
| Molecular Formula | C19H20F3N3O3 |
| XLogP3 | 3.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 7 |
| Exact Mass | 395.14567599 g/mol |
| Monoisotopic Mass | 395.14567599 g/mol |
| Topological Polar Surface Area | 63.7 Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 501 |
| 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 |
Morniflumate is indicated for the treatment of inflammatory conditions affecting the airways, ENT system, urogenital tract and bone and joint systems in adults. In Italy, morniflumate is also indicated for the treatment of pain associated with ear, nose, throat (ENT) and gastrointestinal inflammatory conditions in children. Morniflumate is a well established NSAID that has been in use for over three decades in Italy (particularly for the treatment of upper respiratory tract infections in children), France, Belgium, Austria, Switzerland, Spain and Portugal; it has a generally favorable tolerability profile.
Morniflumate, given at therapeutic dosages to healthy human volunteers, on leukotriene B4 (LTB4) and thromboxane (TXB2) synthesis, both in purified PMNs (polymorphnuclear neutrophils) and in whole blood. In whole blood experiments, morniflumate reduced blood leukotriene B4 (LTB4) synthesis induced by Ca-ionophore A23187 Bx approximately 50%, both after a single dose and at steady state; the level of inhibition showed a pattern similar to the plasma levels of the bioactive metabolite of morniflumate (M1). The inhibition of serum thromboxane B2 (TXB2) levels was higher than 85%. Hence, morniflumate is demonstrated to reduce arachidonic acid metabolism, by exerting its effects on cyclooxygenase and 5-lipoxygenase. This characteristic might provide a better approach for anti-inflammatory therapy. In several animal models orally administered morniflumate, the beta-morpholinoethyl ester of niflumic acid, proved almost equal to the parent compound in anti-inflammatory, analgesic and antipyretic activity with the absence of gastric irritating/ulcerogenic effects of its acidic parent compound.
M - Musculo-skeletal system
M01 - Antiinflammatory and antirheumatic products
M01A - Antiinflammatory and antirheumatic products, non-steroids
M01AX - Other antiinflammatory and antirheumatic agents, non-steroids
M01AX22 - Morniflumate
Route of Elimination
0.12 L /kg on average
Clearance
45 ml/min
The pharmacokinetic availability of niflumic acid in two different pharmaceutical preparations have been studied in 12 subjects after oral administration. Bioavailability and pharmacokinetics studies after oral and intravenous (IV) administration demonstrate that morniflumate is absorbed as from the gastrointestinal tract, followed by rapid hydrolysis in the plasma, releasing the free acidic form, the molecule responsible for its anti-inflammatory effects. The ester displays gastroprotective effect against the ulcerogenic effects of niflumic acid.
2h
The primary mechanism of niflumic acid and its ester is action is inhibition of enzymes involved in the synthesis of inflammatory prostaglandins. This medication inhibits cyclooxygenase and 5-lipoxygenase pathways, which lead to fever and inflammation. Niflumic acid, a calcium-activated Cl- channel blocker, is an analgesic and anti-inflammatory agent used in the treatment of inflammatory conditions. Niflumic acid does directly inhibit calcium channels or activate potassium channels. Niflumic acid selectively reduces noradrenaline- and 5-HT-induced pressor responses by inhibiting a mechanism which leads to the opening of voltage-gated calcium channels. Niflumic acid (NFA) produces biphasic behavior on human CLC-K channels that suggests the presence of two functionally different binding sites: an activating site and a blocking site.
Market Place
