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1. 265114-23-6
2. Cimalgex
3. Cimicoxib [inn]
4. Ur-8880
5. 4-(4-chloro-5-(3-fluoro-4-methoxyphenyl)-1h-imidazol-1-yl)benzenesulfonamide
6. W7fhj107mc
7. 4-[4-chloro-5-(3-fluoro-4-methoxyphenyl)imidazol-1-yl]benzenesulfonamide
8. Chembl435381
9. Chebi:76127
10. Cimicoxib (ema Epar: Veterinary)
11. 4-[4-chloro-5-(3-fluoro-4-methoxyphenyl)-1h-imidazol-1-yl]benzenesulfonamide
12. Ur 8880;ur-8880;ur8880
13. Benzenesulfonamide, 4-[4-chloro-5-(3-fluoro-4-methoxyphenyl)-1h-imidazol-1-yl]-
14. Unii-w7fhj107mc
15. Cimicoxib [mi]
16. Schembl3123310
17. Dtxsid30181093
18. Bcp24933
19. Zinc1494105
20. Bdbm50131593
21. Db05095
22. Ncgc00531794-01
23. Hy-100516
24. Cs-0019655
25. Q5120133
26. 4-[4-chloro-5-(3-fluoro-4-methoxy-phenyl)imidazol-1-yl]benzenesulfonamide
27. 4-[4-chloro-5-(3-fluoro-4-methoxy-phenyl)-imidazol-1-yl]-benzenesulfonamide
28. Cimicoxib;4-(4-chloro-5-(3-fluoro-4-methoxyphenyl)-1h-imidazol-1-yl)benzene Sulfonamide
Molecular Weight | 381.8 g/mol |
---|---|
Molecular Formula | C16H13ClFN3O3S |
XLogP3 | 2.9 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 4 |
Exact Mass | 381.0350183 g/mol |
Monoisotopic Mass | 381.0350183 g/mol |
Topological Polar Surface Area | 95.6 Ų |
Heavy Atom Count | 25 |
Formal Charge | 0 |
Complexity | 553 |
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 |
Investigated for use/treatment in depression.
Relief of pain and inflammation associated with osteoarthritis .
Management of peri-operative pain due to orthopaedic or soft-tissue surgeries.
QM01AH93
Depression and schizophrenia are inflammatory diseases. Increased levels of pro-inflammatory cytokines and prostaglandin E (PGE) have repeatedly been described in major depression. COX-2 inhibitors inhibit production of both. Cimicoxib is a selective COX-2 inhibitor. The mechanism by which some COX-2 inhibitors work in depression could be linked to their anti-inflammatory mechanisms.
ABOUT THIS PAGE
A Cimicoxib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cimicoxib, including repackagers and relabelers. The FDA regulates Cimicoxib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cimicoxib API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Cimicoxib supplier is an individual or a company that provides Cimicoxib active pharmaceutical ingredient (API) or Cimicoxib finished formulations upon request. The Cimicoxib suppliers may include Cimicoxib API manufacturers, exporters, distributors and traders.
Cimicoxib 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 Cimicoxib 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 Cimicoxib GMP manufacturer or Cimicoxib GMP API supplier for your needs.
A Cimicoxib CoA (Certificate of Analysis) is a formal document that attests to Cimicoxib's compliance with Cimicoxib specifications and serves as a tool for batch-level quality control.
Cimicoxib CoA mostly includes findings from lab analyses of a specific batch. For each Cimicoxib 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.
Cimicoxib may be tested according to a variety of international standards, such as European Pharmacopoeia (Cimicoxib EP), Cimicoxib JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cimicoxib USP).
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