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1. 188396-77-2
2. Paliroden [inn]
3. Sr57667b
4. Palirodene
5. Palirodeno
6. Unii-17vj76l90t
7. 17vj76l90t
8. Sr5-7667b
9. 1-(2-(biphenyl-4-yl)ethyl)-4-(3-(trifluoromethyl)phenyl)-1,2,3,6-tetrahydropyridine
10. 1-(2-([1,1'-biphenyl]-4-yl)ethyl)-4-(3-(trifluoromethyl)phenyl)-1,2,3,6-tetrahydropyridine
11. Palirodenum
12. 1-(2-((1,1'-biphenyl)-4-yl)ethyl)-4-(3-(trifluoromethyl)phenyl)-1,2,3,6-tetrahydropyridine
13. 1-(2-{[1,1'-biphenyl]-4-yl}ethyl)-4-[3-(trifluoromethyl)phenyl]-1,2,3,6-tetrahydropyridine
14. 1-[2-([1,1'-biphenyl]-4-yl)ethyl]-4-[3-(trifluoromethyl)phenyl]-1,2,3,6-tetrahydropyridine
15. Refchem:169612
16. Sr57667 Base
17. 1-[2-(4-phenylphenyl)ethyl]-4-[3-(trifluoromethyl)phenyl]-3,6-dihydro-2h-pyridine
18. Orb1706848
19. Schembl4587135
20. Chembl2107767
21. Schembl29375649
22. C26h24f3n
23. Dtxsid60870180
24. Cnewkidcgdxbde-uhfffaoysa-n
25. Nha39677
26. Ex-a12275
27. Mfcd30747895
28. Akos040742362
29. Cs-6710
30. Db05454
31. Da-56559
32. Ms-26996
33. Hy-101580
34. Ns00072159
35. Q27251945
| Molecular Weight | 407.5 g/mol |
|---|---|
| Molecular Formula | C26H24F3N |
| XLogP3 | 6.6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 3.2 |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 555 |
| 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 Alzheimer's disease and Parkinson's disease.
SR 57667 may be an irreversible MAOB inhibitor.
ABOUT THIS PAGE
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PharmaCompass offers a list of Paliroden API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Paliroden manufacturer or Paliroden supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Paliroden manufacturer or Paliroden supplier.
A Paliroden manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paliroden, including repackagers and relabelers. The FDA regulates Paliroden manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paliroden 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 Paliroden supplier is an individual or a company that provides Paliroden active pharmaceutical ingredient (API) or Paliroden finished formulations upon request. The Paliroden suppliers may include Paliroden API manufacturers, exporters, distributors and traders.
Paliroden 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 Paliroden GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Paliroden GMP manufacturer or Paliroden GMP API supplier for your needs.
A Paliroden CoA (Certificate of Analysis) is a formal document that attests to Paliroden's compliance with Paliroden specifications and serves as a tool for batch-level quality control.
Paliroden CoA mostly includes findings from lab analyses of a specific batch. For each Paliroden 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.
Paliroden may be tested according to a variety of international standards, such as European Pharmacopoeia (Paliroden EP), Paliroden JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Paliroden USP).
