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1. Ono-9054
2. Propan-2-yl 4-(6-(4-(2,5-difluorophenoxy)-3-hydroxybut-1-en-1-yl)-7-hydroxyoctahydro-2h-cyclopenta(b)oxepin-3-yl)butanoate
3. Sepetoprost
1. Sepetaprost [inn]
2. Ono-9054
3. De-126
4. 79o7855j4g
5. 1262873-06-2
6. 2-propanyl 4-((3s,5ar,6r,7r,8as)-6-((1e,3r)-4-(2,5-difluorophenoxy)-3-hydroxy-1-buten-1-7-hydroxyoctahydro-2h-cyclopenta(b)oxepin-3-yl)butanoate
7. 2h-cyclopent(b)oxepin-3-butanoic Acid, 6-((1e,3r)-4-(2,5-difluorophenoxy)-3-hydroxy-1-buten-1-yl)octahydro-7-hydroxy-, 1-methylethyl Ester, (3s,5ar,6r,7r,8as)-
8. Sepetoprost
9. Unii-79o7855j4g
10. Sepetaprost [who-dd]
11. Gtpl9875
12. Schembl3702088
13. Chembl4297633
14. Db12043
15. Q27266770
16. Propan-2-yl 4-[(3s,5ar,6r,7r,8as)-6-[(e,3r)-4-(2,5-difluorophenoxy)-3-hydroxybut-1-enyl]-7-hydroxy-3,4,5,5a,6,7,8,8a-octahydro-2h-cyclopenta[b]oxepin-3-yl]butanoate
| Molecular Weight | 482.6 g/mol |
|---|---|
| Molecular Formula | C26H36F2O6 |
| XLogP3 | 3.8 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 11 |
| Exact Mass | 482.24799519 g/mol |
| Monoisotopic Mass | 482.24799519 g/mol |
| Topological Polar Surface Area | 85.2 Ų |
| Heavy Atom Count | 34 |
| Formal Charge | 0 |
| Complexity | 659 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 6 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
49
PharmaCompass offers a list of Sepetaprost 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 Sepetaprost manufacturer or Sepetaprost supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sepetaprost manufacturer or Sepetaprost supplier.
PharmaCompass also assists you with knowing the Sepetaprost API Price utilized in the formulation of products. Sepetaprost API Price is not always fixed or binding as the Sepetaprost Price is obtained through a variety of data sources. The Sepetaprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sepetaprost manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sepetaprost, including repackagers and relabelers. The FDA regulates Sepetaprost manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sepetaprost 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 Sepetaprost supplier is an individual or a company that provides Sepetaprost active pharmaceutical ingredient (API) or Sepetaprost finished formulations upon request. The Sepetaprost suppliers may include Sepetaprost API manufacturers, exporters, distributors and traders.
Sepetaprost 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 Sepetaprost 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 Sepetaprost GMP manufacturer or Sepetaprost GMP API supplier for your needs.
A Sepetaprost CoA (Certificate of Analysis) is a formal document that attests to Sepetaprost's compliance with Sepetaprost specifications and serves as a tool for batch-level quality control.
Sepetaprost CoA mostly includes findings from lab analyses of a specific batch. For each Sepetaprost 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.
Sepetaprost may be tested according to a variety of international standards, such as European Pharmacopoeia (Sepetaprost EP), Sepetaprost JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sepetaprost USP).
