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1. 1192171-69-9
2. Vonafexor [inn]
3. Eyp001
4. Xg6dg6a1un
5. Vonafexor(plx007,eyp-001)
6. 4-chloro-5-[4-(2,6-dichlorophenyl)sulfonylpiperazin-1-yl]-1-benzofuran-2-carboxylic Acid
7. 2-benzofurancarboxylic Acid, 4-chloro-5-(4-((2,6-dichlorophenyl)sulfonyl)-1-piperazinyl)-
8. 4-chloro-5-(4-((2,6-dichlorophenyl)sulfonyl)piperazin-1-yl)benzofuran-2-carboxylic Acid
9. 2156704-25-3
10. Pxl007
11. Unii-xg6dg6a1un
12. Eyp-001
13. Vonafexor [who-dd]
14. Plx007
15. Schembl1893285
16. Bcp33693
17. Ex-a4037
18. Akos040759412
19. Eyp001;eyp 001;eyp-001
20. Ac-36482
21. Ms-29108
22. Hy-109197
23. Cs-0119143
24. F94108
| Molecular Weight | 489.8 g/mol |
|---|---|
| Molecular Formula | C19H15Cl3N2O5S |
| XLogP3 | 4.8 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 4 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 99.4 |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 733 |
| 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 |
Drugs in Development
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PharmaCompass offers a list of Vonafexor 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 Vonafexor manufacturer or Vonafexor supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vonafexor manufacturer or Vonafexor supplier.
PharmaCompass also assists you with knowing the Vonafexor API Price utilized in the formulation of products. Vonafexor API Price is not always fixed or binding as the Vonafexor Price is obtained through a variety of data sources. The Vonafexor Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A F94108 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of F94108, including repackagers and relabelers. The FDA regulates F94108 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. F94108 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 F94108 supplier is an individual or a company that provides F94108 active pharmaceutical ingredient (API) or F94108 finished formulations upon request. The F94108 suppliers may include F94108 API manufacturers, exporters, distributors and traders.
F94108 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 F94108 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 F94108 GMP manufacturer or F94108 GMP API supplier for your needs.
A F94108 CoA (Certificate of Analysis) is a formal document that attests to F94108's compliance with F94108 specifications and serves as a tool for batch-level quality control.
F94108 CoA mostly includes findings from lab analyses of a specific batch. For each F94108 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.
F94108 may be tested according to a variety of international standards, such as European Pharmacopoeia (F94108 EP), F94108 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (F94108 USP).
