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1. Ppar
2. A Agonist
3. Ren-001 Free Acid
4. I9kp509k31
5. 942594-93-6
6. Mavodelpar
7. Mavodelpar [inn]
8. Unii-i9kp509k31
9. Schembl1746564
10. Hy-112597
11. Cs-0058426
12. (4-{[(2e)-3-(4-fluorophenyl)-3-{4-[3-(morpholin-4- Yl)prop-1-yn-1-yl]phenyl}prop-2-en-1-yl]oxy}-2- Methylphenoxy)acetic Acid
13. (e)-[4-[3-(4-fluorophenyl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]allyloxy]-2-methyl-phenoxy]acetic Acid
14. 2-[4-[[(2e)-3-(4-fluorophenyl)-3-[4-[3-(4-morpholinyl)-1-propyn-1-yl]phenyl]-2-propen-1-yl]oxy]-2-methylphenoxy]acetic Acid
15. Acetic Acid, 2-(4-(((2e)-3-(4-fluorophenyl)-3-(4-(3-(4-morpholinyl)-1-propyn-1-yl)phenyl)-2-propen-1-yl)oxy)-2-methylphenoxy)-
| Molecular Weight | 515.6 g/mol |
|---|---|
| Molecular Formula | C31H30FNO5 |
| XLogP3 | 3.5 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 10 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 68.2 |
| Heavy Atom Count | 38 |
| Formal Charge | 0 |
| Complexity | 828 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Drugs in Development
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PharmaCompass offers a list of Mavodelpar 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 Mavodelpar manufacturer or Mavodelpar supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mavodelpar manufacturer or Mavodelpar supplier.
PharmaCompass also assists you with knowing the Mavodelpar API Price utilized in the formulation of products. Mavodelpar API Price is not always fixed or binding as the Mavodelpar Price is obtained through a variety of data sources. The Mavodelpar Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mavodelpar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mavodelpar, including repackagers and relabelers. The FDA regulates Mavodelpar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mavodelpar 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 Mavodelpar supplier is an individual or a company that provides Mavodelpar active pharmaceutical ingredient (API) or Mavodelpar finished formulations upon request. The Mavodelpar suppliers may include Mavodelpar API manufacturers, exporters, distributors and traders.
Mavodelpar 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 Mavodelpar 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 Mavodelpar GMP manufacturer or Mavodelpar GMP API supplier for your needs.
A Mavodelpar CoA (Certificate of Analysis) is a formal document that attests to Mavodelpar's compliance with Mavodelpar specifications and serves as a tool for batch-level quality control.
Mavodelpar CoA mostly includes findings from lab analyses of a specific batch. For each Mavodelpar 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.
Mavodelpar may be tested according to a variety of international standards, such as European Pharmacopoeia (Mavodelpar EP), Mavodelpar JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Mavodelpar USP).
