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1. Castalagin
2. Vescalagin, (33beta)-isomer
3. Vescalene
4. Vescalin
1. Castalagin
2. 24312-00-3
3. 36001-47-5
4. Nsc297535
5. 7,8,9,12,13,14,25,26,27,30,31,32,35,36,37,46-hexadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone
6. Unii-bz58qsx2mq
7. Bz58qsx2mq
8. Ce78qaz4u2
9. Vescalagin, (33beta)-
10. Nsc297812
11. Nsc-297535
12. Nsc-297812
13. Nsc 297535
14. Nsc 297812
15. Unii-ce78qaz4u2
16. Chembl607711
17. Schembl12477174
18. Dtxsid201029283
19. Q5049581
| Molecular Weight | 934.6 g/mol |
|---|---|
| Molecular Formula | C41H26O26 |
| XLogP3 | 0.9 |
| Hydrogen Bond Donor Count | 16 |
| Hydrogen Bond Acceptor Count | 26 |
| Rotatable Bond Count | 0 |
| Exact Mass | 934.07123093 g/mol |
| Monoisotopic Mass | 934.07123093 g/mol |
| Topological Polar Surface Area | 455 Ų |
| Heavy Atom Count | 67 |
| Formal Charge | 0 |
| Complexity | 1960 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 5 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Vescalagin 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 Vescalagin manufacturer or Vescalagin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vescalagin manufacturer or Vescalagin supplier.
PharmaCompass also assists you with knowing the Vescalagin API Price utilized in the formulation of products. Vescalagin API Price is not always fixed or binding as the Vescalagin Price is obtained through a variety of data sources. The Vescalagin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vescalagin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vescalagin, including repackagers and relabelers. The FDA regulates Vescalagin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vescalagin 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 Vescalagin supplier is an individual or a company that provides Vescalagin active pharmaceutical ingredient (API) or Vescalagin finished formulations upon request. The Vescalagin suppliers may include Vescalagin API manufacturers, exporters, distributors and traders.
Vescalagin 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 Vescalagin 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 Vescalagin GMP manufacturer or Vescalagin GMP API supplier for your needs.
A Vescalagin CoA (Certificate of Analysis) is a formal document that attests to Vescalagin's compliance with Vescalagin specifications and serves as a tool for batch-level quality control.
Vescalagin CoA mostly includes findings from lab analyses of a specific batch. For each Vescalagin 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.
Vescalagin may be tested according to a variety of international standards, such as European Pharmacopoeia (Vescalagin EP), Vescalagin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vescalagin USP).
