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1. 72755-25-0
2. F02osn86ge
3. Chebi:9109
4. 21-norsenecionan-11,16-dione, 12-hydroxy-14-methyl-, (12zeta,13zeta)-
5. (1r,5r,6r,7r,17r)-7-hydroxy-5,6,7-trimethyl-4-methylidene-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione
6. Unii-f02osn86ge
7. Ccris 4341
8. Senecivernine, Hplc Grade
9. Chembl3349185
10. Dtxsid20993566
11. Mfcd31693219
12. Hy-133591
13. Cs-0128293
14. Q27108273
15. 21-norsenecionan-11,16-dione, 12-hydroxy-14-methyl-, (14.alpha.)-
16. (4r,5r,6r,14ar,14br)-3,4,5,6,9,11,13,14,14a,14b-decahydro-6-hydroxy-4,5,6-trimethyl-3-methylene(1,6)dioxacyclododecino(2,3,4-gh)pyrrolizine-2,7-dione
| Molecular Weight | 335.4 g/mol |
|---|---|
| Molecular Formula | C18H25NO5 |
| XLogP3 | 1.2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 0 |
| Exact Mass | 335.17327290 g/mol |
| Monoisotopic Mass | 335.17327290 g/mol |
| Topological Polar Surface Area | 76.1 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 613 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 5 |
| Undefined Atom Stereocenter Count | 0 |
| 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 Senecivernine 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 Senecivernine manufacturer or Senecivernine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Senecivernine manufacturer or Senecivernine supplier.
PharmaCompass also assists you with knowing the Senecivernine API Price utilized in the formulation of products. Senecivernine API Price is not always fixed or binding as the Senecivernine Price is obtained through a variety of data sources. The Senecivernine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Senecivernine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Senecivernine, including repackagers and relabelers. The FDA regulates Senecivernine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Senecivernine 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 Senecivernine supplier is an individual or a company that provides Senecivernine active pharmaceutical ingredient (API) or Senecivernine finished formulations upon request. The Senecivernine suppliers may include Senecivernine API manufacturers, exporters, distributors and traders.
Senecivernine 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 Senecivernine 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 Senecivernine GMP manufacturer or Senecivernine GMP API supplier for your needs.
A Senecivernine CoA (Certificate of Analysis) is a formal document that attests to Senecivernine's compliance with Senecivernine specifications and serves as a tool for batch-level quality control.
Senecivernine CoA mostly includes findings from lab analyses of a specific batch. For each Senecivernine 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.
Senecivernine may be tested according to a variety of international standards, such as European Pharmacopoeia (Senecivernine EP), Senecivernine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Senecivernine USP).
