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1. Per977
1. 1438492-26-2
2. Per977
3. Per-977
4. Ciraparantag [usan]
5. Ciraparantag(per977)
6. U2r67kv65q
7. 1438492-26-2 (free Base)
8. Ciraparantag (usan)
9. N1,n1'-(piperazine-1,4-diylbis(propane-1,3-diyl))bis-l-argininamide
10. Pentanamide, N,n'-(1,4-piperazinediyldi-3,1-propanediyl)bis(2-amino-5-((aminoiminomethyl)amino)-, (2s,2's)-
11. Pentanamide, N,n'-(1,4-piperazinediyldi-3,1-propanediyl)bis[2-amino-5-[(aminoiminomethyl)amino]-, (2s,2's)-
12. Aripazine
13. (2s,2's)-n,n'-(piperazine-1,4-diylbis(propane-3,1-diyl))bis(2-amino-5-guanidinopentanamide)
14. Unii-u2r67kv65q
15. Per 977
16. Ciraparantag [inn]
17. Ciraparantag [who-dd]
18. Chembl3544919
19. Schembl14985871
20. Dtxsid701045783
21. Cs-5640
22. Db15199
23. Hy-18660
24. D10868
25. Q27290602
26. (2s)-2-amino-n-[3-[4-[3-[[(2s)-2-amino-5-(diaminomethylideneamino)pentanoyl]amino]propyl]piperazin-1-yl]propyl]-5-(diaminomethylideneamino)pentanamide
Molecular Weight | 512.7 g/mol |
---|---|
Molecular Formula | C22H48N12O2 |
XLogP3 | -4 |
Hydrogen Bond Donor Count | 8 |
Hydrogen Bond Acceptor Count | 8 |
Rotatable Bond Count | 18 |
Exact Mass | 512.40231882 g/mol |
Monoisotopic Mass | 512.40231882 g/mol |
Topological Polar Surface Area | 246 Ų |
Heavy Atom Count | 36 |
Formal Charge | 0 |
Complexity | 629 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 2 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Ciraparantag 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 Ciraparantag manufacturer or Ciraparantag supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ciraparantag manufacturer or Ciraparantag supplier.
PharmaCompass also assists you with knowing the Ciraparantag API Price utilized in the formulation of products. Ciraparantag API Price is not always fixed or binding as the Ciraparantag Price is obtained through a variety of data sources. The Ciraparantag Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aripazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aripazine, including repackagers and relabelers. The FDA regulates Aripazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aripazine 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 Aripazine supplier is an individual or a company that provides Aripazine active pharmaceutical ingredient (API) or Aripazine finished formulations upon request. The Aripazine suppliers may include Aripazine API manufacturers, exporters, distributors and traders.
Aripazine 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 Aripazine 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 Aripazine GMP manufacturer or Aripazine GMP API supplier for your needs.
A Aripazine CoA (Certificate of Analysis) is a formal document that attests to Aripazine's compliance with Aripazine specifications and serves as a tool for batch-level quality control.
Aripazine CoA mostly includes findings from lab analyses of a specific batch. For each Aripazine 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.
Aripazine may be tested according to a variety of international standards, such as European Pharmacopoeia (Aripazine EP), Aripazine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aripazine USP).