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1. Zagociguat [inn]
2. H7ken3o8ai
3. 2201048-82-8
4. Imidazo(1,2-a)pyrazine, 8-((2-fluorophenyl)methyl)-6-(5-(trifluoromethyl)-1h-1,2,4-triazol-3-yl)-
5. Imidazo[1,2-a]pyrazine, 8-[(2-fluorophenyl)methyl]-6-[5-(trifluoromethyl)-1h-1,2,4-triazol-3-yl]-
6. Unii-h7ken3o8ai
7. Zagociguat [usan]
8. Schembl19922804
9. Cy6463
10. Cy-6463
11. Iw-6463
12. Hy-145607
13. Cs-0376702
14. 8-(2-fluorobenzyl)-6-(3-(trifluoromethyl)-1h-1,2,4-triazol-5-yl)imidazo(1,2-a)pyrazine
15. 8-[(2-fluorophenyl)methyl]-6-[5-(trifluoromethyl)-1h-1,2,4-triazol-3-yl]imidazo[1,2-a]pyrazine
16. 8-[(2-fluorophenyl)methyl]-6-[5-(trifluoromethyl)-4h-1,2,4-triazol-3-yl]imidazo[1,2-a]pyrazine
| Molecular Weight | 362.28 g/mol |
|---|---|
| Molecular Formula | C16H10F4N6 |
| XLogP3 | 3.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 3 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 71.8 |
| Heavy Atom Count | 26 |
| Formal Charge | 0 |
| Complexity | 492 |
| 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 Zagociguat 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 Zagociguat manufacturer or Zagociguat supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zagociguat manufacturer or Zagociguat supplier.
PharmaCompass also assists you with knowing the Zagociguat API Price utilized in the formulation of products. Zagociguat API Price is not always fixed or binding as the Zagociguat Price is obtained through a variety of data sources. The Zagociguat Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A IW-6463 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IW-6463, including repackagers and relabelers. The FDA regulates IW-6463 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IW-6463 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 IW-6463 supplier is an individual or a company that provides IW-6463 active pharmaceutical ingredient (API) or IW-6463 finished formulations upon request. The IW-6463 suppliers may include IW-6463 API manufacturers, exporters, distributors and traders.
IW-6463 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 IW-6463 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 IW-6463 GMP manufacturer or IW-6463 GMP API supplier for your needs.
A IW-6463 CoA (Certificate of Analysis) is a formal document that attests to IW-6463's compliance with IW-6463 specifications and serves as a tool for batch-level quality control.
IW-6463 CoA mostly includes findings from lab analyses of a specific batch. For each IW-6463 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.
IW-6463 may be tested according to a variety of international standards, such as European Pharmacopoeia (IW-6463 EP), IW-6463 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (IW-6463 USP).
