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1. Cg-806
2. 1370466-81-1
3. 7w3fgr71nn
4. 1-(3-fluoro-4-(7-(4-methyl-1h-imidazol-2-yl)-1-oxoisoindolin-4-yl)phenyl)-3-(3-(trifluoromethyl)phenyl)urea
5. 1-[3-fluoro-4-[7-(5-methyl-1h-imidazol-2-yl)-1-oxo-2,3-dihydroisoindol-4-yl]phenyl]-3-[3-(trifluoromethyl)phenyl]urea
6. Cg-806 Analog
7. Unii-7w3fgr71nn
8. Schembl1292507
9. Glxc-26135
10. Ex-a2932
11. Nsc810717
12. Cg'806; Cg-806
13. Nsc-810717
14. Hy-112646
15. Cs-0058852
16. 1-(3-fluoro-4-(7-(5-methyl-1h-imidazol-2-yl)-1-oxo-2,3-dihydro-1h-isoindo-1-4-yl)-phenyl)-3-(3-trifluoromethyl-phenyl)-urea
17. 1-(3-fluoro-4-(7-(5-methyl-1h-imidazol-2-yl)-1-oxo-2,3-dihydro-1h-isoindo-1-4-yl)-phenyl)-3-(3-trifluoromethyl-phenyl)urea
18. Urea, N-(4-(2,3-dihydro-7-(5-methyl-1h-imidazol-2-yl)-1-oxo-1h-isoindol-4-yl)-3-fluorophenyl)-n'-(3-(trifluoromethyl)phenyl)
| Molecular Weight | 509.5 g/mol |
|---|---|
| Molecular Formula | C26H19F4N5O2 |
| XLogP3 | 4.1 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 4 |
| Exact Mass | 509.14748751 g/mol |
| Monoisotopic Mass | 509.14748751 g/mol |
| Topological Polar Surface Area | 98.9 Ų |
| Heavy Atom Count | 37 |
| Formal Charge | 0 |
| Complexity | 844 |
| 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 |
ABOUT THIS PAGE
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PharmaCompass offers a list of CG-806 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 CG-806 manufacturer or CG-806 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred CG-806 manufacturer or CG-806 supplier.
PharmaCompass also assists you with knowing the CG-806 API Price utilized in the formulation of products. CG-806 API Price is not always fixed or binding as the CG-806 Price is obtained through a variety of data sources. The CG-806 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CG-806 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CG-806, including repackagers and relabelers. The FDA regulates CG-806 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CG-806 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 CG-806 supplier is an individual or a company that provides CG-806 active pharmaceutical ingredient (API) or CG-806 finished formulations upon request. The CG-806 suppliers may include CG-806 API manufacturers, exporters, distributors and traders.
CG-806 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 CG-806 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 CG-806 GMP manufacturer or CG-806 GMP API supplier for your needs.
A CG-806 CoA (Certificate of Analysis) is a formal document that attests to CG-806's compliance with CG-806 specifications and serves as a tool for batch-level quality control.
CG-806 CoA mostly includes findings from lab analyses of a specific batch. For each CG-806 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.
CG-806 may be tested according to a variety of international standards, such as European Pharmacopoeia (CG-806 EP), CG-806 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (CG-806 USP).
