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1. Etc-159
2. Etc-1922159
1. Etc-159
2. 1638250-96-0
3. Etc-1922159
4. 2-(1,3-dimethyl-2,6-dioxopurin-7-yl)-n-(6-phenylpyridazin-3-yl)acetamide
5. Etc159
6. Chembl3633802
7. 5l854240dq
8. 2-(1,3-dimethyl-2,6-dioxo-2,3,6,7-tetrahydro-1h-purin-7-yl)-n-(6-phenylpyridazin-3-yl)acetamide
9. 7h-purine-7-acetamide, 1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-n-(6-phenyl-3-pyridazinyl)-
10. Unii-5l854240dq
11. Schembl17626176
12. Gtpl11168
13. Etc 159
14. Bcp20688
15. Ex-a2302
16. Bdbm50133866
17. Nsc809251
18. Zinc175660737
19. Cs-5162
20. Etc1922159
21. Nsc-809251
22. Sb18869
23. Ac-35482
24. As-74458
25. Hy-18988
26. S6616
27. A857431
28. 1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-n-(6-phenyl-3-pyridazinyl)-7h-purine-7-acetamide
| Molecular Weight | 391.4 g/mol |
|---|---|
| Molecular Formula | C19H17N7O3 |
| XLogP3 | 0.5 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 4 |
| Exact Mass | 391.13928743 g/mol |
| Monoisotopic Mass | 391.13928743 g/mol |
| Topological Polar Surface Area | 113 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 654 |
| 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 ETC-159 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 ETC-159 manufacturer or ETC-159 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred ETC-159 manufacturer or ETC-159 supplier.
PharmaCompass also assists you with knowing the ETC-159 API Price utilized in the formulation of products. ETC-159 API Price is not always fixed or binding as the ETC-159 Price is obtained through a variety of data sources. The ETC-159 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ETC 159 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ETC 159, including repackagers and relabelers. The FDA regulates ETC 159 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ETC 159 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 ETC 159 supplier is an individual or a company that provides ETC 159 active pharmaceutical ingredient (API) or ETC 159 finished formulations upon request. The ETC 159 suppliers may include ETC 159 API manufacturers, exporters, distributors and traders.
ETC 159 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 ETC 159 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 ETC 159 GMP manufacturer or ETC 159 GMP API supplier for your needs.
A ETC 159 CoA (Certificate of Analysis) is a formal document that attests to ETC 159's compliance with ETC 159 specifications and serves as a tool for batch-level quality control.
ETC 159 CoA mostly includes findings from lab analyses of a specific batch. For each ETC 159 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.
ETC 159 may be tested according to a variety of international standards, such as European Pharmacopoeia (ETC 159 EP), ETC 159 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ETC 159 USP).
