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1. 2248726-53-4
2. Ply98man4c
3. Refchem:1077464
4. Sar-441566
5. Sar441566
6. (7r,14r)-11-[2-(1-aminocyclobutyl)-5-pyrimidinyl]-1-(difluoromethoxy)-6,7-dihydro-6-methyl-7,14-methanobenzimidazo[1,2-b][2,5]benzodiazocin-5(14h)-one
7. Balinatunfib [inn]
8. Balinatunfib [usan]
9. Tnf
10. A Activity Modulator 3
11. Orb2663617
12. Schembl19500617
13. Schembl29664455
14. Gtpl13583
15. Urofxmlqpaucgv-wojbjxkfsa-n
16. Ex-a10231
17. Hy-160412
18. G82253
19. (1r,11r)-5-[2-(1-aminocyclobutyl)pyrimidin-5-yl]-18-(difluoromethoxy)-12-methyl-2,9,12-triazapentacyclo[9.8.1.02,10.03,8.014,19]icosa-3(8),4,6,9,14(19),15,17-heptaen-13-one
20. (7r,14r)-11-[2-(1-aminocyclobutyl)pyrimidin-5-yl]-1-(difluoromethoxy)-6-methyl-6,7-dihydro-7,14-methano[1,3]benzimidazo[1,2-b][2,5]benzodiazocin-5(14h)-one
21. (7r,14r)-11-[2-(1-aminocyclobutyl)pyrimidin-5-yl]-1-(difluoromethoxy)-6-methyl-6,7-dihydro-7,14-methanobenzimidazo[1,2-b][2,5]benzodiazocin-5(14h)-one
22. 7,14-methanobenzimidazo[1,2-b][2,5]benzodiazocin-5(14h)-one, 11-[2-(1-aminocyclobutyl)-5-pyrimidinyl]-1-(difluoromethoxy)-6,7-dihydro-6-methyl-, (7r,14r)-
| Molecular Weight | 502.5 g/mol |
|---|---|
| Molecular Formula | C27H24F2N6O2 |
| XLogP3 | 2.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 4 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 99.2 |
| Heavy Atom Count | 37 |
| Formal Charge | 0 |
| Complexity | 883 |
| 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
99
PharmaCompass offers a list of Balinatunfib API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Balinatunfib manufacturer or Balinatunfib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Balinatunfib manufacturer or Balinatunfib supplier.
A Balinatunfib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Balinatunfib, including repackagers and relabelers. The FDA regulates Balinatunfib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Balinatunfib 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 Balinatunfib supplier is an individual or a company that provides Balinatunfib active pharmaceutical ingredient (API) or Balinatunfib finished formulations upon request. The Balinatunfib suppliers may include Balinatunfib API manufacturers, exporters, distributors and traders.
Balinatunfib 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 Balinatunfib GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Balinatunfib GMP manufacturer or Balinatunfib GMP API supplier for your needs.
A Balinatunfib CoA (Certificate of Analysis) is a formal document that attests to Balinatunfib's compliance with Balinatunfib specifications and serves as a tool for batch-level quality control.
Balinatunfib CoA mostly includes findings from lab analyses of a specific batch. For each Balinatunfib 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.
Balinatunfib may be tested according to a variety of international standards, such as European Pharmacopoeia (Balinatunfib EP), Balinatunfib JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Balinatunfib USP).
