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1. S-222611
1. 908305-13-5
2. Epertinib [inn]
3. 60oik33zqr
4. 2-butyn-1-one, 1-(4-((3-chloro-4-((3-fluorophenyl)methoxy)phenyl)amino)-6-quinazolinyl)-, O-((3r)-3-morpholinylmethyl)oxime, (1z)-
5. N-(3-chloro-4-((3-fluorophenyl)methoxy)phenyl)- 6-((1z)-n-(((3r)-morpholin-3-yl)methoxy)but- 2-ynimidoyl)quinazolin-4-amine
6. N-[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[(z)-n-[[(3r)-morpholin-3-yl]methoxy]-c-prop-1-ynylcarbonimidoyl]quinazolin-4-amine
7. S-22611,epertinib
8. Unii-60oik33zqr
9. Epertinib [who-dd]
10. Schembl9973640
11. Ex-a2701
12. Nsc804521
13. Nsc-804521
14. Ac-36534
15. Hy-107367
16. Cs-0028218
17. S222611
18. S-222611
19. 1831116-77-8
| Molecular Weight | 560.0 g/mol |
|---|---|
| Molecular Formula | C30H27ClFN5O3 |
| XLogP3 | 6.1 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 10 |
| Exact Mass | 559.1786456 g/mol |
| Monoisotopic Mass | 559.1786456 g/mol |
| Topological Polar Surface Area | 89.9 Ų |
| Heavy Atom Count | 40 |
| Formal Charge | 0 |
| Complexity | 899 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Epertinib 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 Epertinib manufacturer or Epertinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Epertinib manufacturer or Epertinib supplier.
PharmaCompass also assists you with knowing the Epertinib API Price utilized in the formulation of products. Epertinib API Price is not always fixed or binding as the Epertinib Price is obtained through a variety of data sources. The Epertinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Epertinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Epertinib, including repackagers and relabelers. The FDA regulates Epertinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Epertinib 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 Epertinib supplier is an individual or a company that provides Epertinib active pharmaceutical ingredient (API) or Epertinib finished formulations upon request. The Epertinib suppliers may include Epertinib API manufacturers, exporters, distributors and traders.
Epertinib 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 Epertinib 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 Epertinib GMP manufacturer or Epertinib GMP API supplier for your needs.
A Epertinib CoA (Certificate of Analysis) is a formal document that attests to Epertinib's compliance with Epertinib specifications and serves as a tool for batch-level quality control.
Epertinib CoA mostly includes findings from lab analyses of a specific batch. For each Epertinib 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.
Epertinib may be tested according to a variety of international standards, such as European Pharmacopoeia (Epertinib EP), Epertinib JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Epertinib USP).
