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1. Crn04894
2. 2392970-97-5
3. Chembl5414447
4. N-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(2-ethoxyphenyl)-3-[(2r)-2-ethyl-4-[1-(trifluoromethyl)cyclobutanecarbonyl]piperazin-1-yl]pyridine-2-carboxamide
5. Atumelnant [inn]
6. Nr57fh6u1n
7. Schembl21700563
8. Gtpl13339
9. Qjrfbkyetdvajq-zeqkjwhpsa-n
10. Crn-0489
11. Bdbm50623115
12. Crn04894?
13. Ex-a10367
14. At43038
15. Compound 17h [pmid: 38628803]
16. Hy-158081
17. Cs-1038003
18. 2-pyridinecarboxamide, N-(3s)-1-azabicyclo[2.2.2]oct-3-yl-6-(2-ethoxyphenyl)-3-[(2r)-2-ethyl-4-[[1-(trifluoromethyl)cyclobutyl]carbonyl]-1-piperazinyl]-
19. N-(3s)-1-azabicyclo[2.2.2]oct-3-yl-6-(2-ethoxyphenyl)-3-[(2r)-2-ethyl-4-[[1-(trifluoromethyl)cyclobutyl]carbonyl]-1-piperazinyl]-2-pyridinecarboxamide
20. N-[(3s)-1-azabicyclo[2.2.2]octan-3-yl]-6-(2-ethoxyphenyl)-3-{(2r)-2-ethyl-4-[1-(trifluoromethyl)cyclobutane-1-carbonyl]piperazin-1-yl}pyridine-2-carboxamide
| Molecular Weight | 613.7 g/mol |
|---|---|
| Molecular Formula | C33H42F3N5O3 |
| XLogP3 | 5.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 8 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 78 |
| Heavy Atom Count | 44 |
| Formal Charge | 0 |
| Complexity | 1020 |
| 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
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PharmaCompass offers a list of Atumelnant 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 Atumelnant manufacturer or Atumelnant supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Atumelnant manufacturer or Atumelnant supplier.
PharmaCompass also assists you with knowing the Atumelnant API Price utilized in the formulation of products. Atumelnant API Price is not always fixed or binding as the Atumelnant Price is obtained through a variety of data sources. The Atumelnant Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Atumelnant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atumelnant, including repackagers and relabelers. The FDA regulates Atumelnant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atumelnant 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 Atumelnant supplier is an individual or a company that provides Atumelnant active pharmaceutical ingredient (API) or Atumelnant finished formulations upon request. The Atumelnant suppliers may include Atumelnant API manufacturers, exporters, distributors and traders.
Atumelnant 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 Atumelnant 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 Atumelnant GMP manufacturer or Atumelnant GMP API supplier for your needs.
A Atumelnant CoA (Certificate of Analysis) is a formal document that attests to Atumelnant's compliance with Atumelnant specifications and serves as a tool for batch-level quality control.
Atumelnant CoA mostly includes findings from lab analyses of a specific batch. For each Atumelnant 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.
Atumelnant may be tested according to a variety of international standards, such as European Pharmacopoeia (Atumelnant EP), Atumelnant JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Atumelnant USP).
