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1. Elismetrep [inn]
2. Elismetrep [usan]
3. Kib8v5ur7d
4. Mt-8554
5. 1400699-64-0
6. 4-(((4-cyclopropyl-3-isoquinolinyl)((4-(trifluoromethoxy)phenyl)methyl)amino)sulfonyl)benzoic Acid
7. Benzoic Acid, 4-(((4-cyclopropyl-3-isoquinolinyl)((4-(trifluoromethoxy)phenyl)methyl)amino)sulfonyl)-
8. Elismetrep (usan/inn)
9. Elismetrep [usan:inn]
10. Unii-kib8v5ur7d
11. Gtpl9774
12. Chembl3682589
13. Schembl12490163
14. Bdbm151677
15. Bcp30294
16. Who 10708
17. Db15287
18. Example 104 [wo2012124825]
19. D11448
20. Us8987445, 104
21. 4-((4-cyclopropylisoquinolin-3-yl) (4-(trifluoromethoxy) Benzyl) Sulfamoyl) Benzoic Acid
22. 4-[(4-cyclopropylisoquinolin-3-yl)-[[4-(trifluoromethoxy)phenyl]methyl]sulfamoyl]benzoic Acid
| Molecular Weight | 542.5 g/mol |
|---|---|
| Molecular Formula | C27H21F3N2O5S |
| XLogP3 | 6.3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 8 |
| Exact Mass | 542.11232743 g/mol |
| Monoisotopic Mass | 542.11232743 g/mol |
| Topological Polar Surface Area | 105 Ų |
| Heavy Atom Count | 38 |
| Formal Charge | 0 |
| Complexity | 922 |
| 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 Elismetrep 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 Elismetrep manufacturer or Elismetrep supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Elismetrep manufacturer or Elismetrep supplier.
PharmaCompass also assists you with knowing the Elismetrep API Price utilized in the formulation of products. Elismetrep API Price is not always fixed or binding as the Elismetrep Price is obtained through a variety of data sources. The Elismetrep Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Elismetrep manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Elismetrep, including repackagers and relabelers. The FDA regulates Elismetrep manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Elismetrep 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 Elismetrep supplier is an individual or a company that provides Elismetrep active pharmaceutical ingredient (API) or Elismetrep finished formulations upon request. The Elismetrep suppliers may include Elismetrep API manufacturers, exporters, distributors and traders.
Elismetrep 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 Elismetrep 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 Elismetrep GMP manufacturer or Elismetrep GMP API supplier for your needs.
A Elismetrep CoA (Certificate of Analysis) is a formal document that attests to Elismetrep's compliance with Elismetrep specifications and serves as a tool for batch-level quality control.
Elismetrep CoA mostly includes findings from lab analyses of a specific batch. For each Elismetrep 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.
Elismetrep may be tested according to a variety of international standards, such as European Pharmacopoeia (Elismetrep EP), Elismetrep JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Elismetrep USP).
