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1. Alrizomadlin
2. Aa-115
3. 1818393-16-6
4. 15qau0si9j
5. Apg-115
6. Apg115
7. Apg 115 [who-dd]
8. Chembl4091801
9. 4-((3'r,4's,5'r)-6''-chloro-4'-(3-chloro-2-fluorophenyl)-1'-ethyl-2''-oxodispiro[cyclohexane-1,2'-pyrrolidine-3',3''-indoline]-5'-carboxamido)bicyclo[2.2.2]octane-1-carboxylic Acid
10. (3'r,4's,5'r)-4-((6-chloro-2-oxo-1,2-dihydro-spiro(indole-3,3'-pyrrolidin)e-4'-(3-chloro-2-fluoro -phenyl)-1'-ethyl-spiro(cyclohexane-1,2'-pyrrolidine)-5'-carbonyl)-amino)-bicyclo(2.2.2)octane-1-carboxylic Acid
11. Alrizomadlin [inn]
12. Unii-15qau0si9j
13. Schembl17189805
14. Bdbm50237739
15. Mfcd32197175
16. Nsc831270
17. Nsc-831270
18. Hy-101518
19. Cs-0021621
Molecular Weight | 642.6 g/mol |
---|---|
Molecular Formula | C34H38Cl2FN3O4 |
XLogP3 | 3.6 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 5 |
Exact Mass | 641.2223403 g/mol |
Monoisotopic Mass | 641.2223403 g/mol |
Topological Polar Surface Area | 98.7 Ų |
Heavy Atom Count | 44 |
Formal Charge | 0 |
Complexity | 1160 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 3 |
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 Alrizomadlin 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 Alrizomadlin manufacturer or Alrizomadlin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Alrizomadlin manufacturer or Alrizomadlin supplier.
PharmaCompass also assists you with knowing the Alrizomadlin API Price utilized in the formulation of products. Alrizomadlin API Price is not always fixed or binding as the Alrizomadlin Price is obtained through a variety of data sources. The Alrizomadlin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Alrizomadlin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alrizomadlin, including repackagers and relabelers. The FDA regulates Alrizomadlin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alrizomadlin 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 Alrizomadlin supplier is an individual or a company that provides Alrizomadlin active pharmaceutical ingredient (API) or Alrizomadlin finished formulations upon request. The Alrizomadlin suppliers may include Alrizomadlin API manufacturers, exporters, distributors and traders.
Alrizomadlin 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 Alrizomadlin 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 Alrizomadlin GMP manufacturer or Alrizomadlin GMP API supplier for your needs.
A Alrizomadlin CoA (Certificate of Analysis) is a formal document that attests to Alrizomadlin's compliance with Alrizomadlin specifications and serves as a tool for batch-level quality control.
Alrizomadlin CoA mostly includes findings from lab analyses of a specific batch. For each Alrizomadlin 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.
Alrizomadlin may be tested according to a variety of international standards, such as European Pharmacopoeia (Alrizomadlin EP), Alrizomadlin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Alrizomadlin USP).