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1. Cirtuvivint [inn]
2. 7t1py32zph
3. 2143917-62-6
4. 4-pyridinecarboxamide, 2-(4-methyl-1-piperazinyl)-n-(6-(1-methyl-1h-pyrazol-4-yl)-3-isoquinolinyl)-
5. Unii-7t1py32zph
6. Chembl4784318
7. Schembl19516414
8. Bdbm293424
9. Ex-a6035
10. Us10106527, Compound 10
11. Nsc835563
12. Us10106527, Compound 142
13. Us10106527, Compound 143
14. Us10106527, Compound 144
15. Us10106527, Compound 459
16. Nsc-835563
17. Sm08502
18. Sm-08502
19. Hy-137435
20. Cs-0138635
21. 2-(4-methylpiperazin-1-yl)-n-[6-(1-methylpyrazol-4-yl)isoquinolin-3-yl]pyridine-4-carboxamide
Molecular Weight | 427.5 g/mol |
---|---|
Molecular Formula | C24H25N7O |
XLogP3 | 2.4 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 4 |
Exact Mass | 427.21205845 g/mol |
Monoisotopic Mass | 427.21205845 g/mol |
Topological Polar Surface Area | 79.2 Ų |
Heavy Atom Count | 32 |
Formal Charge | 0 |
Complexity | 640 |
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
A Cirtuvivint manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cirtuvivint, including repackagers and relabelers. The FDA regulates Cirtuvivint manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cirtuvivint 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 Cirtuvivint supplier is an individual or a company that provides Cirtuvivint active pharmaceutical ingredient (API) or Cirtuvivint finished formulations upon request. The Cirtuvivint suppliers may include Cirtuvivint API manufacturers, exporters, distributors and traders.
Cirtuvivint 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 Cirtuvivint 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 Cirtuvivint GMP manufacturer or Cirtuvivint GMP API supplier for your needs.
A Cirtuvivint CoA (Certificate of Analysis) is a formal document that attests to Cirtuvivint's compliance with Cirtuvivint specifications and serves as a tool for batch-level quality control.
Cirtuvivint CoA mostly includes findings from lab analyses of a specific batch. For each Cirtuvivint 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.
Cirtuvivint may be tested according to a variety of international standards, such as European Pharmacopoeia (Cirtuvivint EP), Cirtuvivint JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cirtuvivint USP).
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