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1. Zurletrectinib [usan]
2. Zvq44e2h6v
3. Icp-723
4. Zurletrectinib [inn]
5. Chembl5095426
6. Schembl23368572
7. Gtpl12389
8. 2403703-30-8
9. Example 1 [us20210147445a1]
10. Hy-148811
11. Cs-0641351
12. 10h-5,7-ethenopyrazolo[4,3-g]pyrido[3,2-m]pyrrolo[1,2-k][1,4,6,9,11]oxatetraazacyclotetradecin-11(12h)-one, 2,18-difluoro-1,2,3,13,14,19b-hexahydro-14-methyl-,(2s,14s,19br)-
| Molecular Weight | 415.4 g/mol |
|---|---|
| Molecular Formula | C19H19F2N7O2 |
| XLogP3 | 1.4 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 0 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 96.7 |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 738 |
| 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 |
Drugs in Development
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PharmaCompass offers a list of Zurletrectinib 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 Zurletrectinib manufacturer or Zurletrectinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zurletrectinib manufacturer or Zurletrectinib supplier.
PharmaCompass also assists you with knowing the Zurletrectinib API Price utilized in the formulation of products. Zurletrectinib API Price is not always fixed or binding as the Zurletrectinib Price is obtained through a variety of data sources. The Zurletrectinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zurletrectinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zurletrectinib, including repackagers and relabelers. The FDA regulates Zurletrectinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zurletrectinib 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 Zurletrectinib supplier is an individual or a company that provides Zurletrectinib active pharmaceutical ingredient (API) or Zurletrectinib finished formulations upon request. The Zurletrectinib suppliers may include Zurletrectinib API manufacturers, exporters, distributors and traders.
Zurletrectinib 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 Zurletrectinib 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 Zurletrectinib GMP manufacturer or Zurletrectinib GMP API supplier for your needs.
A Zurletrectinib CoA (Certificate of Analysis) is a formal document that attests to Zurletrectinib's compliance with Zurletrectinib specifications and serves as a tool for batch-level quality control.
Zurletrectinib CoA mostly includes findings from lab analyses of a specific batch. For each Zurletrectinib 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.
Zurletrectinib may be tested according to a variety of international standards, such as European Pharmacopoeia (Zurletrectinib EP), Zurletrectinib JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zurletrectinib USP).
