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1. Tuvatexib [inn]
2. Hexokinase 2 Modulator Comp-1
3. W17266s02c
4. 2055404-90-3
5. Cyclopentaneacetic Acid, 3-oxo-2-(2z)-2-penten-1-yl-, 8-quinolinyl Ester
6. Schembl2703467
7. Unii-w17266s02c
8. Hy-109140
9. Cs-0086932
| Molecular Weight | 337.4 g/mol |
|---|---|
| Molecular Formula | C21H23NO3 |
| XLogP3 | 3.7 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 7 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 56.3 |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 501 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Tuvatexib 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 Tuvatexib manufacturer or Tuvatexib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tuvatexib manufacturer or Tuvatexib supplier.
PharmaCompass also assists you with knowing the Tuvatexib API Price utilized in the formulation of products. Tuvatexib API Price is not always fixed or binding as the Tuvatexib Price is obtained through a variety of data sources. The Tuvatexib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tuvatexib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tuvatexib, including repackagers and relabelers. The FDA regulates Tuvatexib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tuvatexib 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 Tuvatexib supplier is an individual or a company that provides Tuvatexib active pharmaceutical ingredient (API) or Tuvatexib finished formulations upon request. The Tuvatexib suppliers may include Tuvatexib API manufacturers, exporters, distributors and traders.
Tuvatexib 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 Tuvatexib 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 Tuvatexib GMP manufacturer or Tuvatexib GMP API supplier for your needs.
A Tuvatexib CoA (Certificate of Analysis) is a formal document that attests to Tuvatexib's compliance with Tuvatexib specifications and serves as a tool for batch-level quality control.
Tuvatexib CoA mostly includes findings from lab analyses of a specific batch. For each Tuvatexib 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.
Tuvatexib may be tested according to a variety of international standards, such as European Pharmacopoeia (Tuvatexib EP), Tuvatexib JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tuvatexib USP).
