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1. Schembl6386012
2. Akos022190417
3. Gs-6526
4. Ft-0625594
| Molecular Weight | 580.0 g/mol |
|---|---|
| Molecular Formula | C27H30ClNO11 |
| Hydrogen Bond Donor Count | 7 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 5 |
| Exact Mass | 579.1507385 g/mol |
| Monoisotopic Mass | 579.1507385 g/mol |
| Topological Polar Surface Area | 206 Ų |
| Heavy Atom Count | 40 |
| Formal Charge | 0 |
| Complexity | 977 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 5 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of SCHEMBL6386012 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 SCHEMBL6386012 manufacturer or SCHEMBL6386012 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred SCHEMBL6386012 manufacturer or SCHEMBL6386012 supplier.
PharmaCompass also assists you with knowing the SCHEMBL6386012 API Price utilized in the formulation of products. SCHEMBL6386012 API Price is not always fixed or binding as the SCHEMBL6386012 Price is obtained through a variety of data sources. The SCHEMBL6386012 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SCHEMBL6386012 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SCHEMBL6386012, including repackagers and relabelers. The FDA regulates SCHEMBL6386012 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SCHEMBL6386012 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 SCHEMBL6386012 supplier is an individual or a company that provides SCHEMBL6386012 active pharmaceutical ingredient (API) or SCHEMBL6386012 finished formulations upon request. The SCHEMBL6386012 suppliers may include SCHEMBL6386012 API manufacturers, exporters, distributors and traders.
SCHEMBL6386012 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 SCHEMBL6386012 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 SCHEMBL6386012 GMP manufacturer or SCHEMBL6386012 GMP API supplier for your needs.
A SCHEMBL6386012 CoA (Certificate of Analysis) is a formal document that attests to SCHEMBL6386012's compliance with SCHEMBL6386012 specifications and serves as a tool for batch-level quality control.
SCHEMBL6386012 CoA mostly includes findings from lab analyses of a specific batch. For each SCHEMBL6386012 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.
SCHEMBL6386012 may be tested according to a variety of international standards, such as European Pharmacopoeia (SCHEMBL6386012 EP), SCHEMBL6386012 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (SCHEMBL6386012 USP).
