Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
1. Chembl557172
2. Schembl3377772
| Molecular Weight | 540.4 g/mol |
|---|---|
| Molecular Formula | C28H27Cl2N3O4 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Exact Mass | 539.1378617 g/mol |
| Monoisotopic Mass | 539.1378617 g/mol |
| Topological Polar Surface Area | 82.1 Ų |
| Heavy Atom Count | 37 |
| Formal Charge | 0 |
| Complexity | 821 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
62
PharmaCompass offers a list of CHEMBL557172 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 CHEMBL557172 manufacturer or CHEMBL557172 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred CHEMBL557172 manufacturer or CHEMBL557172 supplier.
PharmaCompass also assists you with knowing the CHEMBL557172 API Price utilized in the formulation of products. CHEMBL557172 API Price is not always fixed or binding as the CHEMBL557172 Price is obtained through a variety of data sources. The CHEMBL557172 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CHEMBL557172 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CHEMBL557172, including repackagers and relabelers. The FDA regulates CHEMBL557172 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CHEMBL557172 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 CHEMBL557172 supplier is an individual or a company that provides CHEMBL557172 active pharmaceutical ingredient (API) or CHEMBL557172 finished formulations upon request. The CHEMBL557172 suppliers may include CHEMBL557172 API manufacturers, exporters, distributors and traders.
CHEMBL557172 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 CHEMBL557172 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 CHEMBL557172 GMP manufacturer or CHEMBL557172 GMP API supplier for your needs.
A CHEMBL557172 CoA (Certificate of Analysis) is a formal document that attests to CHEMBL557172's compliance with CHEMBL557172 specifications and serves as a tool for batch-level quality control.
CHEMBL557172 CoA mostly includes findings from lab analyses of a specific batch. For each CHEMBL557172 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.
CHEMBL557172 may be tested according to a variety of international standards, such as European Pharmacopoeia (CHEMBL557172 EP), CHEMBL557172 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (CHEMBL557172 USP).
