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1. Gly-tyr-lys-dtpa
2. Glycyl-tyrosyl-lysine-dtpa
3. Gyk-dtpa
1. Pendetide [inn]
2. Gyk-dtpa
3. 60c8d1c9uj
4. 148805-91-8
5. Unii-60c8d1c9uj
6. Pendetide [usan]
7. Schembl306050
8. Dtxsid60164112
9. Q1981622
10. Glycyl-l-tyrosyl-n6-[n-[2-[[2-[bis(carboxymethyl)amino]ethyl](carboxymethyl)amino]ethyl]-n-(carboxymethyl)glycyl]-l-lysine
11. L-lysine, Glycyl-l-tyrosyl-n6-[n-[2-[[2-[bis(carboxymethyl)amino]ethyl](carboxymethyl)amino]ethyl]-n-(carboxymethyl)glycyl]-
| Molecular Weight | 741.7 g/mol |
|---|---|
| Molecular Formula | C31H47N7O14 |
| XLogP3 | -11 |
| Hydrogen Bond Donor Count | 10 |
| Hydrogen Bond Acceptor Count | 18 |
| Rotatable Bond Count | 28 |
| Exact Mass | 741.31809920 g/mol |
| Monoisotopic Mass | 741.31809920 g/mol |
| Topological Polar Surface Area | 330 Ų |
| Heavy Atom Count | 52 |
| Formal Charge | 0 |
| Complexity | 1200 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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PharmaCompass offers a list of Capromab Pendetide 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 Capromab Pendetide manufacturer or Capromab Pendetide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Capromab Pendetide manufacturer or Capromab Pendetide supplier.
PharmaCompass also assists you with knowing the Capromab Pendetide API Price utilized in the formulation of products. Capromab Pendetide API Price is not always fixed or binding as the Capromab Pendetide Price is obtained through a variety of data sources. The Capromab Pendetide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Capromab Pendetide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Capromab Pendetide, including repackagers and relabelers. The FDA regulates Capromab Pendetide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Capromab Pendetide 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 Capromab Pendetide supplier is an individual or a company that provides Capromab Pendetide active pharmaceutical ingredient (API) or Capromab Pendetide finished formulations upon request. The Capromab Pendetide suppliers may include Capromab Pendetide API manufacturers, exporters, distributors and traders.
Capromab Pendetide 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 Capromab Pendetide 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 Capromab Pendetide GMP manufacturer or Capromab Pendetide GMP API supplier for your needs.
A Capromab Pendetide CoA (Certificate of Analysis) is a formal document that attests to Capromab Pendetide's compliance with Capromab Pendetide specifications and serves as a tool for batch-level quality control.
Capromab Pendetide CoA mostly includes findings from lab analyses of a specific batch. For each Capromab Pendetide 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.
Capromab Pendetide may be tested according to a variety of international standards, such as European Pharmacopoeia (Capromab Pendetide EP), Capromab Pendetide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Capromab Pendetide USP).
