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1. Azp531
2. Cyclci Dag(6-13)
3. Cyclic Des-acyl Ghrelin (6-13)
1. Azp-531
2. Azp 531
3. 9vhd7j6363
4. 3-((3s,6s,9s,12s,15s,18s,21s,24s)-6,15-bis(3-amino-3-oxo-propyl)-12-(3-guanidinopropyl)-3-(hydroxymethyl)-18-(1h-imidazol-5-ylmethyl)-9-isopropyl-2,5,8,11,14,17,20,23-octaoxo-1,4,7,10,13,16,19,22-octazabicyclo(22.3.0)heptacosan-21-yl)propanoic Acid
5. Livoletide [inn]
6. Unii-9vhd7j6363
7. Azp531
8. Chembl2029605
9. Gtpl10884
10. Cyclo(des-acyl Ghrelin(6-13))
11. Hy-p0231
12. Cs-7528
13. Db15188
14. Q27896244
15. Synthetic Cyclic 8 Amino Acid Analog Of Human Unacylated Ghrelin
16. Cyclo(l-arginyl-l-valyl-l-glutaminyl-l-seryl-l-prolyl-l-.alpha.-glutamyl-l-histidyl-l-glutaminyl)
17. Cyclo(l-arginyl-l-valyl-l-glutaminyl-l-seryl-l-prolyl-l-alpha-glutamyl-l-histidyl-l-glutaminyl)
| Molecular Weight | 962.0 g/mol |
|---|---|
| Molecular Formula | C40H63N15O13 |
| XLogP3 | -5.5 |
| Hydrogen Bond Donor Count | 14 |
| Hydrogen Bond Acceptor Count | 15 |
| Rotatable Bond Count | 17 |
| Exact Mass | 961.47297712 g/mol |
| Monoisotopic Mass | 961.47297712 g/mol |
| Topological Polar Surface Area | 461 Ų |
| Heavy Atom Count | 68 |
| Formal Charge | 0 |
| Complexity | 1900 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 8 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Treatment of Prader-Willi syndrome
ABOUT THIS PAGE
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PharmaCompass offers a list of Livoletide 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 Livoletide manufacturer or Livoletide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Livoletide manufacturer or Livoletide supplier.
PharmaCompass also assists you with knowing the Livoletide API Price utilized in the formulation of products. Livoletide API Price is not always fixed or binding as the Livoletide Price is obtained through a variety of data sources. The Livoletide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Livoletide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Livoletide, including repackagers and relabelers. The FDA regulates Livoletide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Livoletide 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 Livoletide supplier is an individual or a company that provides Livoletide active pharmaceutical ingredient (API) or Livoletide finished formulations upon request. The Livoletide suppliers may include Livoletide API manufacturers, exporters, distributors and traders.
Livoletide 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 Livoletide 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 Livoletide GMP manufacturer or Livoletide GMP API supplier for your needs.
A Livoletide CoA (Certificate of Analysis) is a formal document that attests to Livoletide's compliance with Livoletide specifications and serves as a tool for batch-level quality control.
Livoletide CoA mostly includes findings from lab analyses of a specific batch. For each Livoletide 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.
Livoletide may be tested according to a variety of international standards, such as European Pharmacopoeia (Livoletide EP), Livoletide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Livoletide USP).
