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1. 83-ala-84-lys-89-leu-91-ala-mbp(83-99)
2. Myelin Basic Protein (83-99), Ala(83)-lys(84)-leu(89)-ala(91)-
3. Myelin Basic Protein (83-99), Alanyl(83)-lysyl(84)-leucyl(89)-alanyl(91)-
4. Nbi 5788
5. Nbi-5788
1. Unii-6vn101530y
2. 178823-49-9
3. Nbi-5788
4. Tiplimotide [inn]
5. Nbi5788
6. Nbi 5788
7. 6vn101530y
8. L-proline, D-alanyl-l-lysyl-l-prolyl-l-valyl-l-valyl-l-histidyl-l-leucyl-l-phenylalanyl-l-alanyl-l-asparaginyl-l-isoleucyl-l-valyl-l-threonyl-l-prolyl-l-arginyl-l-threonyl-
9. 83-ala-84-lys-89-leu-91-ala-mbp(83-99)
10. Myelin Basic Protein (83-99), Ala(83)-lys(84)-leu(89)-ala(91)-
11. Myelin Basic Protein (83-99), Alanyl(83)-lysyl(84)-leucyl(89)-alanyl(91)-
12. D-alanyl-l-lysyl-l-prolyl-l-valyl-l-valyl-l-histidyl-l-leucyl-l-phenylalanyl-l-alanyl-l-asparaginyl-l-isoleucyl-l-valyl-l-threonyl-l-prolyl-l-arginyl-l-threonyl-l-prolinamide
| Molecular Weight | 1860.2 g/mol |
|---|---|
| Molecular Formula | C87H142N24O21 |
| XLogP3 | -3.4 |
| Hydrogen Bond Donor Count | 22 |
| Hydrogen Bond Acceptor Count | 25 |
| Rotatable Bond Count | 53 |
| Exact Mass | 1859.07813764 g/mol |
| Monoisotopic Mass | 1859.07813764 g/mol |
| Topological Polar Surface Area | 705 Ų |
| Heavy Atom Count | 132 |
| Formal Charge | 0 |
| Complexity | 3980 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 20 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Tiplimotide 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 Tiplimotide manufacturer or Tiplimotide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tiplimotide manufacturer or Tiplimotide supplier.
PharmaCompass also assists you with knowing the Tiplimotide API Price utilized in the formulation of products. Tiplimotide API Price is not always fixed or binding as the Tiplimotide Price is obtained through a variety of data sources. The Tiplimotide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tiplimotide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiplimotide, including repackagers and relabelers. The FDA regulates Tiplimotide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiplimotide 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 Tiplimotide supplier is an individual or a company that provides Tiplimotide active pharmaceutical ingredient (API) or Tiplimotide finished formulations upon request. The Tiplimotide suppliers may include Tiplimotide API manufacturers, exporters, distributors and traders.
Tiplimotide 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 Tiplimotide 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 Tiplimotide GMP manufacturer or Tiplimotide GMP API supplier for your needs.
A Tiplimotide CoA (Certificate of Analysis) is a formal document that attests to Tiplimotide's compliance with Tiplimotide specifications and serves as a tool for batch-level quality control.
Tiplimotide CoA mostly includes findings from lab analyses of a specific batch. For each Tiplimotide 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.
Tiplimotide may be tested according to a variety of international standards, such as European Pharmacopoeia (Tiplimotide EP), Tiplimotide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tiplimotide USP).
