Synopsis
Synopsis
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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USP
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JP
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1. N-((6-(2,3-dimethoxypropyl)tetrahydro-4-hydroxy-5,5-dimethyl-2h-pyran-2-yl)methoxymethyl)tetrahydro-alpha-hydroxy-2-methoxy-5,6-dimethyl-4-methylene-2h-pyran-2-acetamide
2. Paederine
3. Pederine
1. Pederine
2. 27973-72-4
3. (+)-pederine
4. (+)-pederin
5. B8f7j348gj
6. Nsc-114781
7. (2s)-n-[(s)-[(2s,4r,6r)-6-[(2s)-2,3-dimethoxypropyl]-4-hydroxy-5,5-dimethyloxan-2-yl]-methoxymethyl]-2-hydroxy-2-[(2r,5r,6r)-2-methoxy-5,6-dimethyl-4-methylideneoxan-2-yl]acetamide
8. Nsc 114781
9. Paederine
10. Unii-b8f7j348gj
11. Nsc114781
12. Pederin [mi]
13. Pederin, (+)-
14. Schembl452974
15. Chebi:78591
16. Dtxsid90182248
17. 2h-pyran-2-acetamide, N-(6-(2,3-dimethoxypropyl)tetrahydro-4-hydroxy-5,5-dimethyl-2h-pyran-2-yl)tetrahydro-alpha-hydroxy-2-methoxy-5,6-dimethyl-4-methylene-, (2s-(2alpha(r*(r* (2s*,5s*,6s*))),4beta,6beta(r*)))-
18. 2h-pyran-2-glycolamide, N-((6-(2,3-dimethoxypropyl)tetrahydro-4-hydroxy-5,5-dimethyl-2h-pyran-2-yl)methoxymethyl)tetrahydro-2-methoxy-5,6-dimethyl-4-methylene-
19. D-manno-nonitol, 2,6-anhydro-3,5,7-trideoxy-1-c-(((2s)-hydroxy((2r,5r,6r)-tetrahydro-2-methoxy-5,6-dimethyl-4-methylene-2h-pyran-2-yl)acetyl)amino)-5,5-dimethyl-1,8,9-tri-o-methyl-, (1s)-
20. Q8214251
21. (2s)-n-[(s)-{(2s,4r,6r)-6-[(2s)-2,3-dimethoxypropyl]-4-hydroxy-5,5-dimethyltetrahydro-2h-pyran-2-yl}(methoxy)methyl]-2-hydroxy-2-[(2r,5r,6r)-2-methoxy-5,6-dimethyl-4-methylenetetrahydro-2h-pyran-2-yl]acetamide
22. 2h-puran-2-acetamide,3-dimethoxypropyl)tetrahydro-4-hydroxy-5,5- Dimethyl-2h-pyran-2-yl]tetrahydro-.alpha.-hydroxy-2- Methoxy-5,6-dimethyl-4-methylene-, [2s-[2.alpha.[r*[r* (2s*,5s*,6s*)]],4.beta.,6.beta.(r*)]]-
23. 2h-pyran-2-glycolamide,3-dimethoxypropyl0tetrahydro-3-hydroxy-5,5- Dimethyl-2h-pyran-2-yl]methoxymethyl]tetrahydro-2-methoxy- 5,6-dimethyl-4-methylene-
24. D-manno-nonitol, 2,6-anhydro-3,5,7-trideoxy-1-c-(((2s)-2-hydroxy-2-((2r,5r,6r)-tetrahydro-2-methoxy-5,6-dimethyl-4-methylene-2h-pyran-2-yl)acetyl)amino)-5,5-dimethyl-1,8,9-tri-o-methyl-, (1s)-
| Molecular Weight | 503.6 g/mol |
|---|---|
| Molecular Formula | C25H45NO9 |
| XLogP3 | 1 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 11 |
| Exact Mass | 503.30943201 g/mol |
| Monoisotopic Mass | 503.30943201 g/mol |
| Topological Polar Surface Area | 125 Ų |
| Heavy Atom Count | 35 |
| Formal Charge | 0 |
| Complexity | 717 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 9 |
| 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 Pederin 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 Pederin manufacturer or Pederin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pederin manufacturer or Pederin supplier.
PharmaCompass also assists you with knowing the Pederin API Price utilized in the formulation of products. Pederin API Price is not always fixed or binding as the Pederin Price is obtained through a variety of data sources. The Pederin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A paederine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of paederine, including repackagers and relabelers. The FDA regulates paederine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. paederine 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 paederine supplier is an individual or a company that provides paederine active pharmaceutical ingredient (API) or paederine finished formulations upon request. The paederine suppliers may include paederine API manufacturers, exporters, distributors and traders.
click here to find a list of paederine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A paederine DMF (Drug Master File) is a document detailing the whole manufacturing process of paederine active pharmaceutical ingredient (API) in detail. Different forms of paederine DMFs exist exist since differing nations have different regulations, such as paederine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A paederine DMF submitted to regulatory agencies in the US is known as a USDMF. paederine USDMF includes data on paederine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The paederine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of paederine suppliers with USDMF on PharmaCompass.
paederine 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 paederine 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 paederine GMP manufacturer or paederine GMP API supplier for your needs.
A paederine CoA (Certificate of Analysis) is a formal document that attests to paederine's compliance with paederine specifications and serves as a tool for batch-level quality control.
paederine CoA mostly includes findings from lab analyses of a specific batch. For each paederine 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.
paederine may be tested according to a variety of international standards, such as European Pharmacopoeia (paederine EP), paederine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (paederine USP).
