Synopsis
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
1. 9-(2-(phosphonomethoxy)ethyl)adenine Diphosphate
2. Pmeapp
1. Pmeapp
2. Adefovir Diphosphate
3. 129532-77-0
4. Pmea-dp
5. 9-(meoet)-a-tp
6. 9-(2-(phosphonomethoxy)ethyl)adenine Diphosphate
7. 2-(6-aminopurin-9-yl)ethoxymethyl-[hydroxy(phosphonooxy)phosphoryl]oxyphosphinic Acid
8. N-(2-diphosphorylphosphonylmethoxyethyl)-adenine
9. Diphosphoric Acid, Monoanhydride With ((2-(6-amino-9h-purin-9-yl)ethoxy)methyl)phosphonic Acid
10. Diphosphoric Acid, Monoanhydride With [[2-(6-amino-9h-purin-9-yl)ethoxy]methyl]phosphonic Acid
11. Pmea-pp
12. 1pk0
13. 9-(2-phosphonylmethoxyethyl)adenine Diphosphate
14. Chembl1162433
15. Schembl13394184
16. Dtxsid60156198
17. Bdbm50479983
18. Q27459979
19. [2-(6-amino-9h-purine-9-yl)ethoxy]methylphosphonyldiphosphate
20. 2-(6-aminopurin-9-yl)ethoxymethyl-[hydroxy(phosphonooxy)phosphoryl]oxy-phosphinic Acid
| Molecular Weight | 433.15 g/mol |
|---|---|
| Molecular Formula | C8H14N5O10P3 |
| XLogP3 | -4.2 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 9 |
| Exact Mass | 432.99535265 g/mol |
| Monoisotopic Mass | 432.99535265 g/mol |
| Topological Polar Surface Area | 229 Ų |
| Heavy Atom Count | 26 |
| Formal Charge | 0 |
| Complexity | 632 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Digital Content 
NEWS #PharmaBuzz
ABOUT THIS PAGE
59
PharmaCompass offers a list of Adefovir Diphosphate 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 Adefovir Diphosphate manufacturer or Adefovir Diphosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Adefovir Diphosphate manufacturer or Adefovir Diphosphate supplier.
PharmaCompass also assists you with knowing the Adefovir Diphosphate API Price utilized in the formulation of products. Adefovir Diphosphate API Price is not always fixed or binding as the Adefovir Diphosphate Price is obtained through a variety of data sources. The Adefovir Diphosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EMA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EMA, including repackagers and relabelers. The FDA regulates EMA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EMA 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 EMA supplier is an individual or a company that provides EMA active pharmaceutical ingredient (API) or EMA finished formulations upon request. The EMA suppliers may include EMA API manufacturers, exporters, distributors and traders.
click here to find a list of EMA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EMA DMF (Drug Master File) is a document detailing the whole manufacturing process of EMA active pharmaceutical ingredient (API) in detail. Different forms of EMA DMFs exist exist since differing nations have different regulations, such as EMA USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A EMA DMF submitted to regulatory agencies in the US is known as a USDMF. EMA USDMF includes data on EMA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The EMA USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of EMA suppliers with USDMF on PharmaCompass.
EMA 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 EMA 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 EMA GMP manufacturer or EMA GMP API supplier for your needs.
A EMA CoA (Certificate of Analysis) is a formal document that attests to EMA's compliance with EMA specifications and serves as a tool for batch-level quality control.
EMA CoA mostly includes findings from lab analyses of a specific batch. For each EMA 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.
EMA may be tested according to a variety of international standards, such as European Pharmacopoeia (EMA EP), EMA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (EMA USP).
