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1. 2,5-anhydro-d-glucitol-1,6-diphosphate
2. 4429-47-4
3. [(2r,3s,4s,5s)-3,4-dihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]methyl Dihydrogen Phosphate
4. Schembl20154711
5. Zinc3870733
6. 2,5-anhydroglucitol 1,6-bisphosphate
7. Db02778
8. 2,5-anhydro-d-glucitol1,6-diphosphate
9. 2,5-anhydro-d-glucitol 1,6-diphosphate
10. 2,5-anhydro-1,6-di-o-phosphono-d-glucitol
11. 2,5-anhydro-d-glucitol 1,6-bisphosphoric Acid
12. W-202770
13. 2,5-anhydro-d-glucitol-1,6-diphosphate Is Known As A Phosphofructokinase Inhibitor.
14. Wurcs=2.0/1,1,0/[h2122h_2-5_1*opo/3o/3=o_6*opo/3o/3=o]/1/
| Molecular Weight | 324.12 g/mol |
|---|---|
| Molecular Formula | C6H14O11P2 |
| XLogP3 | -4.8 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 6 |
| Exact Mass | 324.00113525 g/mol |
| Monoisotopic Mass | 324.00113525 g/mol |
| Topological Polar Surface Area | 183 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 351 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| 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 2,5-Anhydroglucitol-1,6-Biphosphate 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 2,5-Anhydroglucitol-1,6-Biphosphate manufacturer or 2,5-Anhydroglucitol-1,6-Biphosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 2,5-Anhydroglucitol-1,6-Biphosphate manufacturer or 2,5-Anhydroglucitol-1,6-Biphosphate supplier.
PharmaCompass also assists you with knowing the 2,5-Anhydroglucitol-1,6-Biphosphate API Price utilized in the formulation of products. 2,5-Anhydroglucitol-1,6-Biphosphate API Price is not always fixed or binding as the 2,5-Anhydroglucitol-1,6-Biphosphate Price is obtained through a variety of data sources. The 2,5-Anhydroglucitol-1,6-Biphosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ESAFOSFINA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ESAFOSFINA, including repackagers and relabelers. The FDA regulates ESAFOSFINA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ESAFOSFINA 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 ESAFOSFINA supplier is an individual or a company that provides ESAFOSFINA active pharmaceutical ingredient (API) or ESAFOSFINA finished formulations upon request. The ESAFOSFINA suppliers may include ESAFOSFINA API manufacturers, exporters, distributors and traders.
ESAFOSFINA 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 ESAFOSFINA 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 ESAFOSFINA GMP manufacturer or ESAFOSFINA GMP API supplier for your needs.
A ESAFOSFINA CoA (Certificate of Analysis) is a formal document that attests to ESAFOSFINA's compliance with ESAFOSFINA specifications and serves as a tool for batch-level quality control.
ESAFOSFINA CoA mostly includes findings from lab analyses of a specific batch. For each ESAFOSFINA 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.
ESAFOSFINA may be tested according to a variety of international standards, such as European Pharmacopoeia (ESAFOSFINA EP), ESAFOSFINA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ESAFOSFINA USP).
