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1. Allocor
2. Cedilanid
3. Ceglunat
4. Celanide
5. Isolanid
6. Lanatigen C
7. Lanatoside C
8. Lanocide
1. Celanide
2. Celanid
3. Lanocide-c
4. Desacetyllanatoside
5. Nsc7533
6. 3-{[hexopyranosyl-(1->4)-3-o-acetyl-2,6-dideoxyhexopyranosyl-(1->4)-2,6-dideoxyhexopyranosyl-(1->4)-2,6-dideoxyhexopyranosyl]oxy}-12,14-dihydroxycard-20(22)-enolide
7. Card-20(22)-enolide,6-dideoxy-.beta.-d-ribo-hexopyranosyl-(1.fwdarw.4)-o-2,6-dideoxy-.beta.-d-ribo-hexopyranosyl-(1.fwdarw.4)-2,6-dideoxy-.beta.-d-ribo-hexopyranosyl)oxy]-12,14-dihydroxy-, (3.beta.,5.beta.,12.beta.)-
8. Mls002207214
9. Chembl110309
10. Schembl18223891
11. Dtxsid20860209
12. Lanatoside C (digoxin Impurity H)
13. Nsc119991
14. Akos026750171
15. Smp1_000175
16. Ncgc00166137-01
17. Ncgc00166137-02
18. Ls-15494
19. Nci60_041651
20. Smr001306767
21. Db-044235
22. Ft-0630440
Molecular Weight | 985.1 g/mol |
---|---|
Molecular Formula | C49H76O20 |
XLogP3 | 0.2 |
Hydrogen Bond Donor Count | 8 |
Hydrogen Bond Acceptor Count | 20 |
Rotatable Bond Count | 12 |
Exact Mass | 984.49299481 g/mol |
Monoisotopic Mass | 984.49299481 g/mol |
Topological Polar Surface Area | 288 Ų |
Heavy Atom Count | 69 |
Formal Charge | 0 |
Complexity | 1870 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 26 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
Market Place
REF. STANDARDS & IMPURITIES
ANALYTICAL
ABOUT THIS PAGE
73
PharmaCompass offers a list of Lanatoside C 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 Lanatoside C manufacturer or Lanatoside C supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lanatoside C manufacturer or Lanatoside C supplier.
PharmaCompass also assists you with knowing the Lanatoside C API Price utilized in the formulation of products. Lanatoside C API Price is not always fixed or binding as the Lanatoside C Price is obtained through a variety of data sources. The Lanatoside C Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lanatoside C manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lanatoside C, including repackagers and relabelers. The FDA regulates Lanatoside C manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lanatoside C 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 Lanatoside C supplier is an individual or a company that provides Lanatoside C active pharmaceutical ingredient (API) or Lanatoside C finished formulations upon request. The Lanatoside C suppliers may include Lanatoside C API manufacturers, exporters, distributors and traders.
Lanatoside C 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 Lanatoside C 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 Lanatoside C GMP manufacturer or Lanatoside C GMP API supplier for your needs.
A Lanatoside C CoA (Certificate of Analysis) is a formal document that attests to Lanatoside C's compliance with Lanatoside C specifications and serves as a tool for batch-level quality control.
Lanatoside C CoA mostly includes findings from lab analyses of a specific batch. For each Lanatoside C 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.
Lanatoside C may be tested according to a variety of international standards, such as European Pharmacopoeia (Lanatoside C EP), Lanatoside C JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lanatoside C USP).