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1. Chembl503
2. Lovastatin Lactone
3. Schembl9612788
4. Bdbm50004774
5. As-14196
6. (lovastatin)2-methyl-butyric Acid 8-[2-(4-hydroxy-6-oxo-tetrahydro-pyran-2-yl)-ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydro-naphthalen-1-yl Ester
7. (s)-2-methyl-butyric Acid (1s,3r,7s,8s,8ar)-8-[2-((r)-4-hydroxy-6-oxo-tetrahydro-pyran-2-yl)-ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydro-naphthalen-1-yl Ester
8. 2-methyl-butyric Acid 8-[2-(4-hydroxy-6-oxo-tetrahydro-pyran-2-yl)-ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydro-naphthalen-1-yl Ester(mevinolin)
| Molecular Weight | 404.5 g/mol |
|---|---|
| Molecular Formula | C24H36O5 |
| XLogP3 | 4.3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Exact Mass | 404.25627424 g/mol |
| Monoisotopic Mass | 404.25627424 g/mol |
| Topological Polar Surface Area | 72.8 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 666 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 7 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Drugs in Development
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A Lovastatin Lactone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lovastatin Lactone, including repackagers and relabelers. The FDA regulates Lovastatin Lactone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lovastatin Lactone 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 Lovastatin Lactone supplier is an individual or a company that provides Lovastatin Lactone active pharmaceutical ingredient (API) or Lovastatin Lactone finished formulations upon request. The Lovastatin Lactone suppliers may include Lovastatin Lactone API manufacturers, exporters, distributors and traders.
Lovastatin Lactone 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 Lovastatin Lactone 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 Lovastatin Lactone GMP manufacturer or Lovastatin Lactone GMP API supplier for your needs.
A Lovastatin Lactone CoA (Certificate of Analysis) is a formal document that attests to Lovastatin Lactone's compliance with Lovastatin Lactone specifications and serves as a tool for batch-level quality control.
Lovastatin Lactone CoA mostly includes findings from lab analyses of a specific batch. For each Lovastatin Lactone 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.
Lovastatin Lactone may be tested according to a variety of international standards, such as European Pharmacopoeia (Lovastatin Lactone EP), Lovastatin Lactone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lovastatin Lactone USP).
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