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1. Olesoxime
2. Tro19622
1. Olesoxime, E-
2. 66538-08-7
3. Tro 19622
4. Olesoxime
5. 8v8ef6094n
6. 22033-87-0
7. (ne)-n-[(8s,9s,10r,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ylidene]hydroxylamine
8. Tro-19622
9. Unii-8v8ef6094n
10. Z-olesoxime
11. Nsc-21311
12. Olesoxime (usan/inn)
13. Olesoxime (tro 19622)
14. Gtpl8542
15. Schembl18870340
16. Qntashoavrslmd-siwswzrqsa-
17. Zinc34035621
18. D11213
19. J-014436
20. Q7086437
| Molecular Weight | 399.7 g/mol |
|---|---|
| Molecular Formula | C27H45NO |
| XLogP3 | 8.8 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 5 |
| Exact Mass | 399.350115059 g/mol |
| Monoisotopic Mass | 399.350115059 g/mol |
| Topological Polar Surface Area | 32.6 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 663 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 7 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Treatment of spinal muscular atrophy
Drugs in Development
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PharmaCompass offers a list of Olesoxime 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 Olesoxime manufacturer or Olesoxime supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Olesoxime manufacturer or Olesoxime supplier.
PharmaCompass also assists you with knowing the Olesoxime API Price utilized in the formulation of products. Olesoxime API Price is not always fixed or binding as the Olesoxime Price is obtained through a variety of data sources. The Olesoxime Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Olesoxime manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Olesoxime, including repackagers and relabelers. The FDA regulates Olesoxime manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Olesoxime 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 Olesoxime supplier is an individual or a company that provides Olesoxime active pharmaceutical ingredient (API) or Olesoxime finished formulations upon request. The Olesoxime suppliers may include Olesoxime API manufacturers, exporters, distributors and traders.
Olesoxime 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 Olesoxime 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 Olesoxime GMP manufacturer or Olesoxime GMP API supplier for your needs.
A Olesoxime CoA (Certificate of Analysis) is a formal document that attests to Olesoxime's compliance with Olesoxime specifications and serves as a tool for batch-level quality control.
Olesoxime CoA mostly includes findings from lab analyses of a specific batch. For each Olesoxime 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.
Olesoxime may be tested according to a variety of international standards, such as European Pharmacopoeia (Olesoxime EP), Olesoxime JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Olesoxime USP).
