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1. Sage-718
2. Sage718
3. Dalzanemdor [inn]
4. 8ens5k3jw8
5. 1629853-48-0
6. (25s)-26,26,26-trifluoro-3alpha-methyl-24-norcholest- 5-ene-3beta,25-diol
7. (3beta,24s)-25,25,25-trifluoro-3-methyl-26,27-dinorergost-5-ene-3,24-diol
8. (3s,8s,9s,10r,13r,14s,17r)-3,10,13-trimethyl-17-[(2r,5s)-6,6,6-trifluoro-5-hydroxy-5-methylhexan-2-yl]-1,2,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol
9. Unii-8ens5k3jw8
10. Schembl16139912
11. Gtpl12050
12. Glxc-25940
13. Ex-a6875
14. Compound 5 [pmid: 35785990]
15. Hy-147260
16. Cs-0542316
17. 26,27-dinorergost-5-ene-3,24-diol, 25,25,25-trifluoro-3-methyl-, (3beta,24s)-
18. (3s,8s,9s,10r,13r,14s,17r)-3,10,13-trimethyl-17-((2r,5s)-6,6,6-trifluoro-5-hydroxy-5-methylhexan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-ol
19. 26,27-dinorergost-5-ene-3,24-diol, 25,25,25-trifluoro-3-methyl-, (3.beta.,24s)-
| Molecular Weight | 456.6 g/mol |
|---|---|
| Molecular Formula | C27H43F3O2 |
| XLogP3 | 7.2 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 40.5 |
| Heavy Atom Count | 32 |
| Formal Charge | 0 |
| Complexity | 763 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 9 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Drugs in Development
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A Dalzanemdor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dalzanemdor, including repackagers and relabelers. The FDA regulates Dalzanemdor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dalzanemdor 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 Dalzanemdor supplier is an individual or a company that provides Dalzanemdor active pharmaceutical ingredient (API) or Dalzanemdor finished formulations upon request. The Dalzanemdor suppliers may include Dalzanemdor API manufacturers, exporters, distributors and traders.
Dalzanemdor 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 Dalzanemdor 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 Dalzanemdor GMP manufacturer or Dalzanemdor GMP API supplier for your needs.
A Dalzanemdor CoA (Certificate of Analysis) is a formal document that attests to Dalzanemdor's compliance with Dalzanemdor specifications and serves as a tool for batch-level quality control.
Dalzanemdor CoA mostly includes findings from lab analyses of a specific batch. For each Dalzanemdor 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.
Dalzanemdor may be tested according to a variety of international standards, such as European Pharmacopoeia (Dalzanemdor EP), Dalzanemdor JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dalzanemdor USP).
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