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1. N-(4-(1-cyclobutylpiperidin-4-yloxy)phenyl)-2-(morpholin-4-yl)acetamide Dihydrochloride
2. Samelisant
3. Suvn-g3031
1. Samelisant
2. 6fzd7vs9ee
3. 1394808-20-8
4. Unii-6fzd7vs9ee
5. Chembl4593911
6. 4-morpholineacetamide, N-(4-((1-cyclobutyl-4-piperidinyl)oxy)phenyl)-, Hydrochloride (1:2)
7. Schembl12486477
8. Lcpqctbhzpmvfx-uhfffaoysa-n
9. Bdbm50517497
10. Akos040754117
11. Ms-28053
12. Hy-120124
13. Cs-0070018
14. N-[4-(1-cyclobutyl Piperidin-4-yloxy)phenyl]-2-(morpholin-4-yl) Acetamide Dihydrochloride
15. N-[4-(1-cyclobutylpiperidin-4-yl)oxyphenyl]-2-morpholin-4-ylacetamide;dihydrochloride
| Molecular Weight | 446.4 g/mol |
|---|---|
| Molecular Formula | C21H33Cl2N3O3 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 6 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 54 |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 463 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Samelisant 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 Samelisant manufacturer or Samelisant supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Samelisant manufacturer or Samelisant supplier.
PharmaCompass also assists you with knowing the Samelisant API Price utilized in the formulation of products. Samelisant API Price is not always fixed or binding as the Samelisant Price is obtained through a variety of data sources. The Samelisant Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Samelisant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Samelisant, including repackagers and relabelers. The FDA regulates Samelisant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Samelisant 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 Samelisant supplier is an individual or a company that provides Samelisant active pharmaceutical ingredient (API) or Samelisant finished formulations upon request. The Samelisant suppliers may include Samelisant API manufacturers, exporters, distributors and traders.
Samelisant 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 Samelisant 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 Samelisant GMP manufacturer or Samelisant GMP API supplier for your needs.
A Samelisant CoA (Certificate of Analysis) is a formal document that attests to Samelisant's compliance with Samelisant specifications and serves as a tool for batch-level quality control.
Samelisant CoA mostly includes findings from lab analyses of a specific batch. For each Samelisant 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.
Samelisant may be tested according to a variety of international standards, such as European Pharmacopoeia (Samelisant EP), Samelisant JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Samelisant USP).
