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1. Azd6765
1. 153322-05-5
2. Azd6765
3. Lanicemine [inn]
4. Lanicemine (free Base)
5. Ar-r15896ar
6. Azd-6765
7. Arl 15896
8. (s)-1-phenyl-2-(pyridin-2-yl)ethanamine
9. 9tmu325rk3
10. (1s)-1-phenyl-2-(pyridin-2-yl)ethan-1-amine
11. (1s)-1-phenyl-2-pyridin-2-ylethanamine
12. Fpl 15896
13. Unii-9tmu325rk3
14. Ar-r 15896
15. Lanicemine(free Base)
16. Lanicemine [who-dd]
17. Chembl467084
18. Gtpl7681
19. Schembl1422817
20. Zinc6163
21. Dtxsid30870011
22. Ar-r-15896ar
23. Zb0597
24. Akos026744074
25. Db11889
26. (+)-2-(s)-beta-aminophenethyl-pyridine
27. (+)-2-((s)-beta-aminophenethyl)pyridine
28. Hy-108235
29. Cs-0027621
30. (+)-2-((s)-.beta.-aminophenethyl)pyridine
31. Q15409412
32. Z2286637868
| Molecular Weight | 198.26 g/mol |
|---|---|
| Molecular Formula | C13H14N2 |
| XLogP3 | 1.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 198.115698455 g/mol |
| Monoisotopic Mass | 198.115698455 g/mol |
| Topological Polar Surface Area | 38.9 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 175 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Lanicemine 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 Lanicemine manufacturer or Lanicemine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lanicemine manufacturer or Lanicemine supplier.
PharmaCompass also assists you with knowing the Lanicemine API Price utilized in the formulation of products. Lanicemine API Price is not always fixed or binding as the Lanicemine Price is obtained through a variety of data sources. The Lanicemine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lanicemine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lanicemine, including repackagers and relabelers. The FDA regulates Lanicemine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lanicemine 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 Lanicemine supplier is an individual or a company that provides Lanicemine active pharmaceutical ingredient (API) or Lanicemine finished formulations upon request. The Lanicemine suppliers may include Lanicemine API manufacturers, exporters, distributors and traders.
Lanicemine 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 Lanicemine 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 Lanicemine GMP manufacturer or Lanicemine GMP API supplier for your needs.
A Lanicemine CoA (Certificate of Analysis) is a formal document that attests to Lanicemine's compliance with Lanicemine specifications and serves as a tool for batch-level quality control.
Lanicemine CoA mostly includes findings from lab analyses of a specific batch. For each Lanicemine 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.
Lanicemine may be tested according to a variety of international standards, such as European Pharmacopoeia (Lanicemine EP), Lanicemine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lanicemine USP).
