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1. 1609452-30-3
2. Sel120
3. Sel-120
4. Se-120-34a
5. Sdm3m518pj
6. Sel120-34a (monohydrochloride)
7. 1609452-30-3 (hcl)
8. 7,8-dibromo-9-methyl-2-piperazin-1-yl-5,6-dihydro-4h-imidazo[4,5,1-ij]quinoline Hydrochloride
9. 4h-imidazo(4,5,1-ij)quinoline, 7,8-dibromo-5,6-dihydro-9-methyl-2-(1-piperazinyl)-, Hydrochloride (1:1)
10. 7,8-dibromo-5,6-dihydro-9-methyl-2-(1-piperazinyl)-4himidazo(4,5,1-ij)quinoline Hydrochloride
11. Unii-sdm3m518pj
12. Chembl4578881
13. Schembl17106021
14. S8840
15. Akos037648926
16. Ex-a2929-1
17. Hy-111388a
18. 7,8-dibromo-9-methyl-2-(piperazin-1-yl)-5,6-dihydro-4h-imidazo[4,5,1-ij]quinoline Hydrochloride
19. Bs-16042
20. Imidazo[4,5,1-ij]quinoline Hydrochloride
21. Cs-0041061
22. A17086
23. D80736
24. Sel120(sel120-34,sel120-34a)
25. 7,8-dibromo-9-methyl-2-piperazin-1-yl-5,6-dihydro-4h-
26. Sel120-34a Monohydrochloride (1609522-33-9 Free Base)
27. 6,7-dibromo-5-methyl-2-piperazin-1-yl-1,3-diazatricyclo[6.3.1.04,12]dodeca-2,4,6,8(12)-tetraene;hydrochloride
| Molecular Weight | 450.6 g/mol |
|---|---|
| Molecular Formula | C15H19Br2ClN4 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 449.96445 g/mol |
| Monoisotopic Mass | 447.96650 g/mol |
| Topological Polar Surface Area | 33.1 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 390 |
| 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 | 2 |
Drugs in Development
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PharmaCompass offers a list of RVU120 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 RVU120 manufacturer or RVU120 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred RVU120 manufacturer or RVU120 supplier.
PharmaCompass also assists you with knowing the RVU120 API Price utilized in the formulation of products. RVU120 API Price is not always fixed or binding as the RVU120 Price is obtained through a variety of data sources. The RVU120 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SEL120 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SEL120, including repackagers and relabelers. The FDA regulates SEL120 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SEL120 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 SEL120 supplier is an individual or a company that provides SEL120 active pharmaceutical ingredient (API) or SEL120 finished formulations upon request. The SEL120 suppliers may include SEL120 API manufacturers, exporters, distributors and traders.
SEL120 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 SEL120 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 SEL120 GMP manufacturer or SEL120 GMP API supplier for your needs.
A SEL120 CoA (Certificate of Analysis) is a formal document that attests to SEL120's compliance with SEL120 specifications and serves as a tool for batch-level quality control.
SEL120 CoA mostly includes findings from lab analyses of a specific batch. For each SEL120 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.
SEL120 may be tested according to a variety of international standards, such as European Pharmacopoeia (SEL120 EP), SEL120 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (SEL120 USP).
