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1. (s)-7-(dimethylphosphoryl)-3-(2-((6,6-dimethylpiperidin- 3-yl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)-1h-indole- 6-carbonitrile
2. Sy-5609
1. Sy-5609
2. Sy5609
3. 2417302-07-7
4. Tw6044c3o6
5. 7-dimethylphosphoryl-3-[2-[[(3s)-6,6-dimethylpiperidin-3-yl]amino]-5-(trifluoromethyl)pyrimidin-4-yl]-1h-indole-6-carbonitrile
6. 1h-indole-6-carbonitrile, 7-(dimethylphosphinyl)-3-(2-(((3s)-6,6-dimethyl-3-piperidinyl)amino)-5-(trifluoromethyl)-4-pyrimidinyl)-
7. 1h-indole-6-carbonitrile, 7-(dimethylphosphinyl)-3-[2-[[(3s)-6,6-dimethyl-3-piperidinyl]amino]-5-(trifluoromethyl)-4-pyrimidinyl]-
8. Cdk7-in-3
9. Unii-tw6044c3o6
10. Schembl22076284
11. Gtpl11841
12. Ex-a6744
13. Nsc837396
14. At32797
15. Nsc-837396
16. Hy-138293
17. Cs-0147167
18. Sy-0005609
| Molecular Weight | 490.5 g/mol |
|---|---|
| Molecular Formula | C23H26F3N6OP |
| XLogP3 | 2.7 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 4 |
| Exact Mass | 490.18578096 g/mol |
| Monoisotopic Mass | 490.18578096 g/mol |
| Topological Polar Surface Area | 107 Ų |
| Heavy Atom Count | 34 |
| Formal Charge | 0 |
| Complexity | 838 |
| 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 SY-5609 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 SY-5609 manufacturer or SY-5609 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred SY-5609 manufacturer or SY-5609 supplier.
PharmaCompass also assists you with knowing the SY-5609 API Price utilized in the formulation of products. SY-5609 API Price is not always fixed or binding as the SY-5609 Price is obtained through a variety of data sources. The SY-5609 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SY-5609 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SY-5609, including repackagers and relabelers. The FDA regulates SY-5609 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SY-5609 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 SY-5609 supplier is an individual or a company that provides SY-5609 active pharmaceutical ingredient (API) or SY-5609 finished formulations upon request. The SY-5609 suppliers may include SY-5609 API manufacturers, exporters, distributors and traders.
SY-5609 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 SY-5609 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 SY-5609 GMP manufacturer or SY-5609 GMP API supplier for your needs.
A SY-5609 CoA (Certificate of Analysis) is a formal document that attests to SY-5609's compliance with SY-5609 specifications and serves as a tool for batch-level quality control.
SY-5609 CoA mostly includes findings from lab analyses of a specific batch. For each SY-5609 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.
SY-5609 may be tested according to a variety of international standards, such as European Pharmacopoeia (SY-5609 EP), SY-5609 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (SY-5609 USP).
