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1. Progerinin
2. Kc-3
3. Unii-426p9hsr8i
4. Slc-d011
5. 2249696-72-6
6. Progerinin (usan)
7. Progerinin [usan]
8. Kc3
9. (7s)-(+)-8,8-dimethyl-7-(3-phenyl-allyloxy)-7,8-dihydro-6h-pyrano(3,2-g)chromen-2-one
10. (7s)-7,8-dihydro-8,8-dimethyl-7-(((2e)-3-phenyl-2-propen-1-yl)oxy)-2h,6h-benzo(1,2-b:5,4-b')dipyran-2-one
11. 2h,6h-benzo(1,2-b:5,4-b')dipyran-2-one, 7,8-dihydro-8,8-dimethyl-7-(((2e)-3-phenyl-2-propen-1-yl)oxy)-, (7s)-
12. (7s)-(+)-8,8-dimethyl-7-(3-phenyl-allyloxy)-7,8-dihydro-6h-pyrano[3,2-g]chromen-2-one
13. (7s)-7,8-dihydro-8,8-dimethyl-7-[[(2e)-3-phenyl-2-propen-1-yl]oxy]-2h,6h-benzo[1,2-b:5,4-b']dipyran-2-one
14. 2h,6h-benzo[1,2-b:5,4-b']dipyran-2-one, 7,8-dihydro-8,8-dimethyl-7-[[(2e)-3-phenyl-2-propen-1-yl]oxy]-, (7s)-
15. Chembl1631723
16. Schembl21681681
17. Schembl21681682
18. D12872
| Molecular Weight | 362.4 g/mol |
|---|---|
| Molecular Formula | C23H22O4 |
| XLogP3 | 4.6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 44.8 |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 587 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Progerinin 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 Progerinin manufacturer or Progerinin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Progerinin manufacturer or Progerinin supplier.
PharmaCompass also assists you with knowing the Progerinin API Price utilized in the formulation of products. Progerinin API Price is not always fixed or binding as the Progerinin Price is obtained through a variety of data sources. The Progerinin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Progerinin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Progerinin, including repackagers and relabelers. The FDA regulates Progerinin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Progerinin 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 Progerinin supplier is an individual or a company that provides Progerinin active pharmaceutical ingredient (API) or Progerinin finished formulations upon request. The Progerinin suppliers may include Progerinin API manufacturers, exporters, distributors and traders.
Progerinin 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 Progerinin 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 Progerinin GMP manufacturer or Progerinin GMP API supplier for your needs.
A Progerinin CoA (Certificate of Analysis) is a formal document that attests to Progerinin's compliance with Progerinin specifications and serves as a tool for batch-level quality control.
Progerinin CoA mostly includes findings from lab analyses of a specific batch. For each Progerinin 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.
Progerinin may be tested according to a variety of international standards, such as European Pharmacopoeia (Progerinin EP), Progerinin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Progerinin USP).
