Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
1. 2439277-80-0
2. 4-amino-1-(2-chlorophenyl)-7-(trifluoromethyl)pyrido(2,3-d)pyrimidin-2(1h)-one
3. 4-amino-1-(2-chlorophenyl)-7-(trifluoromethyl)pyrido[2,3-d]pyrimidin-2(1h)-one
4. Mat2a-in-9?
5. Schembl22103481
6. Ex-a8014k
7. Ide-397
8. Bvnkurjmnqnvao-uhfffaoysa-n
9. Bdbm508034
10. T46p23pk39
11. Us11046691, Compound 167
12. 4-amino-1-(2-chlorophenyl)-7-(trifluoro-methyl)pyrido[2,3-d]pyrimidin-2(1h)-one
13. Ms-25205
14. Db-380487
15. Hy-148499
16. Ide397 (gsk-4362676)
17. Cs-0628754
18. 4-amino-1-(2-chlorophenyl)-7- (trifluoro-methyl)pyrido[2,3- D]pyrimidin-2(1h)-one
19. Pyrido[2,3-d]pyrimidin-2(1h)-one, 4-amino-1-(2-chlorophenyl)-7-(trifluoromethyl)-
| Molecular Weight | 340.69 g/mol |
|---|---|
| Molecular Formula | C14H8ClF3N4O |
| XLogP3 | 2.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 1 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 71.6 |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 513 |
| 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 | 1 |
ABOUT THIS PAGE
75
PharmaCompass offers a list of IDE-397 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 IDE-397 manufacturer or IDE-397 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred IDE-397 manufacturer or IDE-397 supplier.
PharmaCompass also assists you with knowing the IDE-397 API Price utilized in the formulation of products. IDE-397 API Price is not always fixed or binding as the IDE-397 Price is obtained through a variety of data sources. The IDE-397 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A IDE-397 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IDE-397, including repackagers and relabelers. The FDA regulates IDE-397 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IDE-397 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 IDE-397 supplier is an individual or a company that provides IDE-397 active pharmaceutical ingredient (API) or IDE-397 finished formulations upon request. The IDE-397 suppliers may include IDE-397 API manufacturers, exporters, distributors and traders.
IDE-397 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 IDE-397 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 IDE-397 GMP manufacturer or IDE-397 GMP API supplier for your needs.
A IDE-397 CoA (Certificate of Analysis) is a formal document that attests to IDE-397's compliance with IDE-397 specifications and serves as a tool for batch-level quality control.
IDE-397 CoA mostly includes findings from lab analyses of a specific batch. For each IDE-397 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.
IDE-397 may be tested according to a variety of international standards, such as European Pharmacopoeia (IDE-397 EP), IDE-397 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (IDE-397 USP).
