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. Iacs-13909
2. 2160546-07-4
3. 1-[3-(2,3-dichlorophenyl)-2h-pyrazolo[3,4-b]pyrazin-6-yl]-4-methylpiperidin-4-amine
4. 1-(3-(2,3-dichlorophenyl)-1h-pyrazolo[3,4-b]pyrazin-6-yl)-4-methylpiperidin-4-amine
5. 1-(3-(2,3-dichlorophenyl)-2h-pyrazolo[3,4-b]pyrazin-6-yl)-4-methylpiperidin-4-amine
6. Schembl19641152
7. Bbp 398
8. Bbp-398
9. Us10280171, Example 1
10. Bdbm384117
11. Glxc-26922
12. Ex-a4355
13. S9703
14. Akos040759720
15. Ac-36570
16. Ms-26129
17. Hy-137092
18. Cs-0136474
19. F82752
20. U9y
Molecular Weight | 377.3 g/mol |
---|---|
Molecular Formula | C17H18Cl2N6 |
XLogP3 | 3 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 2 |
Exact Mass | g/mol |
Monoisotopic Mass | g/mol |
Topological Polar Surface Area | 83.7 |
Heavy Atom Count | 25 |
Formal Charge | 0 |
Complexity | 472 |
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
77
PharmaCompass offers a list of BBP-398 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 BBP-398 manufacturer or BBP-398 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred BBP-398 manufacturer or BBP-398 supplier.
PharmaCompass also assists you with knowing the BBP-398 API Price utilized in the formulation of products. BBP-398 API Price is not always fixed or binding as the BBP-398 Price is obtained through a variety of data sources. The BBP-398 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A IACS-13909 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IACS-13909, including repackagers and relabelers. The FDA regulates IACS-13909 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IACS-13909 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 IACS-13909 supplier is an individual or a company that provides IACS-13909 active pharmaceutical ingredient (API) or IACS-13909 finished formulations upon request. The IACS-13909 suppliers may include IACS-13909 API manufacturers, exporters, distributors and traders.
IACS-13909 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 IACS-13909 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 IACS-13909 GMP manufacturer or IACS-13909 GMP API supplier for your needs.
A IACS-13909 CoA (Certificate of Analysis) is a formal document that attests to IACS-13909's compliance with IACS-13909 specifications and serves as a tool for batch-level quality control.
IACS-13909 CoA mostly includes findings from lab analyses of a specific batch. For each IACS-13909 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.
IACS-13909 may be tested according to a variety of international standards, such as European Pharmacopoeia (IACS-13909 EP), IACS-13909 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (IACS-13909 USP).