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1. Ft011
1. Ft011
2. 1001288-58-9
3. Ft-011
4. Shp-627
5. Ft-11
6. C6v7zu2npr
7. 2-(3-methoxy-4-propargyloxycinnamoyl)aminobenzoic Acid
8. 2-(((2e)-3-(3-methoxy-4-(2-propyn-1-yloxy)phenyl)-1-oxo-2-propen-1-yl)amino)benzoic Acid
9. Benzoic Acid, 2-(((2e)-3-(3-methoxy-4-(2-propyn-1-yloxy)phenyl)-1-oxo-2-propen-1-yl)amino)-
10. Benzoic Acid, 2-[[(2e)-3-[3-methoxy-4-(2-propyn-1-yloxy)phenyl]-1-oxo-2-propen-1-yl]amino]-
11. Unii-c6v7zu2npr
12. Schembl1590608
13. Schembl1590611
14. Chembl1075834
15. Bqb28858
16. Zinc49050436
17. Cs-5842
18. Ac-35521
19. Hy-100495
20. N17095
21. (e)-2-[[3-(3-methoxy-4-(prop-2-ynyloxy)phenyl)-1-oxo-2-propenyl]amino]benzoic Acid
22. 2-[[(e)-3-(3-methoxy-4-prop-2-ynoxyphenyl)prop-2-enoyl]amino]benzoic Acid
| Molecular Weight | 351.4 g/mol |
|---|---|
| Molecular Formula | C20H17NO5 |
| XLogP3 | 3.3 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Exact Mass | 351.11067264 g/mol |
| Monoisotopic Mass | 351.11067264 g/mol |
| Topological Polar Surface Area | 84.9 Ų |
| Heavy Atom Count | 26 |
| Formal Charge | 0 |
| Complexity | 564 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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 FT011 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 FT011 manufacturer or FT011 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred FT011 manufacturer or FT011 supplier.
PharmaCompass also assists you with knowing the FT011 API Price utilized in the formulation of products. FT011 API Price is not always fixed or binding as the FT011 Price is obtained through a variety of data sources. The FT011 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SHP-627 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SHP-627, including repackagers and relabelers. The FDA regulates SHP-627 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SHP-627 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 SHP-627 supplier is an individual or a company that provides SHP-627 active pharmaceutical ingredient (API) or SHP-627 finished formulations upon request. The SHP-627 suppliers may include SHP-627 API manufacturers, exporters, distributors and traders.
SHP-627 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 SHP-627 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 SHP-627 GMP manufacturer or SHP-627 GMP API supplier for your needs.
A SHP-627 CoA (Certificate of Analysis) is a formal document that attests to SHP-627's compliance with SHP-627 specifications and serves as a tool for batch-level quality control.
SHP-627 CoA mostly includes findings from lab analyses of a specific batch. For each SHP-627 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.
SHP-627 may be tested according to a variety of international standards, such as European Pharmacopoeia (SHP-627 EP), SHP-627 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (SHP-627 USP).
