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1. N-(4-(4-(5-cyano-2-thienyl)phenoxy)tetrahydrofuran-3-yl)propane-2-sulfonamide
2. Pf-04958242
1. Pesampator
2. Pf-04958242
3. 1258963-59-5
4. Pesampator [usan]
5. Pf-4958242
6. 9g1a824cc2
7. 2-propanesulfonamide, N-[(3s,4s)-4-[4-(5-cyano-2-thienyl)phenoxy]tetrahydro-3-furanyl]-
8. N-{(3s,4s)-4-[4-(5-cyanothiophen-2-yl)phenoxy]tetrahydrofuran-3-yl}propane-2-sulfonamide
9. Unii-9g1a824cc2
10. N-((3s,4s)-4-(4-(5-cyanothiophen-2-yl)phenoxy)tetrahydrofuran-3-yl)propane-2-sulfonamide
11. Pesampator [inn]
12. Pf 04958242
13. Biib104
14. Biib-104
15. Schembl1869187
16. Dtxsid001337272
17. Who 11917
18. Zinc72316201
19. Db11843
20. Hy-112781
21. Cs-0064139
22. J3.560.860e
23. Q27272515
24. N-[(3s,4s)-4-[4-(5-cyanothiophen-2-yl)phenoxy]oxolan-3-yl]propane-2-sulfonamide
25. Xpf
| Molecular Weight | 392.5 g/mol |
|---|---|
| Molecular Formula | C18H20N2O4S2 |
| XLogP3 | 2.9 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 6 |
| Exact Mass | 392.08644947 g/mol |
| Monoisotopic Mass | 392.08644947 g/mol |
| Topological Polar Surface Area | 125 Ų |
| Heavy Atom Count | 26 |
| Formal Charge | 0 |
| Complexity | 617 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Drugs in Development
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PharmaCompass offers a list of TTYKUKSFWHEBLI-DLBZAZTESA-N 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 TTYKUKSFWHEBLI-DLBZAZTESA-N manufacturer or TTYKUKSFWHEBLI-DLBZAZTESA-N supplier for your needs.
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TTYKUKSFWHEBLI-DLBZAZTESA-N 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).
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A TTYKUKSFWHEBLI-DLBZAZTESA-N CoA (Certificate of Analysis) is a formal document that attests to TTYKUKSFWHEBLI-DLBZAZTESA-N's compliance with TTYKUKSFWHEBLI-DLBZAZTESA-N specifications and serves as a tool for batch-level quality control.
TTYKUKSFWHEBLI-DLBZAZTESA-N CoA mostly includes findings from lab analyses of a specific batch. For each TTYKUKSFWHEBLI-DLBZAZTESA-N 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.
TTYKUKSFWHEBLI-DLBZAZTESA-N may be tested according to a variety of international standards, such as European Pharmacopoeia (TTYKUKSFWHEBLI-DLBZAZTESA-N EP), TTYKUKSFWHEBLI-DLBZAZTESA-N JP (Japanese Pharmacopeia) and the US Pharmacopoeia (TTYKUKSFWHEBLI-DLBZAZTESA-N USP).
