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1. Gb 0139
2. Gb-0139
3. Gb0139
4. Td-139
1. Td-139
2. Td139
3. 1450824-22-2
4. Td 139
5. Olitigaltin
6. Gb0139
7. Olitigaltin [usan]
8. Gb-0139
9. 60y0guo72b
10. (2s,3r,4s,5r,6r)-4-[4-(3-fluorophenyl)triazol-1-yl]-2-[(2s,3r,4s,5r,6r)-4-[4-(3-fluorophenyl)triazol-1-yl]-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl-6-(hydroxymethyl)oxane-3,5-diol
11. (2r,2'r,3r,3'r,4s,4's,5r,5'r,6s,6's)-6,6'-thiobis(4-(4-(3-fluorophenyl)-1h-1,2,3-triazol-1-yl)-2-(hydroxymethyl)tetrahydro-2h-pyran-3,5-diol)
12. Unii-60y0guo72b
13. Td2
14. Olitigaltin [inn]
15. Gal-3 Inhibitor Gb0139
16. Galectin-3 Inhibitor Gb0139
17. Chembl4297442
18. Schembl15657269
19. Td 139 [who-dd]
20. Gtpl12148
21. Ex-a1688
22. Who 12032
23. Zinc208938373
24. Cs-6265
25. Db12895
26. Gb 0139
27. Ac-35516
28. Beta-d-galactopyranoside, 3-deoxy-3-(4-(3-fluorophenyl)-1h-1,2,3-triazol-1-yl)-beta-d-galactopyranosyl 3-deoxy-3-(4-(3-fluorophenyl)-1h-1,2,3-triazol-1-yl)-1-thio-
29. Bs-15429
30. Bt173009
31. Hy-19940
32. C72753
33. A857944
34. Q27263259
35. Bis-(3-deoxy-3-(3-fluorophenyl-1h-1,2,3-triazol-1-yl)-beta-d-galactopyranosyl)-sulfane
36. .beta.-d-galactopyranoside, 3-deoxy-3-(4-(3-fluorophenyl)-1h-1,2,3-triazol-1-yl)-.beta.-d-galactopyranosyl 3-deoxy-3-(4-(3-fluorophenyl)-1h-1,2,3-triazol-1-yl)-1-thio-
37. 3,3'-dideoxy-3,3'-bis-(4-(3-fluorophenyl)-1h-1,2,3-triazol-1-yl)-1,1'-sulfanediyl-di-.beta.- D-galactopyranoside
38. Bis(3-deoxy-3-(3-fluorophenyl-1h-1,2,3-triazol-1-yl)-.beta.-d-galactopyranosyl)sulfane
| Molecular Weight | 648.6 g/mol |
|---|---|
| Molecular Formula | C28H30F2N6O8S |
| XLogP3 | 0.2 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 15 |
| Rotatable Bond Count | 8 |
| Exact Mass | 648.18138943 g/mol |
| Monoisotopic Mass | 648.18138943 g/mol |
| Topological Polar Surface Area | 227 Ų |
| Heavy Atom Count | 45 |
| Formal Charge | 0 |
| Complexity | 903 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 10 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Olitigaltin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Olitigaltin, including repackagers and relabelers. The FDA regulates Olitigaltin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Olitigaltin 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 Olitigaltin supplier is an individual or a company that provides Olitigaltin active pharmaceutical ingredient (API) or Olitigaltin finished formulations upon request. The Olitigaltin suppliers may include Olitigaltin API manufacturers, exporters, distributors and traders.
Olitigaltin 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 Olitigaltin 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 Olitigaltin GMP manufacturer or Olitigaltin GMP API supplier for your needs.
A Olitigaltin CoA (Certificate of Analysis) is a formal document that attests to Olitigaltin's compliance with Olitigaltin specifications and serves as a tool for batch-level quality control.
Olitigaltin CoA mostly includes findings from lab analyses of a specific batch. For each Olitigaltin 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.
Olitigaltin may be tested according to a variety of international standards, such as European Pharmacopoeia (Olitigaltin EP), Olitigaltin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Olitigaltin USP).
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