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1. 5-(ethylsulfonyl)-2-(naphthalen-2-yl)benzo(d)oxazole
2. 5-ethylsulfonyl-nbo
1. 945531-77-1
2. Smt C1100
3. Bmn-195
4. Bmn 195
5. Smt-c1100
6. Smtc-1100
7. Ezutromid [inn]
8. 5-(ethylsulfonyl)-2-(naphthalen-2-yl)benzo[d]oxazole
9. 5-ethylsulfonyl-nbo
10. 5-ethylsulfonyl-2-naphthalen-2-yl-1,3-benzoxazole
11. 5-(ethylsulfonyl)-2-(naphthalen-2-yl)benzo(d)oxazole
12. 645r07lf0d
13. Benzoxazole, 5-(ethylsulfonyl)-2-(2-naphthalenyl)-
14. Unii-645r07lf0d
15. Smtc1100
16. Smtc 1100
17. Vox-c1100
18. Ezutromid [who-dd]
19. Schembl732212
20. Chembl1773683
21. Gtpl11110
22. Dtxsid30241525
23. Bcp18328
24. Ex-a2333
25. Bdbm50519636
26. Zinc71297091
27. Bmn-195; Smt C1100
28. Akos030527030
29. Cs-5710
30. Db12888
31. Sb19603
32. Ac-30950
33. Hy-17614
34. F20702
35. A901653
36. Q27263708
37. 5-(ethanesulfonyl)-2-(naphthalen-2-yl)-1,3-benzoxazole
| Molecular Weight | 337.4 g/mol |
|---|---|
| Molecular Formula | C19H15NO3S |
| XLogP3 | 4.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 3 |
| Exact Mass | 337.07726451 g/mol |
| Monoisotopic Mass | 337.07726451 g/mol |
| Topological Polar Surface Area | 68.6 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 543 |
| 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 |
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47
PharmaCompass offers a list of Ezutromid 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 Ezutromid manufacturer or Ezutromid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ezutromid manufacturer or Ezutromid supplier.
PharmaCompass also assists you with knowing the Ezutromid API Price utilized in the formulation of products. Ezutromid API Price is not always fixed or binding as the Ezutromid Price is obtained through a variety of data sources. The Ezutromid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ezutromid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ezutromid, including repackagers and relabelers. The FDA regulates Ezutromid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ezutromid 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 Ezutromid supplier is an individual or a company that provides Ezutromid active pharmaceutical ingredient (API) or Ezutromid finished formulations upon request. The Ezutromid suppliers may include Ezutromid API manufacturers, exporters, distributors and traders.
Ezutromid 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 Ezutromid 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 Ezutromid GMP manufacturer or Ezutromid GMP API supplier for your needs.
A Ezutromid CoA (Certificate of Analysis) is a formal document that attests to Ezutromid's compliance with Ezutromid specifications and serves as a tool for batch-level quality control.
Ezutromid CoA mostly includes findings from lab analyses of a specific batch. For each Ezutromid 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.
Ezutromid may be tested according to a variety of international standards, such as European Pharmacopoeia (Ezutromid EP), Ezutromid JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ezutromid USP).
