Synopsis
Synopsis
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API Suppliers
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USDMF
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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EDQM
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USP
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JP
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Others
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
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Listed Dossiers
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Health Canada Patents
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Data Compilation #PharmaFlow
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1. At-007
2. 2170729-29-8
3. Govorestat
4. At007
5. Govorestat [usan]
6. 6jlq8k35kk
7. 2-[4-oxo-3-[[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]methyl]thieno[3,4-d]pyridazin-1-yl]acetic Acid
8. Gavorestat
9. Govorestat [inn]
10. Unii-6jlq8k35kk
11. Chembl4650327
12. Schembl19747408
13. Ex-a3180
14. Mfcd32263046
15. Who 11608
16. Zb1621
17. Akos037649079
18. Ac-36354
19. Bs-16512
20. Hy-129586
21. Cs-0106794
22. D81255
23. (4-oxo-3-{[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]methyl}-3,4- Dihydrothieno[3,4-d]pyridazin-1-yl)acetic Acid
24. Thieno[3,4-d]pyridazine-1-acetic Acid, 3,4-dihydro-4-oxo-3-[[5-(trifluoromethyl)-2-benzothiazolyl]methyl]-
| Molecular Weight | 425.4 g/mol |
|---|---|
| Molecular Formula | C17H10F3N3O3S2 |
| XLogP3 | 3.2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 4 |
| Exact Mass | 425.01156802 g/mol |
| Monoisotopic Mass | 425.01156802 g/mol |
| Topological Polar Surface Area | 139 Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 690 |
| 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 |
Drugs in Development
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PharmaCompass offers a list of Govorestat 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 Govorestat manufacturer or Govorestat supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Govorestat manufacturer or Govorestat supplier.
PharmaCompass also assists you with knowing the Govorestat API Price utilized in the formulation of products. Govorestat API Price is not always fixed or binding as the Govorestat Price is obtained through a variety of data sources. The Govorestat Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Govorestat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Govorestat, including repackagers and relabelers. The FDA regulates Govorestat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Govorestat 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 Govorestat supplier is an individual or a company that provides Govorestat active pharmaceutical ingredient (API) or Govorestat finished formulations upon request. The Govorestat suppliers may include Govorestat API manufacturers, exporters, distributors and traders.
Govorestat 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 Govorestat 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 Govorestat GMP manufacturer or Govorestat GMP API supplier for your needs.
A Govorestat CoA (Certificate of Analysis) is a formal document that attests to Govorestat's compliance with Govorestat specifications and serves as a tool for batch-level quality control.
Govorestat CoA mostly includes findings from lab analyses of a specific batch. For each Govorestat 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.
Govorestat may be tested according to a variety of international standards, such as European Pharmacopoeia (Govorestat EP), Govorestat JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Govorestat USP).
