Synopsis
Synopsis
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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
DRUG PRODUCT COMPOSITIONS
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US Patents
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FDF
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Data Compilation #PharmaFlow
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1. Dtxsid60952839
2. 5-({3-(acetylsulfanyl)-1-[(carboxymethyl)imino]-1-hydroxypropan-2-yl}imino)-5-hydroxynorvaline
3. Refchem:1072301
4. Dtxcid601380912
5. S-acetyl-l-glutathione
6. 5-[[3-acetylsulfanyl-1-(carboxymethylamino)-1-oxopropan-2-yl]amino]-2-amino-5-oxopentanoic Acid
7. C12h19n3o7s
8. 5-[[1-(acetylsulfanylmethyl)-2-(carboxymethylamino)-2-oxo-ethyl]amino]-2-amino-5-oxo-pentanoic Acid
9. Glutathione-s-acetate
10. Schembl420277
11. Orb2279192
12. Fvrwsipjnwxceo-uhfffaoysa-n
13. (2s)-4-{[(1r)-2-(acetylsulfanyl)-1-[(carboxymethyl)carbamoyl]ethyl]carbamoyl}-2-aminobutanoic Acid
14. Bcp09327
15. Akos025404546
16. Ds-9100
17. Fs165201
18. Ns00047864
19. S-acetyl-?-l-glutamyl-l-cysteinyl-glycine;sag
| Molecular Weight | 349.36 g/mol |
|---|---|
| Molecular Formula | C12H19N3O7S |
| XLogP3 | -4.4 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 11 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 201 |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 483 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of S-Acetyl L Glutathione API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right S-Acetyl L Glutathione manufacturer or S-Acetyl L Glutathione supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred S-Acetyl L Glutathione manufacturer or S-Acetyl L Glutathione supplier.
A S-Acetyl L Glutathione manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of S-Acetyl L Glutathione, including repackagers and relabelers. The FDA regulates S-Acetyl L Glutathione manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. S-Acetyl L Glutathione API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of S-Acetyl L Glutathione manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A S-Acetyl L Glutathione supplier is an individual or a company that provides S-Acetyl L Glutathione active pharmaceutical ingredient (API) or S-Acetyl L Glutathione finished formulations upon request. The S-Acetyl L Glutathione suppliers may include S-Acetyl L Glutathione API manufacturers, exporters, distributors and traders.
click here to find a list of S-Acetyl L Glutathione suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
S-Acetyl L Glutathione 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 S-Acetyl L Glutathione GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right S-Acetyl L Glutathione GMP manufacturer or S-Acetyl L Glutathione GMP API supplier for your needs.
A S-Acetyl L Glutathione CoA (Certificate of Analysis) is a formal document that attests to S-Acetyl L Glutathione's compliance with S-Acetyl L Glutathione specifications and serves as a tool for batch-level quality control.
S-Acetyl L Glutathione CoA mostly includes findings from lab analyses of a specific batch. For each S-Acetyl L Glutathione 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.
S-Acetyl L Glutathione may be tested according to a variety of international standards, such as European Pharmacopoeia (S-Acetyl L Glutathione EP), S-Acetyl L Glutathione JP (Japanese Pharmacopeia) and the US Pharmacopoeia (S-Acetyl L Glutathione USP).