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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US Exclusivities
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Health Canada Patents
US Medicaid
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1. Qs 21
2. Qs-21
3. Qs21
4. Saponin Qa-21v1
5. Sq 21a
1. Qs 21
2. Qa 21v1
3. 3lhl0s9kbm
4. Qs-21-api
5. Qs21
6. Saponin Qa 21v1
7. Saponin Qa-21v1
8. Qa 21
9. Unii-3lhl0s9kbm
10. Qs-21-apiose Isomer
11. Qs 21 [who-dd]
12. Qa-21v1
13. Qs-21v1
14. Dtxsid601318719
15. Hy-101092
16. Cs-0020802
| Molecular Weight | 1990.1 g/mol |
|---|---|
| Molecular Formula | C92H148O46 |
| XLogP3 | -2.4 |
| Hydrogen Bond Donor Count | 23 |
| Hydrogen Bond Acceptor Count | 46 |
| Rotatable Bond Count | 38 |
| Exact Mass | 1988.9241772 g/mol |
| Monoisotopic Mass | 1988.9241772 g/mol |
| Topological Polar Surface Area | 717 Ų |
| Heavy Atom Count | 138 |
| Formal Charge | 0 |
| Complexity | 4100 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 51 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Adjuvants, Immunologic
Substances that augment, stimulate, activate, potentiate, or modulate the immune response at either the cellular or humoral level. The classical agents (Freund's adjuvant, BCG, Corynebacterium parvum, et al.) contain bacterial antigens. Some are endogenous (e.g., histamine, interferon, transfer factor, tuftsin, interleukin-1). Their mode of action is either non-specific, resulting in increased immune responsiveness to a wide variety of antigens, or antigen-specific, i.e., affecting a restricted type of immune response to a narrow group of antigens. The therapeutic efficacy of many biological response modifiers is related to their antigen-specific immunoadjuvanticity. (See all compounds classified as Adjuvants, Immunologic.)
ABOUT THIS PAGE
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PharmaCompass offers a list of Stimulon 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 Stimulon manufacturer or Stimulon supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Stimulon manufacturer or Stimulon supplier.
PharmaCompass also assists you with knowing the Stimulon API Price utilized in the formulation of products. Stimulon API Price is not always fixed or binding as the Stimulon Price is obtained through a variety of data sources. The Stimulon Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A QS 21 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of QS 21, including repackagers and relabelers. The FDA regulates QS 21 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. QS 21 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 QS 21 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A QS 21 supplier is an individual or a company that provides QS 21 active pharmaceutical ingredient (API) or QS 21 finished formulations upon request. The QS 21 suppliers may include QS 21 API manufacturers, exporters, distributors and traders.
click here to find a list of QS 21 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
QS 21 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 QS 21 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 QS 21 GMP manufacturer or QS 21 GMP API supplier for your needs.
A QS 21 CoA (Certificate of Analysis) is a formal document that attests to QS 21's compliance with QS 21 specifications and serves as a tool for batch-level quality control.
QS 21 CoA mostly includes findings from lab analyses of a specific batch. For each QS 21 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.
QS 21 may be tested according to a variety of international standards, such as European Pharmacopoeia (QS 21 EP), QS 21 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (QS 21 USP).
