127171-88-4
Chemical Structure
Chitohexaose hexahydrochloride
- CAS No.: 127171-88-4
- Formula:C36H74Cl6N6O25
- Molecular Weight:1203.72
IUPAC Name: (2R,3R,4S,5R)-2-amino-4-(((2S,3R,4R,5S,6R)-3-amino-5-(((2S,3R,4R,5S,6R)-3-amino-5-(((2S,3R,4R,5S,6R)-3-amino-5-(((2S,3R,4R,5S,6R)-3-amino-5-(((2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4-hydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4-hydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4-hydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4-hydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-3,5,6-trihydroxyhexanal hexahydrochloride
InChIKey: YNVCXPBWPOREPI-ATZWJUBSSA-N
SMILES: OC[C@@H](O[C@H]1O[C@@H]([C@@H]([C@H]2N)O)[C@H](O[C@H]2O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)CO)[C@H]([C@@H]([C@H]1N)O)O[C@@H]([C@@H]([C@H]3O)N)O[C@@H]([C@H]3O[C@@H]([C@@H]([C@H]4O)N)O[C@@H]([C@H]4O[C@@H]([C@@H]([C@H]5O)N)O[C@@H]([C@H]5O)CO)CO)CO.Cl.Cl.Cl.Cl.Cl.Cl
Biological Activity: Chitohexaose hexahydrochloride is a small molecular polysaccharide. Chitohexaose hexahydrochloride inhibits the binding of AgW to TLR4. Chitohexaose hexahydrochloride upregulates IL-10, inhibits LPS-induced upregulation of ROS, induces alternative activation of macrophages/monocytes, and suppresses LPS-induced production of TNF-α, IL-1β and IL-6. Chitohexaose hexahydrochloride reverses the mortality of mice challenged with APAP or LPS. Chitohexaose hexahydrochloride can be used in research related to Acetaminophen (HY-66005)-induced hepatotoxicity and endotoxemia[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Chitohexaose hexahydrochloride | 95.0% | Chitohexaose hexahydrochloride is a small molecular polysaccharide. Chitohexaose hexahydrochloride inhibits the binding of AgW to TLR4. Chitohexaose hexahydrochloride upregulates IL-10, inhibits LPS-induced upregulation of ROS, induces alternative activation of macrophages/monocytes, and suppresses LPS-induced production of TNF-α, IL-1β and IL-6. Chitohexaose hexahydrochloride reverses the mortality of mice challenged with APAP or LPS. Chitohexaose hexahydrochloride can be used in research related to Acetaminophen (HY-66005)-induced hepatotoxicity and endotoxemia. | ||||||||||||||||||||
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References
- [1]. Barman PK, et al. Chitohexaose protects against acetaminophen-induced hepatotoxicity in mice. Cell Death Dis. 2016;7(5):e2224. Published 2016 May 12. [Content Brief]
- [2]. Panda SK, et al. Chitohexaose activates macrophages by alternate pathway through TLR4 and blocks endotoxemia. PLoS Pathog. 2012;8(5):e1002717. [Content Brief]
