38854-46-5
Chemical Structure
Hexa-N-acetylchitohexaose
- CAS. Nr.: 38854-46-5
- Formula:C48H80N6O31
- Molecular Weight:1237.17
IUPAC Name: N-((2S,3R,4R,5S,6R)-2-(((2R,3S,4R,5R)-5-acetamido-1,2,4-trihydroxy-6-oxohexan-3-yl)oxy)-5-(((2S,3R,4R,5S,6R)-3-acetamido-5-(((2S,3R,4R,5S,6R)-3-acetamido-5-(((2S,3R,4R,5S,6R)-3-acetamido-5-(((2S,3R,4R,5S,6R)-3-acetamido-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-3-yl)acetamide
InChIKey: FUHDMRPNDKDRFE-LPUYKFNUSA-N
SMILES: CC(N[C@H]([C@H]([C@@H]1O[C@H](O[C@@H]2CO)[C@@H]([C@H]([C@@H]2O[C@H](O[C@@H]3CO)[C@@H]([C@H]([C@@H]3O)O)NC(C)=O)O)NC(C)=O)O)[C@@H](O[C@@H]1CO)O[C@@H]([C@@H]([C@H]4NC(C)=O)O)[C@H](O[C@H]4O[C@@H]([C@@H]([C@H]5NC(C)=O)O)[C@H](O[C@H]5O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)NC(C)=O)CO)CO)=O
Biological Activity: Hexa-N-acetylchitohexaose is an inducer of disease resistance in crop plants, which could elicit an increase of lignification-related and antioxidative enzymes in soybean plants. Hexa-N-acetylchitohexaose is a substrate of lysozyme. Hexa-N-acetylchitohexaose shows antitumor effect[1][2][3].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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Hexa-N-acetylchitohexaose | 99.81% | Hexa-N-acetylchitohexaose is an inducer of disease resistance in crop plants, which could elicit an increase of lignification-related and antioxidative enzymes in soybean plants. Hexa-N-acetylchitohexaose is a substrate of lysozyme. Hexa-N-acetylchitohexaose shows antitumor effect. | ||||||||||||||||||||
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Similarity Score 0.89
HY-N7698APenta-N-acetylchitopentaose -
Similarity Score 0.80
HY-N10629A2G0 Glycan -
Similarity Score 0.78
HY-N7698Tetra-N-acetylchitotetraose -
Similarity Score 0.77
HY-N10630G-NGA2 N-Glycan -
Similarity Score 0.73
HY-N10627NA2 Glycan -
Similarity Score 0.73
HY-N12073Monofucosyllacto-N-hexaose I -
Similarity Score 0.72
HY-N10631Paucimannose -
Similarity Score 0.72
HY-N10511GM1a Ganglioside oligosaccharide -
Similarity Score 0.69
HY-N12074Monofucosyllacto-N-hexaose III -
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References
- [1]. Li K, et al. Access to N-Acetylated Chitohexaose with Well-Defined Degrees of Acetylation. Biomed Res Int. 2017;2017:2486515. [Content Brief]
- [2]. David C. Phillips. THE HEN EGG-WHITE LYSOZYME MOLECULE. Proc Natl Acad Sci U S A. 1967 Mar; 57(3): 483-495.
- [3]. Suzuki K, et al. Antitumor effect of hexa-N-acetylchitohexaose and chitohexaose. Carbohydr Res. 1986;151:403-408. [Content Brief]
