CAS 38854-46-5
:N-Acetylchitohexaose
Description:
N-Acetylchitohexaose is a hexasaccharide composed of repeating units of N-acetylglucosamine and glucosamine, which are derivatives of chitin. This compound is characterized by its structure, which includes six sugar units linked by β(1→4) glycosidic bonds, with N-acetyl groups present on the amino sugars. It is typically soluble in water and exhibits properties associated with polysaccharides, such as viscosity and gel formation. N-Acetylchitohexaose is of interest in various fields, including biochemistry and materials science, due to its potential applications in drug delivery, wound healing, and as a biocompatible material. Additionally, it may exhibit biological activities, such as immunomodulatory effects, making it a subject of research in the context of health and disease. Its CAS number, 38854-46-5, allows for easy identification and reference in scientific literature and databases. Overall, N-acetylchitohexaose represents a significant compound in the study of glycosaminoglycans and their derivatives.
Formula:C48H80N6O31
InChI:InChI=1S/C48H80N6O31/c1-14(62)49-20(7-55)32(69)39(21(68)8-56)81-45-28(51-16(3)64)35(72)41(23(10-58)77-45)83-47-30(53-18(5)66)37(74)43(25(12-60)79-47)85-48-31(54-19(6)67)38(75)42(26(13-61)80-48)84-46-29(52-17(4)65)36(73)40(24(11-59)78-46)82-44-27(50-15(2)63)34(71)33(70)22(9-57)76-44/h7,20-48,56-61,68-75H,8-13H2,1-6H3,(H,49,62)(H,50,63)(H,51,64)(H,52,65)(H,53,66)(H,54,67)/t20-,21+,22+,23+,24+,25+,26+,27+,28+,29+,30+,31+,32+,33+,34+,35+,36+,37+,38+,39+,40+,41+,42+,43+,44-,45-,46-,47-,48-/m0/s1
InChI key:InChIKey=FUHDMRPNDKDRFE-LPUYKFNUSA-N
SMILES:O([C@H]1[C@H](NC(C)=O)[C@@H](O)[C@H](O[C@H]2[C@H](NC(C)=O)[C@@H](O)[C@H](O[C@H]3[C@H](NC(C)=O)[C@@H](O)[C@H](O)[C@@H](CO)O3)[C@@H](CO)O2)[C@@H](CO)O1)[C@@H]4[C@@H](CO)O[C@@H](O[C@@H]5[C@@H](CO)O[C@@H](O[C@@H]([C@@H]([C@@H](NC(C)=O)C=O)O)[C@@H](CO)O)[C@H](NC(C)=O)[C@H]5O)[C@H](NC(C)=O)[C@H]4O
Synonyms:- 2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1->4)-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1->4)-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1->4)-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1->4)-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1->4)-2-(acetylamino)-2-deoxy-D-glucose
- <span class="text-smallcaps">D</smallcap>-Glucose, O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</span>-glucopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-
- Brn 0001006
- Chitohexaose, hexa-N-acetyl (6CI)
- Chitohexaose, hexa-N-acetyl-
- D-Glucose, O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)-2-(acetylamino)-2-deoxy-
- Hexa-N-acetylchitohexaose
- N-Acetylchitohexaose
- N-Acetylglucosamine hexamer
- N-Acetylglucosamine hexasaccharide
- Nacos-6
- O-2-(Acetylamino)-2-deoxy-β-<span class="text-smallcaps">D</smallcap>-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-<smallcap>D</span>-glucose
- O-2-(Acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-D-glucose
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Found 7 products.
Hexa-N-acetylchitohexaose
CAS:Hexa-N-acetylchitohexaose boosts crop immunity, soybean health, and has antitumor effects.Formula:C48H80N6O31Purity:98%Color and Shape:SolidMolecular weight:1237.17N,N'',N'''',N'''''',N'''''''',N''''''''''-Hexaacetylchitohexaose
CAS:Formula:C48H80N6O31Purity:≥ 90.0%Color and Shape:White to off-white powderMolecular weight:1237.18N,N',N'',N''',N'''',N'''''-Hexaacetyl chitohexaose
CAS:Formula:C48H80N6O31Purity:95%~99%Molecular weight:1237.18N,N’,N’’,N’’’,N’’’’,N’’’’’-Hexaacetylchitohexaose
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications Studied for anti-tumor effects.<br>References Suzuki, K., et al.: Carbohydrate Research, 151, 403 (1986)<br></p>Formula:C48H80N6O31Color and Shape:NeatMolecular weight:1237.20N,N',N'',N''',N'''',N'''''-Hexaacetylchitohexaose
CAS:<p>Hexaacetylchitohexaose is a hexamer of N-acetylgucosamine subunits which are linked by β-(1,4)-glucosidic bonds. N-acetylgucosamine is the monomeric unit of the natural polymer chitin which is degraded by chitinases, in mammals, to form smaller fragments that can induce an immune response. Like chitin and some of its derivatives, hexaacetylchitohexaose is a substrate of lysozymes. Hexaacetylchitohexaose has been shown to significantly inhibit tumour growth in mice by the activation of innate and adaptive immune cells.</p>Formula:C48H80N6O31Purity:Min. 90 Area-%Color and Shape:White PowderMolecular weight:1,237.2 g/mol






