CAS 38854-46-5
:N-Acetilquitohexaosa
Descripción:
N-Acetilquitohexaosa es un hexasacárido compuesto por unidades repetitivas de N-acetilglucosamina y glucosamina, que son derivados de la quitina. Este compuesto se caracteriza por su estructura, que incluye seis unidades de azúcar unidas por enlaces glucosídicos β(1→4), con grupos N-acetilo presentes en los azúcares amino. Es típicamente soluble en agua y exhibe propiedades asociadas con los polisacáridos, como la viscosidad y la formación de geles. N-Acetilquitohexaosa es de interés en varios campos, incluida la bioquímica y la ciencia de materiales, debido a sus posibles aplicaciones en la entrega de medicamentos, la curación de heridas y como material biocompatible. Además, puede exhibir actividades biológicas, como efectos inmunomoduladores, lo que lo convierte en un tema de investigación en el contexto de la salud y la enfermedad. Su número CAS, 38854-46-5, permite una fácil identificación y referencia en la literatura científica y bases de datos. En general, N-Acetilquitohexaosa representa un compuesto significativo en el estudio de los glicosaminoglicanos y sus derivados.
Fórmula: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
Clave InChI: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
Sinónimos:- 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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Encontrado 7 productos.
Hexa-N-acetylchitohexaose
CAS:Hexa-N-acetylchitohexaose boosts crop immunity, soybean health, and has antitumor effects.Fórmula:C48H80N6O31Pureza:98%Forma y color:SolidPeso molecular:1237.17N,N'',N'''',N'''''',N'''''''',N''''''''''-Hexaacetylchitohexaose
CAS:Fórmula:C48H80N6O31Pureza:≥ 90.0%Forma y color:White to off-white powderPeso molecular:1237.18N,N',N'',N''',N'''',N'''''-Hexaacetyl chitohexaose
CAS:Fórmula:C48H80N6O31Pureza:95%~99%Peso molecular:1237.18N,N’,N’’,N’’’,N’’’’,N’’’’’-Hexaacetylchitohexaose
CAS:Producto controlado<p>Stability Hygroscopic<br>Applications Studied for anti-tumor effects.<br>References Suzuki, K., et al.: Carbohydrate Research, 151, 403 (1986)<br></p>Fórmula:C48H80N6O31Forma y color:NeatPeso molecular: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>Fórmula:C48H80N6O31Pureza:Min. 90 Area-%Forma y color:White PowderPeso molecular:1,237.2 g/mol






