CAS 38854-46-5
:N-Acetilquitohexaose
Descrição:
N-Acetilquitohexaose é um hexassacarídeo composto por unidades repetitivas de N-acetilglucosamina e glucosamina, que são derivados da quitina. Este composto é caracterizado por sua estrutura, que inclui seis unidades de açúcar ligadas por ligações glicosídicas β(1→4), com grupos N-acetil presentes nos açúcares amino. É tipicamente solúvel em água e exibe propriedades associadas a polissacarídeos, como viscosidade e formação de gel. N-Acetilquitohexaose é de interesse em vários campos, incluindo bioquímica e ciência dos materiais, devido às suas potenciais aplicações em entrega de medicamentos, cicatrização de feridas e como material biocompatível. Além disso, pode exibir atividades biológicas, como efeitos imunomoduladores, tornando-se um assunto de pesquisa no contexto de saúde e doença. Seu número CAS, 38854-46-5, permite fácil identificação e referência na literatura científica e bancos de dados. No geral, N-Acetilquitohexaose representa um composto significativo no estudo de glicosaminoglicanos e seus 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
Chave 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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7 produtos.
Hexa-N-acetylchitohexaose
CAS:Hexa-N-acetylchitohexaose boosts crop immunity, soybean health, and has antitumor effects.Fórmula:C48H80N6O31Pureza:98%Cor e Forma:SolidPeso molecular:1237.17N,N'',N'''',N'''''',N'''''''',N''''''''''-Hexaacetylchitohexaose
CAS:Fórmula:C48H80N6O31Pureza:≥ 90.0%Cor e Forma: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:Produto 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:C48H80N6O31Cor e Forma: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-%Cor e Forma:White PowderPeso molecular:1,237.2 g/mol






