CAS 56501-25-8

Fucosil-lacto-N-neohexose II

Descrição:

Fucosil-lacto-N-neohexose II, identificado pelo seu número CAS 56501-25-8, é um oligossacarídeo complexo que pertence à classe de estruturas de glicosídeos. É caracterizado por sua composição, que inclui unidades de fucose, lactose e hexose, contribuindo para suas propriedades estruturais e funcionais únicas. Este oligossacarídeo está frequentemente envolvido em processos biológicos, particularmente no reconhecimento e sinalização entre células, e pode desempenhar um papel nas respostas imunológicas. Fucosil-lacto-N-neohexose II é tipicamente encontrado em vários fluidos biológicos e pode ser derivado do leite ou sintetizado através de processos enzimáticos. Sua complexidade estrutural permite que interaja com receptores específicos, tornando-o de interesse na pesquisa relacionada à glicobiologia e aplicações terapêuticas potenciais. A estabilidade e solubilidade deste composto podem variar dependendo das condições ambientais, como pH e temperatura, o que pode influenciar sua atividade biológica e interações. No geral, Fucosil-lacto-N-neohexose II representa uma área significativa de estudo dentro do campo da química de carboidratos e suas implicações na saúde e na doença.

Fórmula: C₄₆H₇₈N₂O₃₅

InChI: InChI=1S/C46H78N2O35/c1-11-23(59)29(65)32(68)43(73-11)81-38-19(9-54)77-42(22(48-13(3)56)39(38)82-45-34(70)31(67)26(62)17(7-52)75-45)83-40-27(63)20(78-46(35(40)71)79-36(15(58)5-50)24(60)14(57)4-49)10-72-41-21(47-12(2)55)28(64)37(18(8-53)76-41)80-44-33(69)30(66)25(61)16(6-51)74-44/h4,11,14-46,50-54,57-71H,5-10H2,1-3H3,(H,47,55)(H,48,56)/t11-,14-,15+,16+,17+,18+,19+,20+,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-/m0/s1

Chave InChI: InChIKey=BSVXHMSSYKYLNT-SYJKWMCZSA-N

SMILES: O([C@H]1[C@H](O[C@H]2[C@@H](O)[C@H](O)[C@H](O)[C@H](C)O2)[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](O[C@@H]([C@@H]([C@H](C=O)O)O)[C@@H](CO)O)O[C@H](CO[C@H]4[C@H](NC(C)=O)[C@@H](O)[C@H](O[C@@H]5O[C@H](CO)[C@H](O)[C@H](O)[C@H]5O)[C@@H](CO)O4)[C@@H]3O)[C@@H]1NC(C)=O)[C@@H]6O[C@H](CO)[C@H](O)[C@H](O)[C@H]6O

Sinónimos:

• <span class="text-smallcaps">D</smallcap>-Glucose, O-6-deoxy-α-<smallcap>L</smallcap>-galactopyranosyl-(1→4)-O-[β-<smallcap>D</smallcap>-galactopyranosyl-(1→3)]-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→3)-O-[O-β-<smallcap>D</smallcap>-galactopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→6)]-O-β-<smallcap>D</span>-galactopyranosyl-(1→4)-
• <span class="text-smallcaps">D</smallcap>-Glucose, O-β-<smallcap>D</smallcap>-galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→6)-O-[O-6-deoxy-α-<smallcap>L</smallcap>-galactopyranosyl-(1→4)-O-[β-<smallcap>D</smallcap>-galactopyranosyl-(1→3)]-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→3)]-O-β-<smallcap>D</span>-galactopyranosyl-(1→4)-
• Fucosyllacto-N-neohexaose II
• Lacto-N-fucoheptaose
• O-β-<span class="text-smallcaps">D</smallcap>-Galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→6)-O-[O-6-deoxy-α-<smallcap>L</smallcap>-galactopyranosyl-(1→4)-O-[β-<smallcap>D</smallcap>-galactopyranosyl-(1→3)]-2-(acetylamino)-2-deoxy-β-<smallcap>D</smallcap>-glucopyranosyl-(1→3)]-O-β-<smallcap>D</smallcap>-galactopyranosyl-(1→4)-<smallcap>D</span>-glucose
• O-β-D-Galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→6)-O-[O-6-deoxy-α-L-galactopyranosyl-(1→4)-O-[β-D-galactopyranosyl-(1→3)]-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)]-O-β-D-galactopyranosyl-(1→4)-D-glucose
• D-Glucose, O-β-D-galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→6)-O-[O-6-deoxy-α-L-galactopyranosyl-(1→4)-O-[β-D-galactopyranosyl-(1→3)]-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)]-O-β-D-galactopyranosyl-(1→4)-
• D-Glucose, O-6-deoxy-α-L-galactopyranosyl-(1→4)-O-[β-D-galactopyranosyl-(1→3)]-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-[O-β-D-galactopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→6)]-O-β-D-galactopyranosyl-(1→4)-

Monofucosyllacto-N-hexaose II

CAS: 56501-25-8

Monofucosyllacto-N-hexaose II is a tetraol that is used as a reagent in the synthesis of enantioenriched and synthetically tetrasaccharidic products. Monofucosyllacto-N-hexaose II can be obtained by the reaction of Grignard reagents with glucose or by stereoselective reduction of an alpha, beta unsaturated ketone. The presence of the glucose residue in Monofucosyllacto-N-hexaose II makes it an acceptor for esterification reactions. This compound has chiral centers due to its two stereogenic centers at C2 and C3, which are both beta positions on the glucose residue. Monofucosyllacto-N-hexaose II also has a free hydroxyl group at C5 that can be esterified to produce chiral esters.

Fórmula: C₄₆H₇₈N₂O₃₅

Pureza: Min. 95%

Peso molecular: 1,219.1 g/mol

Ref: 3D-OM31771