CAS 56501-25-8

Fucosil-latto-N-neoesaosio II

Descrizione:

Fucosil-latto-N-neoesaosio II, identificato dal suo numero CAS 56501-25-8, è un oligosaccaride complesso che appartiene alla classe delle strutture glicane. È caratterizzato dalla sua composizione, che include unità di fucosio, lattosio e esoso, contribuendo alle sue uniche proprietà strutturali e funzionali. Questo oligosaccaride è spesso coinvolto in processi biologici, in particolare nel riconoscimento e nella segnalazione tra cellule, e può svolgere un ruolo nelle risposte immunitarie. Fucosil-latto-N-neoesaosio II si trova tipicamente in vari fluidi biologici e può essere derivato dal latte o sintetizzato attraverso processi enzimatici. La sua complessità strutturale gli consente di interagire con recettori specifici, rendendolo di interesse nella ricerca relativa alla glicobiologia e alle potenziali applicazioni terapeutiche. La stabilità e la solubilità di questo composto possono variare a seconda delle condizioni ambientali, come pH e temperatura, che possono influenzare la sua attività biologica e le interazioni. In generale, Fucosil-latto-N-neoesaosio II rappresenta un'area significativa di studio nel campo della chimica dei carboidrati e le sue implicazioni nella salute e nella malattia.

Formula: 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

InChI key: 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

Sinonimi:

• <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.

Formula: C₄₆H₇₈N₂O₃₅

Purezza: Min. 95%

Peso molecolare: 1,219.1 g/mol

Ref: 3D-OM31771