CAS 56501-25-8

Fucosyllacto-N-neohexaose II

Description:

Fucosyllacto-N-neohexaose II, identified by its CAS number 56501-25-8, is a complex oligosaccharide that belongs to the class of glycan structures. It is characterized by its composition, which includes fucose, lactose, and hexose units, contributing to its unique structural and functional properties. This oligosaccharide is often involved in biological processes, particularly in cell-cell recognition and signaling, and may play a role in immune responses. Fucosyllacto-N-neohexaose II is typically found in various biological fluids and can be derived from milk or synthesized through enzymatic processes. Its structural complexity allows it to interact with specific receptors, making it of interest in research related to glycobiology and potential therapeutic applications. The stability and solubility of this compound can vary depending on environmental conditions, such as pH and temperature, which can influence its biological activity and interactions. Overall, Fucosyllacto-N-neohexaose II represents a significant area of study within the field of carbohydrate chemistry and its implications in health and disease.

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

Synonyms:

• <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

Purity: Min. 95%

Molecular weight: 1,219.1 g/mol

Ref: 3D-OM31771