CAS 141342-93-0

O-6-Deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-β-D-galactopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→3)]-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→6)-O-[O-6-deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)]-O-β-D-galactopyranosyl-(1→4)-D-glucose

Description:

The chemical substance known as O-6-Deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-β-D-galactopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→3)]-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→6)-O-[O-6-deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)]-O-β-D-galactopyranosyl-(1→4)-D-glucose, with CAS number 141342-93-0, is a complex glycosylated compound characterized by multiple sugar units linked through various glycosidic bonds. This structure features deoxy and acetylamino groups, indicating modifications that can influence its solubility, reactivity, and biological activity. The presence of multiple galactopyranosyl and glucopyranosyl units suggests potential roles in biological systems, possibly as a component of polysaccharides or glycoproteins. Such compounds may exhibit specific interactions with proteins or other biomolecules, impacting processes like cell signaling, immune response, or microbial adhesion. The intricate arrangement of sugar moieties also implies that this substance could be of interest in research related to carbohydrate chemistry, biochemistry, and potential therapeutic applications.

Formula: C₇₂H₁₂₁N₃O₅₃

InChI: InChI=1S/C72H121N3O53/c1-16-34(89)44(99)49(104)66(110-16)124-58-33(75-21(6)86)63(118-29(14-83)55(58)121-69-52(107)59(42(97)28(13-82)115-69)125-64-31(73-19(4)84)56(40(95)26(11-80)113-64)122-71-61(47(102)38(93)24(9-78)116-71)127-67-50(105)45(100)35(90)17(2)111-67)109-15-30-43(98)60(53(108)70(119-30)120-54(23(88)8-77)37(92)22(87)7-76)126-65-32(74-20(5)85)57(41(96)27(12-81)114-65)123-72-62(48(103)39(94)25(10-79)117-72)128-68-51(106)46(101)36(91)18(3)112-68/h7,16-18,22-72,77-83,87-108H,8-15H2,1-6H3,(H,73,84)(H,74,85)(H,75,86)/t16-,17-,18-,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-,49-,50-,51-,52+,53+,54+,55+,56+,57+,58+,59-,60-,61+,62+,63+,64-,65-,66-,67-,68-,69-,70-,71-,72-/m0/s1

InChI key: InChIKey=VKSOPWNUCGFAPJ-CPFZVZJISA-N

SMILES: O([C@H]1[C@H](O[C@H]2[C@H](O)[C@@H](O[C@H]3[C@H](NC(C)=O)[C@@H](O[C@H]4[C@H](O[C@H]5[C@@H](O)[C@H](O)[C@H](O)[C@H](C)O5)[C@@H](O)[C@@H](O)[C@@H](CO)O4)[C@H](O)[C@@H](CO)O3)[C@@H](O)[C@@H](CO)O2)[C@@H](CO)O[C@@H](OC[C@@H]6[C@H](O)[C@H](O[C@H]7[C@H](NC(C)=O)[C@@H](O[C@H]8[C@H](O[C@H]9[C@@H](O)[C@H](O)[C@H](O)[C@H](C)O9)[C@@H](O)[C@@H](O)[C@@H](CO)O8)[C@H](O)[C@@H](CO)O7)[C@@H](O)[C@H](O[C@@H]([C@@H]([C@H](C=O)O)O)[C@@H](CO)O)O6)[C@@H]1NC(C)=O)[C@H]%10[C@@H](O)[C@H](O)[C@H](O)[C@H](C)O%10

Synonyms:

• D-Glucose, O-6-deoxy-α-L-galactopyranosyl-(1→3)-O-[O-6-deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-β-D-galactopyranosyl-(1→4)]-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→6)-O-[O-6-deoxy-α-L-galactopyranosyl-(1→2)-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→2)-O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-β-D-galactopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→3)]-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→6)-O-[O-6-deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)]-O-β-D-galactopyranosyl-(1→4)-
• O-6-Deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-β-D-galactopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→3)]-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→6)-O-[O-6-deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)]-O-β-D-galactopyranosyl-(1→4)-D-glucose

Trifucosyl (1-2,1-2,1-3)-iso-lacto-N-octaose

CAS: 141342-93-0

Trifucosyl (1-2,1-2,1-3)-iso-lacto-N-octaose is a custom synthesis that is a complex carbohydrate. It is an oligosaccharide that contains three monosaccharides linked by alpha glycosidic bonds. This compound has been modified using methylation and glycosylation reactions. Trifucosyl (1-2,1-2,1-3)-iso-lacto-N-octaose has been fluorinated at the C6 position of the sugar ring to increase its solubility in water and enhance its stability in acid conditions. The product is a high purity synthetic compound.

Formula: C₇₂H₁₂₁N₃O₅₃

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 1,876.72 g/mol

Ref: 3D-OT13725