CAS 141342-93-0

O-6-desossi-α-L-galattopiranosil-(1→2)-O-β-D-galattopiranosil-(1→3)-O-2-(acetilamino)-2-desossi-β-D-glucopiranosil-(1→3)-O-β-D-galattopiranosil-(1→4)-O-[6-desossi-α-L-galattopiranosil-(1→3)]-O-2-(acetilamino)-2-desossi-β-D-glucopiranosil-(1→6)-O-[O-6-desossi-α-L-galattopiranosil-(1→2)-O-β-D-galattopiranosil-(1→3)-2-(acetilamino)-2-desossi-β-D-glucopiranosil-(1→3)]-O-β-D-galattopiranosil-(1→4)-D-glucosio

Descrizione:

La sostanza chimica nota come O-6-desossi-α-L-galattopiranosil-(1→2)-O-β-D-galattopiranosil-(1→3)-O-2-(acetilamino)-2-desossi-β-D-glucopiranosil-(1→3)-O-β-D-galattopiranosil-(1→4)-O-[6-desossi-α-L-galattopiranosil-(1→3)]-O-2-(acetilamino)-2-desossi-β-D-glucopiranosil-(1→6)-O-[O-6-desossi-α-L-galattopiranosil-(1→2)-O-β-D-galattopiranosil-(1→3)-2-(acetilamino)-2-desossi-β-D-glucopiranosil-(1→3)]-O-β-D-galattopiranosil-(1→4)-D-glucosio, con numero CAS 141342-93-0, è un composto glicosilato complesso caratterizzato da più unità di zucchero collegate tramite vari legami glicosidici. Questa struttura presenta gruppi desossi e acetilamino, indicando modifiche che possono influenzare la sua solubilità, reattività e attività biologica. La presenza di più unità di galattopiranosio e glucopiranosio suggerisce ruoli potenziali nei sistemi biologici, possibilmente come componente di polisaccaridi o glicoproteine. Tali composti possono mostrare interazioni specifiche con proteine o altre biomolecole, influenzando processi come la segnalazione cellulare, la risposta immunitaria o l'adesione microbica. La disposizione intricata delle unità di zucchero implica anche che questa sostanza potrebbe essere di interesse nella ricerca relativa alla chimica dei carboidrati, biochimica e potenziali applicazioni terapeutiche.

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

Sinonimi:

• 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

Purezza: Min. 95%

Colore e forma: White Powder

Peso molecolare: 1,876.72 g/mol

Ref: 3D-OT13725