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CAS 1107646-20-7

:

O-2-(Acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-O-α-D-mannopyranosyl-(1→3)-O-[O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-α-D-mannopyranosyl-(1→6)]-O-β-D-mannopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→6)]-2-(acetylamino)-1-[[2-(aminocarbonyl)phenyl]amino]-1,2-dideoxy-D-glucitol

Description:
The chemical substance known as O-2-(Acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-O-α-D-mannopyranosyl-(1→3)-O-[O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-α-D-mannopyranosyl-(1→6)]-O-β-D-mannopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→6)]-2-(acetylamino)-1-[[2-(aminocarbonyl)phenyl]amino]-1,2-dideoxy-D-glucitol, with CAS number 1107646-20-7, is a complex glycosylated compound. It features multiple sugar moieties, including glucopyranosyl and mannosyl units, linked through various glycosidic bonds. The presence of acetylamino groups suggests that it may exhibit solubility in polar solvents and could participate in hydrogen bonding. The intricate structure indicates potential biological activity, possibly as a glycosylated drug or a component in biochemical pathways. Its molecular complexity may also imply specific interactions with biological receptors or enzymes. Overall, this compound's characteristics suggest it could be of interest in medicinal chemistry or biochemistry, particularly in the study of glycosylation effects on biological functions.
Formula:C63H102N6O40
InChI:InChI=1S/C63H102N6O40/c1-18-36(80)46(90)49(93)60(98-18)96-16-26(79)51(37(81)25(66-19(2)75)10-65-24-9-7-6-8-23(24)56(64)95)105-59-35(69-22(5)78)45(89)52(31(15-74)103-59)106-61-50(94)53(107-63-55(48(92)41(85)30(14-73)102-63)109-58-34(68-21(4)77)44(88)39(83)28(12-71)100-58)42(86)32(104-61)17-97-62-54(47(91)40(84)29(13-72)101-62)108-57-33(67-20(3)76)43(87)38(82)27(11-70)99-57/h6-9,18,25-55,57-63,65,70-74,79-94H,10-17H2,1-5H3,(H2,64,95)(H,66,75)(H,67,76)(H,68,77)(H,69,78)/t18-,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-,57-,58-,59-,60+,61-,62-,63+/m0/s1
InChI key:InChIKey=ILUMXYHMNSZLKL-KULVAGPASA-N
SMILES:O([C@@H]1[C@@H](O[C@@H]2[C@H](O)[C@H](O[C@@H]3[C@@H](CO)O[C@@H](O[C@@H]([C@@H]([C@H](CNC4=C(C(N)=O)C=CC=C4)NC(C)=O)O)[C@@H](CO[C@H]5[C@@H](O)[C@H](O)[C@H](O)[C@H](C)O5)O)[C@H](NC(C)=O)[C@H]3O)O[C@H](CO[C@@H]6[C@@H](O[C@H]7[C@H](NC(C)=O)[C@@H](O)[C@H](O)[C@@H](CO)O7)[C@@H](O)[C@H](O)[C@@H](CO)O6)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O)[C@H]8[C@H](NC(C)=O)[C@@H](O)[C@H](O)[C@@H](CO)O8
Synonyms:
  • O-2-(Acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-O-α-D-mannopyranosyl-(1→3)-O-[O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-α-D-mannopyranosyl-(1→6)]-O-β-D-mannopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→6)]-2-(acetylamino)-1-[[2-(aminocarbonyl)phenyl]amino]-1,2-dideoxy-D-glucitol
  • D-Glucitol, O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-O-α-D-mannopyranosyl-(1→3)-O-[O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-α-D-mannopyranosyl-(1→6)]-O-β-D-mannopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→6)]-2-(acetylamino)-1-[[2-(aminocarbonyl)phenyl]amino]-1,2-dideoxy-
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