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  4. Lacto-N-neodifucohexaose II

Lacto-N-neodifucohexaose II  (Synonyms: LNnDFH II)

Cat. No.: HY-N11454
Handling Instructions

Lacto-N-neodifucohexaose II (Compd 9) is a derivative of key human milk tetrasaccharide. Lacto-N-neodifucohexaose II is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

For research use only. We do not sell to patients.

Lacto-N-neodifucohexaose II Chemical Structure

Lacto-N-neodifucohexaose II Chemical Structure

CAS No. : 2583908-45-4

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Description

Lacto-N-neodifucohexaose II (Compd 9) is a derivative of key human milk tetrasaccharide[1]. Lacto-N-neodifucohexaose II is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

Molecular Weight

1125.08

Formula

C44H76N4O29

CAS No.
SMILES

OC[C@@H]([C@H]([C@H]([C@@H]1O)O)O)O[C@@H]1O[C@@H]([C@@H](O[C@@H]([C@H]2NC(C)=O)O[C@H]3[C@@H]([C@H](O[C@H]([C@H]3O)CO)O[C@@H]4[C@H]([C@@H]([C@H](O[C@H]4CO)OCCCCCCN=[N+]=[N-])O)O[C@@H]5[C@@H]([C@H]([C@H]([C@H](O5)C)O)O)O)O)CO)[C@H]2O[C@@H]6[C@@H]([C@H]([C@H]([C@H](O6)C)O)O)O

Structure Classification
Initial Source

Helicobacter pylori

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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