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Lacto-N-neodifucohexaose II

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.

Product Specifications

CAS Number

2583908-45-4

Product Name Alternative

LNnDFH II

UNSPSC

12352005

Target

Others

Type

Natural Products

Related Pathways

Others

Applications

Metabolism-protein/nucleotide metabolism

Field of Research

Metabolic Disease

Assay Protocol

https://www.medchemexpress.com/lacto-n-neodifucohexaose-ii.html

Solubility

10 mM in DMSO

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

Molecular Formula

C44H76N4O29

Molecular Weight

1125.08

References & Citations

[1]Yingying Zhu, et al. Physiological effects, biosynthesis, and derivatization of key human milk tetrasaccharides, lacto- N-tetraose, and lacto- N-neotetraose. Crit Rev Biotechnol. 2022 Jun;42 (4) :578-596.

Shipping Conditions

Room temperature

Scientific Category

Natural Products

Clinical Information

No Development Reported

Frequently Asked Questions

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