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

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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. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

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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. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
Molecular Weight	1125.08
Formula	C₄₄H₇₆N₄O₂₉
CAS No.	2583908-45-4
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	Saccharides Polysaccharides
Initial Source	Microorganisms 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	Data Sheet (269 KB) Handling Instructions (2659 KB)
References	[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. [Content Brief]

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

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