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(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-α-D-mannopyranosyl-(1->3)-[(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-α-D-mannopyranosyl-(1->6)]-β-D-mannopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranosylazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

184916-54-9

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184916-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184916-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,9,1 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 184916-54:
(8*1)+(7*8)+(6*4)+(5*9)+(4*1)+(3*6)+(2*5)+(1*4)=169
169 % 10 = 9
So 184916-54-9 is a valid CAS Registry Number.

184916-54-9Upstream product

184916-54-9Downstream Products

184916-54-9Relevant academic research and scientific papers

Chemoenzymatic synthesis of a sialylated diantennary N-glycan linked to asparagine

Unverzagt, Carlo

, p. 423 - 431 (2007/10/03)

A partial structure of many glycoproteins, a glycosylated asparagine carrying a complex type undecasaccharide N-glycan (Neu5Ac(α2-6)Gal(β1- 4)GlcNAc(β1-2)Manαl3)[Neu5Ac(α2-6)Gal(β1-4)GlcNAc(β1-2)Man(α1- 6)]Man(β1-4)GlcNAc(β1-4)GlcNAcAsn) was obtained by total synthesis. As a starting material served a chemically synthesized diantennary heptasaccharide azide which was deprotected in a three-step sequence in high yield. The reduction of the anomeric azide was accomplished with propanedithiol in methanol-ethyldiisopropylamine. Coupling of the glycosyl amine to an activated aspartic acid gave the benzyl protected asparagine conjugate. After removal of the six benzyl functions the resulting free heptasaccharide asparagine was elongated enzymatically in the oligosaccharide part. The use of β-1,4-galactosyltransferase and α-2,6-sialyltransferase in the presence of alkaline phosphatase allowed the efficient transfer of four sugar units to the acceptor resulting in a full length N-glycan, a sialylated diantennary undecasaccharide-asparagine of the complex type.

Chemoenzymatische Synthese eines sialylierten Undecasaccharid-Asparagins

Unverzagt, Carlo

, p. 2507 - 2510 (2007/10/03)

Keywords: Chemoenzymatische Synthesen; Glycoproteine; Glycoside; Kohlenhydrate; Polysaccharide

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