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O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-(1->4)-O-[6-azido-3-O-benzyl-2-N-(tert-butoxycarbonyl)amino-2,6-di-deoxy-α-D-glucopyranosyl]-(1->6)-2,3:4,5-di-O-cyclohexylidene-D-myoinositol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

251446-01-2

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251446-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 251446-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,4,4 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 251446-01:
(8*2)+(7*5)+(6*1)+(5*4)+(4*4)+(3*6)+(2*0)+(1*1)=112
112 % 10 = 2
So 251446-01-2 is a valid CAS Registry Number.

251446-01-2Upstream product

251446-01-2Downstream Products

251446-01-2Relevant academic research and scientific papers

Synthesis of labeled glycosyl phosphatidyl inositol (GPI) anchors

Mayer, Thomas G.,Weingart, Ralf,Münstermann, Florian,Kawada, Toshinari,Kurzchalia, Teymuras,Schmidt, Richard R.

, p. 2563 - 2571 (1999)

The exploration of the molecular and structural basis for the sorting of GPI-anchored proteins is based on labeled partial structures of GPI's which can be incorporated into the GPI anchor biosynthesis and cellular transport systems. To this end, from mannosyl donor 6 and the D-glucosaminyl-(1→6)D- myo-inositol derivative 7 as acceptor, the pseudotrisaccharide 8 was prepared. Compound 8 was transformed into the GPI partial structures 5a,b which contain the pseudotrisaccharide ligated to two different phosphatidyl residues. Compounds 5a,b have Boc protection at the 2- amino group of the glucosamine residue (2b-position) and a free amino group at the 6b-position. The 6b-amino group was used for the ligation of the 3-(7-nitrobenzofurazan-4- yl)aminopropanoyl group as a fluorescent label, the 5-azido-2-nitrobenzoyl and 4-azidophenylaminothiocarbonyl groups as photolabels, and the 4-azido-2- hydroxybenzoyl group as a radiolabel after the introduction of radioactive iodine by an electrophilic aromatic substitution. Thus, after acid-catalyzed removal of the protective groups, the unprotected target molecules 1-4 were obtained.

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