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GlcNAcβ1→3-Galβ-methyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138492-85-0

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138492-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138492-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,9 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138492-85:
(8*1)+(7*3)+(6*8)+(5*4)+(4*9)+(3*2)+(2*8)+(1*5)=160
160 % 10 = 0
So 138492-85-0 is a valid CAS Registry Number.

138492-85-0Downstream Products

138492-85-0Relevant academic research and scientific papers

Enzymic synthesis of HexNAc-containing disaccharide glycosides.

Nilsson

, p. 79 - 83 (1990)

The following disaccharide glycosides were obtained from the appropriate donor and acceptor glycosides by employing glycosidases from the mollusc Chamelea gallina as catalysts: alpha-D-Galp-OMe (N-acetyl-alpha-D- galactosaminidase), beta-D-GalpNAc-(1----3)-beta-D-Galp-OMe, beta-D-GlcpNAc-(1----3)-beta-D-Galp-OMe, and beta-D-GlcpNAc-(1----6)-alpha-D-Manp-OMe (N-acetyl-beta-D-hexosaminidase). The regioselectivity of the N-acetyl-beta-D-hexosaminidase-catalysed reactions depended on the anomeric configuration of the acceptor. Thus, alpha-D-Galp-OMe gave beta-D-GlcpNAc- (1----6)-alpha-D-Galp-OMe almost exclusively, whereas beta-D-Galp-OMe gave beta-D-GlcpNAc-(1----3)-beta-D-Galp-OMe and beta-D-GlcpNAc-(1----6)-beta-D-Galp-OMe in almost equal amounts. The isolation of the products by chromatography was straightforward.

Novel features of acceptor recognition by β-(1 ← 4)- galactosyltransferase

Kajihara, Yasuhiro,Kodama, Hisashi,Endo, Tsuyoshi,Hashimoto, Hironobu

, p. 361 - 378 (2007/10/03)

In order to understand how β-(1→4)-galactosyltransferase recognizes its glycosyl acceptor, substrate specificities were investigated using synthetic 2-acetamido-2-deoxy-D-glucopyranose (N-acetylglucosamine) derivatives in which the 1-, 2-, 3-, 4-, and 6-p

SYNTHESIS OF DI-, TRI-, AND TETRA-SACCHARIDES CORRESPONDING TO RECEPTOR STRUCTURES RECOGNISED BY Streptococcus pneumoniae

Dahmen, Jan,Gnosspelius, Goesta,Larsson, Ann-Charlott,Lave, Thomas,Noori, Ghazi,et al.

, p. 17 - 28 (2007/10/02)

Syntheses are described for methyl 2-acetamido-2-deoxy-4-O-β-D-galactopyranosyl-α-D-glucopyranoside, methyl 2-acetamido-2-deoxy-4-O-β-D-galactopyranosyl-β-D-glucopyranoside, methyl 3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-β-D-galactopyranoside, methyl

SYNTHETIC MUCIN FRAGMENTS: METHYL 3-O-(2-ACETAMIDO-2-DEOXY-β-D-GLUCOPYRANOSYL)-β-D-GALACTOPYRANOSYDE AND METHYL 3-O-(2-ACETAMIDO-2-DEOXY-3-O-β-D-GALACTOPYRANOSYL-β-D-GLUCOPYRANOSYL)-β-D-GALACTOPYRANOSIDE

Kohata, Katsunori,Abbas, Saeed A.,Matta, Khushi L.

, p. 127 - 136 (2007/10/02)

Methyl 2,4,6-tri-O-benzyl-β-D-galactopyranoside (5) was obtained crystalline by way of its 3-O-allyl derivative, which was in turn obtained by ring-opening of a presumed 3,4-O-stannylene derivative of methyl β-D-galactopyranoside, followed by benzylation.

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