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methyl 2,6,2',3',4',6'-hexa-O-benzyl-β-lactosid-3-ulose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156792-29-9

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156792-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156792-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,9 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 156792-29:
(8*1)+(7*5)+(6*6)+(5*7)+(4*9)+(3*2)+(2*2)+(1*9)=169
169 % 10 = 9
So 156792-29-9 is a valid CAS Registry Number.

156792-29-9Relevant academic research and scientific papers

Involvement of the glucose moiety in the molecular recognition of methyl β-lactoside by ricin: Synthesis, conformational analysis, and binding studies of different derivatives at the C-3 region

Fernandez,Jimenez-Barbero,Martin-Lomas,Solis,Diaz-Maurino

, p. 223 - 244 (1994)

Syntheses of the 3-aminodeoxy (4), 3-deoxy-3-methyl (5), and 3-epi (6) derivatives of methyl β-lactoside (1) have been achieved from 1 in a straightforward way, and their solution conformations in water and dimethyl sulfoxide analysed through molecular mechanics and dynamics calculations and nuclear magnetic resonance data. The overall shape of all the compounds studied is fairly similar and may be described by conformers included in a low energy region with Φ = 15 ± 45° and Ψ = -25 ± 30°, that is ca. 5% of the total potential energy surface for the glycosidic linkages of the disaccharides. The binding of the different compounds to ricin, the galactose-specific toxin from Ricinus communis, has been investigated. The results confirm the involvement of the C-3 region in a nonpolar interaction with the protein at the periphery of the combining site. Syntheses of the 3-aminodeoxy (4), 3-deoxy-3-methyl (5), and 3-epi (6) derivatives of methyl β-lactoside (1) have been achieved from 1 in a straightforward way, and their solution conformations in water and dimethyl sulfoxide analysed through molecular mechanics and dynamics calculations and nuclear magnetic resonance data. The overall shape of all the compounds studied is fairly similar and may be described by conformers included in a low energy region with φ = 15 ± 45° and Ψ = -25 ± 30°, that is ca. 5% of the total potential energy surface for the glycosidic linkages of the disaccharides. The binding of the different compounds to ricin, the galactose-specific toxin from Ricinus communis, has been investigated. The results confirm the involvement of the C-3 region in a nonpolar interaction with the protein at the periphery of the combining site.

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