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The chemical "α-D-GalpA-(1->4)-α-D-GalpA-(1->4)-α-D-GalpA-(1->4)-α-D-GalpA-(1->4)-α-D-GalpA-(1->4)-D-GalpA" is a complex carbohydrate structure, specifically a polysaccharide, composed of α-D-GalpA (α-D-galacturonic acid) units. α-D-GalpA-(1->4)-α-D-GalpA-(1->4)-α-D-GalpA-(1->4)-α-D-GalpA-(1->4)-α-D-GalpA-(1->4)-D-GalpA features a linear sequence of five α-D-GalpA units linked together through 1,4-glycosidic bonds, which means the linkage occurs between the first carbon of one sugar molecule and the fourth carbon of the adjacent sugar molecule. The final α-D-GalpA unit is linked to a D-GalpA (D-galactose) unit, indicating a transition from galacturonic acid to galactose in the polymer chain. This structure is significant in the field of glycobiology and may have implications in various biological processes due to its unique composition and linkage pattern.

40386-95-6

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40386-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40386-95-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,8 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40386-95:
(7*4)+(6*0)+(5*3)+(4*8)+(3*6)+(2*9)+(1*5)=116
116 % 10 = 6
So 40386-95-6 is a valid CAS Registry Number.

40386-95-6Upstream product

40386-95-6Relevant academic research and scientific papers

THE MODE OF ACTION OF THE ISOLATED FORM OF TOMATO ENDO-D-GALACTURONANASE

Markovic, Oskar,Slezarik, Alexander

, p. 525 - 531 (2007/10/02)

The mode of action of the isolated form of tomato endo-D-galacturonanase of molecular weight close to 50 000 was investigated with oligo-D-galactosiduronic acids of polymerization degree 2 - 7 and their derivatives the terminal aldehyde group of which was reduced.The rate of hydrolysis,catalysed by this enzyme decreased with the shortening the chain length of oligo-D-galactosiduronates used; di(D-galactosiduronic) acid was not hydrolyzed by this enzyme at all.Tri(D-galactosiduronic) acid was cleaved into monomer and dimer, tetra(D-galactosiduronic) acid was alternatively cleaved into monomer and trimer, as well as into two dimers.The previously proposed conception that the binding site of the tomato endo-D-galacturonanase contains three subsites and that the catalytic groups are localized close to the first bond from the reducing end of the substrate segment bound in the complex were proved.The mode of hydrolysis of the reduced oligomers is in favour of the mentioned conception.

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