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2-carbobenzyloxyamino-1,3-di-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

809270-15-3

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809270-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 809270-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,9,2,7 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 809270-15:
(8*8)+(7*0)+(6*9)+(5*2)+(4*7)+(3*0)+(2*1)+(1*5)=163
163 % 10 = 3
So 809270-15-3 is a valid CAS Registry Number.

809270-15-3Downstream Products

809270-15-3Relevant academic research and scientific papers

Synthesis and mesogenic properties of a Y-shaped glyco-glycero-lipid

Milkereit,Garamus,Veermans,Willumeit,Vill

, p. 51 - 61 (2004)

We synthesised a new glycoglycerolipid [1,3-di-O-(β-D-glucopyranosyl)- 2-deoxy-2-amino-N-palmitoyl-sn-glycerol] with a Y-shaped structure bearing two sugar head groups and only one fatty acid chain. Instead of an ester linkage between the glycerol and the fatty acid an amido function was introduced. The mesogenic properties were investigated using polarising microscopy and are discussed with respect to similar compounds. The lyotropism was measured using the contact preparation method and small-angle neutron-scattering.

Synthesis of a series of multivalent homo-, and heteroglycosides and their anti-adhesion activities

Li, Qing,Yan, Ting-Ting,Niu, Shan,Zhao, Yue-Tao,Meng, Xiang-Bao,Zhao, Zhi-Hui,Li, Zhong-Jun

, p. 78 - 94 (2013)

Adhesion of leukocytes to endothelium plays an important role in inflammatory diseases. We previously found that the tetravalent lactoside Gu-4 was able to inhibit leukocyte-endothelial cell adhesion significantly and that CD11b was the target of Gu-4 on the surface of leukocytes. In this report, we aimed to explore the relationship between structural characteristics of glycoclusters and anti-adhesion activity. Using selective glycosylation method and convergent strategy, we synthesized a new series of homoglycoclusters and heteroglycoclusters with diverse structures. And the bioactivities of these compounds were assessed by a static state cell-based adhesion assay. We found that when the linked saccharide fragments are the same, the anti-adhesion activities of compounds with flexible linkers were stronger than those with rigid scaffold such as the benzene ring, and the best flexible linker in the tested compounds was L-glutamic acid. When L-glutamic acid was employed as the linker, glycoclusters with four valences, but not other valences, exhibited the most significant anti-adhesion activity; however, no significant differences in anti-adhesion activity were found among the tetravalentglycosides that were made by linking glucose (32), mannose (TMa-4), cellobiose (34), or lactose (Gu-4). Thus, we conclude that a flexible linker with proper length, such as that of L-glutamic acid, and the linking of four saccharide fragments might be the preferable structural characteristics for the glycocluster compounds with potent anti-adhesion activity.

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