6057-48-3 Usage
Uses
Used in Pharmaceutical Industry:
3-O-BETA-D-GALACTO-PYRANOSYL-D-ARABINOSE is used as a pharmaceutical compound for its potential therapeutic properties. The disaccharide structure allows it to interact with specific receptors and enzymes, making it a promising candidate for the development of new drugs targeting various diseases.
Used in Biotechnology Industry:
In the biotechnology sector, 3-O-BETA-D-GALACTO-PYRANOSYL-D-ARABINOSE is used as a key component in the development of bioactive molecules and biomaterials. Its unique structure enables it to be incorporated into various biotechnological applications, such as the creation of novel vaccines, drug delivery systems, and tissue engineering scaffolds.
Used in Food Industry:
3-O-BETA-D-GALACTO-PYRANOSYL-D-ARABINOSE can be utilized in the food industry as a natural sweetener or as an ingredient in the development of functional foods. Its disaccharide structure may provide health benefits, such as promoting gut health and enhancing the immune system.
Used in Cosmetics Industry:
In the cosmetics industry, 3-O-BETA-D-GALACTO-PYRANOSYL-D-ARABINOSE may be used as an active ingredient in skincare products due to its potential moisturizing, anti-aging, and skin-protective properties. Its ability to interact with skin cells and proteins could lead to the development of innovative cosmetic formulations.
Used in Research and Development:
3-O-BETA-D-GALACTO-PYRANOSYL-D-ARABINOSE is also used in research and development for its potential applications in various scientific fields. Its unique disaccharide structure makes it an interesting subject for studying carbohydrate chemistry, glycobiology, and the development of new bioactive compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 6057-48-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6057-48:
(6*6)+(5*0)+(4*5)+(3*7)+(2*4)+(1*8)=93
93 % 10 = 3
So 6057-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O10/c12-1-4(15)10(5(16)2-13)21-11-9(19)8(18)7(17)6(3-14)20-11/h1,4-11,13-19H,2-3H2/t4-,5-,6-,7+,8+,9-,10+,11+/m1/s1
6057-48-3Relevant articles and documents
Characterization of a laminaribiose phosphorylase from Acholeplasma laidlawii PG-8A and production of 1,3-β-d-glucosyl disaccharides
Nihira, Takanori,Saito, Yuka,Kitaoka, Motomitsu,Nishimoto, Mamoru,Otsubo, Ken'Ichi,Nakai, Hiroyuki
, p. 49 - 54 (2013/01/15)
We identified a glycoside hydrolase family 94 homolog (ACL0729) from Acholeplasma laidlawii PG-8A as a laminaribiose (1,3-β-d-glucobiose) phosphorylase (EC 2.4.1.31). The recombinant ACL0729 produced in Escherichia coli catalyzed phosphorolysis of laminar
Characterization of a bacterial laminaribiose phosphorylase
Kitaoka, Motomitsu,Matsuoka, Yasuyuki,Mori, Kiyotaka,Nishimoto, Mamoru,Hayashi, Kiyoshi
, p. 343 - 348 (2012/08/08)
Bacterial laminaribiose phosphorylase (LBPbac) was first identified and purified from cell-free extract of Paenibacillus sp. YM-1. It phosphorolyzed laminaribiose into α-glucose 1-phosphate and glucose, but did not phosphorolyze other glucobioses. It slightly phosphorolyzed laminaritriose and higher laminarioligosaccharides. The specificity of the degree of polymerization of the substrate was clearly different from that of the enzyme of Euglena gracilis (LBPEug): LBPbac was more specific to laminaribiose than LBPEug. It showed acceptor specificity in reverse phosphorolysis similar to LBPEug. Cloning of the gene encoding LBPbac (lbpA) has revealed that LBPbac is a member of the glucoside hydrolase family 94, which includes cellobiose phosphorylase, cellodextrin phosphorylase, and N,N0-diacetylchitobiose phosphorylase. The genes that encode the components of an ATP-binding cassette sugar transporter specific to laminarioligosaccharides were identified upstream of lbpA, suggesting that the role of LBPbac is to utilize laminaribiose generated outside the cell. This role is different from that of LBPEug, which participates in the utilization of paramylon, the intracellular storage 1,3-β-glucan.
