98302-29-5 Usage
Description
BETA-D-GAL-[1->4]-BETA-D-GLC-1->OPR is a chemical compound that consists of two sugar molecules, beta-D-galactose and beta-D-glucose, connected by a glycosidic bond. It is commonly found in various biological systems and plays a significant role in important physiological processes such as cell signaling and energy metabolism. The unique structure of BETA-D-GAL-[1->4]-BETA-D-GLC-1->OPR enables it to participate in the formation of complex carbohydrates, including glycoproteins and glycolipids, which are crucial for cell recognition and signaling. Furthermore, this compound can act as a substrate for enzymes involved in carbohydrate metabolism, making it an essential component in the intricate network of biochemical pathways within living organisms.
Uses
Used in Biochemical Research:
BETA-D-GAL-[1->4]-BETA-D-GLC-1->OPR is used as a research tool for studying the structure and function of complex carbohydrates, glycoproteins, and glycolipids. Its involvement in cell recognition and signaling makes it a valuable compound for understanding the underlying mechanisms of various biological processes.
Used in Pharmaceutical Development:
Due to its role in carbohydrate metabolism and its ability to serve as a substrate for enzymes, BETA-D-GAL-[1->4]-BETA-D-GLC-1->OPR can be used in the development of pharmaceuticals targeting carbohydrate-related metabolic pathways. This may include the development of drugs for the treatment of diabetes, obesity, and other metabolic disorders.
Used in Food Industry:
BETA-D-GAL-[1->4]-BETA-D-GLC-1->OPR, being a natural sugar compound, can be utilized in the food industry as a sweetener or as a component in the development of novel food products with potential health benefits related to carbohydrate metabolism and cell signaling.
Used in Cosmetics and Personal Care Products:
BETA-D-GAL-[1->4]-BETA-D-GLC-1->OPR's role in cell recognition and signaling, as well as its involvement in the formation of complex carbohydrates, may make BETA-D-GAL-[1->4]-BETA-D-GLC-1->OPR a useful ingredient in cosmetics and personal care products. It could potentially be employed in the development of products aimed at improving skin health, hydration, and overall skin appearance by modulating cell signaling pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 98302-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,0 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98302-29:
(7*9)+(6*8)+(5*3)+(4*0)+(3*2)+(2*2)+(1*9)=145
145 % 10 = 5
So 98302-29-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H28O11/c1-2-3-23-14-12(22)10(20)13(7(5-17)25-14)26-15-11(21)9(19)8(18)6(4-16)24-15/h6-22H,2-5H2,1H3
98302-29-5Relevant articles and documents
Stereoselective enzymatic galactosylation of C-glucosides
Panza, Luigi,Chiappini, Pietro L.,Russo, Giovanni,Monti, Daniela,Riva, Sergio
, p. 1255 - 1256 (1997)
The enzyme β-1,4-galactosyl transferase from bovine colostrum (GalT) is able stereoselectively to galactosylate C-glucosides (i.e. 1 and 4), precursors of stable glycoconjugate analogues, and a systematic investigation of the structural modifications at C
Studies on the synthesis of propyl 4-O-beta-D-galactopyranosyl-alpha-D-galactopyranoside.
El-Shenawy,Schuerch
, p. 227 - 238 (2007/10/02)
2-O-Benzoyl-3,6-di-O-benzyl-4-O-(chloroacetyl)-, 4-O-acetyl-2-O-benzoyl-3,6-di-O-benzyl-, and 2-O-benzoyl-3,4,6-tri-O-benzyl-alpha-D-galactopyranosyl chloride were converted into the corresponding 2,2,2-trifluoroethanesulfonates, and these were treated wi
