2788-56-9 Usage
Uses
Used in Biochemical Research:
P-Nitrophenyl-thio-beta-D-glucopyranoside is used as a substrate for the detection and measurement of beta-glucosidase activity, which is vital for understanding the enzyme's role in carbohydrate metabolism and its involvement in various metabolic and biochemical processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, P-Nitrophenyl-thio-beta-D-glucopyranoside is employed for the development of new drugs and therapeutic agents targeting carbohydrate metabolism. Its application aids in the discovery and optimization of compounds that can modulate or inhibit beta-glucosidase activity, potentially leading to treatments for diseases associated with carbohydrate metabolism dysregulation.
Used in Biotechnology Industry:
Similarly, in the biotechnology sector, P-Nitrophenyl-thio-beta-D-glucopyranoside is utilized for the development of biotechnological applications targeting carbohydrate metabolism. This includes the engineering of enzymes or the creation of biosensors for monitoring beta-glucosidase activity, which can be applied in various diagnostic and therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2788-56-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,8 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2788-56:
(6*2)+(5*7)+(4*8)+(3*8)+(2*5)+(1*6)=119
119 % 10 = 9
So 2788-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO7S/c14-5-8-9(15)10(16)11(17)12(20-8)21-7-3-1-6(2-4-7)13(18)19/h1-4,8-12,14-17H,5H2
2788-56-9Relevant academic research and scientific papers
Direct transformation of unprotected sugars to aryl 1-thio-β- glycosides in aqueous media using 2-chloro-l, 3-dimethylimidazolinium chloride
Tanaka, Tomonari,Matsumoto, Takeshi,Noguchi, Masato,Kobayashi, Atsushi,Shoda, Shin-Ichiro
supporting information; experimental part, p. 458 - 459 (2010/03/04)
Aryl 1-thioglycosides have directly been synthesized in good yields from the corresponding unprotected sugars and thiols without protection of the hydroxy groups by using 2-chloro-l, 3-dimethylirnidazolinium chloride (DMC) as dehydrative condensing agent.
Thio-arylglycosides with various aglycon para-substituents: A probe for studying chemical glycosylation reactions
Li, Xiaoning,Huang, Lijun,Hu, Xiche,Huang, Xuefei
experimental part, p. 117 - 127 (2009/04/08)
Three series of thioglycosyl donors differing only in their respective aglycon substituents within each series have been prepared as representatives of typical glycosyl donors. The relative anomeric reactivities of these donors were quantified under compe
