3180-78-7 Usage
Chemical structure
A derivative of the nucleoside uridine, consisting of a sugar molecule (glucopyranosyl) attached to a pyrimidine base (5-methylpyrimidine-2,4(1H,3H)-dione).
Monosaccharide component
The sugar molecule in the compound is β-D-glucopyranosyl, which is a monosaccharide derived from glucose.
Pyrimidine base
The base in the compound is 5-methylpyrimidine-2,4(1H,3H)-dione, which is a modified version of the pyrimidine base found in uridine.
Glycosidic linkage
The sugar molecule is attached to the pyrimidine base through a glycosidic linkage, specifically at the 1' position of the sugar and the N-1 position of the base.
Natural occurrence
This compound is commonly found in natural sources such as plants and microorganisms.
Pharmaceutical and research applications
It is used in the pharmaceutical industry and research for its potential roles in various biological processes and therapeutic applications.
Biochemical and medicinal importance
Due to its presence in natural sources and potential therapeutic applications, 1-(β-D-Glucopyranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione is considered an important compound in the fields of biochemistry and medicinal chemistry.
Potential roles in biological processes
The compound has been studied for its potential roles in various biological processes, which may include cellular signaling, gene regulation, and other cellular functions.
Therapeutic applications
Research is ongoing to explore the compound's potential therapeutic applications, such as in the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 3180-78-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3180-78:
(6*3)+(5*1)+(4*8)+(3*0)+(2*7)+(1*8)=77
77 % 10 = 7
So 3180-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O7/c1-4-2-13(11(19)12-9(4)18)10-8(17)7(16)6(15)5(3-14)20-10/h2,5-8,10,14-17H,3H2,1H3,(H,12,18,19)
3180-78-7Relevant articles and documents
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Visser et al.
, p. 1926 (1948)
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SELECTIVE VALORIZATION OF BIOMASS SUGARS
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, (2021/06/26)
Disclosed are methods of forming an epimer or a dehydrated isomer of a pyranose monosaccharide or a pyranose saccharide residue in an oligosaccharide or a glycoside.
Oligodeoxyribonucleosides containing 1-β-D-glucopyranosylthymine: Synthesis and substrate properties
Ermolinsky, Boris S.,Fomitcheva, Marina V.,Efimtseva, Ekaterina,Meshkov, Sergey E.,Mikhailov, Sergey N.,Esipov, Dmitriy S.,Boldyreva, Elena F.,Korobko, Vyacheslav G.
, p. 1619 - 1634 (2007/10/03)
Regioselective method for 1-β-D-glucopyranosylthymine incorporation into oligonucleotides has been developed and substrate properties of the latters in DNA synthesis and hydrolysis reactions were investigated.
Stereospecific Vorbrueggen-like Reactions of 1,2-Anhydro Sugars. An Alternative Route to the Synthesis of Nucleosides
Chow, Ken,Danishefsky, Samuel
, p. 4211 - 4214 (2007/10/02)
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