107537-94-0 Usage
General Description
Galactostatin is a chemical compound that belongs to the class of glycosidase inhibitors. It is known for its ability to inhibit the enzyme α-galactosidase, which is involved in the metabolism of complex carbohydrates such as galactose-containing substrates. By inhibiting this enzyme, galactostatin can interfere with the breakdown of certain carbohydrates in the body, potentially leading to altered metabolic processes. As a result, it has potential applications in research and medicine for studying carbohydrate metabolism and related diseases. Additionally, galactostatin may have potential as a therapeutic agent for conditions such as Fabry disease, where the inhibition of α-galactosidase is beneficial. However, further research is needed to fully understand the effects and potential applications of galactostatin.
Check Digit Verification of cas no
The CAS Registry Mumber 107537-94-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,5,3 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107537-94:
(8*1)+(7*0)+(6*7)+(5*5)+(4*3)+(3*7)+(2*9)+(1*4)=130
130 % 10 = 0
So 107537-94-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO5/c8-1-2-3(9)4(10)5(11)6(12)7-2/h2-12H,1H2/t2-,3+,4+,5-,6?/m1/s1
107537-94-0Relevant articles and documents
The structures of a β-galactosidase inhibitor, galactostatin, and its derivatives
Miyake,Ebata
, p. 661 - 666 (1988)
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Synthesis of (+)-Galactostatin and (+)-1-Deoxygalactostatin utilizing L-Quebrachitol as a Chiral Building Block
Chida, Noritaka,Tanikawa, Tetsuya,Tobe, Takahiko,Ogawa, Seiichiro
, p. 1247 - 1248 (2007/10/02)
The stereoselective conversion of the naturally occurring optically active cyclitol, L-quebrachitol 1, into galactosidase inhibitors, (+)-galactostatin 2 and (+)-1-deoxygalactostatin 3 is described; the key steps in this synthesis are (i) stereoselective
Stereocontrolled Total Synthesis of Galactostasin from Serine
Dondoni, Alessandro,Merino, Pedro,Perrone, Daniela
, p. 1576 - 1578 (2007/10/02)
An efficient stereoselective total synthesis of (-)-galactostasin (-)-1 from N-tert-butoxycarbonyl-2,3-isopropylidene L-serine methyl ester (21percent overall yield) is described via thiazole intermediates serving as protected aldehydes; the parallel synt
