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methyl 4-acetoxy-2-(4-acetoxy-3-(3-methylbut-2-enyl)benzyl)-3-(4-acetoxyphenyl)-5-oxo-2,5-dihydrofuran-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156002-95-8

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156002-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156002-95-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,0,0 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 156002-95:
(8*1)+(7*5)+(6*6)+(5*0)+(4*0)+(3*2)+(2*9)+(1*5)=108
108 % 10 = 8
So 156002-95-8 is a valid CAS Registry Number.

156002-95-8Downstream Products

156002-95-8Relevant academic research and scientific papers

Effect on α-glucosidase inhibition and antioxidant activities of butyrolactone derivatives from Aspergillus terreus MC751

Dewi, Rizna Triana,Tachibana, Sanro,Darmawan, Ahmad

, p. 454 - 460 (2014)

Butyrolactone I and II from Aspergillus terreus MC751 as well as three synthetic butyrolactone I derivatives were assessed for α-glucosidase inhibitory and antioxidant activities. Butyrolactone I (1), which has a prenyl side chain and an alpha hydroxy-lactone group, was the most potent α-glucosidase inhibitor and also had antioxidant activities with IC 50 values of 52.17 ± 5.68 and 51.39 ± 3.68 μM, respectively. In contrast, butyrolactone II (2) lacking a prenyl side chain was the most potent antioxidant with an IC50 of 17.64 ± 6.41 μM, but was less active against α-glucosidase. Acetylation of all hydroxyl groups of butyrolactone I significantly decreased both the α-glucosidase inhibitory and antioxidant activity. The prenyl and alpha hydroxy-lactone groups seem to have a synergic effect on the inhibitory activity but not antioxidant activity. This is the first structure-activity relationship report on the α-glucosidase inhibition and antioxidant activity by butyrolactone derivatives.

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