6920-38-3 Usage
Uses
Used in Pharmaceutical and Nutraceutical Industries:
LUTEOLIN-4'-O-GLUCOSIDE is used as a bioactive compound for its antioxidant and anti-inflammatory properties, which can contribute to the development of health supplements and medications aimed at reducing inflammation and oxidative stress.
Used in Anticancer Applications:
LUTEOLIN-4'-O-GLUCOSIDE is utilized as a potential anticancer agent, with research indicating its ability to inhibit the growth of cancer cells. It is being studied for its potential to be incorporated into cancer treatment protocols or as a preventive measure against the development of cancer.
Used in Cardiovascular Health Applications:
LUTEOLIN-4'-O-GLUCOSIDE is used as a component in products designed to promote cardiovascular health. Its potential to reduce the risk of chronic diseases makes it a candidate for inclusion in dietary supplements and functional foods that support heart health.
Used in Functional Food and Beverage Industry:
LUTEOLIN-4'-O-GLUCOSIDE is used as a functional ingredient in food and beverages, capitalizing on its health-promoting properties to enhance the nutritional value and appeal of these products to health-conscious consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 6920-38-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6920-38:
(6*6)+(5*9)+(4*2)+(3*0)+(2*3)+(1*8)=103
103 % 10 = 3
So 6920-38-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)31-13-2-1-8(3-10(13)24)14-6-12(26)17-11(25)4-9(23)5-15(17)30-14/h1-6,16,18-25,27-29H,7H2/t16-,18-,19+,20-,21-/m1/s1
6920-38-3Relevant academic research and scientific papers
Biological synthesis of isorhamnetin 3-O-glucoside using engineered glucosyltransferase
Kim, Bong-Gyu,Sung, Su Hyun,Jung, Na Ri,Chong, Youhoon,Ahn, Joong-Hoon
experimental part, p. 194 - 199 (2010/10/18)
The gene for one of the glycosyltransferases from Populus deltoids, PGT-3, was cloned and was expressed as a glutathione S-transferase fusion protein in Escherichia coli. Various flavonoids were used as potential substrates of the purified recombinant PGT-3. Flavones having two adjacent hydroxyl groups were served as substrate. The regioselectivity of PGT-3 depends on the hydroxyl groups of the substrate. Flavones having two adjacent hydroxyl groups in the B ring were glucosylated at the 4′-hydroxyl group. However, PGT-3 transferred a glucose group to the 3-hydroxyl group of isorhamnetin. Molecular modeling and docking and site-directed mutagenesis were carried out to engineer a PGT-3 having a specificity for isorhamnetin but not for quercetin. Glu82Leu turned out to display this activity. Using the Glu82Leu mutant and a quercetin 3′- O-methyltransferase, isorhamnetin 3- O-glucoside was synthesized.
