61775-19-7 Usage
General Description
5-O-Methylnaringenin is a chemical compound, specifically a flavanone, naturally found in select citrus fruits, barley, and hops. It is recognized for its potential health benefits, including antioxidant, anti-inflammatory, and anticancer effects. Its unique structure allows it to easily attach to cell membranes, potentially inhibiting the growth of harmful cells. The compound also stands out for its possible role in brewing, as its presence might affect the taste of beer due, in part, to its antioxidative qualities. However, while research on 5-O-Methylnaringenin indicates promising results, more extensive studies are needed to further understand its comprehensive properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 61775-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,7 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61775-19:
(7*6)+(6*1)+(5*7)+(4*7)+(3*5)+(2*1)+(1*9)=137
137 % 10 = 7
So 61775-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O5/c1-20-14-6-11(18)7-15-16(14)12(19)8-13(21-15)9-2-4-10(17)5-3-9/h2-7,13,17-18H,8H2,1H3/t13-/m0/s1
61775-19-7Relevant articles and documents
A chalcone glycoside from Clerodendron phlomidis
Roy,Pandey
, p. 1775 - 1776 (1994)
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Novel flavanone and chalcone glycosides from Clerondendron phlomidis (Verbenaceae)
Anam, Edet M.
, p. 1307 - 1310 (2007/10/03)
Oven dried ground roots and flowers of Clerodendron phlomidis yield two flavonoidglycosides, ∞-L-Rhamnopyranosyl-(1→2)-∞-D-glucopyranosyl-7-O- naringin-4'-O-∞-D-glucopyranoside-5-methyl ether 1 and 4, 2', 4'-trihydroxy- 6'-methoxychalcone-4, 4'-∞-D-diglucoside 5.
Novel flavone and chalcone glycosides from clerodendron phlomidis (verbenaceae)
Anam, Edet M.
, p. 897 - 900 (2007/10/03)
Photochemical investigation of oven dried ground roots and flowers of Clerodendron phlomidis lead to the isolation of two flavonoidglycosides, α-L-Rhamnopyranosyl-(1→2)-α-.D-Glucopyranosyl-7-0-naringin-4-0- α-D-glucopyranoside-5-methylether 1 and 4, 2′, 4′-trihydroxy-6′-methoxy chalcone-4,4′-α-D-diglucoside 5.Their structures have been established by spectroscopic studies . . .