Computational Studies Applied to Flavonoids against Alzheimer’s and Parkinson’s Diseases

Table 1

Structure, name, structural formula, and molar mass of the flavonoids present in the study.

No.	Structure	Molecular name	Molecular formula	Mass
1		3-O-Methylquercetin	C16H12O7	316.058
2		8-Prenylnaringenin	C20H20O5	340.131
3		Afzelechin	C15H14O5	274.084
4		Ampelopsin	C15H12O8	320.053
5		Aromadendrin	C15H12O6	288.063
6		Aspalathin	C21H24O11	452.131
7		Aurantinidin	C15H11O6	287.055
8		Butin	C15H12O5	272.068
9		Capensinidin	C18H17O7	345.097
10		Chrysin	C15H10O4	254.057
11		Delphinidin	C15H11O7	303.050
12		Di-hydrogossypetin	C15H12O8	320.053
13		Di-hydromorin	C15H12O7	304.058
14		Epicatechin	C15H14O6	290.07
15		Eriodictyol	C15H12O6	288.063
16		Europinidin	C17H15O7	331.081
17		Fisetin	C15H10O6	286.047
18		Fisetinidol	C15H14O5	274.084
19		Fustin	C15H12O6	288.063
20		Epicatechin gallate	C22H18O10	442.090
21		Genistein	C15H10O5	270.052
22		Gossypetin	C15H10O8	318.037
23		Hesperidin	C28H34O15	610.189
24		Hibiscetin	C15H10O9	334.032
25		Homoeriodictyol	C16H14O6	302.079
26		Isosakuranetin	C16H14O5	286.084
27		Luteolinidin	C15H11O5	271.060
28		Meciadanol	C16H16O6	304.094
29		Mesquitol	C15H14O6	290.079
30		Morin	C15H10O7	302.042
31		Norartocarpetin	C15H10O6	286.047
32		Pinocembrin	C15H12O4	256.073
33		Procyanidins	C45H38O18	866.205
34		Rhamnetin	C16H12O7	316.058
35		Robinetidinol	C15H14O6	290.079
36		Rosinidin	C17H15O6	315.086
37		Sakuranetin	C16H14O5	286.084
38		Sterubin	C16H14O6	302.079
39		Taxifolin	C15H12O7	304.058
40		Control 4TG-Aden2A-Parkinson	C17H27N3O15P2	575.357
41		Control CLR01–Parkinson	C42H32O8P2	726.658
42		Control BIA–Parkinson	C16H20N4O2	300.360
43		Control ladostigil-Parkinson	C16H20N2O2	272.340
44		Control rivastigmine-Alzheimer	C14H22N2O2	250.337
45		Control galantamine-Alzheimer	C17H21NO3	287.340
46		Control donepezil-Alzheimer	C24H29NO3	379.480