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. 2021 Dec 30;11(1):94. doi: 10.3390/antiox11010094

Table 1.

Structural characteristics of the tested substances related to the magnitude of protection (%) determined according to the time of their administration in relation to the exposure to X-rays, as well as modifications that could be due to a possible additive effect of the substances dissolved in DMSO.

No COMPOUND %MP BEFORE %MP AFTER DMSO %MP BEFORE
COMPENSATE
%MP AFTER
COMPENSATE *
STRUCTURAL CONSIDERATIONS
1 Grape seed Ex. 68 42 N 68 42 (−38%) Flavonoid: flavan-3-ols (catechins); mixture of monomers, dimers and polymers C1-C15 catechin units. Presence of catechol and gallic groups. Water soluble
2 P medium 68 42 N 68 42 (−38%) Flavonoid: flavan-3-ols (catechins); mixture of monomers, dimers and polymers C1-C15 catechin units. Presence of catechol and gallic groups. Water soluble. 10% of monomers and dimers
3 Rosmarinic acid 63 16 N 63 16 (−75%) Di-Caffeoyl compound; free carboxilic group. Water soluble
4 Citrus Ex. 58 47 N 58 47 (−19%) Flavonoid: flavanone glycosides (naringin and neohesperidin). NO C2 = C3 double bond, NO catechol group. Water soluble.
5 Carnosic acid 53 42 Y 27 42 (+56%) Diterpene: free carboxilic group; catechol group. NO water soluble, lipid soluble.
6 Rutin 47 0 Y 21 0 (−100%) Flavonoid: flavonol glycoside; C2 = C3 double bond; catechol group. NO water soluble.
7 P long 47 26 N 47 26 (−45%) Flavonoid: flavan-3-ols (catechins); mixture of monomers, dimers and polymers C1-C15 catechin units. Presence of catechol and gallic groups. Sligthy watersoluble. 1% of monomers and dimers
8 P short 47 53 N 47 53 (+13%) Flavonoid: flavan-3-ols (catechins); mixture of monomers, dimers and polymers C1-C15 catechin units. Presence of catechol and gallic groups. Watwr soluble,25% of monomers and dimers
9 Apigenin 42 37 Y 16 37 (+131%) Flavonoid: flavone aglycon; C2 = C3 double bond; NO catechol group. NO water soluble.
10 Olive leaf Ex. 42 26 Y 16 26 (+63%) Secoiridoid + minor flavonoids: oleuropein; catechol group and sterified carbonyl groups. Partially water soluble.
11 Vitamin C 42 15 N 42 15 (−64%) (R)-3,4-dihydroxy-5-((S)-1,2-dihydroxyethyl) furan-2(5H)-one. Presence of orto-dihydroxy structure, Water soluble.
12 Amifostine 37 −5 N 37 −5 (−114%) S-phospho derivative of 2-[(3-aminopropyl) amino] ethanethiol. Organothiophosphate with a free amino group. Water soluble
13 Diosmin 37 16 Y 11 16 (+45%) Flavonoid: flavone glycoside; C2 = C3 double bond; NO catechol group. NO water soluble.
14 PASE 32 26 Y 6 26 (+333%) Sargahydroquinoic acid ((2Z,6E,10E)-12-(2,5-dihydroxy-3-methylphenyl)-6,10-dimethyl-2-(4-methylpent-3-enyl) dodeca-2,6,10-trienoic acid, Structure para-hydroxy phenolic and free carboxilic group. NO water soluble.
15 PTU 32 −5 N 32 −5 (−116%) Propylthiouracil. Water soluble (after dissolution in NaOH 0.15N adjusting to pH 8.5).
16 Green tea Ex. 26 16 Y 0 16 (>+100%) Flavonoid: flavan-3-ols (catechins: EGCG, EGC. ECG….all are monomers); presence of catechol and mainly gallic groups. Sligthy watersoluble
17 DMSO 26 0 Y Dimethylsulfoxide. Water soluble
18 Quercetin −16 −26 Y −42 −26 Flavonoid: flavonol aglycon; C2 = C3 double bond; catechol group, five free hydroxyl groups (can be pro-oxidant). NO water soluble
19 Zoledronic acid −32 −26 N −58 −26 Imidazole (biphosphonate): 2,2-bis(phosphono)-2-hydroxyethane-1-yl. Sparingly soluble

* % relative modification vs. % MP Before Compensate.