Research Article

Antioxidant and Wound Healing Activity of Polyherbal Fractions of Clinacanthus nutans and Elephantopus scaber

Table 5

List of flavonoids tentatively identified in ethyl acetate fractions.

CharacteristicsEthyl acetate fraction MS+/MS
Sequence123456789101112131415

9.069.3339.5989.69410.35410.60211.98412.81612.95315.02111.30811.31611.4611.85714.089
M−H ()580.1439564.1492448.1018534.1379516.1279402.0963286.0485330.0746362.1373358.1422546.1368432.1426446.1597636.1493390.1325
Error (ppm)−1.91−2.3−2.7−1.05−2.16−3.05−2.49−1.9−1.95−1.591.03−1.31−4.59−2.26−2.73
Molecular formulaC26H28O15C26H28O14C21H20O11C25H26O13C25H24O12C20H18O9C15H10O6C17H14O7C19H22O7C20H22O6C26H26O13C22H24O9C23H26O9C32H28O14C20H22O8
Proposed compoundABCDEFGHIJKLMNO

A: isoorientin 2′′-O-apiofuranoside 1; B: vitexin 2′′-O-xyloside 2; C: scutellarein 6-glucoside 3; D: 6,8-Di-C-beta-D-arabinopyranosylapigenin 4; E: apigenin 7-(2′′,3′′-diacetylglucoside) 5; F: cerarvensin 6; G: 5,7,2′,3′-tetrahydroxyflavone 7; H: 5,2′,4′-trihydroxy-6,8-dimethoxyflavone (rehderianin I) 8; I: machaerol B 9; J: brosimacutin B 10; K: isorhamnetin 3-[6′′-(2-(E)-butenoyl)-glucoside] 11; L: 3,5,6,7,3′,4′,5′-heptamethoxyflavone 12; M: 5-hydroxy-7,8-dimethoxyflavanone 5-rhamnoside 13; N: kaempferol 3-(4′′-acetyl-6′′-p-coumarylglucoside) 14; O: apigeniflavan 5-O-xyloside 15.