Leaf Extracts of Moringa oleifera Cultivated in Baghdad: Characterization and Antimicrobial Potential against Endodontic Pathogens

Figure 1

Thin layer chromatogram plate for phenolic compounds under UV 254 nm (a), 366 nm (b): caffeic acid (Ca), catechin (Cat), chlorogenic acid (Ch), gallic acid (G), epicatechin (Ep), hydroquinone (H), paracumaric acid (Pc), pyrogallol (P), ethanolic extract (E), and aqueous extract (W). Note: Spots indicating the presence of another isomer of chlorogenic acid can be visualized at wavelength of 366 nm.

(a)

(b)