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Research Article

The components from aerial parts of Sarcosperma affinis Gagnep. and their antibacterial activities

, , , , , , & | (Reviewing Editor) show all
Article: 1254421 | Received 28 Jul 2016, Accepted 25 Oct 2016, Published online: 15 Nov 2016

Figures & data

Figure 1. Chemical structures of isolated compounds (116): (E)-phytol (1), heptadecan-1-ol (2), lupeol (3), oleanolic acid (4), 3β-hexadecanoyloleanolic acid (5), pomolic acid (6), euscaphic acid (7), myrianthic acid (8), (+)-pinoresinol (9), (+)-medioresinol (10), (+)-syringaresinol (11), quercetin-3-O-β-D-galactopyranoside (12), epicatechin (13), bis-(2-ethylhexyl) phthalate (14), 3-prenyl-4-O-β-D-glucopyranosyloxy-4-hydroxylbenzoic acid (15), icariside E5 (16).

Figure 1. Chemical structures of isolated compounds (1–16): (E)-phytol (1), heptadecan-1-ol (2), lupeol (3), oleanolic acid (4), 3β-hexadecanoyloleanolic acid (5), pomolic acid (6), euscaphic acid (7), myrianthic acid (8), (+)-pinoresinol (9), (+)-medioresinol (10), (+)-syringaresinol (11), quercetin-3-O-β-D-galactopyranoside (12), epicatechin (13), bis-(2-ethylhexyl) phthalate (14), 3-prenyl-4-O-β-D-glucopyranosyloxy-4-hydroxylbenzoic acid (15), icariside E5 (16).

Table 1. Antibacterial activities of compounds 1, 4, 6, and 7

Figure 2. Fractination of methanol extract (A) and isolation of compounds from chloroform (B), ethyl acetate (C) extracts, and water residue (D) of Sarcosperma affinis.

Figure 2. Fractination of methanol extract (A) and isolation of compounds from chloroform (B), ethyl acetate (C) extracts, and water residue (D) of Sarcosperma affinis.