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Fig. 3 in ABCG transporter proteins with beneficial activity on plants

Fig. 3. Arabidopsis plants grown in medium containing different concentrations of Cd and Pb. (a) Decrease in growth of plants with AtPDR8-RNAi (8i-2) and AtPDR8 knockout plants(ko-1), whereas normal growth occurs in wild-type plants(WT) in media containing different concentrations of CdCl2. (b) Decreased resistance to Pb in Arabidopsis plants with 8i-2 and knockout of AtPDR8 (ko-2) when grown in Pb(NO3)2 containing medium (Kim et al., 2007).

Fig. 6 in ABCG transporter proteins with beneficial activity on plants

Fig. 6. Mutants of AtABCG26 with loss of function (abcg26-1) show less amount of self-pollination due to impaired sporopollenin formation whereas wild type plants with normal AtABCG26 perform usual self-pollination (Choi et al., 2011).

Fig. 2 in ABCG transporter proteins with beneficial activity on plants

Fig. 2. Transport of Abscisic acid (ABA) during water stress in plant mediated by AtABCG25 and AtABCG40 (Kang et al., 2011).

Fig. 5 in ABCG transporter proteins with beneficial activity on plants

Fig. 5. ABCG transporters that play important role in cuticle development by transporting cuticular wax/cutin (Kang et al., 2011).

Fig. 7 in HRESIMS-guided isolation of aspidosperma-scandine type bisindole alkaloids from Melodinus cochinchinensis and their anti-inflammatory and cytotoxic activities

Fig. 7. Effect of BIAs 1 and 6 on LPS-stimulated NO (A), IL-6 (B) and TNF-α (C) production in RAW 264.7 macrophages. DXM was used as a positive control at 30 μM concentration. The values are presented as mean SD of triplicate replicates. Statically significant difference was determined by ANOVA and Tukey test (#p <0.05, ± compared with control group, *p<0.05, compared with model group).

Fig. 1 in HRESIMS-guided isolation of aspidosperma-scandine type bisindole alkaloids from Melodinus cochinchinensis and their anti-inflammatory and cytotoxic activities

Fig. 1. (A) Total ion chromatogram of the extract of M. cochinchinensis. (B) UV absorption bands of compounds 1–3. (C) HRESIMS data of melokhanines KM (1–3).

Fig. 6 in HRESIMS-guided isolation of aspidosperma-scandine type bisindole alkaloids from Melodinus cochinchinensis and their anti-inflammatory and cytotoxic activities

Fig. 6. Key HMBC (single arrows in red), 1 H– 1 H COSY (bold in blue) and ROESY (double-headed arrows in red) correlations of BIA 3. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 6 in Glycoglycerolipids from the leaves of Perilla frutescens (L.) Britton (Labiatae) and their anti-inflammatory activities in lipopolysaccharide-stimulated RAW264.7 cells

Fig. 6. Inhibitory effects of three glycoglycerolipids on pro-inflammatory cytokines (IL-6, TNF-α, and IL-1β) secretion in 200 ng/ml LPS-stimulated murine macrophages RAW 264.7 cells after 24 h incubation. Different lowercase letters above the bars represented the significant difference (P <0.05) (+: presence; -: absence).

Fig. 5 in Glycoglycerolipids from the leaves of Perilla frutescens (L.) Britton (Labiatae) and their anti-inflammatory activities in lipopolysaccharide-stimulated RAW264.7 cells

Fig. 5. Inhibitory effects of three glycoglycerolipids from Perilla frutescens leaves on the production of NO in 200 ng/ml LPS-stimulated murine macrophages RAW 264.7 cells. Different lowercase letters above the bars represented the significant difference (P <0.05) (+: presence; -: absence).

Fig. 3 in HRESIMS-guided isolation of aspidosperma-scandine type bisindole alkaloids from Melodinus cochinchinensis and their anti-inflammatory and cytotoxic activities

Fig. 3. Key HMBC (single arrows in red), 1H–1H COSY (bold in blue) and ROESY (double-headed arrows in red) correlations of BIA 1. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 5 in HRESIMS-guided isolation of aspidosperma-scandine type bisindole alkaloids from Melodinus cochinchinensis and their anti-inflammatory and cytotoxic activities

Fig. 5. Key HMBC (single arrows in red), 1H–1H COSY (bold in blue) and ROESY (double-headed arrows in red) correlations of BIA 2. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 3. 2D in Glycoglycerolipids from the leaves of Perilla frutescens (L.) Britton (Labiatae) and their anti-inflammatory activities in lipopolysaccharide-stimulated RAW264.7 cells

Fig. 3. 2D NMR spectra of compounds 1, 2 and 3 and structure of compounds 1. (A) Partial HMQC NMR spectrum of compound 1 (CDCl3, 600 MHz), see Supplementary Figs. 6 for the complete HMQC NMR spectrum of compound 1; (B) TCOSY NMR spectrum of compound 1 (CDCl3, 600 MHz); (C) HMBC NMR spectrum of compound 1 (CDCl, 600 MHz); (D) Structure of compound 1. (E) Key 1H–1H TCOSY (─) and HMBC (→) correlations in compound 2. (F) Key 1H–1H TCOSY (─) and 3 HMBC (→) correlations in compound 3.

Fig. 2 in Glycoglycerolipids from the leaves of Perilla frutescens (L.) Britton (Labiatae) and their anti-inflammatory activities in lipopolysaccharide-stimulated RAW264.7 cells

Fig. 2. Positive-ion MALDI-TOF/TOF-MS/MS spectrum of MGDG and DGDG from Perilla frutescens leaves. (A) Compound 1 (MGDG); (B) Compound 2 (DGDG); and (C) Compound 3 (DGDG).

Fig. 8 in Guaiane-type sesquiterpenoids from the roots of Stellera chamaejasme L. and their neuroprotective activities

Fig. 8. Neuroprotective effects of 1–16 on H2O2-induced damage of human neuroblastoma SH-SY5Y cells. The percentage of surviving cells is presented as the percentage of viable cells compared to the control group (cell viability 100%). All data are presented as the means ± SD of three independent experiments. *p <0.05, **p <0.01, ***p <0.001 compared with the model.

Fig. 5 in Guaiane-type sesquiterpenoids from the roots of Stellera chamaejasme L. and their neuroprotective activities

Fig. 5. The calculated and experimental ECD curves of compounds 1–4 and 6–9 at B3LYP/6-31G(d)//B3LYP/6–311++ G(2d,p) level.

Fig. 2 in Panduratins Q-Y, dimeric metabolites from Boesenbergia rotunda and their antiausterity activities against the PANC-1 human pancreatic cancer cell line

Fig. 2. Connectivities (bold lines) deduced by the COSY spectrum and significant HMBC correlations (solid arrows) observed for 1–9.

Fig. 3. X in Structurally diverse steroids with nitric oxide inhibitory activities from Aglaia lawii leaves

Fig. 3. X-ray structure of 1 (A) and the assembly of molecules of 1 in the crystals (hydrogen-bonds are shown as dashed lines) (B).

Fig. 9 in Guaiane-type sesquiterpenoids from the roots of Stellera chamaejasme L. and their neuroprotective activities

Fig. 9. Flow cytometry analysis of the protective effect of 13 on H2O2-induced (400 μM) SH-SY5Y cell apoptosis. All data were presented as the mean ± SD (n = 3). **p <0.05 compared with the control group. #p <0.1 compared with the H O group.

Fig. 2 in Guaiane-type sesquiterpenoids from the roots of Stellera chamaejasme L. and their neuroprotective activities

Fig. 2. Key HMBC correlations (blue) of compounds 1–9 (Magenta line represents part A, red line represents part B, and green line represents part C). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 2 in Polyoxygenated germacranes from Daucus carota and their antimalarial transmission blocking activity

Fig. 2. Left: COSY (red) and HMBC (arrows) correlations of 4; right: ROESY correlations of 4. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)