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8 results for “Heteroscyphus”
FIG. 22. — Heteroscyphus supinopsis J.J in A taxonomic revision of the Lophocoleaceae Vanden Berghen (Marchantiophyta) of New Caledonia
FIG. 22. — Heteroscyphus supinopsis J.J.Engel, Thouvenot & Frank Müll.: A, G, leaves; B, pair of leaves with associated underleaf, ventral view; C, F, underleaves; D, cells from leaf median portion; E, shoot portion, ventral view; H, dorsal leaf connation, dorsal view. All drawn from the holotype. Scale bars: A-C, F, G, 500 µm; D, 50 µm; E, 1 mm; H, 200 µm.
FIG. 6. — Heteroscyphus assurgentissimus J.J in A taxonomic revision of the Lophocoleaceae Vanden Berghen (Marchantiophyta) of New Caledonia
FIG. 6. — Heteroscyphus assurgentissimus J.J.Engel, Thouvenot & Frank Müll.: A-D, leaves; E, shoot habit in dry condition, lateral view; F-H, K, L, underleaves; I, shoot portion, ventral view; J, leaf cells. All illustrated from the holotype. Scale bars: A-D, F-H, K, L, 500 µm; E, I, 1 mm; J, 20 µm.
Fig. 6 in Terpenoids from the Chinese liverwort Heteroscyphus coalitus and their antivirulence activity against Candida albicans
Fig. 6. The inhibitory effect of the compound 13 on C. albicans morphological transition. A. C. albicans DSY654 were grown in RPMI 1640 medium with a series of concentrations of 13. After 6 h incubation at 37 ̊C, the images were obtained using a microscope (scale bars: 25 μm). B. The A549 cells were co-incubated with C. albicans DSY654-TDH3-GFP cells for 90 min. Finally, cells were observed using a fluorescence microscope (scale bars: 50 μm). C. The number of adherent cells was determined by counting the cells in the pictures. Bars represent means ± SD. *P <0.05, **P <0.01, **P <0.001. D. After incubation of 24 h, the biofilm was washed three times with PBS and photographed by a microscope (scale bars: 50 μm). E. The biofilm was detected with an XTT reduction assay. Bars represent means ± SD. *P <0.05, **P <0.01, **P <0.001. F. C. albicans DSY654 was treated with 4 μg/ml of 13 for 6 h at 37 ̊C. The transcriptional levels of genes related to hyphal formation and adhesion were determined by qPCR and showed as a fold change relative to the negative group. Bars represent means ± SD. *P <0.05, **P <0.01, **P <0.001.
Fig. 3 in Terpenoids from the Chinese liverwort Heteroscyphus coalitus and their antivirulence activity against Candida albicans
Fig. 3. Selected NOESY correlations (H↔H) of 1, 2, 10 and 14.
Fig. 4. X in Terpenoids from the Chinese liverwort Heteroscyphus coalitus and their antivirulence activity against Candida albicans
Fig. 4. X-ray crystallographic structure of 1.
Fig. 2 in Terpenoids from the Chinese liverwort Heteroscyphus coalitus and their antivirulence activity against Candida albicans
Fig. 2. Selected HMBC (H 1 – 1 ▬ →C) and H H COSY (H H) correlations of 1, 2, 10, and 14.
Fig. 5 in Terpenoids from the Chinese liverwort Heteroscyphus coalitus and their antivirulence activity against Candida albicans
Fig. 5. Experimental ECD and calculated ECD curves of 4 (1:1).
Fig. 1 in Terpenoids from the Chinese liverwort Heteroscyphus coalitus and their antivirulence activity against Candida albicans
Fig. 1. Structures of compounds 1–15.
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