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15 results for “Pseudopestalotiopsis theae”
Fig. 5 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 5. Phytotoxic effects of different metabolites on seed germination and seedling growth of S. viridis in Petri dishes of experiment: (a) control; (b) 1; (c) 2; (d) 3; (e) 4; (f) 8.
Fig. 3 in Prenylated cyclohexene-type meroterpenoids and sulfur-containing xanthones produced by Pseudopestalotiopsis theae
Fig. 3. Mosher model for (methoxyphenyl)acetic acid MPA ester and Δδ (δR – δS) values (in ppm) derived from the chemical shifts of the (R)-MPA and (S)-MPA esters of 1A.
Fig. 6 in Prenylated cyclohexene-type meroterpenoids and sulfur-containing xanthones produced by Pseudopestalotiopsis theae
Fig. 6. Experimental ECD spectrum of 3 measured in MeCN compared with the Boltzmann-weighted PBE0/TZVP PCM/MeCN ECD spectrum of (1R,2R,3S,4S)-3 computed for the ωB97X/TZVP PCM/MeCN conformers. Bars represent the rotational strength values of the lowest-energy conformer.
Fig. 4 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 4. Experimental and calculated ECD spectra of 1–4 and 8.
Fig. 7 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 7. Symptoms of 1–4 and 8 against the weed seeding growth of S. viridis.
Fig. 3 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 3. Key NOE correlations of 1–5 and 8.
Fig. 6 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 6. Effect of different specialized metabolites on seed germination of S. viridis.
Fig. 1 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 1. Chemical structures of 1–8.
Fig. 2. Key 1H–1H in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 2. Key 1H–1H COSY, and HMBC correlations of 1–5 and 8.
Fig. 7. 1H–1H in Prenylated cyclohexene-type meroterpenoids and sulfur-containing xanthones produced by Pseudopestalotiopsis theae
Fig. 7. 1H–1H COSY (bold) and selected HMBC (plain) correlations of 3–5.
Fig. 5. Keys NOE correlations for compounds 3, 4, 5 in Prenylated cyclohexene-type meroterpenoids and sulfur-containing xanthones produced by Pseudopestalotiopsis theae
Fig. 5. Keys NOE correlations for compounds 3, 4, 5.
Fig. 4. Plausible biosynthetic pathway for sydoxanthones D and E in Prenylated cyclohexene-type meroterpenoids and sulfur-containing xanthones produced by Pseudopestalotiopsis theae
Fig. 4. Plausible biosynthetic pathway for sydoxanthones D and E.
Fig. 2. 1H-1H in Prenylated cyclohexene-type meroterpenoids and sulfur-containing xanthones produced by Pseudopestalotiopsis theae
Fig. 2. 1H-1H COSY (bold) and HMBC (plain) correlations of1.
Fig. 1 in Prenylated cyclohexene-type meroterpenoids and sulfur-containing xanthones produced by Pseudopestalotiopsis theae
Fig. 1. Structures of compounds 1–10.
Fig. 8 in Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
Fig. 8. Effect of different specialized metabolites on seedling growth (germ and radicle length) of S. viridis.
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International Brain Laboratory public data
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OpenNeuro
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