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34 results for “Cyathus”

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zenodo32/100

Fig. 6 in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134

Fig. 6. (A) The four possible stereoisomers of 9. (B), (C) The comparisons of the experimental CD and calculated ECD of 9.

opennotspecifiedMar 2022View details →
zenodo32/100

Fig. 7 in Thirteen cyathane diterpenoids with acetylcholinesterase inhibitory effects from the fungus Cyathus africanus

Fig. 7. The binding modes of 9 (A), 10 (B) and 11 (C) with human AChE (PDB ID: 4M0F). Hydrogen bond interactions were depicted with red dotted lines in Å. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedJan 2022View details →
dryad32/100

Data from: Inbreeding depression in urban environments of the bird's nest fungus Cyathus stercoreus (Nidulariaceae: Basidiomycota)

Open the record for dataset details and reuse information.

publicOct 2012View details →
zenodo28/100

Fig. 3 in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134

Fig. 3. ECD and NMR of 1 and 2.

opennotspecifiedMar 2022View details →
zenodo28/100

Fig. 2. Key 2D in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134

Fig. 2. Key 2D NMR correlations of compounds 1–9.

opennotspecifiedMar 2022View details →
zenodo28/100

Fig. 1 in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134

Fig. 1. The chemical structures of compounds 1–13.

opennotspecifiedMar 2022View details →
zenodo28/100

Fig. 3 in Thirteen cyathane diterpenoids with acetylcholinesterase inhibitory effects from the fungus Cyathus africanus

Fig. 3. Key NOESY correlations and ECD spectra of 2 and 4.

opennotspecifiedJan 2022View details →
zenodo28/100

Fig. 5 in Thirteen cyathane diterpenoids with acetylcholinesterase inhibitory effects from the fungus Cyathus africanus

Fig. 5. ORTEP drawing of neocyathin K (12).

opennotspecifiedJan 2022View details →
zenodo28/100

Fig. 1 in Thirteen cyathane diterpenoids with acetylcholinesterase inhibitory effects from the fungus Cyathus africanus

Fig. 1. Chemical structures of 1–13 isolated from C. africanus.

opennotspecifiedJan 2022View details →
zenodo28/100

Fig. 4. Key 1H–1H in Thirteen cyathane diterpenoids with acetylcholinesterase inhibitory effects from the fungus Cyathus africanus

Fig. 4. Key 1H–1H COSY and HMBC correlations of 1 8.

opennotspecifiedJan 2022View details →
zenodo28/100

Fig. 6 in Thirteen cyathane diterpenoids with acetylcholinesterase inhibitory effects from the fungus Cyathus africanus

Fig. 6. ORTEP drawing of cyathin I (13) and its configuration correction.

opennotspecifiedJan 2022View details →
zenodo20/100

Fig. 5 in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134

Fig. 5. Comparison of the experimental CD and calculated ECD of (A) (+)-5 and ()-5, and (B) (+)-8 and ()-8.

opennotspecifiedMar 2022View details →
zenodo20/100

Fig. 4 in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134

Fig. 4. Chiral analyses of four racemates 5–8 by the column CHIRALPAK AS-H, (flow rate = 1 mL min 1). (A) (±)-5 (n-hexane/2-propanol = 90/10). (B) (±)-6 (n- hexane/2-propanol = 90/10). (C) (±)-7 (n-hexane/2-propanol = 95/5). (D) (±)-8 (n-hexane/2-propanol = 85/15). (150 MHz, CDCl3) data, see Table 2; HRESIMS m/z 217.15858 [M H O + H]+ (calcd for C H O, 217.15869). 2 15 21

opennotspecifiedMar 2022View details →
zenodo16/100

Fig. 2 in Thirteen cyathane diterpenoids with acetylcholinesterase inhibitory effects from the fungus Cyathus africanus

Fig. 2. ORTEP drawings of 1 and 3.

opennotspecifiedJan 2022View details →

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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Last verified 2026-04-29Open record