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Fig. 4 in Decalintetracids A and B, two pairs of unusual 3-decalinoyltetramic acid derivatives with phytotoxicity from Fusarium equiseti D39
Fig. 4. Comparison between calculated and experimental ECD spectra of compounds 1 and 2.
Fig. 5 in Phialocetones A-J, C lactones from the rhizospheric soil-derived fungus Phialocephala sp. YUD18001 associated with Gastrodia elata
Fig. 5. Reactions of compound 5 with Mosher esters.
Fig. 3 in Phialocetones A-J, C lactones from the rhizospheric soil-derived fungus Phialocephala sp. YUD18001 associated with Gastrodia elata
Fig. 3. Conformations and key NOESY correlations of 1–3 and 5–10.
Fig. 1 in Phialocetones A-J, C lactones from the rhizospheric soil-derived fungus Phialocephala sp. YUD18001 associated with Gastrodia elata
Fig. 1. Structures of compounds of 1–10.
Fig. 4 in Phialocetones A-J, C lactones from the rhizospheric soil-derived fungus Phialocephala sp. YUD18001 associated with Gastrodia elata
Fig. 4. Experimental and calculated ECD spectra of compounds 1–10 (A–J).
Fig. 1 in Polychlorinated cyclopentenes from a marine derived Periconia sp. (strain G1144)
Fig. 1. Structures of Compounds 1–4 isolated from Periconia sp. (strain G1144).
Fig. 1 in Polyketides, diketopiperazines and an isochromanone from the marine-derived fungal strain Fusarium graminearum FM1010 from Hawaii
Fig. 1. Chemical structures of compounds 1–6.
Fig. 3 in Polyketides, diketopiperazines and an isochromanone from the marine-derived fungal strain Fusarium graminearum FM1010 from Hawaii
Fig. 3. Experimental and calculated ECD of compound 6.
Fig. 4 in Structures and absolute configurations of butenolide derivatives from the isopod-associated fungus Pidoplitchkoviella terricola
Fig. 4. Comparison of the calculated vs experimental ECD spectra in MeOH for compound 5.
Fig. 3 in Structures and absolute configurations of butenolide derivatives from the isopod-associated fungus Pidoplitchkoviella terricola
Fig. 3. Δδ values (in ppm) = δS - δR obtained for (S)- and (R)- MPTA esters (1a–5a and 1b–5b).
Fig. 2 in Structures and absolute configurations of butenolide derivatives from the isopod-associated fungus Pidoplitchkoviella terricola
Fig. 2. Key COSY and HMBC correlations of compounds 1–7.
Fig. 1 in Structures and absolute configurations of butenolide derivatives from the isopod-associated fungus Pidoplitchkoviella terricola
Fig. 1. The structures of compounds 1–20.
Fig. 6 in Structures and absolute configurations of butenolide derivatives from the isopod-associated fungus Pidoplitchkoviella terricola
Fig. 6. Comparison of the calculated and experimental ECD spectra in MeOH for compound 6.
Fig. 8 in Three unusual hybrid sorbicillinoids with anti-inflammatory activities from the deep-sea derived fungus Penicillium sp. SCSIO06868
Fig. 8. NO production inhibitory effects of compounds 1 and 2.
Fig. 5 in Three unusual hybrid sorbicillinoids with anti-inflammatory activities from the deep-sea derived fungus Penicillium sp. SCSIO06868
Fig. 5. Comparation of the experimental ECD curves of compounds 1–3.
Fig. 3 in Three unusual hybrid sorbicillinoids with anti-inflammatory activities from the deep-sea derived fungus Penicillium sp. SCSIO06868
Fig. 3. Chemical structures of compounds 1–11.
Fig. 4. Key 1H–1H in Three unusual hybrid sorbicillinoids with anti-inflammatory activities from the deep-sea derived fungus Penicillium sp. SCSIO06868
Fig. 4. Key 1H–1H COSY (¡), HMBC (→), and NOESY (↔) correlations of compound 1.
Fig. 7. A in Three unusual hybrid sorbicillinoids with anti-inflammatory activities from the deep-sea derived fungus Penicillium sp. SCSIO06868
Fig. 7. A suggested biosynthesis pathway of compounds 1–3.
Fig. 1 in Three unusual hybrid sorbicillinoids with anti-inflammatory activities from the deep-sea derived fungus Penicillium sp. SCSIO06868
Fig. 1. Typical monomeric-, di-, tri- and hybrid sorbicillinoids.
Fig. 3 in Feruloyl sucrose derivatives from the root of Xerophyllum tenax
Fig. 3. Isomerization of double bond in compound 1, as shown by change in 1H-NMR over time (CD OD).
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.