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193 results for “Penicillium”
Fig. 3 in Metabolites isolated from the human intestinal fungus Penicillium oxalicum SL2 and their agonistic effects on PXR and FXR
Fig. 3. Selected NOESY correlations of compounds 1 and 8.
Fig. 2. Selected HMBC and 1H–1H in Metabolites isolated from the human intestinal fungus Penicillium oxalicum SL2 and their agonistic effects on PXR and FXR
Fig. 2. Selected HMBC and 1H–1H COSY correlations of compounds 1, 2, 5, and 8.
Fig. 2. Key 1H–1H in Fungal polyketides from a rhizospheric soil-derived Penicillium sp. YUD17004 associated with Gastrodia elata
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of 1–5.
Fig. 1 in Fungal polyketides from a rhizospheric soil-derived Penicillium sp. YUD17004 associated with Gastrodia elata
Fig. 1. Chemical structures of compounds 1–6.
Fig. 3 in Fungal polyketides from a rhizospheric soil-derived Penicillium sp. YUD17004 associated with Gastrodia elata
Fig. 3. Experimental and calculated ECD spectra in MeOH of 1–3 (A–C) and 5 (D).
Fig. 5. Key 1H–1H in Polyketides with antimicrobial activities from Penicillium canescens DJJ-1
Fig. 5. Key 1H–1H COSY, HMBC and NOE correlations of 2 and 3.
Fig. 6 in Polyketides with antimicrobial activities from Penicillium canescens DJJ-1
Fig. 6. DP4+ results for two possible isomers 6′R*- and 6′S*-2.
Fig. 1 in Polyketides with antimicrobial activities from Penicillium canescens DJJ-1
Fig. 1. Structures of 1–15.
Fig. 2. 1H – 1H in Meroterpenoids from the fungus Penicillium sclerotiorum GZU-XW03-2 and their anti-inflammatory activity
Fig. 2. 1H – 1H COSY and key HMBC correlations of compounds 1–7.
Fig. 1 in Meroterpenoids from the fungus Penicillium sclerotiorum GZU-XW03-2 and their anti-inflammatory activity
Fig. 1. Structures of compounds 1–7.
Fig. 4 in Meroterpenoids from the fungus Penicillium sclerotiorum GZU-XW03-2 and their anti-inflammatory activity
Fig. 4. The experimental and calculated ECD spectra of compounds 1–7.
Fig. 3 in Meroterpenoids from the fungus Penicillium sclerotiorum GZU-XW03-2 and their anti-inflammatory activity
Fig. 3. Key NOESY correlations of compounds 1–7.
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. 4 in Two pairs of undescribed enantiomers isolated from the fungus Penicillium griseofulvum
Fig. 4. Comparing of experimental and calculated ECD spectra of (±)-1 in MeOH.
Fig. 2. Key 1H–1H in Two pairs of undescribed enantiomers isolated from the fungus Penicillium griseofulvum
Fig. 2. Key 1H–1H COSY, HMBC, NOESY, and 1H– 15 N HMBC correlations of compound 1 and 2.
Fig. 1 in Two pairs of undescribed enantiomers isolated from the fungus Penicillium griseofulvum
Fig. 1. Chemical structures of compounds 1–7.
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.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.
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.