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193 results for “Penicillium”
Fig. 5 in Meroterpenoids from the fungus Penicillium sclerotiorum GZU-XW03-2 and their anti-inflammatory activity
Fig. 5. Effects of compound 4 on COX-2 (A), IL-6 (B) and IL-1β (C) release from LPS-stimulated RAW264.7 cells. Data are presented as means ± SD (n = 3). ###p <0.001 versus the control group. *p <0.05, **p <0.01 versus the LPS group.
Fig. 5 in Two pairs of undescribed enantiomers isolated from the fungus Penicillium griseofulvum
Fig. 5. The binding modes of 4 (A) and 7 (B) with human α-glucosidase (PDB ID: 3TOP). 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.)
Fig. 3. Linear correlation between the experimental and calculated 13C in Two pairs of undescribed enantiomers isolated from the fungus Penicillium griseofulvum
Fig. 3. Linear correlation between the experimental and calculated 13C NMR chemical shift of 1A and 1B and their compared 13C NMR data (Δδ δ δ). = adj_calcd – expt MG857577) is 99% identical to P. griseofulvum isolate M12 (KX302025.1) and P. griseofulvum strain Yup08 (HQ262520.1).
Fig. 2 in Three unusual hybrid sorbicillinoids with anti-inflammatory activities from the deep-sea derived fungus Penicillium sp. SCSIO06868
Fig. 2. Global natural products social molecular networking analysis of HR- MS/MS of culture extracts derived from Penicillium sp. SCSIO06868 and the cluster corresponding to undescribed sorbicillinoids in this study.
Fig. 6 in Three unusual hybrid sorbicillinoids with anti-inflammatory activities from the deep-sea derived fungus Penicillium sp. SCSIO06868
Fig. 6. Linear regression analysis of calculated 13C NMR shifts of (1′S)-1 (right) and (1′R)-1 (left) against the experimental shifts of 1 and the DP4 probability for + assignment of 1 to the candidate stereoisomers.
Fig. 5 in Biotransformation of artemisinic acid to bioactive derivatives by endophytic Penicillium oxalicum B4 from Artemisia annua L.
Fig. 5. Time course for the biotransformation of artemisinic acid (AA) by Penicillium oxalicum B4. AA (3.50 mg/50 mL) was added to 2-day-old culture for the biotransformation.
Fig. 4 in Biotransformation of artemisinic acid to bioactive derivatives by endophytic Penicillium oxalicum B4 from Artemisia annua L.
Fig. 4. Time course of mycelial biomass (A) and the biotransformation of artemisinic acid (AA) by Penicillium oxalicum B4. AA (3.50 mg/50 mL) was added to 2-day-old culture for the biotransformation. Data presented are the means ± SD of results from three independent experiments.
Fig. 7 in Biotransformation of artemisinic acid to bioactive derivatives by endophytic Penicillium oxalicum B4 from Artemisia annua L.
Fig. 7. Inhibitory effects of metabolite 4 (A) and 7 (B) on cell viability and LPSinduced nitrite production in RAW 264.7 cells. Normal cells were incubated for 24 h with metabolite 4 and 7 at indicated concentrations. Cells were pretreated with the indicated concentrations of metabolite 4 and 7 for 1 h followed by treatment with LPS (1.0 μg/mL). After 24 h of incubation, the amount of nitrite in the culture supernatants and cell viability were measured. Data presented are the means ± SD of results from three independent experiments (###p <0.001 versus untreated group; *p <0.05, **p <0.01 versus LPS treated group. The small letters indicate the significant difference (p <0.05) between groups).
Fig. 6 in Three diketomorpholines from a Penicillium sp. (strain G1071)
Fig. 6. Proposed methanolysis products of 1–4. The R1 and R2 groups for compounds 1–4 are as noted in Fig. 5.
Fig. 7 in Piperazine-2,5-dione derivatives and an α-pyrone polyketide from Penicillium griseofulvum and their immunosuppression activity
Fig. 7. DP4 probabilities of 13C NMR data for both diastereoisomers of 4; comparing of experimental and calculated ECD spectra of 4-A and 4-B.
Fig. 4. Linear correlation between the experimental and calculated 13C in Piperazine-2,5-dione derivatives and an α-pyrone polyketide from Penicillium griseofulvum and their immunosuppression activity
Fig. 4. Linear correlation between the experimental and calculated 13C NMR chemical shift of 1-A and 1-B and their compared 13C NMR data (Δδ δ – δ).
Fig. 5 in Pyrrolyl 4-quinolone alkaloids from the mangrove endophytic fungus Penicillium steckii SCSIO 41025: Chiral resolution, configurational assignment, and enzyme inhibitory activities
Fig. 5. Molecular docking result of (+)-1 in α-glucosidase (PDB ID: 5NN8). (A) 3D structure of the enzyme docked with (+)-1. (B) Detail analysis of the 2D binding model of (+)-1 with the residues surrounding the binding pocket of α-glucosidase.
Fig. 7. Selected 1H–1H in Kadanguslactones A-E, further oxygenated terpenoids from Kadsura angustifolia fermented by a symbiotic endophytic fungus, Penicillium ochrochloron SWUKD4.1850
Fig. 7. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) correlations of compound 6. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 6. Selected 1H–1H in Kadanguslactones A-E, further oxygenated terpenoids from Kadsura angustifolia fermented by a symbiotic endophytic fungus, Penicillium ochrochloron SWUKD4.1850
Fig. 6. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) correlations of compound 5. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 5. Selected 1H–1H in Kadanguslactones A-E, further oxygenated terpenoids from Kadsura angustifolia fermented by a symbiotic endophytic fungus, Penicillium ochrochloron SWUKD4.1850
Fig. 5. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) correlations of compound 4. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3. Selected 1H–1H in Kadanguslactones A-E, further oxygenated terpenoids from Kadsura angustifolia fermented by a symbiotic endophytic fungus, Penicillium ochrochloron SWUKD4.1850
Fig. 3. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) correlations of compound 3. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2. Selected 1H–1H in Kadanguslactones A-E, further oxygenated terpenoids from Kadsura angustifolia fermented by a symbiotic endophytic fungus, Penicillium ochrochloron SWUKD4.1850
Fig. 2. Selected 1H–1H COSY (red bold), HMBC (blue arrow), and ROESY (blue double-headed arrow) correlations of compound 2. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2. Key 1H–1H in Pesimquinolones produced by Penicillium simplicissimum and their inhibitory activity on nitric oxide production
Fig. 2. Key 1H–1H COSY (bold), HMBC (arrow), and NOESY (double-headed arrow) correlations of compounds 1, 4, and 8.
FIGURE 1 in Penicillium thailandense (Aspergillaceae, Eurotiales), a new species isolated from soil in northern Thailand
FIGURE 1. Phylogram derived from maximum likelihood analysis of a combined ITS, BenA, CaM, and rpb2 genes of 51 sequences. Penicillium corylophilum CBS 312.48 and P. rubefaciens CBS 145.83 were used as outgroups. The numbers above branches represent bootstrap percentages (left) and Bayesian posterior probabilities (right). Bootstrap values ≥ 75% and Bayesian posterior probabilities ≥ 0.90 are shown. The scale bar represents the expected number of nucleotide substitutions per site. Sequences of fungal species obtained in this study are in red. Superscript "T" and "NT" represents type strains.
FIGURE 2 in Penicillium thailandense (Aspergillaceae, Eurotiales), a new species isolated from soil in northern Thailand
FIGURE 2. Penicillium thailandense (SDBR-CMU442, holotype). Colonies incubated at 25°C for one week. a. PDA; b. CYA; c. CYAS; d. CZA; e. DG18; f. MEA; g. OA; h. YES; i. CREA; j–m. Conidiophores; n. Conidia. Scale bars: a–i = 10 mm, j–n = 5 µm.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.