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606 results for “Bioactivation”
Fig. 3 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 3. Key NOE correlations of 1–6.
Fig. 1 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 1. Chemical structures of 1–21.
Fig. 8 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 8. Experimental and calculated ECD spectra of 4 in MeCN.
Fig. 6 in Phytochemical and biological studies on rare and endangered plants endemic to China. Part XXII. Structurally diverse diterpenoids from the leaves and twigs of the endangered conifer Torreya jackii and their bioactivities
Fig. 6. Experimental and calculated ECD spectra of 3 in MeCN.
Fig. 3. Key 1H–1H in Bioactive polyketide derivatives from the endophytic fungus Phaeosphaeriopsis musa
Fig. 3. Key 1H–1H COSYs and HMBCs of 3–8.
Fig. 6 in Bioactive polyketide derivatives from the endophytic fungus Phaeosphaeriopsis musa
Fig. 6. Experimental and calculated ECD spectra of 4, and 9–10.
Fig. 4. Key 1H–1H in Bioactive polyketide derivatives from the endophytic fungus Phaeosphaeriopsis musa
Fig. 4. Key 1H–1H COSYs and HMBCs of 9 and 10.
Fig. 2. Key 1H–1H in Bioactive polyketide derivatives from the endophytic fungus Phaeosphaeriopsis musa
Fig. 2. Key 1H–1H COSYs and HMBCs of 1 and 2.
Fig. 5 in Bioactive polyketide derivatives from the endophytic fungus Phaeosphaeriopsis musa
Fig. 5. Key NOESY correlations of 9 and 10.
Fig. 1 in Bioactive polyketide derivatives from the endophytic fungus Phaeosphaeriopsis musa
Fig. 1. Structures of compounds 1–10 isolated from Phaeosphaeriopsis musae.
Psychochemical properties and bioactivity of biogenic nano-hydroxyapatite derived from scallop shell waste
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Supplementary material 1 from: Veloso T, Reboleira AS, Oliveira H, Gonçalves F, Marques S (2018) Accessing bioactive potential of cave bacterial extracts. ARPHA Conference Abstracts 1: e30109. https://doi.org/10.3897/aca.1.e30109
Accessing bioactive potential of cave bacterial extracts
Figure 7 in Bioactivity and chemical screening of endophytic fungi associated with the seaweed Ulva sp. of the Bay of Bengal, Bangladesh
Figure 7: Antioxidant and cytotoxic potential of the crude extracts of fungi associated with Ulva sp. (A) DPPH (2,2-diphenyl1-picrylhydrazyl) radical scavenging activity, and (B) brine shrimp lethality bioassay. Values are mean ± standard deviation, n = 3. Bars with different letters are significantly different according to Tukey's post hoc test at p = 0.05.
Fig. 2 in Repellency and bioactivity of Caatinga biome plant powders against Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae)
Fig. 2. Percentage of Callosobruchus maculatus (Coleoptera: Chrysomelidae) that moved toward bean seeds untreated and treated with leaf (A) and stem (B) powders. An asterisk by a bar indicates a significant difference in repellency between leaf powder–treated and untreated bean seeds (binomial test, P <0.01). The following plant species were tested:Amburana cearensis ("cumaru"), Croton sonderianus ("marmeleiro"), Cleome spinosa ("mussambê"), Mimosa tenuiflora ("jurema-preta"), Anadenanthera macrocarpa ("angico-vermelho"), Aspidosperma pyrifolium ("pereiro"), Senna occidentalis ("manjerioba"), Hyptis suaveolens ("alfazema-brava"), and Ziziphus joazeiro ("juazeiro").
Fig. 4 in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 4. Experimental and calculated ECD spectra of compounds 1–4 and 6–11.
Fig. 2. Key 1H–1H in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–11.
Fig. 4 in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 4. (continued).
Fig. 7 in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 7. (continued).
Fig. 1 in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 1. Structures of compounds 1–18.
Fig. 5. Single-crystal X in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 5. Single-crystal X-ray structure of compound 5.
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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.