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58 results for “Achillea millefolium”
Achillea millefolium (Asteraceae) - whole plant - in flower - general view
Image of Achillea millefolium (Asteraceae) - whole plant - in flower - general view
Achillea millefolium (Asteraceae) - inflorescence - whole - unspecified
Image of Achillea millefolium (Asteraceae) - inflorescence - whole - unspecified
Achillea millefolium (Asteraceae) - inflorescence - frontal view of flower
Image of Achillea millefolium (Asteraceae) - inflorescence - frontal view of flower
Achillea millefolium (Asteraceae) - leaf - basal or on lower stem
Image of Achillea millefolium (Asteraceae) - leaf - basal or on lower stem
Fig. 5 in Guaianolide sesquiterpene lactones from Achillea millefolium L
Fig. 5. The effects of compounds 6, 7, 10, and 8-MOP on the melanin content (A) and compounds 6, 7 and 10, and 8-MOP on tyrosinase activity (B) of B16 melanoma cells at the concentrations of 1, 10, 50 μM. Each value represents the mean ± SE (n = 3). *P <0.05, **P <0.01, ***P <0.001.
Achillea millefolium L. (BR0000015240545V)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Achillea millefolium L. (BR0000015267276V)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Achillea millefolium L. (BR0000024578585)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Fig. 2. 1H–1H in Guaianolide sesquiterpene lactones from Achillea millefolium L
Fig. 2. 1H–1H COSY, key HMBC and NOSEY correlations of compounds 1–7.
Fig. 6 in Guaianolide sesquiterpene lactones from Achillea millefolium L
Fig. 6. The anti-inflammatory activity of compounds 1, 3, 4 and 10.
Fig. 4 in Guaianolide sesquiterpene lactones from Achillea millefolium L
Fig. 4. Experimental and calculated ECD spectra of 1 7.
Fig. 3 in Guaianolide sesquiterpene lactones from Achillea millefolium L
Fig. 3. ORTEP drawing of compounds 1, 4 and 6.
Fig. 1 in Guaianolide sesquiterpene lactones from Achillea millefolium L
Fig. 1. Structures of compounds 1–12.
Fig. 5 in Chlorine-containing guaianolide sesquiterpenoids from Achillea millefolium L. with inhibitory effects against LPS-induced NO release in BV-2 microglial cells
Fig. 5. ORTEP diagrams of compounds 1, 4, 6 and 8.
Fig. 3. Key 1 H– 1 H in Chlorine-containing guaianolide sesquiterpenoids from Achillea millefolium L. with inhibitory effects against LPS-induced NO release in BV-2 microglial cells
Fig. 3. Key 1 H– 1 H COSY, HMBC, and NOESY correlations of compound 6.
Fig. 1 in Chlorine-containing guaianolide sesquiterpenoids from Achillea millefolium L. with inhibitory effects against LPS-induced NO release in BV-2 microglial cells
Fig. 1. Structures of Millefolactons B1–B9 (1–9) isolated from A. millefolium L.
Fig. 4 in Chlorine-containing guaianolide sesquiterpenoids from Achillea millefolium L. with inhibitory effects against LPS-induced NO release in BV-2 microglial cells
Fig. 4. Experimental ECD spectra of compounds 1–9.
Fig. 2. Key 1H–1H in Chlorine-containing guaianolide sesquiterpenoids from Achillea millefolium L. with inhibitory effects against LPS-induced NO release in BV-2 microglial cells
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compound 1.
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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.