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72 results for “acetylcholinesterase”
Fig. 1 in Diterpenoid alkaloids from Aconitum anthoroideum that offer protection against MPP -Induced apoptosis of SH-SY5Y cells and acetylcholinesterase inhibitory activity
Fig. 1. Structures of compounds 1–24.
Fig. 5 in Diterpenoid alkaloids from Aconitum anthoroideum that offer protection against MPP -Induced apoptosis of SH-SY5Y cells and acetylcholinesterase inhibitory activity
Fig. 5. ORTEP drawing of 19.
Fig. 3 in Diterpenoid alkaloids from Aconitum anthoroideum that offer protection against MPP -Induced apoptosis of SH-SY5Y cells and acetylcholinesterase inhibitory activity
Fig. 3. Plausible biosynthetic pathway of anthoroidine B (2).
Fig. 4 in Diterpenoid alkaloids from Aconitum anthoroideum that offer protection against MPP -Induced apoptosis of SH-SY5Y cells and acetylcholinesterase inhibitory activity
Fig. 4. ORTEP drawing of 7.
Fig. 4 in (þ/¡)-Dievodialetins A¡G: Seven pairs of enantiomeric coumarin dimers with anti-acetylcholinesterase activity from the roots of Evodia lepta Merr.
Fig. 4. Plausible biosynthetic pathway of (+/)-1 7.
Fig. 1 in (þ/¡)-Dievodialetins A¡G: Seven pairs of enantiomeric coumarin dimers with anti-acetylcholinesterase activity from the roots of Evodia lepta Merr.
Fig. 1. Chemical structures of 1 9.
Fig. 9 in Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
Fig. 9. ORTEP drawing of the X-ray structures of haemanthamine (18) and (+)-tazettine (24).
Fig. 1 in Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
Fig. 1. Chemical structures of the isolated alkaloids 1–26.
Fig. 5 in Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
Fig. 5. Proposed biosynthetic pathway of zephyranine A (1).
Fig. 2. 1H–1H in Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
Fig. 2. 1H–1H COSY, key HMBC, and key NOESY correlations of zephyranines A D (1–4).
Fig. 2. 1H–1H in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 2. 1H–1H COSY, key HMBC correlations of 1, 4, and 9.
Fig. 6 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 6. ORTEP drawing of compound 4.
Fig. 5 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 5. Comparison of the experimental and calculated ECD spectra of 3.
Fig. 8. Plausible biogenetic pathway for rauvomitorine A in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 8. Plausible biogenetic pathway for rauvomitorine A (1).
Fig. 4 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 4. Comparison of the experimental ECD spectra of 1 and 18 in MeOH.
Fig. 3 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 3. Key NOESY correlations of 1, 4, and 9.
Fig. 1 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 1. Chemical structures of MIAs 1−20.
Fig. 7 in Monoterpene indole alkaloids with diverse skeletons from the stems of Rauvolfia vomitoria and their acetylcholinesterase inhibitory activities
Fig. 7. ORTEP drawing of compound 11.
Fig. 1 in Gigantelline, gigantellinine and gigancrinine, cherylline- and crinine-type alkaloids isolated from Crinum jagus with anti-acetylcholinesterase activity
Fig. 1. Structures of the isolated compounds (1–9).
Fig. 2 in Gigantelline, gigantellinine and gigancrinine, cherylline- and crinine-type alkaloids isolated from Crinum jagus with anti-acetylcholinesterase activity
Fig. 2. The key correlations observed in the HMBC and NOESY spectra of alkaloids 1–3.
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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)
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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.