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402 results for “ABSOLUTE”
Fig. 1 in Lanostane triterpenoids from cultivated fruiting bodies of Ganoderma sichuanense: Determination of the C-25 absolute configuration of ganoderic acid A and its derivatives using the phenylglycine methyl ester (PGME) method
Fig. 1. Structures of compounds 1–15.
Fig. 5 in Lanostane triterpenoids from cultivated fruiting bodies of Ganoderma sichuanense: Determination of the C-25 absolute configuration of ganoderic acid A and its derivatives using the phenylglycine methyl ester (PGME) method
Fig. 5. Δδ-Values (δ(S) – δ(R)) of the bis-MTPA esters 28a/28b.
Fig. 6 in Bisabolane-type sesquiterpenes from Vernonia amygdalina: Absolute configuration and anti-inflammatory activity
Fig. 6. Experimental and calculated ECD spectra of (A) 7′ and (B) 8.
Fig. 2. Key 2D in Bisabolane-type sesquiterpenes from Vernonia amygdalina: Absolute configuration and anti-inflammatory activity
Fig. 2. Key 2D NMR correlations of 1, 3, 5 and 7.
Fig. 3 in Bisabolane-type sesquiterpenes from Vernonia amygdalina: Absolute configuration and anti-inflammatory activity
Fig. 3. Key NOESY correlations of 1, 3, 5 and 7.
Fig. 4 in Bisabolane-type sesquiterpenes from Vernonia amygdalina: Absolute configuration and anti-inflammatory activity
Fig. 4. Relative configuration analysis of the C6–C7 segment in 1, 3, 5 and 7 by Newman projection.
Fig. 4 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 4. Rh2(OCOCF3)4-induced ECD spectrum of compounds 1–3.
Fig. 5 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 5. Experimental and calculated ECD spectra of compounds 1–9.
Fig. 2 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 2. Selective oxidation reaction of the double bond (Δ11,12) in compound 1.
Fig. 3 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 3. Stereochemical determination by acetonide formation of azaphilones.
Fig. 6. X in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 6. X-ray ORTEP drawing of compounds 1–3.
Fig. 1 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 1. Structures of compounds 1–9.
Fig. 5 in Polyhydroxylated bergamotane-type sesquiterpenoids from cultures of Paraconiothyrium sporulosum YK-03 and their absolute configurations
Fig. 5. Experimental and calculated ECD spectra of 3 in CH3OH.
Fig. 3 in Polyhydroxylated bergamotane-type sesquiterpenoids from cultures of Paraconiothyrium sporulosum YK-03 and their absolute configurations
Fig. 3. NOESY correlations of compounds 1 8.
Fig. 1 in Polyhydroxylated bergamotane-type sesquiterpenoids from cultures of Paraconiothyrium sporulosum YK-03 and their absolute configurations
Fig. 1. Chemical structures of compounds 1–11.
Fig. 4 in Polyhydroxylated bergamotane-type sesquiterpenoids from cultures of Paraconiothyrium sporulosum YK-03 and their absolute configurations
Fig. 4. Diamond plot of X-ray crystal structure of 1.
Fig. 4 in Structures and absolute configurations of butenolide derivatives from the isopod-associated fungus Pidoplitchkoviella terricola
Fig. 4. Comparison of the calculated vs experimental ECD spectra in MeOH for compound 5.
Fig. 3 in Structures and absolute configurations of butenolide derivatives from the isopod-associated fungus Pidoplitchkoviella terricola
Fig. 3. Δδ values (in ppm) = δS - δR obtained for (S)- and (R)- MPTA esters (1a–5a and 1b–5b).
Fig. 2 in Structures and absolute configurations of butenolide derivatives from the isopod-associated fungus Pidoplitchkoviella terricola
Fig. 2. Key COSY and HMBC correlations of compounds 1–7.
Fig. 1 in Structures and absolute configurations of butenolide derivatives from the isopod-associated fungus Pidoplitchkoviella terricola
Fig. 1. The structures of compounds 1–20.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.