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415 results for “diterpenoid”
Fig. 2. Key 2D in Undescribed abietane-type diterpenoids and oleanane-type triterpenoids from the stem and branch of Tripterygium wilfordii
Fig. 2. Key 2D NMR correlations of 1 and 7.
Fig. 1 in Undescribed abietane-type diterpenoids and oleanane-type triterpenoids from the stem and branch of Tripterygium wilfordii
Fig. 1. Chemical structures of compounds 1–11.
Fig. 4 in Undescribed abietane-type diterpenoids and oleanane-type triterpenoids from the stem and branch of Tripterygium wilfordii
Fig. 4. Calculated and experimental CD spectra of 2.
Fig. 4. Key 1H–1H in Thirteen cyathane diterpenoids with acetylcholinesterase inhibitory effects from the fungus Cyathus africanus
Fig. 4. Key 1H–1H COSY and HMBC correlations of 1 8.
Fig. 6 in Thirteen cyathane diterpenoids with acetylcholinesterase inhibitory effects from the fungus Cyathus africanus
Fig. 6. ORTEP drawing of cyathin I (13) and its configuration correction.
Fig. 3. X in Undescribed abietane-type diterpenoids and oleanane-type triterpenoids from the stem and branch of Tripterygium wilfordii
Fig. 3. X-ray crystallographic structures of 1, 2, 5 and 7.
Fig. 1 in Diterpenoids from Zhumeria majdae roots as potential heat shock protein 90 (HSP90) modulators
Fig. 1. Structures of compounds 1–21.
Fig. 2. 1H–1H in Ingenane and jatrophane-type diterpenoids from Euphorbia kansui with multidrug resistance reversal activity
Fig. 2. 1H–1H COSY and key HMBC (A) and ROESY (B) correlations of 1.
Fig. 1 in Ingenane and jatrophane-type diterpenoids from Euphorbia kansui with multidrug resistance reversal activity
Fig. 1. Structures of compounds 1–32 isolated from Euphorbia kansui.
Fig. 4. Key HMBC and 1H-1H in Antifeedant, cytotoxic, and anti-inflammatory neo-clerodane diterpenoids in the peltate glandular trichomes and fresh leaves of Ajuga forrestii
Fig. 4. Key HMBC and 1H-1H COSY correlations of compounds 8a/b and 9a/b.
Fig. 3 in Antifeedant, cytotoxic, and anti-inflammatory neo-clerodane diterpenoids in the peltate glandular trichomes and fresh leaves of Ajuga forrestii
Fig. 3. Proposed biosynthetic pathway of the neo-clerodane diterpenoids in A. forrestii.
Fig. 12. Tigliane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 12. Tigliane diterpenoids isolated from E. ebracteolata.
Fig. 10. Lathyrane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 10. Lathyrane diterpenoids isolated from E. ebracteolata.
Fig. 8. Kaurane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 8. Kaurane diterpenoids isolated from E. ebracteolata.
Fig. 5. Rosane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 5. Rosane diterpenoids isolated from E. ebracteolata.
Fig. 6. Pimarane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 6. Pimarane diterpenoids isolated from E. ebracteolata.
Fig. 7. Atisane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 7. Atisane diterpenoids isolated from E. ebracteolata.
Fig. 4. Abietane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 4. Abietane diterpenoids isolated from E. ebracteolata.
Fig. 11. Ingenane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 11. Ingenane diterpenoids isolated from E. ebracteolata.
Fig. 13. Dimeric diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 13. Dimeric diterpenoids isolated from E. ebracteolata.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.