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38 results for “Lanostanes”
Fig. 2. Key 1H–1H in Lanostane-type triterpenoids from the mycelial mat of Ganoderma lucidum and their hepatoprotective activities
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–10.
Fig. 1 in Lanostane-type triterpenoids from the mycelial mat of Ganoderma lucidum and their hepatoprotective activities
Fig. 1. Structures of compounds 1–31.
Fig. 1 in Lanostane triterpenoids from the fruiting bodies of Fomitopsis pinicola and their anti-inflammatory activities
Fig. 1. The structures of compounds 1–13.
Fig. 3. X in Lanostane triterpenoids from the fruiting bodies of Fomitopsis pinicola and their anti-inflammatory activities
Fig. 3. X-ray crystal structure of 1.
Fig. 2. COSY and HMBC correlations for 1, 4, 5 in Lanostane triterpenoids from cultivated fruiting bodies of basidiomycete Ganoderma mbrekobenum
Fig. 2. COSY and HMBC correlations for 1, 4, 5, and 9.
Fig. 1 in Lanostane triterpenoids from cultivated fruiting bodies of the wood-rot basidiomycete Ganoderma casuarinicola
Fig. 1. Structures of compounds 1–21.
Fig. 5 in Lanostane-type triterpenoids from Ganoderma applanatum and their inhibitory activities on NO production in LPS-induced BV-2 cells
Fig. 5. Putative biosynthetic pathway of 1 and 2.
Fig. 2. Key 1H–1H in Lanostane-type triterpenoids from Ganoderma applanatum and their inhibitory activities on NO production in LPS-induced BV-2 cells
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of 1.
Fig. 1 in Lanostane-type triterpenoids from Ganoderma applanatum and their inhibitory activities on NO production in LPS-induced BV-2 cells
Fig. 1. Structures of the compounds from G. applanatum.
Fig. 3 in Lanostane triterpenoids with anti-inflammatory activities from Ganoderma lucidum
Fig. 3. Key NOESY correlations of compounds 1–5, 7 and 8.
Fig. 2. Key HMBC and 1H–1H in Lanostane triterpenoids with anti-inflammatory activities from Ganoderma lucidum
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–8.
Fig. 1 in Lanostane triterpenoids with anti-inflammatory activities from Ganoderma lucidum
Fig. 1. Structures of compounds 1–15.
Fig. 4. Single-crystal X in Lanostane triterpenoids with anti-inflammatory activities from Ganoderma lucidum
Fig. 4. Single-crystal X-ray structure of 5.
Fig. 7 in Lanostane triterpenoids from cultivated fruiting bodies of basidiomycete Ganoderma mbrekobenum
Fig. 7. Comparison of the chemical shifts (δН, ppm) of Hα-16, Hβ-16, and H3-18.
Fig. 1 in Lanostane triterpenoids from cultivated fruiting bodies of basidiomycete Ganoderma mbrekobenum
Fig. 1. Structures of compounds 1–11.
Fig. 3. Key NOESY correlations for 1, 2 in Lanostane triterpenoids from cultivated fruiting bodies of the wood-rot basidiomycete Ganoderma casuarinicola
Fig. 3. Key NOESY correlations for 1, 2, and 4.
Fig. 2. COSY and HMBC correlations for 1, 2 in Lanostane triterpenoids from cultivated fruiting bodies of the wood-rot basidiomycete Ganoderma casuarinicola
Fig. 2. COSY and HMBC correlations for 1, 2, and 4.
Fig. 3 in Lanostane-type triterpenoids from Ganoderma applanatum and their inhibitory activities on NO production in LPS-induced BV-2 cells
Fig. 3. ORTEP drawings of 1 and 2.
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