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50 results for “Triterpenes”
Fig. 6 in Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
Fig. 6. CD spectrum of 4 in DMSO containing Mo2(OAc)4 with the inherent CDs subtracted.
Fig. 4. X in Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
Fig. 4. X-ray crystallographic diagram and experimental CD/calculated ECD spectra of 1.
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 and 4–7 in Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 and 4–7.
Fig. 3 in Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
Fig. 3. Key NOE correlations of compounds 1, 3, 6, and 7.
Fig. 5. 1H in Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
Fig. 5. 1H NMR spectra and assignments of compounds 1–3.
Fig. 2 in Biosynthetic diversity in triterpene cyclization within the Boswellia genus
Fig. 2. (continued).
Fig. 5 in Triterpene glycosides and phenylpropane derivatives from Staurogyne concinnula possessing anti-angiogenic activity
Fig. 5. Inhibition of FAK/paxillin/MMP signaling pathway treated with 4.
Fig. 1 in Triterpene glycosides and phenylpropane derivatives from Staurogyne concinnula possessing anti-angiogenic activity
Fig. 1. Structures of isolated compounds 1–9 from S. concinnula.
Fig. 2. Key HMBC and 1H–1H COSY correlations for 1–3 and 5 in Triterpene glycosides and phenylpropane derivatives from Staurogyne concinnula possessing anti-angiogenic activity
Fig. 2. Key HMBC and 1H–1H COSY correlations for 1–3 and 5.
Fig. 6. X in Pentacyclic Triterpenes from the resin of Liquidambar formosana have anti-angiogenic properties
Fig. 6. X-ray ORTEP drawing of 3 with ellipsoids drawn at the 30% probability level.
Fig. 3 in Pentacyclic Triterpenes from the resin of Liquidambar formosana have anti-angiogenic properties
Fig. 3. Key NOSEY correlations of compounds 1, 3, 4, and 5.
Fig. 1 in Pentacyclic Triterpenes from the resin of Liquidambar formosana have anti-angiogenic properties
Fig. 1. Structures of compounds 1–15.
Fig. 5. X in Pentacyclic Triterpenes from the resin of Liquidambar formosana have anti-angiogenic properties
Fig. 5. X-ray ORTEP drawing of 2 with ellipsoids drawn at the 30% probability level.
Fig. 2. Key 1H–1H in Pentacyclic Triterpenes from the resin of Liquidambar formosana have anti-angiogenic properties
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–5.
Fig. 4. X in Pentacyclic Triterpenes from the resin of Liquidambar formosana have anti-angiogenic properties
Fig. 4. X-ray ORTEP drawing of 1 with ellipsoids drawn at the 30% probability level.
Fig. 2 in Triterpene saponins from the seeds of Erythrophleum fordii and their cytotoxic activities
Fig. 2. COSY (bold lines) and key HMBC (H→C) correlations of 1 and 2.
Fig. 1 in Triterpene glycosides from Silene odontopetala
Fig. 1. Triterpene saponins from Silene odontopetala.
Fig. 2 in Triterpene glycosides from Silene odontopetala
Fig. 2. (A) 1H–1H COSY and key HMBC correlations for 1; (B) Selected ROESY correlations for 1.
Fig. 1 in Triterpene glycosides from Blighia welwitschii and evaluation of their antibody recognition capacity in multiple sclerosis
Fig. 1. Structures of new triterpene saponins 1–7 isolated from the fruits of B. welwitschii.
Fig. 1 in Triterpene saponins from Silene gallica collected in North-Eastern Algeria
Fig. 1. Chemical structures of compounds 1–11 isolated from Silene gallica.
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