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570 results for “Euphorbia”

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Fig. 3 in Euphorbia helioscopia L.: A phytochemical and pharmacological overview

Fig. 3. Graphical summary of pharmacological properties of E. helioscopia.

opennotspecifiedApr 2021View details →
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Fig. 2 in Euphorbia helioscopia L.: A phytochemical and pharmacological overview

Fig. 2. (continued).

opennotspecifiedApr 2021View details →
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Fig. 2 in Euphorbia helioscopia L.: A phytochemical and pharmacological overview

Fig. 2. Chemical structures of terpenoids and flavonoids.

opennotspecifiedApr 2021View details →
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Fig. 2 in Euphorbia helioscopia L.: A phytochemical and pharmacological overview

Fig. 2. (continued).

opennotspecifiedApr 2021View details →
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Fig. 4. A in Euphorbia helioscopia L.: A phytochemical and pharmacological overview

Fig. 4. A schematic representation of the main molecular mechanisms of E. helioscopia.

opennotspecifiedApr 2021View details →
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Fig. 5. ORTEP drawing for compound 6 in Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities

Fig. 5. ORTEP drawing for compound 6.

opennotspecifiedMar 2021View details →
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Fig. 1 in Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities

Fig. 1. Structure of compounds 1–15.

opennotspecifiedMar 2021View details →
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Fig. 3. ORTEP drawing for compound 1 in Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities

Fig. 3. ORTEP drawing for compound 1.

opennotspecifiedMar 2021View details →
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Fig. 2 in Eupholides A H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities

Fig. 2. The key HMBC (a), 1H–1H COSY (a), and NOESY (b) correlations of compound 1.

opennotspecifiedMar 2021View details →
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Fig. 3 in Antiproliferative diterpenoids and acetophenone glycoside from the roots of Euphorbia fischeriana

Fig. 3. Key NOE correlations of Compounds 1 and 5.

opennotspecifiedSep 2020View details →
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Fig. 2 in Antiproliferative diterpenoids and acetophenone glycoside from the roots of Euphorbia fischeriana

Fig. 2. Key HMBC correlations of Compounds 1, 5 and 9.

opennotspecifiedSep 2020View details →
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Fig. 1 in Antiproliferative diterpenoids and acetophenone glycoside from the roots of Euphorbia fischeriana

Fig. 1. Chemical structures of compounds 1–12 isolated from E. fischeriana.

opennotspecifiedSep 2020View details →
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Fig. 4 in Antiproliferative diterpenoids and acetophenone glycoside from the roots of Euphorbia fischeriana

Fig. 4. The experimental ECD and calculated ECD spectra of compounds 1, 5.

opennotspecifiedSep 2020View details →
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Fig. 8 in Diterpenoids from Euphorbia royleana reverse P-glycoprotein-mediated multidrug resistance in cancer cells

Fig. 8. Effects of 15 on the expression of P-gp.

opennotspecifiedAug 2020View details →
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Fig. 3 in Diterpenoids from Euphorbia royleana reverse P-glycoprotein-mediated multidrug resistance in cancer cells

Fig. 3. Key NOESY correlations () of compounds 1, 2, 4, 5, 6, and 8.

opennotspecifiedAug 2020View details →
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Fig. 1 in Diterpenoids from Euphorbia royleana reverse P-glycoprotein-mediated multidrug resistance in cancer cells

Fig. 1. The structures of compounds 1–30 and 8a.

opennotspecifiedAug 2020View details →
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Fig. 4. Single-crystal X in Diterpenoids from Euphorbia royleana reverse P-glycoprotein-mediated multidrug resistance in cancer cells

Fig. 4. Single-crystal X-ray structures of 1, 6, 7, and 8a.

opennotspecifiedAug 2020View details →
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Fig. 1 in Bioactive ent-isopimarane diterpenoids from Euphorbia neriifolia

Fig. 1. Structures of compounds 1–12 isolated from Euphorbia neriifolia.

opennotspecifiedJul 2020View details →
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Fig. 4. X in Bioactive ent-isopimarane diterpenoids from Euphorbia neriifolia

Fig. 4. X-ray crystallographic ORTEP diagram of compound 1.

opennotspecifiedJul 2020View details →
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Fig. 2. 1 H– 1 H in Bioactive ent-isopimarane diterpenoids from Euphorbia neriifolia

Fig. 2. 1 H– 1 H COSY and key HMBC correlations of compounds 1–3.

opennotspecifiedJul 2020View details →

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