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77 results for “coumarin”

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zenodo28/100

Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10 in Sesquiterpene coumarins from Ferula samarkandica Korovin and their bioactivity

Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10.

opennotspecifiedJul 2021View details →
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Fig. 3 in Sesquiterpene coumarins from Ferula sinkiangensis K.M.Shen and their cytotoxic activities

Fig. 3. Key NOESY correlations of compounds 1–5.

opennotspecifiedDec 2020View details →
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Fig. 2. Key 1H–1H in Sesquiterpene coumarins from Ferula sinkiangensis K.M.Shen and their cytotoxic activities

Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–6.

opennotspecifiedDec 2020View details →
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Fig. 1 in Sesquiterpene coumarins from Ferula sinkiangensis K.M.Shen and their cytotoxic activities

Fig. 1. Structures of compounds 1–31 isolated from the resin of F. sinkiangensis K.M.Shen.

opennotspecifiedDec 2020View details →
zenodo28/100

Fig. 4 in (þ/¡)-Dievodialetins A¡G: Seven pairs of enantiomeric coumarin dimers with anti-acetylcholinesterase activity from the roots of Evodia lepta Merr.

Fig. 4. Plausible biosynthetic pathway of (+/)-1 7.

opennotspecifiedFeb 2021View details →
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Fig. 1 in (þ/¡)-Dievodialetins A¡G: Seven pairs of enantiomeric coumarin dimers with anti-acetylcholinesterase activity from the roots of Evodia lepta Merr.

Fig. 1. Chemical structures of 1 9.

opennotspecifiedFeb 2021View details →
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Fig. 8 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities

Fig. 8. The docked view of interactions between compound 5 with iNOS protein.

opennotspecifiedSep 2020View details →
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Fig. 1 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities

Fig. 1. Structures of compounds 1–19.

opennotspecifiedSep 2020View details →
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Fig. 4 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities

Fig. 4. The NOE correlations (A), CD spectrum, UV spectrum, and the exciton chirality (B) of 5.

opennotspecifiedSep 2020View details →
zenodo28/100

Fig. 7 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities

Fig. 7. The Rh2(OCOCF3)4 induced CD spectrum of 11.

opennotspecifiedSep 2020View details →
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Fig. 6 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities

Fig. 6. The dihedral angles of four preferred conformations of 8 and 9.

opennotspecifiedSep 2020View details →
zenodo28/100

Fig. 3 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities

Fig. 3. The calculated and experimental ECD spectra of compounds 1a and 1b.

opennotspecifiedSep 2020View details →
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Fig. 1 in Terpenylated coumarins from the root bark of Ailanthus altissima (Mill.) Swingle

Fig. 1. Chemical structure of compounds 1–14.

opennotspecifiedJul 2020View details →
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Fig. 5 in Terpenylated coumarins from the root bark of Ailanthus altissima (Mill.) Swingle

Fig. 5. ΔδS-R value (ppm) of MTPA ester of 3, 5, 6 and 10.

opennotspecifiedJul 2020View details →
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Fig. 3 in Benzofuran and coumarin derivatives from the root of Angelica dahurica and their PPAR-γ ligand-binding activity

Fig. 3. Key HMBC correlations and ORTEP drawing of the crystal structure of 7.

opennotspecifiedMay 2020View details →
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Fig. 2 in Benzofuran and coumarin derivatives from the root of Angelica dahurica and their PPAR-γ ligand-binding activity

Fig. 2. Key HMBC correlations of 1.

opennotspecifiedMay 2020View details →
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Fig. 1 in Benzofuran and coumarin derivatives from the root of Angelica dahurica and their PPAR-γ ligand-binding activity

Fig. 1. Structures of 1–21 isolated from the root of Angelica dahurica.

opennotspecifiedMay 2020View details →
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Fig. 2 in Coumarin and spirocyclopentenone derivatives from the leaves and stems of Murraya paniculata (L.) Jack

Fig. 2. Key HMBC correlations of compounds 1–5.

opennotspecifiedApr 2020View details →
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Fig. 1 in Coumarin and spirocyclopentenone derivatives from the leaves and stems of Murraya paniculata (L.) Jack

Fig. 1. Structures of compounds 1–19.

opennotspecifiedApr 2020View details →
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Fig. 4 in Coumarin and spirocyclopentenone derivatives from the leaves and stems of Murraya paniculata (L.) Jack

Fig. 4. Putative biosynthesis pathway to 1.

opennotspecifiedApr 2020View details →

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