2021
DOI: 10.1016/j.phytochem.2021.112935
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Prenylated C6–C3 derivatives from the stems and branches of Illicium ternstroemioides A. C. Smith with antiviral activity

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Cited by 7 publications
(2 citation statements)
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“…The genus Illicium has been regarded as a rich source of sesquiterpenes [1][2][3][4][5][6][7][8][9], especially seco-prezizaanetype sesquiterpenes and prenylated C6-C3 compound derivatives [10][11][12][13][14][15][16], which have distinct structural features and various carbon skeletons. Some of the sesquiterpenes have exhibited intriguing antiviral, neuroprotective, and neurotrophic activities [7,[17][18][19][20][21], while many prenylated C6-C3 compounds were found to exhibit increased choline acetyltransferase, cytotoxic and antiviral activities [12][13][14]22].…”
Section: Introductionmentioning
confidence: 99%
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“…The genus Illicium has been regarded as a rich source of sesquiterpenes [1][2][3][4][5][6][7][8][9], especially seco-prezizaanetype sesquiterpenes and prenylated C6-C3 compound derivatives [10][11][12][13][14][15][16], which have distinct structural features and various carbon skeletons. Some of the sesquiterpenes have exhibited intriguing antiviral, neuroprotective, and neurotrophic activities [7,[17][18][19][20][21], while many prenylated C6-C3 compounds were found to exhibit increased choline acetyltransferase, cytotoxic and antiviral activities [12][13][14]22].…”
Section: Introductionmentioning
confidence: 99%
“…Crystal data for diacorone B(16). C30H50O2 (M =442.70 g/mol): tetragonal, space group P43 (no.78), a = 10.14050(10) Å, c = 26.2081(4) Å, V = 2694.97(6) Å 3 , Z = 4, T = 100.00(10) K, μ (CuKα) = 0.495 mm -1 , Dcalc = 1.091 g/cm 3 , 19678 reflections measured (8.72 ° ≤ 2Θ ≤ 147.4 °), and 5316 unique reflections (Rint = 0.0274, Rsigma = 0.0222), which were used in all calculations.…”
mentioning
confidence: 99%