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Journal articles on the topic 'Phenylpropanoi͏̈de glycoside'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Arnold, Ulrike W., Christian Zidorn, Ernst P. Ellmerer, and Hermann Stuppner. "Iridoid and Phenolic Glycosides from Wulfenia carinthiaca." Zeitschrift für Naturforschung C 57, no. 11-12 (2002): 969–75. http://dx.doi.org/10.1515/znc-2002-11-1202.

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Two new phenylpropanoid glycosides (2′-O-acetylplantamajoside and 2′-O, 6″-O-diacetylplantamajoside), a new iridoid glycoside (10-O-(cinnamoyl)-6′-O-(desacetylalpinosidyl)-catalpol), the two known iridoid glycosides globularin and isoscrophularioside, and the known phenylpropanoid glycoside platamajoside were isolated from the methanolic extract of the underground parts of Wulfenia carinthiaca. Structure elucidations were based on high-resolution mass spectrometry and extensive 1-D and 2-D NMR spectroscopy.

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2

Santos, Javier de, Ana M. Díaz Lanza, Lidia Fernández, and Angel Rumbero. "Isoangoroside C, a Phenylpropanoid Glycoside from Scrophularia scorodonia Roots." Zeitschrift für Naturforschung C 55, no. 5-6 (2000): 333–36. http://dx.doi.org/10.1515/znc-2000-5-606.

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A new phenylpropanoid glycoside isoangoroside C was isolated from the roots of Scrophularia scorodonia. Its structure was determined on the basis of spectral data as: 3-hydroxy- 4-methoxy-β-phenylethoxy-O-α-ʟ-arabinopyranosyl-(1→6)α ʟ-rhamnopyranosyl-(l→3)-4-O- Z-feruloyl-β-ᴅ -glucopyranoside. Additionally, one known phenylpropanoid, angoroside C, and five known iridoid glycosides, harpagoside, bartsioside, 8-O-acetyl-harpagide, aucuboside and harpagide were isolated and identified.

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3

Zhang, San-Qi, Zhong-Jun Li, An-Bang Wang, Meng-Shen Cai, and Rui Feng. "Synthesis of a phenylpropanoid glycoside, Osmanthuside B611Studies on Glycosides XXIV." Carbohydrate Research 308, no. 3-4 (1998): 281–85. http://dx.doi.org/10.1016/s0008-6215(98)00092-5.

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4

Chu, Hong-Biao, Ning-Hua Tan, and Yu-Mei Zhanga. "Chemical Constituents from Pedicularis rex C. B. Clarke." Zeitschrift für Naturforschung B 62, no. 11 (2007): 1465–70. http://dx.doi.org/10.1515/znb-2007-1117.

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One new ionone glycoside, pedicurexoside (1), one new flavonoid, 5, 4′-dihydroxy-3′-methoxyflavone- 7-O-6″-n-butyryl-β -D-glucopyranoside (2), two new iridoid glycosides, 6-O-ethyl-aucubin (7), 6-O-ethyl-epiaucubin (8), and one new phenylpropanoid glycoside, 4-hydroxy-phenylpropenyl- α-L-rhamnopyranosyl-(1→3)-4-O- feruloyl-β -D-glucopyranoside (13), together with eleven known compounds, apigenin (3), luteolin (4), chrysoeriol (5), luteolin-7-O-β -D-glucopyranoside (6), aucubin (9), yuheinoside (10), euphroside (11), mussaenoside (12), verbascoside (14), martynoside (15) and isomartynoside (16)

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5

Liu, Shi-Qiao, Li-Ping Kang, Jie Zhang, et al. "New sesquiterpenoid glycoside and phenylpropanoid glycosides from the tuber of Ophiopogon japonicus." Journal of Asian Natural Products Research 18, no. 6 (2015): 520–27. http://dx.doi.org/10.1080/10286020.2015.1121996.

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6

Skrzypek, Zuzanna, Halina Wysokińska, Lucjan Świa̧tek, and Andrzej E. Wróblewski. "Phenylpropanoid Glycosides fromPenstemonserrulatus." Journal of Natural Products 62, no. 1 (1999): 127–29. http://dx.doi.org/10.1021/np970465b.

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7

ZHANG, S. Q., Z. J. LI, A. B. WANG, M. S. CAI, and R. FENG. "ChemInform Abstract: Studies on Glycosides. Part 24. Synthesis of a Phenylpropanoid Glycoside, Osmanthuside B6." ChemInform 29, no. 46 (2010): no. http://dx.doi.org/10.1002/chin.199846236.

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8

Abdallah, O. M., M. S. Kamel, and M. H. Mohamed. "Phenylpropanoid glycosides ofPrunus ssiori." Phytochemistry 37, no. 6 (1994): 1689–92. http://dx.doi.org/10.1016/s0031-9422(00)89593-x.

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9

Seidel, V., F. Bailleul, and F. Tillequin. "Phenylpropanoid Glycosides fromBallota nigra." Planta Medica 62, no. 02 (1996): 186–87. http://dx.doi.org/10.1055/s-2006-957854.

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10

Fauvel, M., K. Taoubi, J. Gleye, and I. Fourasté. "Phenylpropanoid Glycosides fromAvicennia marina." Planta Medica 59, no. 04 (1993): 387. http://dx.doi.org/10.1055/s-2006-959711.

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11

ZHANG, S. Q., Z. J. LI, A. B. WANG, M. S. CAI, and R. FENG. "ChemInform Abstract: Studies on Glycosides. Part 20. Total Synthesis of the Phenylpropanoid Glycoside, Grayanoside A." ChemInform 28, no. 34 (2010): no. http://dx.doi.org/10.1002/chin.199734250.

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12

Ono, Masateru, Yoshie Takatsu, Tetsuya Ochiai, et al. "Two New Nortriterpenoid Glycosides and a New Phenylpropanoid Glycoside from the Bulbs of Scilla scilloides." Chemical and Pharmaceutical Bulletin 60, no. 10 (2012): 1314–19. http://dx.doi.org/10.1248/cpb.c12-00457.

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13

Seidel, Veronique, François Bailleul, Francine Libot, and François Tillequin. "A phenylpropanoid glycoside from Ballota nigra." Phytochemistry 44, no. 4 (1997): 691–93. http://dx.doi.org/10.1016/s0031-9422(96)00578-x.

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14

Sang, Shengmin, Aina Lao, Hongcheng Wang, Zhongliang Chen, Jun Uzawa, and Yasuo Fujimoto. "A phenylpropanoid glycoside from Vaccaria segetalis." Phytochemistry 48, no. 3 (1998): 569–71. http://dx.doi.org/10.1016/s0031-9422(97)00896-0.

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15

Huong, Nguyen Thi Hong, Nguyen Khac Quynh Cu, Trinh Van Quy, Christian Zidorn, Markus Ganzera, and Hermann Stuppner. "A new phenylpropanoid glycoside fromJasminum subtriplinerveBlume." Journal of Asian Natural Products Research 10, no. 11 (2008): 1035–38. http://dx.doi.org/10.1080/10286020802320897.

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16

Khan, I., C. Erdelmeier, and O. Sticher. "A New Phenylpropanoid Glycoside fromEurya tigang." Planta Medica 56, no. 06 (1990): 573. http://dx.doi.org/10.1055/s-2006-961170.

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17

Cervellati, Rinaldo, Ester Speroni, Paolo Govoni, et al. "Wulfenia carinthiaca Jacq., Antioxidant and Pharmacological Activities." Zeitschrift für Naturforschung C 59, no. 3-4 (2004): 255–62. http://dx.doi.org/10.1515/znc-2004-3-424.

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Relative antioxidant activities of a methanolic extract of three phenylpropanoid glycosides and three iridoid glycosides from Wulfenia carinthiaca were evaluated using the Briggs- Rauscher (BR) reaction method. This method is based on the inhibitory effects by antioxidants on oscillations of the BR reaction. The total extract showed a certain antioxidant activity with respect to resorcinol chosen as standard. The three phenylpropanoid glycosides showed a very high relative antioxidant activity while iridoid glycosides had practically no activity. These experimental results were confirmed by em

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18

Brito, José Assis Gomes de, Luciano da Silva Pinto, Cintia Folly Chaves, Antônio Jorge Ribeiro da Silva, Maria Fátima das Graças Fernandes da Silva, and Fernando Cotinguiba. "Chemophenetic Significance of Anomalocalyx uleanus Metabolites Are Revealed by Dereplication Using Molecular Networking Tools." Molecules 26, no. 4 (2021): 925. http://dx.doi.org/10.3390/molecules26040925.

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Anomalocalyx uleanus (Pax & K. Hoffm.) Ducke (Euphorbiaceae) is a singular species in the genus and is restricted and exclusive to the Brazilian Amazon. A phytochemical study of A. uleanus leaves was performed, yielding the isolation of five major compounds: catechin/epicatechin, afzelin, quercetin 3-O-α-L-rhamnopyranoside, and astilbin. The phytochemical compositions of the methanolic extracts of leaves, roots, bark, and stem bark were determined using a dereplication approach. Forty-six compounds were annotated from the liquid chromatography-mass spectrometry (LC-MS/MS) data, while four

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19

Judeh, Zaher, and Duc Khong. "Short Synthesis of Phenylpropanoid Glycosides Calceolarioside A and Syringalide B." Synlett 29, no. 08 (2018): 1079–83. http://dx.doi.org/10.1055/s-0036-1591753.

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An efficient and practical three-step synthesis of phenylpropanoid glycosides calceolarioside A and syringalide B in >62% overall yield is disclosed. The key step involves the chemoselective and regioselective direct O-4 cinnamoylation of unprotected 2-phenylethyl-β-d-glucosides with cinnamic anhydrides using a chiral 4-pyrrolidinopyridine organocatalyst. This approach serves as a model for the short synthesis of phenylpropanoid glycosides acylated at O-4 without protection/deprotection steps.

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20

Jin, Changdong, Ronald G. Micetich, and Mohsen Daneshtalab. "Phenylpropanoid glycosides from Stellera chamaejasme." Phytochemistry 50, no. 4 (1999): 677–80. http://dx.doi.org/10.1016/s0031-9422(98)00586-x.

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21

Yi, Jin-Hai, Guo-Lin Zhang, Bo-Gang Li, and Yao-Zu Chen. "Phenylpropanoid glycosides from Lamiophlomis rotata." Phytochemistry 51, no. 6 (1999): 825–28. http://dx.doi.org/10.1016/s0031-9422(99)00027-8.

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22

Chen, Ting, Jian-Xin Li, and Qiang Xu. "Phenylpropanoid glycosides from Smilax glabra." Phytochemistry 53, no. 8 (2000): 1051–55. http://dx.doi.org/10.1016/s0031-9422(99)00522-1.

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23

Jimenez, Carlos, Mary Carmen Villaverde, Ricardo Riguera, Luis Castedo, and Frank R. Stermitz. "Three phenylpropanoid glycosides from Mussatia." Phytochemistry 26, no. 6 (1987): 1805–10. http://dx.doi.org/10.1016/s0031-9422(00)82293-1.

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24

Li, Yi-Ming, Shan-Hao Jiang, Wen-Yun Gao, and Da-Yuan Zhu. "Phenylpropanoid glycosides from Scrophularia ningpoensis." Phytochemistry 54, no. 8 (2000): 923–25. http://dx.doi.org/10.1016/s0031-9422(00)00171-0.

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25

Munkombwe, Namboole Moses, Pelotshweu Galebotswe, Kabelo Modibesane, and Nametso Morebodi. "Phenylpropanoid glycosides of Gnidia polycephala." Phytochemistry 64, no. 8 (2003): 1401–4. http://dx.doi.org/10.1016/s0031-9422(03)00211-5.

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26

Taoubi, K., M. Fauvel, J. Gleye, C. Moulis, and I. Fourasté. "Phenylpropanoid Glycosides fromLantana camaraandLippia multiflora." Planta Medica 63, no. 02 (1997): 192–93. http://dx.doi.org/10.1055/s-2006-957647.

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27

Houghton, Peter J. "Phenylpropanoid Glycosides in Buddleja davidii." Journal of Natural Products 48, no. 6 (1985): 1005–6. http://dx.doi.org/10.1021/np50042a033.

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28

Jiménez, Carlos, Mary Carmen Villaverde, Ricardo Riguera, Luis Castedo, and Frank Stermitz. "Phenylpropanoid Glycosides from Mussatia hyacinthina." Journal of Natural Products 52, no. 2 (1989): 408–10. http://dx.doi.org/10.1021/np50062a036.

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29

Jimenez, Carlos, Mary Carmen Villaverde, Ricardo Riguera, Luis Castedo, and Frank R. Stermitz. "Five phenylpropanoid glycosides from Mussatia." Phytochemistry 27, no. 9 (1988): 2947–51. http://dx.doi.org/10.1016/0031-9422(88)80694-0.

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30

Nicoletti, M., C. Galeffi, I. Messana, G. B. Marini-Bettolo, J. A. Garbarino, and V. Gambaro. "Phenylpropanoid glycosides from Calceolaria hypericina." Phytochemistry 27, no. 2 (1988): 639–41. http://dx.doi.org/10.1016/0031-9422(88)83164-9.

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31

ULLAH, Nisar, Saeed AHMAD, and Abdul MALIK. "Phenylpropanoid Glycosides from Daphne oleoides." CHEMICAL & PHARMACEUTICAL BULLETIN 47, no. 1 (1999): 114–15. http://dx.doi.org/10.1248/cpb.47.114.

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32

Tolonen, Ari, Minna Pakonen, Anja Hohtola, and Jorma Jalonen. "Phenylpropanoid Glycosides from Rhodiola rosea." CHEMICAL & PHARMACEUTICAL BULLETIN 51, no. 4 (2003): 467–70. http://dx.doi.org/10.1248/cpb.51.467.

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33

Çaliş, İhsan, Mohammed Hosny, Taha Khalifa, and Peter Rüedi. "Phenylpropanoid glycosides from Marrubium alysson." Phytochemistry 31, no. 10 (1992): 3624–26. http://dx.doi.org/10.1016/0031-9422(92)83740-p.

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34

Çaliş, İhsan, Tayfun Erso¨z, Den⌝z Taşdem⌝r, and Peter Ru¨edi. "Two phenylpropanoid glycosides fromLeonurus glaucescens." Phytochemistry 31, no. 1 (1992): 357–59. http://dx.doi.org/10.1016/0031-9422(91)83078-y.

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35

Hu, Jiang, Xiaodong Shi, Wei Ding, Jiangang Chen, and Changsheng Li. "Phenylpropanoid glycosides from Conyza japonica." Chemistry of Natural Compounds 48, no. 5 (2012): 782–84. http://dx.doi.org/10.1007/s10600-012-0381-3.

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36

Oganesyan, G. B., A. M. Galstyan, V. A. Mnatsakanyan, A. S. Shashkov, and P. V. Agababyan. "Phenylpropanoid glycosides of Teucrium polium." Chemistry of Natural Compounds 27, no. 5 (1991): 556–59. http://dx.doi.org/10.1007/bf00630353.

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37

Comte, Gilles, Albert Chulia, Joseph Vercauteren, and Daovy Allais. "Phenylpropane Glycosides fromJuniperus phœnicea." Planta Medica 62, no. 01 (1996): 88–89. http://dx.doi.org/10.1055/s-2006-957817.

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38

Wang, Yu, Wen Yuan Gao, Tie Jun Zhang, and Yuan Qiang Guo. "A novel phenylpropanoid glycosides and a new derivation of phenolic glycoside from Paris Polyphylla var. yunnanensis." Chinese Chemical Letters 18, no. 5 (2007): 548–50. http://dx.doi.org/10.1016/j.cclet.2007.03.011.

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39

Ravasi, Juliana Mourão, Giuseppina Negri, Antonio Salatino, Maria Luiza Faria Salatino, and Marco Aurelio Sivero Mayworm. "GC-MS and HPLC-ESI-MS-MS Characterization of Sanchezia oblonga (Acanthaceae) Extracts." Journal of Food Research 9, no. 1 (2020): 57. http://dx.doi.org/10.5539/jfr.v9n1p57.

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The genus Sanchezia (Acanthaceae) comprises neotropical herbs and shrubs with showy flowers. Sanchezia oblonga (syn. S. nobilis) is a shrub of the rainforests of central and south America. The ethanolic extracts of leaves and stems from S. oblonga were analyzed by GC-EI-MS and RPHPLC-DAD-ESI-MS/MS. Fatty acids (free and esterified) and phytosterols were detected by the former method. Benzyl alcohol glycosides (21 and 25), sinapic acid glycoside esters (29 and 31), ethyl rosmarinate (24), sinapic acid-O-glucoside (28), dihydrosinapic acid-O-glucoside (26), catechin-O-arabinoside (36), in additi

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40

Afifi, M., M. Lahloub, S. El-Khayaat, C. Anklin, H. Rüegger, and O. Sticher. "Crenatoside: A Novel Phenylpropanoid Glycoside fromOrobanche crenata1." Planta Medica 59, no. 04 (1993): 359–62. http://dx.doi.org/10.1055/s-2006-959701.

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41

Kawada, Toshinari, Ryuji Asano, Shiho Hayashida, and Tomoyasu Sakuno. "Total Synthesis of the Phenylpropanoid Glycoside, Acteoside." Journal of Organic Chemistry 64, no. 25 (1999): 9268–71. http://dx.doi.org/10.1021/jo9906983.

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42

Başaran, Arif Ahmet, İhsan Çaliş, Clemens Anklin, Sansei Nishibe, and Otto Sticher. "Lavandulifolioside: A New Phenylpropanoid Glycoside fromStachys lavandulifolia." Helvetica Chimica Acta 71, no. 6 (1988): 1483–90. http://dx.doi.org/10.1002/hlca.19880710612.

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43

Çaliş, İhsan, Deniz Taşdemir, Anthony D. Wright, and Otto Sticher. "Lagotoside: A New Phenylpropanoid Glycoside fromLagotis stolonifera." Helvetica Chimica Acta 74, no. 6 (1991): 1273–77. http://dx.doi.org/10.1002/hlca.19910740615.

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44

Gross, G. A., M. F. Lahloub, C. Anklin, H. R. Schulten, and O. Sticher. "Teucrioside, a phenylpropanoid glycoside from Teucrium chamaedrys." Phytochemistry 27, no. 5 (1988): 1459–63. http://dx.doi.org/10.1016/0031-9422(88)80215-2.

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45

Lahloub, M., H. Rüegger, S. El-Khayaat, M. Affifi, and O. Sticher. "Crenatoside, a Novel Phenylpropanoid Glycoside fromOrobanche crenata." Planta Medica 55, no. 07 (1989): 612–13. http://dx.doi.org/10.1055/s-2006-962164.

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46

Baudouin, Geneviève, Alexios-Léandros Skaltsounis, François Tillequin, and Michel Koch. "Lugrandoside: A New Phenylpropanoid Glycoside from VariousDigitalisSpecies." Planta Medica 54, no. 04 (1988): 321–23. http://dx.doi.org/10.1055/s-2006-962445.

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47

Çaliş, İ., D. Taşdemir, and O. Sticher. "Lagotoside: A New Phenylpropanoid Glycoside fromLagotis stolonifera." Planta Medica 56, no. 06 (1990): 574. http://dx.doi.org/10.1055/s-2006-961173.

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48

Lahloub, M., G. A. Gross, O. Sticher, T. Winkler, and H. R. Schulten. "Ehrenoside, a New Phenylpropanoid Glycoside fromVeronica bellidioides1." Planta Medica 52, no. 05 (1986): 352–55. http://dx.doi.org/10.1055/s-2007-969182.

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49

Zheng-Dan, He, and Yang Chong-Ren. "Brandioside, a phenylpropanoid glycoside from Brandisia hancei." Phytochemistry 30, no. 2 (1991): 701–2. http://dx.doi.org/10.1016/0031-9422(91)83759-e.

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50

Song, Xun, Jiang He, Hong Xu та ін. "The antiviral effects of acteoside and the underlying IFN-γ-inducing action". Food & Function 7, № 7 (2016): 3017–30. http://dx.doi.org/10.1039/c6fo00335d.

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