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Journal articles on the topic 'Hopeaphenol'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Atun, Sri. "HOPEAPHENOL-O-GLYCOSIDE, A COMPOUND ISOLATED FROM STEM BARK Anisoptera marginata (Dipterocarpaceae)." Indonesian Journal of Chemistry 9, no. 1 (2010): 151–57. http://dx.doi.org/10.22146/ijc.21578.

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Isolation and structure elucidation of some compounds from stem bark of Anisoptera marginata had been done. The isolation of those compounds was carried out by chromatographyc method and structure elucidation was performed by interpretation of spectroscopic data, including UV, IR, 1H and 13C NMR 1D and 2D, and FABMS. From acetone extract stem bark A. marginata we isolated five known compounds namely bergenin (1), (-)-ε-vinipherin (2), (-)-ampelopsin A (3), vaticanol B (4), (-)-hopeaphenol (5), and a glycoside compound namely hopeaphenol-O- glycoside (6). Keywords: Dipterocarpaceae; Anisoptera

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2

Hikita, Kiyomi, Norikazu Seto, Yusuke Takahashi, et al. "Effect of Resveratrol Dimers and Tetramers Isolated from Vitaceous and Dipterocarpaceous Plants on Human SIRT1 Enzyme Activity." Natural Product Communications 13, no. 11 (2018): 1934578X1801301. http://dx.doi.org/10.1177/1934578x1801301130.

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SIRT1 is a mammalian ortholog of the yeast enzyme Sir2, which is an NAD+-dependent deacetylase of histones, p53, FOXO, NF-κB, PGC-1α, and other transcription factors. The Sir2 protein is reported as a longevity protein in yeast. Resveratrol, a polyphenol isolated from various types of plant families, particularly the Vitaceae family, is a known naturally occurring SIRT1 activator. In this study, we evaluated the effects of four types of resveratrol dimers and four types of tetramers isolated from vitaceous plants, and one type of resveratrol tetramer isolated from a dipterocarpaceous plant on

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3

Sahidin, Sahidin. "ISOLATION AND STRUCTURE ELUCIDATIONS OF RESVERATROL OLIGOMERS FROM STEM BARK OF Dryobalanops lanceolata." Indonesian Journal of Chemistry 9, no. 2 (2010): 315–20. http://dx.doi.org/10.22146/ijc.21549.

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Five resveratrol oligomers which consist of two resveratrol dimers, balanocarpol (1) and e-viniferin (2), a resveratrol trimer i.e. a-viniferin (3), and two resveratrol tetramers, vaticanol B (4), and hopeaphenol (5) have been isolated from acetone extract of the stem bark of Dryobalanops lanceolata. These compounds were isolated by vacuum liquid chromatography method. Furthermore, the compound structures were determined based on the spectroscopic evidence, including UV, IR, 1-D and 2D NMR spectra, and comparing with those related data reported previously. Keywords: Balanocarpol, e-Viniferin,

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4

Dávid, Csilla Zsuzsanna, Norbert Kúsz, Orinamhe Godwin Agbadua, et al. "Phytochemical Investigation of Carex praecox Schreb. and ACE-Inhibitory Activity of Oligomer Stilbenes of the Plant." Molecules 29, no. 14 (2024): 3427. http://dx.doi.org/10.3390/molecules29143427.

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Phenolic compounds are the main special metabolites of Cyperaceae species from phytochemical, pharmacological, and chemotaxonomical points of view. The present study focused on the isolation, structure determination, and pharmacological investigation of constituents from Carex praecox. Twenty-six compounds, including lignans, stilbenes, flavonoids, megastigmanes, chromenes, and phenylpropanoids, were identified from the methanol extract of the plant. Five of these compounds, namely, carexines A–E, are previously undescribed natural products. All compounds were isolated for the first time from

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5

I, Sahidin, Wahyuni W, Muh Hajrul Malaka, and Imran I. "ANTIBACTERIAL AND CYTOTOXIC POTENCIES OF STILBENE OLIGOMERS FROM STEM BARKS OF BAOTI (DRYOBALANOPS LANCEOLATA) GROWING IN KENDARI, INDONESIA." Asian Journal of Pharmaceutical and Clinical Research 10, no. 8 (2017): 139. http://dx.doi.org/10.22159/ajpcr.2017.v10i8.18664.

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Objective: The purpose of the research is to isolate and to identify compounds from stem barks of Dryobalanops lanceolata and to evaluate their activities toward bacteria and cancer cell lines.Methods: Isolation of the compounds worked with chromatography methods including thin-layer chromatography, vacuum liquid chromatography, and radial chromatography. All compound structures were determined based on the spectroscopic evidence including ultraviolet (UV), Infrared, and one-dimension and two-dimension nuclear magnetic resonance spectra and comparison the spectroscopy data with related data fr

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6

Chen, Lih-Geeng, Ching-Chiung Wang, Yi-Shan Lee, Yi-Yan Sie, Chi-I. Chang, and Wen-Chi Hou. "Vitisin A, a Resveratrol Tetramer, Improves Scopolamine-Induced Impaired Learning and Memory Functions in Amnesiac ICR Mice." Biomedicines 10, no. 2 (2022): 273. http://dx.doi.org/10.3390/biomedicines10020273.

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Resveratrol has been reported to exhibit neuroprotective activities in vitro and in vivo. However, little is known about resveratrol tetramers of hopeaphenol, vitisin A, and vitisin B with the same molecular mass in the improvement of degenerative disorders. In this study, two 95% ethanol extracts (95EE) from stem parts of Vitis thunbergii Sieb. & Zucc. (VT-95EE) and from the root (R) parts of Vitis thunbergii var. taiwaniana (VTT-R-95EE) showed comparable acetylcholinesterase (AChE) inhibitory activities. It was found that VT-95EE and VTT-R-95EE showed different distribution patterns of i

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7

Aja, Iris, M. Begoña Ruiz-Larrea, Arnaud Courtois, Stéphanie Krisa, Tristan Richard, and José-Ignacio Ruiz-Sanz. "Screening of Natural Stilbene Oligomers from Vitis vinifera for Anticancer Activity on Human Hepatocellular Carcinoma Cells." Antioxidants 9, no. 6 (2020): 469. http://dx.doi.org/10.3390/antiox9060469.

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The characterization of bioactive resveratrol oligomers extracted from Vitis vinifera canes has been recently reported. Here, we screened six of these compounds (ampelopsin A, trans-ε-viniferin, hopeaphenol, isohopeaphenol, R2-viniferin, and R-viniferin) for their cytotoxic activity to human hepatocellular carcinoma (HCC) cell lines p53 wild-type HepG2 and p53-null Hep3B. The cytotoxic efficacy depended on the cell line. R2-viniferin was the most toxic stilbene in HepG2, with inhibitory concentration 50 (IC50) of 9.7 ± 0.4 µM at 72 h, 3-fold lower than for resveratrol, while Hep3B was less sen

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8

Surapinit, Serm, Jonkolnee Jong-aramruang, Pongpun Siripong, Suttira Khumkratok, and Santi Tip-pyang. "Dipterostilbenosides A and B, Oligostilbene Glycosides from Dipterocarpus tuberculatus." Natural Product Communications 9, no. 9 (2014): 1934578X1400900. http://dx.doi.org/10.1177/1934578x1400900926.

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From the chemical investigation of the methanolic extract of the roots of the Thai dipterocarp, Dipterocarpus tuberculatus, two new oligostilbene glycosides, dipterostilbenes A (1) and B (2), were isolated together with four known stilbenes. Their structures and relative configurations were determined on the basis of spectroscopic data. From an evaluation of cytotoxic activity against KB and HeLa cell lines, α-viniferin (5) and (-)-hopeaphenol (6) showed potent activity, but less than that of doxorubicin.

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9

Hakim, Euis H., Lia D. Juliawaty, Yana M. Syah, et al. "Cytotoxic Properties of Oligostilbenoids from the Tree Barks of Hopea dryobalanoides." Zeitschrift für Naturforschung C 60, no. 9-10 (2005): 723–27. http://dx.doi.org/10.1515/znc-2005-9-1011.

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Abstract A new modified stilbene dimer, diptoindonesin D (1), was isolated from the acetone extract of the tree bark of Hopea dryobalanoides, together with seven known compounds, parviflorol (2), (D)-balanocarpol (3), heimiol A (4), hopeafuran (5), (+)-α-viniferin (6), vaticanol B (7) and (D)-hopeaphenol (8). Cytotoxic properties of compounds 1-8 were evaluated against murine leukemia P-388 cells. Compound 8 was found to be the most active with IC50 of 5.7 μm

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10

Guebailia, Habiba Amira, Kleopatra Chira, Tristan Richard, et al. "Hopeaphenol: The First Resveratrol Tetramer in Wines from North Africa." Journal of Agricultural and Food Chemistry 54, no. 25 (2006): 9559–64. http://dx.doi.org/10.1021/jf062024g.

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11

Tietjen, I., Z. Haq, M. Naidu, et al. "Persistent HIV reservoir suppression by (-)-hopeaphenol, a plant-derived stilbenoid." Journal of Virus Eradication 5 (December 2019): 44. http://dx.doi.org/10.1016/s2055-6640(20)30190-4.

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12

Subramanian, R., V. Raj, K. Manigandan, and N. Elangovan. "Antioxidant activity of hopeaphenol isolated from Shorea roxburghii stem bark extract." Journal of Taibah University for Science 9, no. 2 (2015): 237–44. http://dx.doi.org/10.1016/j.jtusci.2014.11.004.

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13

Loisruangsin, Arthorn, Kiyomi Hikita, Norikazu Seto, Masatake Niwa, Yoshiaki Takaya, and Norio Kaneda. "Structural analysis of the inhibitory effects of polyphenols, (+)‐hopeaphenol and (−)‐isohopeaphenol, on human SIRT1." BioFactors 45, no. 2 (2018): 253–58. http://dx.doi.org/10.1002/biof.1479.

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14

RAMESHWAR, DAYAL. "Phytochemical Investigation of Vateria indica." Journal of Indian Chemical Society Vol. 64, Apr 1987 (1987): 259. https://doi.org/10.5281/zenodo.6217446.

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Chemistry of Forest Products Branch, Forest Research Institute & Colleges, Dehra Dun-248 006 <em>Manuscript received 23 June 1986, accepted 9 March 1987</em> Phytochemical Investigation of \(Vateria\) \(indica\).

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15

Yu, Zaiqiang, Xu Liu, Tadaatsu Imaizumi та ін. "(+)-Hopeaphenol inhibits Poly IC-induced innate immunity activation via IFN-β in human cerebral microvascular endothelial cells". Proceedings for Annual Meeting of The Japanese Pharmacological Society 95 (2022): 3—P—194. http://dx.doi.org/10.1254/jpssuppl.95.0_3-p-194.

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16

Kawabata, Jun, Eri Fukushi, Masato Hara, and Junya Mizutani. "Detection of connectivity between equivalent carbons in aC2 molecule using isotopomeric asymmetry: Identification of hopeaphenol inCarex pumila." Magnetic Resonance in Chemistry 30, no. 1 (1992): 6–10. http://dx.doi.org/10.1002/mrc.1260300103.

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17

Anna Malinowska, Magdalena, Kévin Billet, Samantha Drouet, et al. "Grape Cane Extracts as Multifunctional Rejuvenating Cosmetic Ingredient: Evaluation of Sirtuin Activity, Tyrosinase Inhibition and Bioavailability Potential." Molecules 25, no. 9 (2020): 2203. http://dx.doi.org/10.3390/molecules25092203.

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Grape canes are waste biomass of viticulture containing bioactive polyphenols valuable in cosmetics. Whereas several studies reported the cosmetic activities of E-resveratrol, only few described the potential of E-ε-viniferin, the second major constituent of grape cane extracts (GCE), and none of them investigated GCE as a natural blend of polyphenols for cosmetic applications. In this study, we considered the potential of GCE from polyphenol-rich grape varieties as multifunctional cosmetic ingredients. HPLC analysis was performed to quantify major polyphenols in GCE i.e., catechin, epicatechi

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18

Zetterström, Caroline E., Jenny Hasselgren, Olli Salin, et al. "The Resveratrol Tetramer (-)-Hopeaphenol Inhibits Type III Secretion in the Gram-Negative Pathogens Yersinia pseudotuberculosis and Pseudomonas aeruginosa." PLoS ONE 8, no. 12 (2013): e81969. http://dx.doi.org/10.1371/journal.pone.0081969.

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19

Schrader, Kevin, Mohamed Ibrahim, Howaida Abd-Alla, Charles Cantrell, and David Pasco. "Antibacterial Activities of Metabolites from Vitis rotundifolia (Muscadine) Roots against Fish Pathogenic Bacteria." Molecules 23, no. 11 (2018): 2761. http://dx.doi.org/10.3390/molecules23112761.

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Enteric septicemia of catfish, columnaris disease and streptococcosis, caused by Edwardsiella ictaluri, Flavobacterium columnare and Streptococcus iniae, respectively, are the most common bacterial diseases of economic significance to the pond-raised channel catfish Ictalurus punctatus industry. Certain management practices are used by catfish farmers to prevent large financial losses from these diseases such as the use of commercial antibiotics. In order to discover environmentally benign alternatives, using a rapid bioassay, we evaluated a crude extract from the roots of muscadine Vitis rotu

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20

Kuete, Victor, Ean-Jeong Seo, Benjamin Krusche, et al. "Cytotoxicity and Pharmacogenomics of Medicinal Plants from Traditional Korean Medicine." Evidence-Based Complementary and Alternative Medicine 2013 (2013): 1–14. http://dx.doi.org/10.1155/2013/341724.

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Aim. The present study was designed to investigate the cytotoxicity of a panel of 280 Korean medicinal plants belonging to 73 families and 198 species against human CCRF-CEM leukemia cells. Selected phytochemicals were investigated in more detail for their mode of action.Methods. The resazurin assay was used to determine cytotoxicity of the plant extracts. Microarray-based mRNA expression profiling, COMPARE, and hierarchical cluster analyses were applied to identify which genes correlate with sensitivity or resistance to selected phytochemicals of the Korean plants.Results. The results of the

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21

Labois, Clément, Kim Wilhelm, Hélène Laloue, et al. "Wood Metabolomic Responses of Wild and Cultivated Grapevine to Infection with Neofusicoccum parvum, a Trunk Disease Pathogen." Metabolites 10, no. 6 (2020): 232. http://dx.doi.org/10.3390/metabo10060232.

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Grapevine trunk diseases (GTDs), which are associated with complex of xylem-inhabiting fungi, represent one of the major threats to vineyard sustainability currently. Botryosphaeria dieback, one of the major GTDs, is associated with wood colonization by Botryosphaeriaceae fungi, especially Neofusicoccum parvum. We used GC-MS and HPLC-MS to compare the wood metabolomic responses of the susceptible Vitis vinifera subsp. vinifera (V. v. subsp. vinifera) and the tolerant Vitis vinifera subsp. sylvestris (V. v. subsp. sylvestris) after artificial inoculation with Neofusicoccum parvum (N. parvum). N

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22

Seya, Kazuhiko, Kouta Kanemaru, Chiharu Sugimoto, et al. "Opposite Effects of Two Resveratrol (trans-3,5,4′-Trihydroxystilbene) Tetramers, Vitisin A and Hopeaphenol, on Apoptosis of Myocytes Isolated from Adult Rat Heart." Journal of Pharmacology and Experimental Therapeutics 328, no. 1 (2008): 90–98. http://dx.doi.org/10.1124/jpet.108.143172.

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23

Alam, Saiyad Shah, Waseem Ahmad, Md Rizwanullah, and Mohammad Muzammil. "HEALING OF A TRAUMATIC WOUND WITH HERBO-MEDICINAL OINTMENT; MARHAM-E-RAAL: A CASE STUDY." Journal of Pharmaceutical and Scientific Innovation 9, no. 6 (2020): 152–55. http://dx.doi.org/10.7897/2277-4572.096188.

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Introduction: A wound can be defined as the discontinuity in skin or mucus membrane. Healing is nothing but neogranulation in the depth and neo-epithelialization at the edges of the wound which ultimately results in the complete repair of such discontinuity. This case report deals with a patient of traumatic large wound at the heel who receives Unani management for wound healing. He was diagnosed as avulsion of pad of right heel with type-II diabetes mellitus. The treatment plan included mechanical debridement, cleaning with solution of alum powder (Sufuf-e-zaaj/alusol) and dressing with Marha

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24

Goufo, Piebiep, Rupesh Kumar Singh, and Isabel Cortez. "A Reference List of Phenolic Compounds (Including Stilbenes) in Grapevine (Vitis vinifera L.) Roots, Woods, Canes, Stems, and Leaves." Antioxidants 9, no. 5 (2020): 398. http://dx.doi.org/10.3390/antiox9050398.

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Due to their biological activities, both in plants and in humans, there is a great interest in finding natural sources of phenolic compounds or ways to artificially manipulate their levels. During the last decade, a significant amount of these compounds has been reported in the vegetative organs of the vine plant. In the roots, woods, canes, stems, and leaves, at least 183 phenolic compounds have been identified, including 78 stilbenes (23 monomers, 30 dimers, 8 trimers, 16 tetramers, and 1 hexamer), 15 hydroxycinnamic acids, 9 hydroxybenzoic acids, 17 flavan-3-ols (of which 9 are proanthocyan

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25

Empl, M. T., S. Macke, P. Winterhalter, et al. "The growth of the canine glioblastoma cell line D-GBM and the canine histiocytic sarcoma cell line DH82 is inhibited by the resveratrol oligomers hopeaphenol and r2-viniferin." Veterinary and Comparative Oncology 12, no. 2 (2012): 149–59. http://dx.doi.org/10.1111/j.1476-5829.2012.00349.x.

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26

Sasikumar, P., B. Prabha, T. R. Reshmitha, et al. "Comparison of antidiabetic potential of (+) and (−)-hopeaphenol, a pair of enantiomers isolated from Ampelocissus indica (L.) and Vateria indica Linn., with respect to inhibition of digestive enzymes and induction of glucose uptake in L6 myotubes." RSC Advances 6, no. 80 (2016): 77075–82. http://dx.doi.org/10.1039/c6ra14334b.

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The remarkable α-glucosidase inhibition exhibited by the acetone extract of the rhizome of Ampelocissus indica (L.) and stem bark of Vateria indica Linn. (IC<sub>50</sub> 23.2 and 1.47 μg mL<sup>−1</sup>) encouraged us to isolate the phytochemicals from these plants.

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27

Kang, Ji Eun, Sungmin Hwang, Nayeon Yoo, Beom Seok Kim, and Eui-Hwan Chung. "A resveratrol oligomer, hopeaphenol suppresses virulence activity of Pectobacterium atrosepticum via the modulation of the master regulator, FlhDC." Frontiers in Microbiology 13 (October 28, 2022). http://dx.doi.org/10.3389/fmicb.2022.999522.

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Pectobacterium atrosepticum (P. atrosepticum: Pba) which causes potato soft rot and blackleg is a notorious plant pathogen worldwide. Discovery of new types of antimicrobial chemicals that target specifically to virulence factors such as bacterial motility and extracellular enzymes is required for protecting crops from pathogenic infection. A transcriptomic analysis of Pba upon hopeaphenol treatment revealed that bacterial motility-related gene expression, including a master regulator flhDC genes, was significantly influenced by hopeaphenol. We further generated a double knock-out mutant of fl

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28

Tietjen, Ian, Joel Cassel, Emery T. Register, et al. "The natural stilbenoid (–)-hopeaphenol inhibits cellular entry of SARS-CoV-2 USA-WA1/2020, B.1.1.7 and B.1.351 variants." Antimicrobial Agents and Chemotherapy, September 20, 2021. http://dx.doi.org/10.1128/aac.00772-21.

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Antivirals are urgently needed to combat the global SARS-CoV-2/COVID-19 pandemic, supplement existing vaccine efforts, and target emerging SARS-CoV-2 variants of concern. Small molecules that interfere with binding of the viral spike receptor binding domain (RBD) to the host ACE2 receptor may be effective inhibitors of SARS-CoV-2 cell entry. Here we screened 512 pure compounds derived from natural products using a high-throughput RBD/ACE2 binding assay and identified (–)-hopeaphenol, a resveratrol tetramer, in addition to vatalbinoside A and vaticanol B, as potent and selective inhibitors of R

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29

Sundin, Charlotta, Caroline E. Zetterström, Duc Duy Vo, Robert Brkljača, Sylvia Urban, and Mikael Elofsson. "Exploring resveratrol dimers as virulence blocking agents – Attenuation of type III secretion in Yersinia pseudotuberculosis and Pseudomonas aeruginosa." Scientific Reports 10, no. 1 (2020). http://dx.doi.org/10.1038/s41598-020-58872-0.

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AbstractBacterial infections continue to threaten humankind and the rapid spread of antibiotic resistant bacteria is alarming. Current antibiotics target essential bacterial processes and thereby apply a strong selective pressure on pathogenic and non-pathogenic bacteria alike. One alternative strategy is to block bacterial virulence systems that are essential for the ability to cause disease but not for general bacterial viability. We have previously show that the plant natural product (-)-hopeaphenol blocks the type III secretion system (T3SS) in the Gram-negative pathogens Yersinia pseudotu

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30

Tietjen, Ian, Cole Schonhofer, Amanda Sciorillo та ін. "The Natural Stilbenoid (–)-Hopeaphenol Inhibits HIV Transcription by Targeting Both PKC and NF-κB Signaling and Cyclin-Dependent Kinase 9". Antimicrobial Agents and Chemotherapy, 28 березня 2023. http://dx.doi.org/10.1128/aac.01600-22.

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Despite effective combination antiretroviral therapy (cART), people living with HIV (PLWH) continue to harbor replication-competent and transcriptionally active virus in infected cells, which in turn can lead to ongoing viral antigen production, chronic inflammation, and increased risk of age-related comorbidities. To identify new agents that may inhibit postintegration HIV beyond cART, we screened a library of 512 pure compounds derived from natural products and identified (–)-hopeaphenol as an inhibitor of HIV postintegration transcription at low to submicromolar concentrations without cytot

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31

Ramli, Rohaity, Nor Hadiani Ismail, and Nurhuda Manshoor. "IDENTIFICATION OF OLIGOSTILBENES FROM Dipterocarpus semivestitus THROUGH DEREPLICATION TECHNIQUE." Jurnal Teknologi 77, no. 2 (2015). http://dx.doi.org/10.11113/jt.v77.5992.

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Three oligostilbenes have been identified in stems extract of Dipterocarpus semivestitus through dereplication strategy. The stems extract was injected to liquid chromatography tandem mass spectroscopy. Two tetramer, hopeaphenol and hemsleyanol D, were identified by comparing their mass fragmentation patterns with in-house library. A trimer, a-viniferin was isolated by various separation techniques and its structure was confirmed by NMR analyses and comparison with published data.

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32

Decendit, Alain. "Identification and quantification of stilbenes in some Tunisian red wines using UPLC-MS and HPLC-DAD." OENO One 51, no. 2 (2017). http://dx.doi.org/10.20870/oeno-one.2017.51.2.1673.

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<p>Seven Tunisian red wines mainly from the Mornag appellation were analyzed for resveratrol and analogues. The wines of each variety were evaporated, concentrated, and then subjected to fractionation and purification using XAD16 and DOWEX column chromatography. In addition to resveratrol, seven stilbenes were identified by UPLC-MS. The stilbenes derived were shown to be piceatannol, piceid, <strong> </strong>α-viniferin, e-viniferin, hopeaphenol and isohopeaphenol. From the point of view of the presence of resveratrol derivatives, one wine, Sidi Zahia, was the richest qualit

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33

Atun, Sri. "TEST ACTIVITIES SOME COMPOUNDS OLIGORESVERATROL RESULT OF INSULATION OF SKIN HOPEA ODORATA PLANT AS PREVENT 2-DEOKSIRIBOSE DEGRADATION." Jurnal Penelitian Saintek 13, no. 1 (2010). http://dx.doi.org/10.21831/jps.v13i1.183.

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The objective of the study were measured inhibitory of 2-deoxyribose degradation activity of balanocarpol (1), ampelopsin H (2), hopheaphenol (3), and hemlesyanol C (4) which are resveratrol compounds from isolation of stem bark of Hopea odorata, and to study of different activity as 2-deoxyribose degradation activity from this compounds. Methods of this study to measured 2-deoxyribose degradation activity test with Fenton reaction method. Activity of 2-deoxyribose degradation activity calculated as percentage absorbansi decreased sample with bioactive compounds compared with a blank. As posit

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34

Wallis, Christopher M. "Microplate bioassay to examine the effects of grapevine-isolated stilbenoids on survival of root knot nematodes." BMC Research Notes 15, no. 1 (2022). http://dx.doi.org/10.1186/s13104-022-06106-z.

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Abstract Objectives Root knot nematodes can be major pests in vineyards and cause significant yield losses over time. Control involves the use of different resistant grapevine rootstocks, but it remains unclear the mechanisms that such rootstocks possess to limit root knot nematode infections. Defense-associated compounds called stilbenoids, a type of phenolic compound, are present in relatively substantial amounts in grapevine root tissues. Therefore, experiments were performed to assess how different stilbenoid compounds impact nematode survival in microplate assays. Data generated were part

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35

Xu, Liu, Zaiqiang Yu, Yoshinori Uekusa, et al. "Elucidation of the inhibitory effect of (+)-hopeaphenol on polyinosinic–polycytidylic acid-induced innate immunity activation in human cerebral microvascular endothelial cells." Journal of Pharmacological Sciences, May 2022. http://dx.doi.org/10.1016/j.jphs.2022.04.011.

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36

Huy, Nguyen Quang, and Phan Tuan Nghia. "Effects of hopeaphenol and malibatol a isolated from bark of Hopea odorata Roxb on membrane enzymes and glycolysis of Streptococcus mutans." TAP CHI SINH HOC 31, no. 3 (2014). http://dx.doi.org/10.15625/0866-7160/v31n3.5228.

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37

Xu, Liu, Zaiqiang Yu, Yoshinori Uekusa, et al. "Corrigendum to “Elucidation of the inhibitory effect of (+)-hopeaphenol on polyinosinicepolycytidylic acid-induced innate immunity activation in human cerebral microvascular endothelial cells” [Journal of Pharmacological Sciences 149 (2022) 147–157]." Journal of Pharmacological Sciences, September 2022. http://dx.doi.org/10.1016/j.jphs.2022.09.001.

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