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Journal articles on the topic 'Stilbenoidy'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Kambiranda, Devaiah, Sheikh Basha, Stephen Stringer, James Obuya, and Janana Snowden. "Multi-year Quantitative Evaluation of Stilbenoids Levels Among Selected Muscadine Grape Cultivars." Molecules 24, no. 5 (2019): 981. http://dx.doi.org/10.3390/molecules24050981.

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Stilbenoids such as t-piceid, t-resveratrol, ε-viniferins, and t-pterostilbene can differ significantly among grape cultivars and years due to variation in environmental conditions and subsequent stressors encountered during a year. This study evaluated diverse muscadine grape cultivars for their ability to consistently produce four major stilbenoids such as t-piceid, t-resveratrol, ε-viniferins, and t-pterostilbene irrespective of environmental changes that can impact their production. Berries from forty-two muscadine grape cultivars were collected for three years (2013, 2014, and 2015) to me

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2

Pawlus, Alison D., Pierre Waffo-Téguo, Jonah Shaver, and Jean-Michel Mérillon. "Stilbenoid chemistry from wine and the genus Vitis, a review." OENO One 46, no. 2 (2012): 57. http://dx.doi.org/10.20870/oeno-one.2012.46.2.1512.

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<p style="text-align: justify;">Stilbenoids are of great interest on account of their many promising biological activities, especially in regards to prevention and potential treatment of many chronic diseases associated with aging. The simple stilbenoid monomer, <em>E</em>-resveratrol, has received the most attention due to early<em> in vitro</em> and <em>in vivo</em> biological activities in anti-aging assays. Since <em>Vitis vinifera</em>, primarily in the form of wine, is a major dietary source of these compounds, there is a tremendous a

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3

Chai, Yuan-yuan, Fang Wang, Yan-li Li, Ke Liu, and Hui Xu. "Antioxidant Activities of Stilbenoids fromRheum emodiWall." Evidence-Based Complementary and Alternative Medicine 2012 (2012): 1–7. http://dx.doi.org/10.1155/2012/603678.

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Rheum emodiWall has been reported to possess protective effect in many inflammatory diseases and oxidative stress-related injuries. This study aims to investigate antioxidant power of stilbenoids fromR. emodiand then explore the material basis for its antioxidant potential. The most abundant stilbenoid piceatannol-4′-O-β-D-glucopyranoside (PICG) and its aglycon piceatannol (PICE) were isolated fromR. emodirhizome. Using well-accepted antioxidant chemicals as reference, antioxidant activity of these stilbenoids was examined by measuring DPPH and superoxide anion radical scavenging, ferric reduc

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4

Rathore, Rajendra, and Jay K. Kochi. "Vicinal-diaryl interactions in stilbenoid hydrocarbons as observed in the through-space charge delocalization of their cation radicals." Canadian Journal of Chemistry 77, no. 5-6 (1999): 913–21. http://dx.doi.org/10.1139/v99-081.

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The conformational preference of vicinal or 1,2-phenyl groups is probed in two classes of ring-substituted 1,2-diphenylbicyclooctene (stilbenoid) hydrocarbons 1a-1d and 2a-2c. UV-vis spectroscopy reveals, and X-ray crystallography verifies, the intramolecular (edge-to-face) orientation for the phenyl-phenyl interaction in stilbenoids 1a-1d. Most importantly, when two pairs of ortho-methyl substituents are present, the cofacial phenyl groups in the stilbenoid donors are established by X-ray crystallography and spectrally observed in the cation radicals (2a+.-2c+.) by the appearance of new bands

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5

Billet, Kévin, Magdalena Anna Malinowska, Thibaut Munsch, et al. "Semi-Targeted Metabolomics to Validate Biomarkers of Grape Downy Mildew Infection Under Field Conditions." Plants 9, no. 8 (2020): 1008. http://dx.doi.org/10.3390/plants9081008.

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Grape downy mildew is a devastating disease worldwide and new molecular phenotyping tools are required to detect metabolic changes associated to plant disease symptoms. In this purpose, we used UPLC-DAD-MS-based semi-targeted metabolomics to screen downy mildew symptomatic leaves that expressed oil spots (6 dpi, days post-infection) and necrotic lesions (15 dpi) under natural infections in the field. Leaf extract analyses enabled the identification of 47 metabolites belonging to the primary metabolism including 6 amino acids and 1 organic acid, as well as an important diversity of specialized

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6

Ball, Judith M., Fabricio Medina-Bolivar, Katelyn Defrates, et al. "Investigation of Stilbenoids as Potential Therapeutic Agents for Rotavirus Gastroenteritis." Advances in Virology 2015 (2015): 1–10. http://dx.doi.org/10.1155/2015/293524.

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Rotavirus (RV) infections cause severe diarrhea in infants and young children worldwide. Vaccines are available but cost prohibitive for many countries and only reduce severe symptoms. Vaccinated infants continue to shed infectious particles, and studies show decreased efficacy of the RV vaccines in tropical and subtropical countries where they are needed most. Continuing surveillance for new RV strains, assessment of vaccine efficacy, and development of cost effective antiviral drugs remain an important aspect of RV studies. This study was to determine the efficacy of antioxidant and anti-inf

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7

Mattio, Luce Micaela, Giorgia Catinella, Sabrina Dallavalle, and Andrea Pinto. "Stilbenoids: A Natural Arsenal against Bacterial Pathogens." Antibiotics 9, no. 6 (2020): 336. http://dx.doi.org/10.3390/antibiotics9060336.

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The escalating emergence of resistant bacterial strains is one of the most important threats to human health. With the increasing incidence of multi-drugs infections, there is an urgent need to restock our antibiotic arsenal. Natural products are an invaluable source of inspiration in drug design and development. One of the most widely distributed groups of natural products in the plant kingdom is represented by stilbenoids. Stilbenoids are synthesised by plants as means of protection against pathogens, whereby the potential antimicrobial activity of this class of natural compounds has attract

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8

Treml, Leláková, Šmejkal, et al. "Antioxidant Activity of Selected Stilbenoid Derivatives in a Cellular Model System." Biomolecules 9, no. 9 (2019): 468. http://dx.doi.org/10.3390/biom9090468.

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The stilbenoids, a group of naturally occurring phenolic compounds, are found in a variety of plants, including some berries that are used as food or for medicinal purposes. They are known to be beneficial for human health as anti-inflammatory, chemopreventive, and antioxidative agents. We have investigated a group of 19 stilbenoid substances in vitro using a cellular model of THP-1 macrophage-like cells and pyocyanin-induced oxidative stress to evaluate their antioxidant or pro-oxidant properties. Then we have determined any effects that they might have on the expression of the enzymes catala

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9

Laavola, Mirka, Tiina Leppänen, Mari Hämäläinen, et al. "IL-6 in Osteoarthritis: Effects of Pine Stilbenoids." Molecules 24, no. 1 (2018): 109. http://dx.doi.org/10.3390/molecules24010109.

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Interleukin-6 (IL-6) is involved in the pathogenesis of various inflammatory diseases, like rheumatoid arthritis (RA). In the present study, we investigated the role of IL-6 in osteoarthritis (OA) patients and the effects of the stilbenoids monomethyl pinosylvin and pinosylvin on the expression of the cartilage matrix components aggrecan and collagen II and the inflammatory cytokine IL-6 in human OA chondrocytes. Synovial fluid and plasma samples were obtained from 100 patients with severe OA [BMI 29.7 (8.3) kg/m2, age 72 (14) years, median (IQR); 62/38 females/males] undergoing total knee rep

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10

Kivimäki, Konsta, Tiina Leppänen, Mari Hämäläinen, Katriina Vuolteenaho, and Eeva Moilanen. "Pinosylvin Shifts Macrophage Polarization to Support Resolution of Inflammation." Molecules 26, no. 9 (2021): 2772. http://dx.doi.org/10.3390/molecules26092772.

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Pinosylvin is a natural stilbenoid found particularly in Scots pine. Stilbenoids are a group of phenolic compounds identified as protective agents against pathogens for many plants. Stilbenoids also possess health-promoting properties in humans; for instance, they are anti-inflammatory through their suppressing action on proinflammatory M1-type macrophage activation. Macrophages respond to environmental changes by polarizing towards proinflammatory M1 phenotype in infection and inflammatory diseases, or towards anti-inflammatory M2 phenotype, mediating resolution of inflammation and repair. In

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11

Yang, Tony, Cayla Boycott, Katarzyna Lubecka, and Barbara Stefanska. "BRUNOL5 as a Novel Oncogene Is Epigenetically Regulated by Stilbenoids in Primary Liver Cancer Cells." Current Developments in Nutrition 5, Supplement_2 (2021): 287. http://dx.doi.org/10.1093/cdn/nzab036_029.

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Abstract Objectives We previously discovered that a novel gene, BRUNOL5, is hypomethylated at the promoter region and upregulated in patients with primary liver cancer. Since DNA hypomethylation was shown to underlie up-regulation of genes with oncogenic functions, BRUNOL5 could potentially act as an oncogene. Interestingly, certain dietary compounds such as polyphenols with a stilbenoid ring have been demonstrated by us and others to suppress hypomethylated cancer-driving genes. In the present study, we investigate BRUNOL5 oncogenic functions and the role of two stilbenoids, resveratrol (RSV)

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12

Wen, Haichao, Zheng Fu, Yangji Wei, et al. "Antioxidant Activity and Neuroprotective Activity of Stilbenoids in Rat Primary Cortex Neurons via the PI3K/Akt Signalling Pathway." Molecules 23, no. 9 (2018): 2328. http://dx.doi.org/10.3390/molecules23092328.

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Antioxidant activity and neuroprotective activity of three stilbenoids, namely, trans-4-hydroxystilbene (THS), trans-3,5,4′-trihydroxy-stilbene (resveratrol, RES), and trans-3′,4′,3,5-tetrahydroxy-stilbene (piceatannol, PIC), against β-amyloid (Aβ)-induced neurotoxicity in rat primary cortex neurons were evaluated. THS, RES, and PIC significantly scavenged DPPH• and •OH radicals. All three stilbenoids were able to inhibit Aβ neurotoxicity by decreasing intracellular reactive oxygen species (ROS) via the PI3K/Akt signalling pathway. Specifically, stilbenoids significantly promoted Akt phosphory

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13

Jarosova, Veronika, Ondrej Vesely, Petr Marsik, et al. "Metabolism of Stilbenoids by Human Faecal Microbiota." Molecules 24, no. 6 (2019): 1155. http://dx.doi.org/10.3390/molecules24061155.

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Stilbenoids are dietary phenolics with notable biological effects on humans. Epidemiological, clinical, and nutritional studies from recent years have confirmed the significant biological effects of stilbenoids, such as oxidative stress protection and the prevention of degenerative diseases, including cancer, cardiovascular diseases, and neurodegenerative diseases. Stilbenoids are intensively metabolically transformed by colon microbiota, and their corresponding metabolites might show different or stronger biological activity than their parent molecules. The aim of the present study was to det

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14

Fang, Lingling, Tianhong Yang, and Fabricio Medina-Bolivar. "Production of Prenylated Stilbenoids in Hairy Root Cultures of Peanut (Arachis hypogaea) and Its Wild Relatives A. ipaensis and A. duranensis via an Optimized Elicitation Procedure." Molecules 25, no. 3 (2020): 509. http://dx.doi.org/10.3390/molecules25030509.

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Prenylated stilbenoids are phenolic compounds produced in a small number of plants such as peanut (Arachis hypogaea) to counteract biotic and abiotic stresses. In addition to their role in plant defense, they exhibit biological activities with potential application in human health. Whereas non-prenylated stilbenoids such as resveratrol are commercially available, the availability of prenylated stilbenoids is limited. To this end, hairy root cultures of peanut were developed as an elicitor-controlled bioproduction platform for prenylated stilbenoids. An orthogonal array design approach led to t

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15

Meier, Herbert, and Matthias Lehmann. "Stilbenoide Dendrimere." Angewandte Chemie 110, no. 5 (1998): 666–69. http://dx.doi.org/10.1002/(sici)1521-3757(19980302)110:5<666::aid-ange666>3.0.co;2-0.

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16

Meier, Herbert, and Matthias Lehmann. "Stilbenoid Dendrimers." Angewandte Chemie International Edition 37, no. 5 (1998): 643–45. http://dx.doi.org/10.1002/(sici)1521-3773(19980316)37:5<643::aid-anie643>3.0.co;2-4.

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17

Meier, Herbert, Matthias Lehmann, and Ute Kolb. "Stilbenoid Dendrimers." Chemistry - A European Journal 6, no. 13 (2000): 2462–69. http://dx.doi.org/10.1002/1521-3765(20000703)6:13<2462::aid-chem2462>3.0.co;2-a.

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18

Yang, Xin-Zhou, Chun-Ping Tang, and Yang Ye. "Stilbenoids fromStemona japonica." Journal of Asian Natural Products Research 8, no. 1-2 (2006): 47–53. http://dx.doi.org/10.1080/10286020500382678.

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19

Chichioco Hernandez, Christine L., Irene M. Villaseñor, Frank C. Schroeder, Henry Paulus, and Jon Clardy. "Stilbenoids fromHopea acuminata." Journal of Herbs, Spices & Medicinal Plants 22, no. 1 (2016): 92–104. http://dx.doi.org/10.1080/10496475.2015.1042618.

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20

Waterman, Peter G. "Biochemistry of Stilbenoids." Biochemical Systematics and Ecology 23, no. 5 (1995): 579. http://dx.doi.org/10.1016/0305-1978(95)90006-3.

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21

Packter, N. M. "Biochemistry of stilbenoids." Biochemical Education 23, no. 3 (1995): 179. http://dx.doi.org/10.1016/0307-4412(95)90235-x.

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22

Basri, Dayang Fredalina, Lee Wee Xian, Nur Indah Abdul Shukor, and Jalifah Latip. "Bacteriostatic Antimicrobial Combination: Antagonistic Interaction between Epsilon-Viniferin and Vancomycin against Methicillin-ResistantStaphylococcus aureus." BioMed Research International 2014 (2014): 1–8. http://dx.doi.org/10.1155/2014/461756.

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Stilbenoids have been considered as an alternative phytotherapeutic treatment against methicillin-resistantStaphylococcus aureus(MRSA) infection. The combined effect ofε-viniferin and johorenol A with the standard antibiotics, vancomycin and linezolid, was assessed against MRSA ATCC 33591 and HUKM clinical isolate. The minimum inhibitory concentration (MIC) value of the individual tested compounds and the fractional inhibitory concentration index (FICI) value of the combined agents were, respectively, determined using microbroth dilution test and microdilution checkerboard (MDC) method. Only s

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23

Vesely, Ondrej, Simona Baldovska, and Adriana Kolesarova. "Enhancing Bioavailability of Nutraceutically Used Resveratrol and Other Stilbenoids." Nutrients 13, no. 9 (2021): 3095. http://dx.doi.org/10.3390/nu13093095.

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Stilbenoids are interesting natural compounds with pleiotropic in vitro and in vivo activity. Their well-documented biological properties include anti-inflammatory effects, anticancer effects, effects on longevity, and many others. Therefore, they are nowadays commonly found in foods and dietary supplements, and used as a part of treatment strategy in various types of diseases. Bioactivity of stilbenoids strongly depends on different types of factors such as dosage, food composition, and synergistic effects with other plant secondary metabolites such as polyphenols or vitamins. In this review,

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24

Dávid, Csilla Zsuzsanna, Judit Hohmann, and Andrea Vasas. "Chemistry and Pharmacology of Cyperaceae Stilbenoids: A Review." Molecules 26, no. 9 (2021): 2794. http://dx.doi.org/10.3390/molecules26092794.

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Cyperaceae is a cosmopolitan plant family with approx. 5000 species distributed worldwide. Several members of this family are used in traditional medicines for the treatment of different diseases. In the last few decades, constituents with great chemical diversity were isolated from sedges, and a wide range of biological activities were detected either for crude extracts or for pure compounds. Among the isolated compounds, phenolic derivatives are the most important, especially stilbenoids, and flavonoids. To date, more than 60 stilbenoids were isolated from 28 Cyperaceae species. Pharmacologi

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25

Ewald, Philipp, Ulf Delker, and Peter Winterhalter. "Quantification of stilbenoids in grapevine canes and grape cluster stems with a focus on long-term storage effects on stilbenoid concentration in grapevine canes." Food Research International 100 (October 2017): 326–31. http://dx.doi.org/10.1016/j.foodres.2017.08.003.

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26

Rätsep, Reelika, Kadri Karp, Mariana Maante-Kuljus, Alar Aluvee, Hedi Kaldmäe, and Rajeev Bhat. "Recovery of Polyphenols from Vineyard Pruning Wastes—Shoots and Cane of Hybrid Grapevine (Vitis sp.) Cultivars." Antioxidants 10, no. 7 (2021): 1059. http://dx.doi.org/10.3390/antiox10071059.

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Grapevine shoots and canes represent a significant amount of biomass, considered as a waste in viticulture. In cooler climates, grapevines are pruned in the autumn (October) and spring (March) due to harsh winter conditions (e.g., snow, low temperatures), and large amounts of biomass are produced at these different pruning times. This work was undertaken in order to investigate the potential of vineyard pruning waste for recovery of polyphenolic compounds for biomass valorization. Qualitative and quantitative analyses of grapevine shoot and cane polyphenols, including flavonoids and stilbenoid

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27

Komaikul, Jukrapun, Supachoke Mangmool, Waraporn Putalun, and Tharita Kitisripanya. "Preparation of Readily-to-Use Stilbenoids Extract from Morus alba Callus Using a Natural Deep Eutectic Solvent." Cosmetics 8, no. 3 (2021): 91. http://dx.doi.org/10.3390/cosmetics8030091.

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The consumer and cosmetic industries have recently placed a greater emphasis on ecofriendly solvents for botanical extraction, including natural deep eutectic solvents (NADES). In this study, NADES were prepared for Morus alba callus extraction. The efficiency of extraction from the NADES and methanol was investigated by comparison of the stilbenoids yield and anti-melanogenesis activity. Prior to testing the irritability of a suitable NADES on the reconstructed human epidermis (RhE), the effect of the selected NADES on stilbenoids stability was determined. The results showed that the highest

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28

Akinwumi, Bolanle, Kimberly-Ann Bordun, and Hope Anderson. "Biological Activities of Stilbenoids." International Journal of Molecular Sciences 19, no. 3 (2018): 792. http://dx.doi.org/10.3390/ijms19030792.

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29

Zidorn, Christian, Sandra Grass, Ernst P. Ellmerer, Karl-Hans Ongania, and Hermann Stuppner. "Stilbenoids from Tragopogon orientalis." Phytochemistry 67, no. 19 (2006): 2182–88. http://dx.doi.org/10.1016/j.phytochem.2006.06.031.

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30

Baba, Kimiye, Tadashi Kido, Masahiko Taniguchi, and Mitsugi Kozawaqa. "Stilbenoids from Cassia garrettiana." Phytochemistry 36, no. 6 (1994): 1509–13. http://dx.doi.org/10.1016/s0031-9422(00)89752-6.

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31

Yang, X. Z., C. P. Tang, C. Q. Ke, and Y. Ye. "Stilbenoids from Stemona sessilifolia." Journal of Asian Natural Products Research 9, no. 3 (2007): 261–66. http://dx.doi.org/10.1080/10286020600604310.

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32

Zhang, Ya-Zhong, Guo-Bing Xu, and Tong Zhang. "Antifungal stilbenoids fromStemona japonica." Journal of Asian Natural Products Research 10, no. 7 (2008): 634–39. http://dx.doi.org/10.1080/10286020802133555.

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33

Pacher, T., C. Seger, D. Engelmeier, S. Vajrodaya, O. Hofer, and H. Greger. "Antifungal Stilbenoids fromStemona collinsae." Journal of Natural Products 65, no. 6 (2002): 820–27. http://dx.doi.org/10.1021/np0105073.

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34

Bai, Li, Tomoko Kato, Keiko Inoue, Masae Yamaki, and Shuzo Takagi. "Stilbenoids from Bletilla striata." Phytochemistry 33, no. 6 (1993): 1481–83. http://dx.doi.org/10.1016/0031-9422(93)85115-8.

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35

Bai, Li, Masae Yamaki, and Shuzo Takagi. "Stilbenoids from Pleione bulbocodioides." Phytochemistry 42, no. 3 (1996): 853–56. http://dx.doi.org/10.1016/0031-9422(95)00068-2.

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36

Kimura, Mutsumi, Hirotoshi Narikawa, Kazuchika Ohta, Kenji Hanabusa, Hirofusa Shirai, and Nagao Kobayashi. "Star-Shaped Stilbenoid Phthalocyanines." Chemistry of Materials 14, no. 6 (2002): 2711–17. http://dx.doi.org/10.1021/cm020222r.

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37

MEIER, H., and M. LEHMANN. "ChemInform Abstract: Stilbenoid Dendrimers." ChemInform 29, no. 26 (2010): no. http://dx.doi.org/10.1002/chin.199826122.

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38

Bai, Li, Noriko Masukawa, Masae Yamaki, and Shuzo Takagi. "Four stilbenoids from Pleione bulbocodioides." Phytochemistry 48, no. 2 (1998): 327–31. http://dx.doi.org/10.1016/s0031-9422(97)01110-2.

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39

Polunin, K. E., P. N. Kolotilov, V. M. Voitova, A. V. Larin, and I. A. Polunina. "Adsorption of stilbenoids on silica." Protection of Metals and Physical Chemistry of Surfaces 46, no. 1 (2010): 64–70. http://dx.doi.org/10.1134/s2070205110010090.

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40

Kang, Yun-Yao, Yan-Bei Tu, Chao Zhu, et al. "Two new stilbenoids fromBletilla striata." Journal of Asian Natural Products Research 21, no. 12 (2018): 1170–76. http://dx.doi.org/10.1080/10286020.2018.1526787.

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41

Liu, Xin-Qiao, Qiao-Yu Yuan, and Yuan-Qiang Guo. "Two new stilbenoids fromPleione bulbocodioides." Journal of Asian Natural Products Research 11, no. 2 (2009): 116–21. http://dx.doi.org/10.1080/10286020802573370.

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42

Hu, Hao-Bin, Hai-Peng Liang, Xu-Dong Zheng, Yun Wu, and Xiao-Wei Zhang. "Stilbenoids and Phenols inAcanthopanax brachypus." Helvetica Chimica Acta 98, no. 10 (2015): 1466–73. http://dx.doi.org/10.1002/hlca.201500227.

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43

Baba, Kimiye, Tadashi Kido, Kaoru Maeda, Masahiko Taniguchi, and Mitsugi Kozawa. "Two stilbenoids from Cassia garrettiana." Phytochemistry 31, no. 9 (1992): 3215–18. http://dx.doi.org/10.1016/0031-9422(92)83478-h.

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44

Tomás-Barberán, Francisco A. "The biochemistry of the stilbenoids." Phytochemistry 40, no. 3 (1995): 1007. http://dx.doi.org/10.1016/0031-9422(95)90181-7.

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45

Yamaki, Masae, and Chie Honda. "The stilbenoids from Dendrobium plicatile." Phytochemistry 43, no. 1 (1996): 207–8. http://dx.doi.org/10.1016/0031-9422(96)00270-1.

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46

Yamaki, Masae, Tomoko Kato, Li Bai, Keiko Inoue, and Shuzo Takagi. "Methylated stilbenoids from Bletilla striata." Phytochemistry 30, no. 8 (1991): 2759–60. http://dx.doi.org/10.1016/0031-9422(91)85139-q.

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47

Zhao, Ning-Dong, Guang-Yu Yang, Yan Zhang, Li-Jun Chen, and Ye-Gao Chen. "Stilbenoids from Bulbophyllum emarginatum (Orchidaceae)." Biochemical Systematics and Ecology 58 (February 2015): 285–87. http://dx.doi.org/10.1016/j.bse.2014.12.027.

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48

Yang, Xinzhou, Jing Yang, Chan Xu, Jingnan Lv, Chao Wang, and Ping Song. "Antimicrobial Stilbenoids from Bletilla yunnanensis." Chemistry of Natural Compounds 52, no. 1 (2016): 19–22. http://dx.doi.org/10.1007/s10600-016-1537-3.

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49

Estrada, S., J. J. López-Guerrero, R. Villalobos-Molina, and R. Mata. "Spasmolytic stilbenoids from Maxillaria densa." Fitoterapia 75, no. 7-8 (2004): 690–95. http://dx.doi.org/10.1016/j.fitote.2004.08.004.

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50

Meier, Herbert, Thorsten Lifka, and Annette Oehlhof. "Comparison of Alkoxy-substituted 4,4´-Distyrylbiphenyls and the Corresponding 4,4´-Distyrylbenzenes." Zeitschrift für Naturforschung B 63, no. 10 (2008): 1187–91. http://dx.doi.org/10.1515/znb-2008-1008.

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AbstractConfigurationally highly pure (E,E)-4,4´-bis(styryl)biphenyls 2a - e were obtained by Siegrist reactions of 4,4´-dimethylbiphenyl 3 and alkoxy-substituted benzaldimines (4a - e). DSC measurements have indicated different crystalline modifications of these conjugated compounds. The stilbenoid chromophores of 2a - e are compared to the stilbenoid chromophores in the OPV series, which have a similar length of conjugation. The intense fluorescence and the high transparency in the visible region are promising properties for an application of the donor-substituted compounds 2a - e in twophot

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