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Journal articles on the topic '-methoxycinnamate'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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1

Suzana, Suzana, Nunuk Irawati, and Tutuk Budiati. "Synthesis Octyl P-Methoxycinnamate as Sunblock by Transesterification Reaction with the Starting Material Ethyl P- Methoxycinnamate." Indonesian Journal of Cancer Chemoprevention 2, no. 2 (2011): 217. http://dx.doi.org/10.14499/indonesianjcanchemoprev2iss2pp217-221.

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Synthesis octyl p-methoxycinnamate substance as sunblock, has been done by transesterification reaction. The starting material of the reaction was ethyl p-methoxycinnamate isolated from Kaempferia galanga L.The transesterification reaction was carried out by reacting ethyl p-methoxycinnamate with octanol. The product was identified by UV-VIS,Infra Red and Mass Spectroscopy. The result of measurements on erythemic %T at various concentrations demonstrate that octyl p-methoxycinnamate is applicable as a sunblock compound.Keywords: octyl p-methoxycinnamate, transesterification, ethyl p-methoxycin

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2

&NA;. "Methoxycinnamate/oxybenzone." Reactions Weekly &NA;, no. 911 (2002): 12. http://dx.doi.org/10.2165/00128415-200209110-00038.

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3

Ekowati, Juni, Marcellino Rudyanto, Shigeru Sasaki, et al. "Structure Modification of Ethyl p-methoxycinnamate Isolated from Kaempferia galanga Linn. and Citotoxicity Assay of The Products on WiDr Cells." Indonesian Journal of Cancer Chemoprevention 1, no. 1 (2010): 12. http://dx.doi.org/10.14499/indonesianjcanchemoprev1iss1pp12-18.

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Ethyl p-methoxycinnamate, major ingredient of Kaempferia galanga rhizome, have been reported not only has analgesic – anti inflammatory activities like NSAIDs which inhibited cyclooxygenase, but also inhibit tumor cell proliferation in specimen of mouse epidermis. Therefore, it will be interesting to carry out synthetic studies on the derivates of ethyl p-methoxycinnamate and searching their citotoxic activity on WiDr cell. We wish to report of structure modification on carboxyl moiety of ethyl p-methoxycinnamate and evaluation on their citotoxic activity on WiDr cell. Isolation of ethyl p-met

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4

Gong, Sheng Zhao, Xiao Xi Tai, and Yun Er Yang. "Inhibitory Kinetics of Isooctyl 4-Hydroxy-3-Methoxycinnamate on Tyrosinase-Catalyzing Reaction." Advanced Materials Research 634-638 (January 2013): 655–58. http://dx.doi.org/10.4028/www.scientific.net/amr.634-638.655.

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The inhibitory kinetics of isooctyl 4-hydroxy-3-methoxycinnamate on the activity of monophenolase and diphenolase contained in tyrosinase was studied by enzymological kinetic method with Na2HPO4-NaH2PO4 buffer solution (pH=6.8) at 30 °C. Isooctyl 4-hydroxy-3-methoxycinnamate was found to inhibit the monophenolase and diphenolase activity of tyrosinase well. The isooctyl 4-hydroxy-3-methoxycinnamate concentrations leading to 50 % inhibitory rate (IC50) were 0.24 mmol/L for monophenolase and 0.45 mmol/L for diphenolase, much less than that of arbutin (IC50 =5.3 mmol/L for diphenolase activity).

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5

Ohba, Shigeru, and Yoshikatsu Ito. "Ammonium 4-methoxycinnamate." Acta Crystallographica Section C Crystal Structure Communications 60, no. 6 (2004): o393—o394. http://dx.doi.org/10.1107/s0108270104008261.

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6

Aulia, Pidia, Saprini Hamdiani, and Iwan Sumarlan. "Synthesis of Rice Husk Mesoporous Silica as pH Responsive Release Material." Acta Chimica Asiana 2, no. 2 (2019): 103. http://dx.doi.org/10.29303/aca.v2i2.21.

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The synthesis of mesoporous silica as a delivery agent for the ethyl para-methoxycinnamate has been carried out. The study aims to determine the process of mesoporous silica synthesis from sodium silicate from the smelting of rice husk ash, determine the adsorption capacity of mesoporous silica in the ethyl para-methoxycinnamate and the pH responsive release of ethyl para-methoxycinnamate with mesoporous silica as a delivery agent in simulated intestinal and gastric fluids. It was found that mesoporous silica can be synthesized from rice husk ash with a 30% tartaric acid template. Characteriza

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7

Pattanaargson, Supason, Thitinun Munhapol, Piyawan Hirunsupachot, and Pamornwan Luangthongaram. "Photoisomerization of octyl methoxycinnamate." Journal of Photochemistry and Photobiology A: Chemistry 161, no. 2-3 (2004): 269–74. http://dx.doi.org/10.1016/s1010-6030(03)00282-x.

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8

Sugihartini, Nining. "Curcumin and Extract of Plantago major, L Increased SPF Value of Cold Cream Base." Indonesian Journal of Cancer Chemoprevention 1, no. 1 (2010): 43. http://dx.doi.org/10.14499/indonesianjcanchemoprev1iss1pp43-47.

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Octyl methoxycinnamate as the active material of the sunscreen would be degradated after being exposed to the sunlight. Curcumin, rice flour and the extract of Plantago major, L was the material that could function as the sunscreen. The aim of this research was to know the SPF value and the physical characteristics of cream of the sunscreen with the active material octyl methoxycinnamate after the addition of the optimum composition of curcumin and the extract of Plantago major, L and the optimum composition of rice flour and the extract of Plantago major, L.In this research three formulas was

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9

Arianto, Anayanti, Gra Cella, and Hakim Bangun. "Preparation and Evaluation of Sunscreen Nanoemulsions with Synergistic Efficacy on SPF by Combination of Soybean Oil, Avobenzone, and Octyl Methoxycinnamate." Open Access Macedonian Journal of Medical Sciences 7, no. 17 (2019): 2751–56. http://dx.doi.org/10.3889/oamjms.2019.745.

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BACKGROUND: Soybean oil contains vitamin E and acts as a natural sunscreen which can absorb Ultra Violet (UV) B light and has antioxidant properties to reduce the photooxidative damage that results from UV-induced Reactive Oxygen Species production. The UV blocking from most natural oils is insufficient to obtain a high UV protection. The strategies for preparations of sunscreen products with high SPF can be done by nanoemulsion formulation and Ultra Violet filter combinations of Soybean Oil, Avobenzone and Octyl methoxycinnamate. AIM: The purpose of this study was to prepare and in vitr

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10

Umar, Muhammad Ihtisham, Muhammad Adnan Iqbal, Mohamed B. Khadeer Ahamed, et al. "Cytotoxic and Pro-Apoptotic Properties of Ethyl-p-Methoxycinnamate and Its Hydrophilic Derivative Potassium-p-Methoxycinnamate." Chemistry Africa 1, no. 1-2 (2018): 87–95. http://dx.doi.org/10.1007/s42250-018-0010-z.

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11

Hanson, Kerry M., Swathi Narayanan, Valerie M. Nichols, and Christopher J. Bardeen. "Photochemical degradation of the UV filter octyl methoxycinnamate in solution and in aggregates." Photochemical & Photobiological Sciences 14, no. 9 (2015): 1607–16. http://dx.doi.org/10.1039/c5pp00074b.

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12

Fareza, Muhamad Salman, Rehana Rehana, Nuryanti Nuryanti, and Didin Mujahidin. "TRANSFORMATION OF ETHYL-P-METHOXYCINNAMATE TO P –METHOXYCINNAMIC ACID FROM KENCUR (Kaempheria galanga L.) AND THEIR ANTIBACTERIAL ACTIVITY." ALCHEMY Jurnal Penelitian Kimia 13, no. 2 (2017): 176. http://dx.doi.org/10.20961/alchemy.13.2.8472.176-190.

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This study aimed to evaluate the antibacterial properties of ethyl-<em>p</em>-methoxycinnamate and <em>p</em>-methoxycinnamate acid from Kaempheria galanga L. Ethyl-<em>p</em>-methoxycinnamate was isolated from the <em>n</em>-hexane rhizome extract of <em>Kaempheria galanga L</em>. Separation and purification of this compound was carried out with vacuum liquid chromatography and column chromatography. Hydrolysis of ethyl-<em>p</em>-methoxycinnamic under alkaline conditions obtained <em>p</em>-methoxycinnamic ac

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13

Kudlek, Edyta. "Toxicological analysis of water mixtures of organic micropollutants subjected to UV irradiation." E3S Web of Conferences 44 (2018): 00084. http://dx.doi.org/10.1051/e3sconf/20184400084.

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The paper presents the toxicological analysis of water solutions of micropollutants from different groups i.e. industrial additives, pharmaceutical compounds, hormones, UV blockers and pesticides before and after their exposure to UV light. The toxicological response of both Microtox® and Daphtoxkit F® test, increased with the increase of the compound concentration. Triclosan water solution was considered as the most toxic. The lowest toxic effect was observed for Imidacloprid and Octyl-methoxycinnamate solutions. The exposure of Benzocaine, Octyl-methoxycinnamate and Triclosan water solutions

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14

Stein, Hannah V., Courtney J. Berg, Jessica N. Maung, et al. "Photolysis and cellular toxicities of the organic ultraviolet filter chemical octyl methoxycinnamate and its photoproducts." Environmental Science: Processes & Impacts 19, no. 6 (2017): 851–60. http://dx.doi.org/10.1039/c7em00059f.

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15

Herzog, Bernd, Jochen Giesinger, and Volker Settels. "Insights into the stabilization of photolabile UV-absorbers in sunscreens." Photochemical & Photobiological Sciences 19, no. 12 (2020): 1636–49. http://dx.doi.org/10.1039/d0pp00335b.

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Butyl methoxy dibenzoylmethane and ethylhexyl methoxycinnamate as photolabile UV-filter molecules can be stabilized in the presence of photostable UV-absorbers by quenching effects and by spectral stabilization.

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16

Hanson, Kerry M., Swathi Narayanan, Valerie M. Nichols, and Christopher J. Bardeen. "Correction: Photochemical degradation of the UV filter octyl methoxycinnamate in solution and in aggregates." Photochemical & Photobiological Sciences 15, no. 9 (2016): 1212. http://dx.doi.org/10.1039/c6pp90025a.

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17

Herzog, Bernd, Lola Amorós-Galicia, Myriam Sohn, Melanie Hofer, Katja Quass, and Jochen Giesinger. "Analysis of photokinetics of 2′-ethylhexyl-4-methoxycinnamate in sunscreens." Photochemical & Photobiological Sciences 18, no. 7 (2019): 1773–81. http://dx.doi.org/10.1039/c9pp00084d.

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18

Choi, In-Ho, Ju-Yong Park, Sang-Chul Shin, and Il-Kwon Park. "Nematicidal activity of medicinal plant extracts and two cinnamates isolated from Kaempferia galanga L. (Proh Hom) against the pine wood nematode, Bursaphelenchus xylophilus." Nematology 8, no. 3 (2006): 359–65. http://dx.doi.org/10.1163/156854106778493402.

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Abstract Extracts from 40 medicinal plant species in 27 families were tested for their nematicidal activity against the pine wood nematode, Bursaphelenchus xylophilus, in 96-well plate bioassays. Responses varied with plant material and concentration. Extracts of Acorus gramineus (Araceae), Asiasarum sieboldi (Aristolochiaceae), Illicium verum (Illicaiceae) and Kaempferia galanga (Zingiberaceae) showed nematicidal activity against male, female and juvenile nematodes of B. xylophilus at 2000 μg ml−1. Among test plant species, Kaempferia galanga showed the most potent nematicidal activity. As K.

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19

Silva do Nascimento, Danielle, Verónica Volpe, Matías Insausti, and Marcos Grünhut. "On line kinetic analysis of permeation profiles for UV filter loaded microemulsions using an automatic system with spectroscopic detection and a chemometric approach." RSC Advances 11, no. 26 (2021): 15528–38. http://dx.doi.org/10.1039/d1ra01067k.

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On-line and green automatic methods with spectrophotometric detection were developed to the obtention of permeation kinetic constants of octyl p-methoxycinnamate in o/w microemulsions. The effect of interferences was overcome using chemometric tools.

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20

Singh, Pahup, Durga K. Mewara, and Mahesh C. Sharma. "A New Ferulic Ester and Related Compounds from Bombax Malabaricum DC." Natural Product Communications 3, no. 2 (2008): 1934578X0800300. http://dx.doi.org/10.1177/1934578x0800300223.

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A new ferulic ester, trans-triacontyl-4-acetoxy-3-methoxycinnamate (2), was isolated, along with related known ferulates and triterpenes, from the spines of stem bark of Bombax malabaricum DC. The structures were elucidated from chemical and spectroscopic data.

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21

Gogna, Deepak, Sunil Jain, Awesh Yadav, and G. Agrawal. "Microsphere Based Improved Sunscreen Formulation of Ethylhexyl Methoxycinnamate." Current Drug Delivery 4, no. 2 (2007): 153–59. http://dx.doi.org/10.2174/156720107780362285.

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22

Murphy, G. M., and I. R. White. "Photoallergic contact dermatitis to 2-ethoxyethyl-p-methoxycinnamate." Contact Dermatitis 16, no. 5 (1987): 296. http://dx.doi.org/10.1111/j.1600-0536.1987.tb01470.x.

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23

Alves, Leonardo F., Ricardo Gargano, Silvia K. B. Alcanfor, Luiz A. S. Romeiro, and João B. L. Martins. "A chromophoric study of 2-ethylhexyl p-methoxycinnamate." Chemical Physics Letters 516, no. 4-6 (2011): 162–65. http://dx.doi.org/10.1016/j.cplett.2011.09.078.

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24

Hasegawa, Toshio, Momohiro Hashimoto, Takashi Fujihara, and Hideo Yamada. "Aroma Profile of Galangal Composed of Cinnamic Acid Derivatives and Their Structure-Odor Relationships." Natural Product Communications 11, no. 10 (2016): 1934578X1601101. http://dx.doi.org/10.1177/1934578x1601101012.

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Cinnamic acid derivatives are important odorants due to their characteristic scent. Some fragrance materials, such as cinnamon bark, matsutake mushrooms, and Kaempferia galanga L. rhizome (galangal), contain several cinnamic acid derivatives as important odor constituents. The main odor constituent of galangal is ( E)-ethyl 4-methoxycinnamate, but the odor of this compound is different from that of galangal. We investigated the aroma profile of galangal using our previously described method that considers the intermolecular interactions of the odorant compounds with their receptors. Odorant co

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25

Pattanaargson, Supason, Nantawan Hongchinnagorn, Piyawan Hirunsupachot, and Yongsak Sritana-anant. "UV Absorption and Photoisomerization of p-Methoxycinnamate Grafted Silicone¶." Photochemistry and Photobiology 80, no. 2 (2004): 322. http://dx.doi.org/10.1562/2003-11-14-ra-007.1.

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26

Kim, Min-Hwa, Seong-Gwang Lim, Min-Kook Kim, Hyo-Sun Suh, Seol-Hwa Baek, and Byung-Mu Lee. "Risk assessment of isoamyl p-Methoxycinnamate in cosmetic products." Toxicology Letters 280 (October 2017): S104. http://dx.doi.org/10.1016/j.toxlet.2017.07.288.

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27

Luger, P., M. Weber, N. X. Dung, and N. T. B. Tuyet. "Ethyl p-Methoxycinnamate from Kaempferia galanga L. in Vietnam." Acta Crystallographica Section C Crystal Structure Communications 52, no. 5 (1996): 1255–57. http://dx.doi.org/10.1107/s0108270195016027.

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28

He, Zhi-Heng, Grace Gar-Lee Yue, Clara Bik-San Lau, Wei Ge, and Paul Pui-Hay But. "Antiangiogenic Effects and Mechanisms oftrans-Ethylp-Methoxycinnamate fromKaempferia galangaL." Journal of Agricultural and Food Chemistry 60, no. 45 (2012): 11309–17. http://dx.doi.org/10.1021/jf304169j.

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29

Pattanaargson, Supason, Nantawan Hongchinnagorn, Piyawan Hirunsupachot, and Yongsak Sritana-anant. "UV Absorption and Photoisomerixation of p-Methoxycinnamate Grafted Silicone¶." Photochemistry and Photobiology 80, no. 2 (2007): 322–25. http://dx.doi.org/10.1111/j.1751-1097.2004.tb00090.x.

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30

Fois, Ettore, Mario Oriani, and Gloria Tabacchi. "A post-HF approach to the sunscreen octyl methoxycinnamate." Journal of Chemical Physics 154, no. 14 (2021): 144304. http://dx.doi.org/10.1063/5.0046118.

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31

Ekowati, Juni, Suko Hardjono, and Iwan Sahrial Hamid. "Ethyl p-methoxycinnamate from Kaempferia galanga inhibits angiogenesis through tyrosine kinase." Universa Medicina 34, no. 1 (2016): 43. http://dx.doi.org/10.18051/univmed.2015.v34.43-51.

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BACKGROUND<br />Many tumors express on their receptor tyrosine kinases vascular endothelial<br />growth factor activity associated with angiogenesis. Inhibition of<br />angiogenesis through reduction of tyrosine kinase activity is a promising<br />strategy for cancer therapy. The present study aimed to determine the<br />mechanism and potency of ethyl p-methoxycinnamate (EPMC) isolated<br />from Kaempferia galanga as angiogenesis inhibitor.<br />METHODS<br />A laboratory experimental study was conducted using chorio-allantoic<br />membranes

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32

MacManus-Spencer, Laura A., Monica L. Tse, Jacob L. Klein, and Alison E. Kracunas. "Aqueous Photolysis of the Organic Ultraviolet Filter Chemical Octyl Methoxycinnamate." Environmental Science & Technology 45, no. 9 (2011): 3931–37. http://dx.doi.org/10.1021/es103682a.

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33

Chimichi, Stefano, Piero Sarti-Fantoni, Giacomo Coppini, Franca Perghem, and Giovanni Renzi. "Solid-state photoreactivity of ethyl (E)-.alpha.-cyano-2-methoxycinnamate." Journal of Organic Chemistry 52, no. 23 (1987): 5124–26. http://dx.doi.org/10.1021/jo00232a013.

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34

Omar, Muhammad, Nor Hasali, and Mohd Yarmo. "Cytotoxicity Activity of Biotransformed Ethyl p-methoxycinnamate by Aspergillus niger." Oriental Journal of Chemistry 32, no. 5 (2016): 2731–34. http://dx.doi.org/10.13005/ojc/320547.

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35

Necasova, Anezka, and Pavel Cupr. "Genotoxicity evaluation of UV sunscreen Ethylhexyl methoxycinnamate and its photoproducts." ISEE Conference Abstracts 2013, no. 1 (2013): 5158. http://dx.doi.org/10.1289/isee.2013.p-2-26-12.

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36

Jiménez, M. M., J. Pelletier, M. F. Bobin, M. C. Martini, and H. Fessi. "Poly‐Epsilon‐Caprolactone Nanocapsules Containing Octyl Methoxycinnamate: Preparation and Characterization." Pharmaceutical Development and Technology 9, no. 3 (2004): 329–39. http://dx.doi.org/10.1081/pdt-200031456.

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37

Ko, Hyun-Ju, Hae Jong Kim, Su Yeon Kim, et al. "Hypopigmentary Effects of Ethyl P -Methoxycinnamate Isolated from Kaempferia galanga." Phytotherapy Research 28, no. 2 (2013): 274–79. http://dx.doi.org/10.1002/ptr.4995.

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38

Kikuchi, Azusa, Shinsuke Yukimaru, Nozomi Oguchi, Kazuyuki Miyazawa, and Mikio Yagi. "Excited Triplet State of a UV-B Absorber, Octyl Methoxycinnamate." Chemistry Letters 39, no. 6 (2010): 633–35. http://dx.doi.org/10.1246/cl.2010.633.

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39

Noomane, Ayed, Souhaira Hbaieb, Marie-Alexandrine Bolzinger, Stéphanie Briançon, Yves Chevalier, and Rafik Kalfat. "Effectiveness of grafting modes of methoxycinnamate sunscreen onto silica particles." Colloids and Surfaces A: Physicochemical and Engineering Aspects 441 (January 2014): 653–63. http://dx.doi.org/10.1016/j.colsurfa.2013.10.029.

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40

Khalfaoui, Ouafa, Adel Beghidja, Jérôme Long, Chahrazed Beghidja, Yannick Guari, and Joulia Larionova. "Field-Induced Slow Relaxation in a Dinuclear Dysprosium(III) Complex Based on 3-Methoxycinnamic Acid." Inorganics 6, no. 1 (2018): 35. http://dx.doi.org/10.3390/inorganics6010035.

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We report the synthesis, structure, and magnetic properties of a new dinuclear dysprosium(III) complex based on a 3-methoxycinnamate ligand. The centrosymmetric complex exhibits a field-induced SMM behavior. In contrast to the previously reported lanthanide-based systems with cinnamate derivatives that relax through a combination of Raman and direct processes, an Orbach process is also involved in highlighting the role of the structural organization over the spin-lattice relaxations.

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41

Wang, Tao, Osamu Shirota, Koji Nakanishi, et al. "Absolute stereochemistry of the spiroxins." Canadian Journal of Chemistry 79, no. 11 (2001): 1786–91. http://dx.doi.org/10.1139/v01-153.

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The absolute configuration of spiroxin A has been determined by exciton-coupled circular dichroism (CD). Namely, the difference CD between spiroxin A bis-methoxycinnamate, as well as that between spiroxin A bis-retinoate, both exhibit negative exciton couplings between the acylated phenolic hydroxyl group chromophores. This establishes the absolute configuration as 2S,3R,4S,2'S,3'R,4'S.Key words: circular dichroism, exciton coupling, spiroxins, antitumor, antifungal.

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42

., Nurmeilis, Azrifitria ., Nita Fitriani, and Ismiarni Komala. "SEDATIVE-HYPNOTICACTIVITYOF ETHYL- P-METHOXYCINNAMATE AND N-(2-HYDROXYETHYL)-P-METHOXYCINNAMAMIDE." International Research Journal Of Pharmacy 9, no. 10 (2018): 43–46. http://dx.doi.org/10.7897/2230-8407.0910223.

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43

Pattanaargson, S., and P. Limphong. "Stability of octyl methoxycinnamate and identification of its photo-degradation product." International Journal of Cosmetic Science 23, no. 3 (2001): 153–60. http://dx.doi.org/10.1046/j.1467-2494.2001.00071.x.

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44

Yang, Jiang, Huafang Yang, Guo Rong, Ann L. Harder, and Stig E. Friberg. "Phase Behavior of Ethylhexyl P-Methoxycinnamate, Nonylphenol Ethoxylates-8 and Water." Journal of Dispersion Science and Technology 18, no. 4 (1997): 407–21. http://dx.doi.org/10.1080/01932699708943744.

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45

Harry-O’kuru, Rogers E. "4-hydroxy-3-methoxycinnamate esters of milkweed oil: Synthesis and characterization." Lipids 40, no. 11 (2005): 1179–83. http://dx.doi.org/10.1007/s11745-005-1483-0.

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46

Kapingu, Modest C., Joseph J. Magadula, Zakaria H. Mbwambo, and Dulcie A. Mulholland. "Puguflavanones A and B; Prenylated Flavanones from Baphia Puguensis." Natural Product Communications 3, no. 5 (2008): 1934578X0800300. http://dx.doi.org/10.1177/1934578x0800300514.

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Two new flavanones, puguflavanone A [5,4′-dihydroxy-6-(1″,1″-dimethylprop-2-enyl)-2″’,2″'-dimethylpyrano-(5″’,6″’:7,8)flavanone] (1) and puguflavanone B [5,7,4′-trihydroxy-6-(1″,1″-dimethylprop-2-enyl)-8-(3-methylbut-2-enyl)flavanone] (2) were isolated from the ethyl acetate extract of the root bark of Baphia puguensis, together with four known compounds, erythrisenegalone (3), 3-methoxy-8,9-methylenedioxypterocarpene, alkyl trans-4-hydroxy-3-methoxycinnamate, and stigmasterol. Structures were established using NMR and MS techniques.

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47

Komala, Ismiarni, Supandia, Nurhasnib та ін. "Microwave Assisted Synthesis of p-Methoxycinnamamides and p-Methoxy-β-nitrostyrenes from Ethyl p-methoxycinnamate and Screening their Anti-inflammatory Activity". Natural Product Communications 12, № 8 (2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200830.

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A new modification reaction of ethyl p-methoxycinnamate (1) to afford a series of p-methoxycinnamamide and p-methoxy-β-nitrostyrene has been developed by using the assistance of the unmodified microwave oven. The synthesized compounds were characterized by using various spectroscopic techniques and furthermore screened for their anti-inflammatory activity by using anti-denaturation of heat bovine serum albumin (BSA) method. The result of bioassay indicated that p-methoxycinnamamide derivatives and p-methoxy-β-nitrostyrenes showed interesting anti-inflammatory activity.

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48

Wang, Chang Qing, Su Juan Pan, Xin You Lei, and Guo Fang Zuo. "Chemical Compositions of the Flower Essential Oils of Elaeagnuslanceolata Warb. apud Diels." Advanced Materials Research 524-527 (May 2012): 2246–49. http://dx.doi.org/10.4028/www.scientific.net/amr.524-527.2246.

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The flower essential oil in Elaeagnus lanceolata Warb. apud Diels flowers is extracted by water-steaming method. The extraction rate is 0.53%. The chemical compositions of the essential oil have been identified with the optimum separating and analyzing conditions by means of the GC-MS. The result shows 31 compounds are separated. The represention rate of total essential oil is 83.9％. The major chemical compositions of essential oil in Elaeagnus lanceolata Warb. apud Diels are octyl 4-methoxycinnamate，pelargonic acid , linoleic acid , palmitic acid , Germacrene D，hydrocarbon etc.

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Klammer, Holger, Christiane Schlecht, Wolfgang Wuttke, and Hubertus Jarry. "Multi-organic risk assessment of estrogenic properties of octyl-methoxycinnamate in vivo." Toxicology 215, no. 1-2 (2005): 90–96. http://dx.doi.org/10.1016/j.tox.2005.06.026.

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Bányiová, K., A. Sharma, and P. Čupr. "The impact of isomerization on overall human dermal exposure to ethylhexyl methoxycinnamate." Toxicology Letters 258 (September 2016): S209. http://dx.doi.org/10.1016/j.toxlet.2016.06.1759.

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