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Journal of Asian Natural Products Research Volume 4, 2002 - Issue 3
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Original Articles

New thiophenes from Echinops grijisii

Yue Liu The State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100083, China
,
Min Ye The State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100083, China
,
Hong-Zhu Guo The State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100083, China
,
Yu-Ying Zhao The State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100083, China
&
De-An Guo The State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100083, China
Pages 175-178 | Published online: 09 Sep 2010

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Peng Zhang, Wen-Rong Jin, Qiang Shi, Hua He, Zhong-Jun Ma & Hai-Bin Qu. (2008) Two novel thiophenes from Echinops grijissi Hance. Journal of Asian Natural Products Research 10:10, pages 977-981.
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Ariaya hymete, Jens rohloff, Helge kjØsen & Tor-henning iversen. (2005) Acetylenic thiophenes from the roots of Echinops ellenbeckii from Ethiopia. Natural Product Research 19:8, pages 755-761.
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Articles from other publishers (22)

祥宇 孔. (2023) Application and Research Progress of Echinops latifolius Tausch in Mongolian Pharmacology in China. Advances in Clinical Medicine 13:02, pages 1589-1600.
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Amel Bouzabata, Paola Montoro, Katarzyna Angelika Gil, Sonia Piacente, Fadia S. Youssef, Nawal M. Al Musayeib, Geoffrey A. Cordell, Mohamed L. Ashour & Carlo Ignazio Giovanni Tuberoso. (2022) HR-LC-ESI-Orbitrap-MS-Based Metabolic Profiling Coupled with Chemometrics for the Discrimination of Different Echinops spinosus Organs and Evaluation of Their Antioxidant Activity. Antioxidants 11:3, pages 453.
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Mohamed A. Ismail, Mahmoud M. Shaban, Ehab Abdel-Latif, Fatma H. Abdelhamed, Mohamed A. Migahed, Mahmoud N. El-Haddad & Ashraf S. Abousalem. (2022) Novel cationic aryl bithiophene/terthiophene derivatives as corrosion inhibitors by chemical, electrochemical and surface investigations. Scientific Reports 12:1.
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Helen Bitew & Ariaya Hymete. (2019) The Genus Echinops: Phytochemistry and Biological Activities: A Review. Frontiers in Pharmacology 10.
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Nikolaos Tsafantakis, Konstantinos Zelianeos, Aikaterini Termentzi, Argyro Vontzalidou, Nektarios Aligiannis & Nikolas Fokialakis. (2019) Triterpenes from Echinops spinosissimus Turra subsp. spinosissimus. Phytochemistry Letters 30, pages 273-277.
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Liang-Bo Li, Guang-Da Xiao, Wei Xiang, Xing Yang, Ke-Xin Cao & Rong-Shao Huang. (2019) Novel Substituted Thiophenes and Sulf-Polyacetylene Ester from Echinops ritro L.. Molecules 24:4, pages 805.
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Abdelaziz S. Fouda, Mohamed A. Ismail, Aliaa M. Temraz & Ashraf S. Abousalem. (2019) Comprehensive investigations on the action of cationic terthiophene and bithiophene as corrosion inhibitors: experimental and theoretical studies. New Journal of Chemistry 43:2, pages 768-789.
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Mei Zhao, Qi Liu, Qiyong Liu & Zhi Liu. (2017) Identification of Larvicidal Constituents of the Essential Oil of Echinops grijsii Roots against the Three Species of Mosquitoes. Molecules 22:2, pages 205.
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Sabrin R. M. Ibrahim, Hossam M. Abdallah, Ali M. El-Halawany & Gamal A. Mohamed. (2015) Naturally occurring thiophenes: isolation, purification, structural elucidation, and evaluation of bioactivities. Phytochemistry Reviews 15:2, pages 197-220.
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Roberto Negri. (2015) Polyacetylenes from terrestrial plants and fungi: Recent phytochemical and biological advances. Fitoterapia 106, pages 92-109.
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Fatma Belkessam, Aidene Mohand, Jean-François Soulé, Abdelhamid Elias & Henri Doucet. (2014) Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives. Beilstein Journal of Organic Chemistry 10, pages 2912-2919.
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Niko S. Radulović & Marija S. Denić. (2013) Essential Oils from the Roots of Echinops bannaticus Rochel ex Schrad . and Echinops sphaerocephalus L. (Asteraceae): Chemotaxonomic and Biosynthetic Aspects . Chemistry & Biodiversity 10:4, pages 658-676.
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Krishna C. Majumdar & Shovan Mondal. 2011. Heterocycles in Natural Product Synthesis. Heterocycles in Natural Product Synthesis 377 401 .
Eun-Jung Kim, Kwang-Ju Jung, In-Hye Lee, Bo-Ram Kim, Jeum-Jong Kim, Jong-Keun Park, Sang-Gyeong Lee & Yong-Jin Yoon. (2010) Rapid and Effective Multihalogenations of 2,2',5',2''-Terthiophene with 2-Halo-4,5-dichloropyridazin-3(2H)-ones under Ambient Conditions. Bulletin of the Korean Chemical Society 31:10, pages 2985-2988.
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Xue Qiao, Jian Han, Wen-ni He, Tao Wu, Bao-rong Wang, Min Ye & De-an Guo. (2010) Chemical fingerprint of commercial Radix Echinopsis and quantitative analysis of α-terthienyl . Journal of Separation Science 33:4-5, pages 530-538.
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Wenrong Jin, Qiang Shi, Chengtao Hong, Yiyu Cheng, Zhongjun Ma & Haibin Qu. (2008) Cytotoxic properties of thiophenes from Echinops grijissi Hance. Phytomedicine 15:9, pages 768-774.
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Manuel A.V. Ribeiro da Silva & Ana Filipa L.O.M. Santos. (2008) Experimental study on the thermochemistry of 2,5-dimethylthiophene and its acetyl derivative. The Journal of Chemical Thermodynamics 40:8, pages 1217-1221.
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Guodong Yin, Zihua Wang, Aihua Chen, Meng Gao, Anxin Wu & Yuanjiang Pan. (2008) A New Facile Approach to the Synthesis of 3-Methylthio-Substituted Furans, Pyrroles, Thiophenes, and Related Derivatives. The Journal of Organic Chemistry 73:9, pages 3377-3383.
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J. Schatz, T. Brendgen & D. Schühle. 2008. Comprehensive Heterocyclic Chemistry III. Comprehensive Heterocyclic Chemistry III 931 974 .
Hai‐Li Liu & Yue‐Wei Guo. (2008) Three New Thiophene Acetylenes from Rhaponticum uniflorum (L.) DC. . Helvetica Chimica Acta 91:1, pages 130-135.
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Ariaya Hymete, Jens Rohloff, Tor-Henning Iversen & Helge Kjøsen. (2007) Volatile constituents of the roots ofEchinops kebericho Mesfin. Flavour and Fragrance Journal 22:1, pages 35-38.
Crossref
A. Hymete, T.-H. Iversen, J. Rohloff & B. Erko. (2005) Screening of Echinops ellenbeckii and Echinops longisetus for biological activities and chemical constituents. Phytomedicine 12:9, pages 675-679.
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