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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Nine 2‐(2‐Phenylethyl)chromone Derivatives from the Resinous Wood of Aquilaria sinensis and Their Inhibition of LPS‐Induced NO Production in RAW 264.7 Cells
Dong Chen, Zhengren Xu, Xingyun Chai, et al.
European Journal of Organic Chemistry (2012) Vol. 2012, Iss. 27, pp. 5389-5397
Closed Access | Times Cited: 92

Showing 1-25 of 92 citing articles:

Chromone: A Valid Scaffold in Medicinal Chemistry
Alexandra Gaspar, María João Matos, Jorge Garrido, et al.
Chemical Reviews (2014) Vol. 114, Iss. 9, pp. 4960-4992
Closed Access | Times Cited: 658
Chromones as a privileged scaffold in drug discovery: A review
Rangappa S. Keri, Srinivasa Budagumpi, Ranjith Krishna Pai, et al.
European Journal of Medicinal Chemistry (2014) Vol. 78, pp. 340-374
Closed Access | Times Cited: 431
Aquilaria spp. (agarwood) as source of health beneficial compounds: A review of traditional use, phytochemistry and pharmacology
Yumi Zuhanis Has-Yun Hashim, Philip G. Kerr, Phirdaous Abbas, et al.
Journal of Ethnopharmacology (2016) Vol. 189, pp. 331-360
Closed Access | Times Cited: 206
Overview of the Antioxidant and Anti-Inflammatory Activities of Selected Plant Compounds and Their Metal Ions Complexes
Paulina Mucha, Anna Skoczyńska, Magdalena Małecka, et al.
Molecules (2021) Vol. 26, Iss. 16, pp. 4886-4886
Open Access | Times Cited: 149
Natural products in agarwood andAquilariaplants: chemistry, biological activities and biosynthesis
Wei Li, Huiqin Chen, Hao Wang, et al.
Natural Product Reports (2020) Vol. 38, Iss. 3, pp. 528-565
Closed Access | Times Cited: 145
Chemical Constituents and Pharmacological Activity of Agarwood and Aquilaria Plants
Shuai Wang, Zhang‐Xin Yu, Canhong Wang, et al.
Molecules (2018) Vol. 23, Iss. 2, pp. 342-342
Open Access | Times Cited: 142
Chromones: A Promising Ring System for New Anti‐inflammatory Drugs
Carlos F. M. Silva, Diana C. G. A. Pinto, Artur M. S. Silva
ChemMedChem (2016) Vol. 11, Iss. 20, pp. 2252-2260
Closed Access | Times Cited: 114
2-(2-Phenylethyl)chromone derivatives from Chinese agarwood induced by artificial holing
Wei Li, Cai-Hong Cai, Wen-Hua Dong, et al.
Fitoterapia (2014) Vol. 98, pp. 117-123
Closed Access | Times Cited: 99
Identification of a diarylpentanoid-producing polyketide synthase revealing an unusual biosynthetic pathway of 2-(2-phenylethyl)chromones in agarwood
Xiaohui Wang, Bowen Gao, Yu Nakashima, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 48
Euchrestifolines A–O, fifteen novel carbazole alkaloids with potent anti-ferroptotic activity from Murraya euchrestifolia
Yue-Mei Chen, Nankai Cao, Si-Si Zhu, et al.
Natural Products and Bioprospecting (2025) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Anti-inflammatory 2-(2-phenylethyl)chromone derivatives from Chinese agarwood
Hui-Xia Huo, Yufan Gu, Hui Sun, et al.
Fitoterapia (2017) Vol. 118, pp. 49-55
Closed Access | Times Cited: 70
Anti-inflammatory Dimeric 2-(2-Phenylethyl)chromones from the Resinous Wood of Aquilaria sinensis
Hui-Xia Huo, Zhixiang Zhu, Yuelin Song, et al.
Journal of Natural Products (2017) Vol. 81, Iss. 3, pp. 543-553
Closed Access | Times Cited: 70
Overview of sesquiterpenes and chromones of agarwood originating from four main species of the genus Aquilaria
Mei Gao, Xiaomin Han, Ying Sun, et al.
RSC Advances (2019) Vol. 9, Iss. 8, pp. 4113-4130
Open Access | Times Cited: 68
Agarwood—The Fragrant Molecules of a Wounded Tree
Pooja Shivanand, Nurul Fadhila Arbie, Sarayu Krishnamoorthy, et al.
Molecules (2022) Vol. 27, Iss. 11, pp. 3386-3386
Open Access | Times Cited: 37
Characterization and Determination of 2-(2-Phenylethyl)chromones in Agarwood by GC-MS
Wen-Li Mei, De‐Lan Yang, Hao Wang, et al.
Molecules (2013) Vol. 18, Iss. 10, pp. 12324-12345
Open Access | Times Cited: 68
A review of chemistry, quality and analysis of infected agarwood tree (Aquilaria sp.)
Rishu Kalra, Nutan Kaushik
Phytochemistry Reviews (2017) Vol. 16, Iss. 5, pp. 1045-1079
Closed Access | Times Cited: 56
Natural occurring 2-(2-phenylethyl) chromones, structure elucidation and biological activities
Sabrin R. M. Ibrahim, Gamal A. Mohamed
Natural Product Research (2014) Vol. 29, Iss. 16, pp. 1489-1520
Closed Access | Times Cited: 54
2-(2-Phenylethyl)chromone derivatives in artificial agarwood from Aquilaria sinensis
Ge Liao, Wen-Li Mei, Wen-Hua Dong, et al.
Fitoterapia (2016) Vol. 110, pp. 38-43
Closed Access | Times Cited: 54
Salinity stress induces the production of 2-(2-phenylethyl)chromones and regulates novel classes of responsive genes involved in signal transduction in Aquilaria sinensis calli
Xiaohui Wang, Bowen Gao, Xiao Liu, et al.
BMC Plant Biology (2016) Vol. 16, Iss. 1
Open Access | Times Cited: 51
Health benefits of chromones: common ingredients of our daily diet
Ruchi Badoni Semwal, Deepak Kumar Semwal, Sandra Combrinck, et al.
Phytochemistry Reviews (2020) Vol. 19, Iss. 4, pp. 761-785
Closed Access | Times Cited: 48
Natural chromones as potential anti-inflammatory agents: Pharmacological properties and related mechanisms
Luı́za Carolina França Opretzka, Renan Fernandes do Espírito Santo, Olívia Azevedo Nascimento, et al.
International Immunopharmacology (2019) Vol. 72, pp. 31-39
Open Access | Times Cited: 44
Occurrence, synthesis and biological activity of 2-(2-phenyethyl)chromones
Meiyan Fan, Wei Yang, Min He, et al.
European Journal of Medicinal Chemistry (2022) Vol. 237, pp. 114397-114397
Closed Access | Times Cited: 26
Anatomical, chemical and endophytic fungal diversity of a Qi-Nan clone of Aquilaria sinensis (Lour.) Spreng with different induction times
Xiaofei Li, Xiaoying Fang, Zhiyi Cui, et al.
Frontiers in Plant Science (2024) Vol. 15
Open Access | Times Cited: 5
5,6,7,8-Tetrahydro-2-(2-phenylethyl)chromones from artificial agarwood of Aquilaria sinensis and their inhibitory activity against acetylcholinesterase
Ge Liao, Wen-Li Mei, Fan‐Dong Kong, et al.
Phytochemistry (2017) Vol. 139, pp. 98-108
Closed Access | Times Cited: 48
Anti-neuroinflammatory sesquiterpenes from Chinese eaglewood
Hui-Xia Huo, Zhixiang Zhu, Dao-Ran Pang, et al.
Fitoterapia (2015) Vol. 106, pp. 115-121
Closed Access | Times Cited: 47
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