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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:

Five new eudesmane-type sesquiterpenoids from Chinese agarwood induced by artificial holing
Wei Li, Cai-Hong Cai, Zhi‐Kai Guo, et al.
Fitoterapia (2014) Vol. 100, pp. 44-49
Closed Access | Times Cited: 73

Showing 1-25 of 73 citing articles:

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
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
Acetylcholinesterase Inhibitory Potential of Various Sesquiterpene Analogues for Alzheimer’s Disease Therapy
Ashwani Arya, Rubal Chahal, Rekha Rao, et al.
Biomolecules (2021) Vol. 11, Iss. 3, pp. 350-350
Open Access | Times Cited: 85
Antibacterial and Antifungal Sesquiterpenoids: Chemistry, Resource, and Activity
Hang-Ying Li, Wenqian Yang, Xinzhu Zhou, et al.
Biomolecules (2022) Vol. 12, Iss. 9, pp. 1271-1271
Open Access | Times Cited: 43
Agarwood (Aquilaria malaccensis L.) a quality fragrant and medicinally significant plant based essential oil with pharmacological potentials and genotoxicity
Roktim Gogoi, Neelav Sarma, Twahira Begum, et al.
Industrial Crops and Products (2023) Vol. 197, pp. 116535-116535
Closed Access | Times Cited: 43
Essential oil from Aquilaria spp. (agarwood): a comprehensive review on the impact of extraction methods on yield, chemical composition, and biological activities
Xin Wang, Sook Wah Chan, Nallammai Singaram, et al.
Journal of Essential Oil Research (2025) Vol. 37, Iss. 1, pp. 110-144
Closed Access | Times Cited: 1
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
Formation of agarwood from Aquilaria malaccensis in response to inoculation of local strains of Fusarium solani
Ahmad Faizal, Rizkita Rachmi Esyanti, Elfa Norisda Aulianisa, et al.
Trees (2016) Vol. 31, Iss. 1, pp. 189-197
Closed Access | Times Cited: 67
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: 38
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
Understanding Agarwood Formation and Its Challenges
Saiema Rasool, Rozi Mohamed
Tropical forestry (2016), pp. 39-56
Closed Access | Times Cited: 52
Sesquiterpenoids and 2-(2-phenylethyl)chromones respectively acting as α-glucosidase and tyrosinase inhibitors from agarwood of an Aquilaria plant
Li Yang, Yiling Yang, Wen-Hua Dong, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2019) Vol. 34, Iss. 1, pp. 853-862
Open Access | Times Cited: 49
Aquilariperoxide A, a Sesquiterpene Dimer from Agarwood of Aquilaria sinensis with Dual Antitumor and Antimalarial Effects
Xiaoling Huang, Dan Cai, Peng Gao, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 13, pp. 8352-8359
Closed Access | Times Cited: 14
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
Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing
Wei Li, Ge Liao, Wen-Hua Dong, et al.
Molecules (2016) Vol. 21, Iss. 3, pp. 274-274
Open Access | Times Cited: 44
Three new sesquiterpenoids from agarwood of Aquilaria crassna
Hong-Ni Wang, Wen-Hua Dong, Sheng‐Zhuo Huang, et al.
Fitoterapia (2016) Vol. 114, pp. 7-11
Closed Access | Times Cited: 41
Aquilanols A and B, Macrocyclic Humulene-Type Sesquiterpenoids from the Agarwood of Aquilaria malaccensis
Chi Thanh, Taeyong Eom, Eunji Cho, et al.
Journal of Natural Products (2017) Vol. 80, Iss. 11, pp. 3043-3048
Closed Access | Times Cited: 40
Review: Secondary Metabolites of Aquilaria, a Thymelaeaceae Genus
Alfinda Novi Kristanti, Mulyadi Tanjung, Nanik Siti Aminah
Mini-Reviews in Organic Chemistry (2017) Vol. 15, Iss. 1
Open Access | Times Cited: 40
How Closely Does Induced Agarwood’s Biological Activity Resemble That of Wild Agarwood?
Sheng Ma, Manqin Huang, Yunlin Fu, et al.
Molecules (2023) Vol. 28, Iss. 7, pp. 2922-2922
Open Access | Times Cited: 11
GC-MS Study of the Chemical Components of Different Aquilaria sinensis (Lour.) Gilgorgans and Agarwood from Different Asian Countries
Meng‐Ru Wang, Wei Li, Sha Luo, et al.
Molecules (2018) Vol. 23, Iss. 9, pp. 2168-2168
Open Access | Times Cited: 38
Four new bi-phenylethylchromones from artificial agarwood
Pan Xiang, Wen-Li Mei, Huiqin Chen, et al.
Fitoterapia (2017) Vol. 120, pp. 61-66
Closed Access | Times Cited: 37
Anti-Cancer Effect of Sesquiterpene and Triterpenoids from Agarwood of Aquilaria sinensis
Lili Chen, Yunyun Liu, Yifei Li, et al.
Molecules (2022) Vol. 27, Iss. 16, pp. 5350-5350
Open Access | Times Cited: 17
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