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:

Selective inhibition of monoamine oxidase A by hispidol
Seung Cheol Baek, Hyun-Woo Lee, Hyung Won Ryu, et al.
Bioorganic & Medicinal Chemistry Letters (2018) Vol. 28, Iss. 4, pp. 584-588
Closed Access | Times Cited: 63

Showing 1-25 of 63 citing articles:

Natural Products Inhibitors of Monoamine Oxidases—Potential New Drug Leads for Neuroprotection, Neurological Disorders, and Neuroblastoma
Narayan D. Chaurasiya, Francisco León, Ilias Muhammad, et al.
Molecules (2022) Vol. 27, Iss. 13, pp. 4297-4297
Open Access | Times Cited: 40

Development of Isopropyl-Tailed Chalcones as a New Class of Selective MAO-B Inhibitors for the Treatment of Parkinson’s Disorder
Sunil Kumar, Jong‐Min Oh, Mohamed A. Abdelgawad, et al.
ACS Omega (2023) Vol. 8, Iss. 7, pp. 6908-6917
Open Access | Times Cited: 26

Rhamnocitrin isolated from Prunus padus var. seoulensis: A potent and selective reversible inhibitor of human monoamine oxidase A
Seung Cheol Baek, Mi Hyeon Park, Hyung Won Ryu, et al.
Bioorganic Chemistry (2018) Vol. 83, pp. 317-325
Closed Access | Times Cited: 66

Design, synthesis and biological evaluation of oxygenated chalcones as potent and selective MAO-B inhibitors
Della Grace Thomas Parambi, Jong‐Min Oh, Seung Cheol Baek, et al.
Bioorganic Chemistry (2019) Vol. 93, pp. 103335-103335
Closed Access | Times Cited: 60

Potent inhibition of acetylcholinesterase by sargachromanol I from Sargassum siliquastrum and by selected natural compounds
Jae Pil Lee, Myung-Gyun Kang, Joon Yeop Lee, et al.
Bioorganic Chemistry (2019) Vol. 89, pp. 103043-103043
Closed Access | Times Cited: 58

Bioactive Aurones, Indanones, and Other Hemiindigoid Scaffolds: Medicinal Chemistry and Photopharmacology Perspectives
Leticia M. Lazinski, Guy Royal, Maxime Robin, et al.
Journal of Medicinal Chemistry (2022) Vol. 65, Iss. 19, pp. 12594-12625
Open Access | Times Cited: 35

Introduction of benzyloxy pharmacophore into aryl/heteroaryl chalcone motifs as a new class of monoamine oxidase B inhibitors
Sachithra Thazhathuveedu Sudevan, Jong‐Min Oh, Mohamed A. Abdelgawad, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 27

Potent and highly selective dual‐targeting monoamine oxidase‐B inhibitors: Fluorinated chalcones of morpholine versus imidazole
Bijo Mathew, Seung Cheol Baek, Della Grace Thomas Parambi, et al.
Archiv der Pharmazie (2019) Vol. 352, Iss. 4
Closed Access | Times Cited: 52

Novel Class of Chalcone Oxime Ethers as Potent Monoamine Oxidase-B and Acetylcholinesterase Inhibitors
Jong‐Min Oh, T. M. Rangarajan, Reeta Chaudhary, et al.
Molecules (2020) Vol. 25, Iss. 10, pp. 2356-2356
Open Access | Times Cited: 46

Calycosin and 8-O-methylretusin isolated from Maackia amurensis as potent and selective reversible inhibitors of human monoamine oxidase-B
Jong‐Min Oh, Hyun‐Jae Jang, Won Jun Kim, et al.
International Journal of Biological Macromolecules (2020) Vol. 151, pp. 441-448
Closed Access | Times Cited: 43

Piperazine-substituted chalcones: a new class of MAO-B, AChE, and BACE-1 inhibitors for the treatment of neurological disorders
Bijo Mathew, Jong‐Min Oh, Roua S. Baty, et al.
Environmental Science and Pollution Research (2021) Vol. 28, Iss. 29, pp. 38855-38866
Open Access | Times Cited: 38

Morpholine-based chalcones as dual-acting monoamine oxidase-B and acetylcholinesterase inhibitors: synthesis and biochemical investigations
Rani Sasidharan, Bo Hyun Eom, Jeong Hyun Heo, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2021) Vol. 36, Iss. 1, pp. 188-197
Open Access | Times Cited: 33

Roles of selected non-P450 human oxidoreductase enzymes in protective and toxic effects of chemicals: review and compilation of reactions
Slobodan Rendić, Rachel D. Crouch, F. Peter Guengerich
Archives of Toxicology (2022) Vol. 96, Iss. 8, pp. 2145-2246
Open Access | Times Cited: 24

Synthesis of 4-substituted benzyl-2-triazole-linked-tryptamine-paeonol derivatives and evaluation of their selective inhibitions against butyrylcholinesterase and monoamine oxidase-B
Jong‐Min Oh, Yujung Kang, Ji Hyun Hwang, et al.
International Journal of Biological Macromolecules (2022) Vol. 217, pp. 910-921
Closed Access | Times Cited: 23

Selected aryl thiosemicarbazones as a new class of multi-targeted monoamine oxidase inhibitors
Bijo Mathew, Seung Cheol Baek, Della Grace Thomas Parambi, et al.
MedChemComm (2018) Vol. 9, Iss. 11, pp. 1871-1881
Open Access | Times Cited: 45

Imidazole bearing chalcones as a new class of monoamine oxidase inhibitors
Rani Sasidharan, Seung Cheol Baek, Manju Sreedharannair Leelabaiamma, et al.
Biomedicine & Pharmacotherapy (2018) Vol. 106, pp. 8-13
Closed Access | Times Cited: 43

Inhibition of Butyrylcholinesterase and Human Monoamine Oxidase-B by the Coumarin Glycyrol and Liquiritigenin Isolated from Glycyrrhiza uralensis
Geum Seok Jeong, Myung-Gyun Kang, Joon Yeop Lee, et al.
Molecules (2020) Vol. 25, Iss. 17, pp. 3896-3896
Open Access | Times Cited: 33

Development of morpholine ring-bearing halogenated α,β-unsaturated ketones as selective monoamine oxidase-B inhibitors
Jiseong Lee, Saranya Kattil Parmbil, Nagendar Kumar Pandit, et al.
Applied Biological Chemistry (2024) Vol. 67, Iss. 1
Open Access | Times Cited: 3

Selective inhibition of monoamine oxidase A by chelerythrine, an isoquinoline alkaloid
Seung Cheol Baek, Hyung Won Ryu, Myung-Gyun Kang, et al.
Bioorganic & Medicinal Chemistry Letters (2018) Vol. 28, Iss. 14, pp. 2403-2407
Closed Access | Times Cited: 32

Design, synthesis and evaluation of 2-(indolylmethylidene)-2,3-dihydro-1-benzofuran-3-one and 2-(indolyl)-4H-chromen-4-one derivatives as novel monoamine oxidases inhibitors
Koichi Takao, U Shiori, Hitoshi Kamauchi, et al.
Bioorganic Chemistry (2019) Vol. 87, pp. 594-600
Closed Access | Times Cited: 32

Ethyl Acetohydroxamate Incorporated Chalcones: Unveiling a Novel Class of Chalcones for Multitarget Monoamine Oxidase-B Inhibitors Against Alzheimer’s Disease
Reeta Reeta, Seung Cheol Baek, Jae Pil Lee, et al.
CNS & Neurological Disorders - Drug Targets (2019) Vol. 18, Iss. 8, pp. 643-654
Closed Access | Times Cited: 31

Acetylcholinesterase and monoamine oxidase-B inhibitory activities by ellagic acid derivatives isolated from Castanopsis cuspidata var. sieboldii
Jong‐Min Oh, Hyun‐Jae Jang, Myung-Gyun Kang, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 23

Development of a Novel Class of Pyridazinone Derivatives as Selective MAO-B Inhibitors
Mehmet Abdullah Alagöz, Jong‐Min Oh, Yaren Nur Zenni, et al.
Molecules (2022) Vol. 27, Iss. 12, pp. 3801-3801
Open Access | Times Cited: 16

Positional scanning of natural product hispidol’s ring-B: discovery of highly selective human monoamine oxidase-B inhibitor analogues downregulating neuroinflammation for management of neurodegenerative diseases
Ahmed H.E. Hassan, Hyeon Jeong Kim, Min Sung Gee, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2022) Vol. 37, Iss. 1, pp. 768-780
Open Access | Times Cited: 15

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