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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:

Kinetically selective and potent inhibitors of HDAC8
Markus Schweipert, Niklas Jänsch, Wisely Oki Sugiarto, et al.
Biological Chemistry (2018) Vol. 400, Iss. 6, pp. 733-743
Closed Access | Times Cited: 9

Showing 9 citing articles:

Are inhibitors of histone deacetylase 8 (HDAC8) effective in hematological cancers especially acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL)?
Sk. Abdul Amin, Samima Khatun, Shovanlal Gayen, et al.
European Journal of Medicinal Chemistry (2023) Vol. 258, pp. 115594-115594
Closed Access | Times Cited: 19
Discovery of 5-naphthylidene-2,4-thiazolidinedione derivatives as selective HDAC8 inhibitors and evaluation of their cytotoxic effects in leukemic cell lines
Kalpana Tilekar, Neha Upadhyay, Niklas Jänsch, et al.
Bioorganic Chemistry (2019) Vol. 95, pp. 103522-103522
Closed Access | Times Cited: 43
Discovery of novel N-substituted thiazolidinediones (TZDs) as HDAC8 inhibitors: in-silico studies, synthesis, and biological evaluation
Neha Upadhyay, Kalpana Tilekar, Niklas Jänsch, et al.
Bioorganic Chemistry (2020) Vol. 100, pp. 103934-103934
Open Access | Times Cited: 43
Non-Hydroxamate Zinc-Binding Groups as Warheads for Histone Deacetylases
Anton Frühauf, Franz‐Josef Meyer‐Almes
Molecules (2021) Vol. 26, Iss. 17, pp. 5151-5151
Open Access | Times Cited: 31
Rapid Determination of Kinetic Constants for Slow-Binding Inhibitors and Inactivators of Human Histone Deacetylase 8
Aleksandra Kopranovic, Franz‐Josef Meyer‐Almes
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 11, pp. 5593-5593
Open Access | Times Cited: 2
HDAC8 As an Emerging Target in Drug Discovery With Special Emphasis on Medicinal Chemistry
S. Rajaraman, Ranjani Balakrishnan, Dhruv Deshmukh, et al.
Future Medicinal Chemistry (2023) Vol. 15, Iss. 10, pp. 885-908
Closed Access | Times Cited: 6
Design and synthesis of peptides as stabilizers of histone deacetylase 4
Annika Lill, Markus Schweipert, Thomas Nehls, et al.
Journal of Peptide Science (2024) Vol. 30, Iss. 9
Open Access | Times Cited: 1
Mechanistic Exploration of Methionine 274 Acting as a “Switch” of the Selective Pocket Involved in HDAC8 Inhibition: An in Silico Study
Yao Peng, Qiushuang Gao, Ying Wang, et al.
ChemMedChem (2021) Vol. 16, Iss. 12, pp. 1933-1944
Closed Access | Times Cited: 3
Futuristic Approaches Towards Designing of Isozyme-Selective Histone Deacetylase Inhibitors Against Zinc-Dependent Histone Deacetylases
Shabir Ahmad Ganai
(2020), pp. 241-258
Closed Access | Times Cited: 1
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