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:

Discovery of Highly Potent p53-MDM2 Antagonists and Structural Basis for Anti-Acute Myeloid Leukemia Activities
Yijun Huang, Siglinde Wolf, Barbara Beck, et al.
ACS Chemical Biology (2014) Vol. 9, Iss. 3, pp. 802-811
Open Access | Times Cited: 40

Showing 26-50 of 40 citing articles:

Indoles
Navriti Chadha, Om Silakari
Elsevier eBooks (2018), pp. 285-321
Closed Access | Times Cited: 17

p53–MDM2 and MDMX Antagonists
Constantinos G. Neochoritis, Natalia Estrada‐Ortiz, Kareem Khoury, et al.
Annual reports in medicinal chemistry (2014), pp. 167-187
Closed Access | Times Cited: 17

Multicomponent Reactions in Medicinal Chemistry
Zefeng Wang, Alexander Dömlingꝉ
(2021), pp. 91-137
Closed Access | Times Cited: 13

Design of indole- and MCR-based macrocycles as p53-MDM2 antagonists
Constantinos G. Neochoritis, Maryam Kazemi Miraki, Eman M. M. Abdelraheem, et al.
Beilstein Journal of Organic Chemistry (2019) Vol. 15, pp. 513-520
Open Access | Times Cited: 13

Hitting on the move: Targeting intrinsically disordered protein states of the MDM2-p53 interaction
Constantinos G. Neochoritis, Jack Atmaj, Aleksandra Twarda‐Clapa, et al.
European Journal of Medicinal Chemistry (2019) Vol. 182, pp. 111588-111588
Open Access | Times Cited: 10

Two‐Step Synthesis of Complex Artificial Macrocyclic Compounds
Rudrakshula Madhavachary, Eman M. M. Abdelraheem, Arianna Rossetti, et al.
Angewandte Chemie (2017) Vol. 129, Iss. 36, pp. 10865-10869
Open Access | Times Cited: 10

Nano structured spinel Co 3 O 4 -catalyzed four component reaction: A novel synthesis of Ugi adducts from aryl alcohols as a key reagent
Priya Chacko, Kalegowda Shivashankar
Chinese Chemical Letters (2017) Vol. 28, Iss. 7, pp. 1619-1624
Closed Access | Times Cited: 9

Discovery of a Potent Allosteric Kinase Modulator by Combining Computational and Synthetic Methods
Edwin Kroon, Jörg O. Schulze, Evelyn Süß, et al.
Angewandte Chemie (2015) Vol. 127, Iss. 47, pp. 14139-14142
Open Access | Times Cited: 7

Development of a novel immunoassay to detect interactions with the transactivation domain of p53: application to screening of new drugs
Yufeng Xiong, Yingsong Wu, Shuhong Luo, et al.
Scientific Reports (2017) Vol. 7, Iss. 1
Open Access | Times Cited: 6

Proposing novel MDM2 inhibitors: Combined physics‐driven high‐throughput virtual screening and in vitro studies
Gulsah Aydin, Maide Nur Paksoy, Müge Didem Orhan, et al.
Chemical Biology & Drug Design (2020) Vol. 96, Iss. 1, pp. 684-700
Closed Access | Times Cited: 6

Focusing on shared subpockets – new developments in fragment-based drug discovery
Eman M. M. Abdelraheem, Carlos J. Camacho, Alexander Dömlingꝉ
Expert Opinion on Drug Discovery (2015) Vol. 10, Iss. 11, pp. 1179-1187
Open Access | Times Cited: 5

Multicomponent Assembly of the Kinesin Spindle Protein Inhibitor CPUYJ039 and Analogues as Antimitotic Agents
Carlos Carbajales, Jun‐ichi Sawada, Giovanni Marzaro, et al.
ACS Combinatorial Science (2017) Vol. 19, Iss. 3, pp. 153-160
Closed Access | Times Cited: 5

Daunorubicin for the treatment of acute myeloid leukemia
Clara Bertuzzi, Stefania Paolini, Giuseppe Visani, et al.
Expert Opinion on Orphan Drugs (2014) Vol. 2, Iss. 10, pp. 1075-1087
Closed Access | Times Cited: 1

Hot Spot-Based Design of Small-Molecule Inhibitors for Protein-Protein Interactions
Haitao Ji
Springer eBooks (2018), pp. 53-71
Closed Access | Times Cited: 1

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