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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:

New cell cycle checkpoint pathways regulators with 2-Oxo-indoline scaffold as potential anticancer agents: Design, synthesis, biological activities and in silico studies
Hend A. A. Abd El-wahab, Hany S. Mansour, Ahmed M. Ali, et al.
Bioorganic Chemistry (2022) Vol. 120, pp. 105622-105622
Closed Access | Times Cited: 9

Showing 9 citing articles:

New 2-Indolinone-Indole Hybrid Compounds Carrying a Benzoyl Moiety as Tyrosine Kinase Inhibitors
Merve Camci, Tuğçe Cinek, Gökçe Cihan‐Üstündağ, et al.
(2025)
Closed Access
New 2-indolinone-indole hybrid compounds carrying a benzoyl moiety as tyrosine kinase inhibitors
Merve Camcı-Eren, Tuğçe Cinek, Gökçe Cihan‐Üstündağ, et al.
Bioorganic Chemistry (2025) Vol. 156, pp. 108203-108203
Closed Access
Therapeutic Insights of Indole Scaffold‐Based Compounds as Protein Kinase Inhibitors
Dina H. Dawood
ChemistrySelect (2025) Vol. 10, Iss. 5
Open Access
2‐Indolinone: An Anticancer Scaffold, Overview of the Studies and Approaches (2017–2024)
Taha Koulani, Asu Büşra Temizer, Nilgün Karalı
ChemistrySelect (2025) Vol. 10, Iss. 5
Closed Access
Novel Azine Linked Hybrids of 2-Indolinone and Thiazolodinone Scaffolds as CDK2 Inhibitors with Potential Anticancer Activity: In Silico Design, Synthesis, Biological, Molecular Dynamics and Binding Free Energy Studies
Wesam S. Qayed, Mostafa A. Hassan, Wael M. El‐Sayed, et al.
Bioorganic Chemistry (2022) Vol. 126, pp. 105884-105884
Closed Access | Times Cited: 12
Synthesis, cytotoxic evaluation, apoptosis, cell cycle, and molecular docking studies of some new 5-(arylidene/heteroarylidene)-2-(morpholinoimino)-3-phenylthiazolidin-4-ones
Mohammed A. Assiri, Tarik E. Ali, Maha N. Alqahtani, et al.
Synthetic Communications (2023) Vol. 53, Iss. 15, pp. 1240-1261
Closed Access | Times Cited: 6
Design, synthesis, and molecular docking of novel 1,3, 4-triaryl pyrazole derivatives bearing methylsulfonyl moiety with anticancer activity through dual targeting CDK2 and COX-2 enzymes
Ahmed Shaker, Mai I. Shahin, Asmaa M. AboulMagd, et al.
Journal of Molecular Structure (2023) Vol. 1301, pp. 137323-137323
Closed Access | Times Cited: 6
One-Pot, Five-Component Condensation Reaction of Isatin, Secondary Amines, Malononitrile, Alcohols, and Molecular Oxygen to Access 3-Functionalized 2-Oxindoles
Kaushik Bora, Uma Devi Newar, Ram Awatar Maurya
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 19, pp. 14216-14221
Closed Access | Times Cited: 3
Pyrrolizine/indolizine-bearing (un)substituted isoindole moiety: design, synthesis, antiproliferative and MDR reversal activities, and in silico studies
Amr L. AbdelSamad, Mohammed T. El‐Saadi, Ahmed M. Gouda, et al.
RSC Advances (2023) Vol. 13, Iss. 44, pp. 30753-30770
Open Access | Times Cited: 2
New and efficient one-pot method for the synthesis of spiro[indoline-2,1′-isobenzofuran] derivatives and evaluation of their anticancer activity by in vitro and in silico studies
Maryam Alborz, Mohammad R. Mohammadizadeh, Pegah Mardaneh, et al.
Journal of Molecular Structure (2024), pp. 140164-140164
Closed Access
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