| S1525 |
Adavosertib (AZD1775, MK-1775)
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Adavosertib (MK-1775, AZD1775) is a potent and selective Wee1 inhibitor with IC50 of 5.2 nM in a cell-free assay; hinders G2 DNA damage checkpoint. Phase 2.
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Cancer Cell, 2025, 43(8):1530-1548.e9
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Nat Cancer, 2025, 10.1038/s43018-025-00960-z
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Cell Rep Med, 2025, S2666-3791(25)00102-8
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| S8148 |
PD0166285
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PD0166285 is a potent Wee1 and Chk1 inhibitor with activity at nanomolar concentrations (IC50=24 nM for Wee1 and 72 nM for Myt1). This compound is also a novel G2 checkpoint abrogator. It induces apoptosis.
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iScience, 2025, 28(5):112292
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Signal Transduct Target Ther, 2024, 9(1):181.
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Nat Commun, 2024, 15(1):2089
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| S9778 |
Debio 0123
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WEE1-IN-5 (Debio 0123) is a potent Wee1 inhibitor that inhibits phospho-CDC2 and abrogates the G2 check point.
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J Clin Invest, 2025, 135(11)e188165
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medRxiv, 2024, 2023.05.17.23290140
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| E1000 |
Azenosertib (Zn-C3)
|
Azenosertib (Zn-C3) is an oral active, highly effective and selective Wee1 inhibitor with IC50 of 3.9 nM, which can be used in cancer research.
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bioRxiv, 2025, 2025.05.28.656693
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medRxiv, 2024, 2023.05.17.23290140
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| E4737 |
Potrasertib
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Potrasertib (IMP7068, WEE1-IN-10) is a potent and selective inhibitor of WEE1 Kinase. It displays antitumor activity and is well-tolerated in patients with advanced solid tumors.
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|
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| E1175 |
RP-6306 (lunresertib)
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lunresertib (RP-6306) is a Protein Kinase, Membrane Associated Tyrosine/Threonine 1 (PKMYT1) inhibitor, which can be used for the research of cancer.
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Cell Rep, 2025, 44(8):116019
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BMC Cancer, 2024, 24(1):1333
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