Design, synthesis, and biological evaluation of novel azaspirooxindolinone derivatives as potent inhibitors of ITK and BTK-dependent cancers

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15640%2F25%3A73630462" target="_blank" >RIV/61989592:15640/25:73630462 - isvavai.cz</a>

Alternative codes found

RIV/00098892:_____/25:10159169 RIV/61989592:15110/25:73630462

Result on the web

<a href="https://www.sciencedirect.com/science/article/pii/S0968089625000574?ref=pdf_download&fr=RR-2&rr=9255ba02da81f9a0" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0968089625000574?ref=pdf_download&fr=RR-2&rr=9255ba02da81f9a0</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.bmc.2025.118116" target="_blank" >10.1016/j.bmc.2025.118116</a>

Result language

angličtina

Original language name

Design, synthesis, and biological evaluation of novel azaspirooxindolinone derivatives as potent inhibitors of ITK and BTK-dependent cancers

Original language description

Interleukin-2-inducible T-cell kinase (ITK) and Bruton&apos;s tyrosine kinase (BTK) are two important members of the Tec family with crucial roles in immune system function. Deregulation in ITK and BTK activity is linked to several hematological malignancies, making them key targets for cancer immunotherapy. In this study, we synthesized a series of azaspirooxindolinone derivatives and evaluated their cytotoxic activity against ITK/BTK-negative and positive cancer cell lines, followed by enzymatic inhibition studies to assess the ITK/BTK kinase selectivity of two hit compounds. Several compounds demonstrated selective cytotoxicity against ITK- or BTK-expressing cells. Compound 3d exhibited high cytotoxicity in ITK-positive Jurkat (IC50 = 3.58 mu M) and BTK-positive Ramos (IC50 = 3.06 mu M) cells, while compound 3j showed strong cytotoxicity in Ramos (IC50 = 1.38 mu M) and Jurkat (IC50 = 4.16 mu M) cells. Compounds 3a and 3e were selectively cytotoxic in Jurkat cells (IC50 = 9.36 mu M and 10.85 mu M, respectively), while compounds 3f and 3g were highly cytotoxic in Ramos cells (IC50 = 1.82 mu M and 1.42 mu M, respectively). None of the active compounds exhibited cytotoxicity in non-cancer cell lines (IC50 &gt; 50 mu M), demonstrating their selectivity for malignant cells. Enzyme inhibition assay showed that 3d is a selective ITK inhibitor (IC50 = 0.91 mu M) with no detectable BTK inhibition, aligning with its strong activity in ITK-positive cells. In contrast, compound 3j did not inhibit ITK or BTK enzymatically, suggesting an alternative mechanism of action. These findings highlight 3d as a promising ITK inhibitor and warrant further investigation to elucidate its mechanism of action.

Czech name

—

Czech description

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Type

J_imp - Article in a specialist periodical, which is included in the Web of Science database

CEP classification

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OECD FORD branch

10608 - Biochemistry and molecular biology

Project

Result was created during the realization of more than one project. More information in the Projects tab.

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year

2025

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Bioorganic and Medicinal Chemistry

ISSN

0968-0896

e-ISSN

1464-3391

Volume of the periodical

121

Issue of the periodical within the volume

15.4.2025

Country of publishing house

GB - UNITED KINGDOM

Number of pages

9

Pages from-to

nestránkováno

UT code for WoS article

001436890700001

EID of the result in the Scopus database

2-s2.0-85218503979