Recent contributions of pyridazine as a privileged scaffold of anticancer agents in medicinal chemistry: An updated review

ZQ Liu, Q Zhang, YL Liu, XQ Yu, RH Chui… - Bioorganic & Medicinal …, 2024 - Elsevier
Pyridazine, as a privileged scaffold, has been extensively utilized in drug development due
to its multiple biological activities. Especially around its distinctive anticancer property, a …

Is It Still Possible to Think about HSP70 as a Therapeutic Target in Onco-Hematological Diseases?

N Mouawad, G Capasso, E Ruggeri, L Martinello… - Biomolecules, 2023 - mdpi.com
The search for molecules to be targeted that are involved in apoptosis resistance/increased
survival and pathogenesis of onco-hematological malignancies is ongoing since these …

Reengineering ponatinib to minimize cardiovascular toxicity

AP Hnatiuk, AAN Bruyneel, D Tailor, M Pandrala… - Cancer research, 2022 - AACR
Small molecule tyrosine kinase inhibitors (TKI) have revolutionized cancer treatment and
greatly improved patient survival. However, life-threatening cardiotoxicity of many TKIs has …

Overcoming the imatinib-resistant BCR-ABL mutants with new ureidobenzothiazole chemotypes endowed with potent and broad-spectrum anticancer activity

AK El-Damasy, H Jin, JW Park, HJ Kim… - Journal of Enzyme …, 2023 - Taylor & Francis
The design of kinase inhibitors targeting the oncogenic kinase BCR-ABL constitutes a
promising paradigm for treating chronic myeloid leukaemia (CML). Nevertheless, the …

Discovery of 3-((3-amino-1H-indazol-4-yl)ethynyl)-N-(4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide (AKE-72), a potent Pan-BCR-ABL …

AK El-Damasy, HJ Kim, JW Park, Y Nam… - Journal of Enzyme …, 2023 - Taylor & Francis
BCR-ABL inhibition is an effective therapeutic approach for the treatment of chronic myeloid
leukaemia (CML). Herein, we report the discovery of AKE-72 (5), a diarylamide 3 …

[HTML][HTML] In Silico Molecular Modeling of Four New Afatinib Derived Molecules Targeting the Inhibition of the Mutated Form of BCR-ABL T315I

KML Rocha, ÉCM Nascimento, RCC de Jesus… - Molecules, 2024 - mdpi.com
Four afatinib derivatives were designed and modeled. These derivatives were compared to
the known tyrosine-kinase inhibitors in treating Chronic Myeloid Leukemia, ie, imatinib and …

Heterocyclic Compounds as Bcr-Abl Tyrosine Kinase Inhibitors Against Chronic Myeloid Leukemia

S Gado, MAK Hassan, MM Kisla… - Medicinal …, 2024 - benthamdirect.com
Despite significant progress in oncology therapeutics, cancer remains a leading cause of
mortality worldwide. Chronic myeloid leukemia, which accounts for 15% of all adult leukemia …

Exploring the Potential of Azo Compounds in Leukemia Treatment: Synthesis and Characterization of New Derivatives with Dimedone and Meldrum's Acid End …

Y Güney, Ö Dilek, B Sezgin, T Tilki - ChemistrySelect, 2023 - Wiley Online Library
This scholarly investigation presents pioneering drug candidates for combating leukemia,
distinguished by reduced side effects and elevated efficacy. The study focuses on azo …

Molecular docking and ADMET profiling of Carbazole-rhodanine hybrid as anticancer agent

EA Erazua, AA Olaseinde, AK Oyebamiji… - … of phytomedicine and …, 2024 - ajol.info
Drug resistance and lack of specificity of currently available chemotherapeutics for cancer
cells contribute to the failure of cancer chemotherapy. This highlights the pressing need to …

[HTML][HTML] Subsets of natural killer cells in chronic myeloid leukemia and their relation with some inflammatory cytokines

YF Faraj, KM Salih, A Khelif… - Iraqi Journal of …, 2023 - journals.lww.com
BACKGROUND: As in other malignancies, different subsets of natural killer (NK) cells play a
crucial role in the recognition and lysing of malignant cells in chronic myeloid leukemia …