[HTML][HTML] FLT3 inhibitors in acute myeloid leukemia

M Wu, C Li, X Zhu - Journal of hematology & oncology, 2018 - Springer
FLT3 mutations are one of the most common findings in acute myeloid leukemia (AML).
FLT3 inhibitors have been in active clinical development. Midostaurin as the first-in-class …

Genetic biomarkers of drug resistance: A compass of prognosis and targeted therapy in acute myeloid leukemia

L Long, YG Assaraf, ZN Lei, H Peng, L Yang… - Drug Resistance …, 2020 - Elsevier
Acute myeloid leukemia (AML) is a highly aggressive hematological malignancy with
complex heterogenous genetic and biological nature. Thus, prognostic prediction and …

Discovery of a benzimidazole-based dual FLT3/TrKA inhibitor targeting acute myeloid leukemia

EME Dokla, AK Abdel-Aziz, SN Milik… - Bioorganic & Medicinal …, 2022 - Elsevier
FMS-like tyrosine kinase 3 (FLT3) enzyme overexpression and mutations are the most
common molecular abnormalities associated with acute myeloid leukemia (AML). In …

Novel selective TOPK inhibitor SKLB-C05 inhibits colorectal carcinoma growth and metastasis

T Gao, Q Hu, X Hu, Q Lei, Z Feng, X Yu, C Peng… - Cancer letters, 2019 - Elsevier
The mitogen-activated protein kinase (MAPK) signaling pathway member T-LAK cell–
originated protein kinase/PDZ-binding kinase (TOPK/PBK) is closely involved in …

Dual FLT3 inhibitors: Against the drug resistance of acute myeloid leukemia in recent decade

T Yuan, B Qi, Z Jiang, W Dong, L Zhong, L Bai… - European Journal of …, 2019 - Elsevier
Acute myeloid leukemia (AML) is a malignant disease characterized by abnormal growth
and differentiation of hematopoietic stem cells. Although the pathogenesis has not been fully …

Potently inhibiting cancer cell migration with novel 3H-pyrazolo [4, 3-f] quinoline boronic acid ROCK inhibitors

N Dayal, CG Mikek, D Hernandez, GA Naclerio… - European journal of …, 2019 - Elsevier
Rho-associated protein kinases (ROCKs) are ubiquitously expressed in most adult tissues,
and are involved in modulating the cytoskeleton, protein synthesis and degradation …

[HTML][HTML] Targeting proliferation signals and the cell cycle machinery in acute leukemias: novel molecules on the horizon

A Ghelli Luserna di Rorà, M Jandoubi, G Martinelli… - Molecules, 2023 - mdpi.com
Uncontrolled proliferative signals and cell cycle dysregulation due to genomic or functional
alterations are important drivers of the expansion of undifferentiated blast cells in acute …

3H-Pyrazolo[4,3-f]quinoline-Based Kinase Inhibitors Inhibit the Proliferation of Acute Myeloid Leukemia Cells In Vivo

N Dayal, E Reznickova, DE Hernandez… - Journal of Medicinal …, 2021 - ACS Publications
The 3 H-pyrazolo [4, 3-f] quinoline moiety has been recently shown to be a privileged kinase
inhibitor core with potent activities against acute myeloid leukemia (AML) cell lines in vitro …

HSD1787, a Tetrahydro-3H-Pyrazolo[4,3-f]Quinoline Compound Synthesized via Povarov Reaction, Potently Inhibits Proliferation of Cancer Cell Lines at Nanomolar …

N Dayal, M Wang, HO Sintim - ACS omega, 2020 - ACS Publications
Multicomponent reaction (MCR) is often used to rapidly assemble complex compounds for
drug screening. Povarov MCR has been used to prepare a new library containing tetrahydro …

STING antagonists, synthesized via Povarov–Doebner type multicomponent reaction

WWS Ong, N Dayal, R Chaudhuri, J Lamptey… - RSC Medicinal …, 2023 - pubs.rsc.org
The cGAS–STING axis plays an important role in protecting higher organisms against
invading pathogens or cancer by promoting the production of cytokines and interferons …