Small-molecule fms-like tyrosine kinase 3 inhibitors: an attractive and efficient method for the treatment of acute myeloid leukemia
Y Zhong, RZ Qiu, SL Sun, C Zhao, TY Fan… - Journal of medicinal …, 2020 - ACS Publications
Fms-like tyrosine kinase 3 (FLT3) is an important member of the class III receptor tyrosine
kinase (RTK) family, which is involved in the proliferation of hematopoietic cells and …
kinase (RTK) family, which is involved in the proliferation of hematopoietic cells and …
[HTML][HTML] Indole-based FLT3 inhibitors and related scaffolds as potential therapeutic agents for acute myeloid leukemia
Fms-like tyrosine kinase 3 (FLT3) mutation mechanisms are among the most common
genetic abnormalities detected in about 30% of acute myeloid leukemia (AML) patients …
genetic abnormalities detected in about 30% of acute myeloid leukemia (AML) patients …
Design, synthesis, and biological evaluation of carbonyl-hydrazine-1-carboxamide derivatives as anti-hepatic fibrosis agents targeting Nur77
H Hu, G Lin, F He, J Liu, R Jia, K Li, W Hong, M Fang… - Bioorganic …, 2023 - Elsevier
Hepatic fibrosis remains a great challenge clinically. The orphan nuclear receptor Nur77 is
recently suggested as the critical regulator of transforming growth factor-β (TGF-β) signaling …
recently suggested as the critical regulator of transforming growth factor-β (TGF-β) signaling …
[HTML][HTML] The MNK1/2-eIF4E axis as a potential therapeutic target in melanoma
SA Prabhu, O Moussa, WH Miller Jr… - International Journal of …, 2020 - mdpi.com
Melanoma is a type of skin cancer that originates in the pigment-producing cells of the body
known as melanocytes. Most genetic aberrations in melanoma result in hyperactivation of …
known as melanocytes. Most genetic aberrations in melanoma result in hyperactivation of …
In silico approach of novel HPPD/PDS dual target inhibitors by pharmacophore, AILDE and molecular docking
J Shi, HF Cao, CF Wang, S Gao, JY Wang… - Journal of the Taiwan …, 2023 - Elsevier
Background Phytoene dehydrogenase (PDS) and p-hydroxyphenylpyruvate dioxygenase
(HPPD) are two important herbicides targets in photosynthesis. If inhibiting the activity of …
(HPPD) are two important herbicides targets in photosynthesis. If inhibiting the activity of …
The MAP kinase-interacting kinases (MNKs) as targets in oncology
Introduction: The mitogen-activated protein kinase (MAPK)-interacting kinases (MNKs) are
switched on by the oncogenic MAPK (ERK) signalling pathway. They phosphorylate …
switched on by the oncogenic MAPK (ERK) signalling pathway. They phosphorylate …
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 …
and differentiation of hematopoietic stem cells. Although the pathogenesis has not been fully …
[HTML][HTML] An orally bioavailable and highly efficacious inhibitor of CDK9/FLT3 for the treatment of acute myeloid leukemia
AT Anshabo, L Bantie, S Diab, J Lenjisa, A Kebede… - Cancers, 2022 - mdpi.com
Simple Summary CDDD11-8 is an orally bioactive pharmacological inhibitor of CDK9. In
AML cells, CDDD11-8 suppressed the proliferation and caused robust inhibition of tumor …
AML cells, CDDD11-8 suppressed the proliferation and caused robust inhibition of tumor …
[HTML][HTML] Identification of a dual FLT3 and MNK2 inhibitor for acute myeloid leukemia treatment using a structure-based virtual screening approach
Fms-like tyrosine kinase 3 (FLT3) is considered a promising therapeutic target for acute
myeloid leukemia (AML) in the clinical. However, monotherapy with FLT3 inhibitor is usually …
myeloid leukemia (AML) in the clinical. However, monotherapy with FLT3 inhibitor is usually …
Design, synthesis and activity of Mnk1 and Mnk2 selective inhibitors containing thieno [2, 3-d] pyrimidine scaffold
The mitogen-activated protein kinase-interacting kinases 1 and 2 (MNK1 and MNK2)
phosphorylate eukaryotic initiation factor 4E (eIF4E) and play important roles in promoting …
phosphorylate eukaryotic initiation factor 4E (eIF4E) and play important roles in promoting …