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 …

[HTML][HTML] Indole-based FLT3 inhibitors and related scaffolds as potential therapeutic agents for acute myeloid leukemia

HAA Ezelarab, TFS Ali, SH Abbas, HA Hassan… - BMC chemistry, 2023 - Springer
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 …

Discovery of trypanocidal coumarins with dual inhibition of both the glycerol kinase and alternative oxidase of Trypanosoma brucei brucei

EO Balogun, DK Inaoka, T Shiba, C Tsuge… - The FASEB …, 2019 - Wiley Online Library
African trypanosomiasis, sleeping sickness in humans or nagana in animals, is a potentially
fatal neglected tropical disease and a threat to 65 million human lives and 100 million small …

Facile synthesis of new N1-alkylated 1H-indazole-3-carboxamide derivatives as potential anticancer agents: In vitro, ADMET prediction, and SAR studies

S Puri, K Juvale - Journal of Molecular Structure, 2022 - Elsevier
This work is focused on the synthesis and characterization by spectroscopic methods of new
indazole compounds containing carboxamide and acetamido N-substituted moieties on C 3 …

Discovery of dual inhibitors of topoisomerase I and Cyclooxygenase-2 for colon cancer therapy

X Hu, J Li, H Zhang, Q Yu, Y Wang, X Li, L Long… - European Journal of …, 2022 - Elsevier
Novel tolfenamic acid derivatives based on the structure of I-1 were designed and
synthesized to improve its poor target inhibition and solubility. Among them, W10 was …

Palladium-catalyzed carbonylative synthesis of indole-3-carboxamides from 2-ethynylanilines and nitroarenes

J Zhang, S Wang, JS Wang, J Ying… - Organic Chemistry …, 2022 - pubs.rsc.org
A palladium-catalyzed carbonylative cyclization of 2-ethynylanilines with nitroarenes has
been developed for the rapid synthesis of indole-3-carboxamide skeletons. By using …

Chemoselective Cu-catalyzed synthesis of diverse N-arylindole carboxamides, β-oxo amides and N-arylindole-3-carbonitriles using diaryliodonium salts

MK Mehra, M Malik, B Kumar, D Kumar - Organic & Biomolecular …, 2021 - pubs.rsc.org
Chemoselective copper-catalyzed synthesis of diverse N-arylindole-3-carboxamides, β-oxo
amides and N-arylindole-3-carbonitriles from readily accessible indole-3-carbonitriles, α …

Multi‐target Fragments Display Versatile Binding Modes

MN Drwal, G Bret, E Kellenberger - Molecular Informatics, 2017 - Wiley Online Library
Promiscuity is an interesting concept in fragment‐based drug design as fragments with low
specificity can be advantageous for finding many screening hits. We present a PDB‐wide …

重氮化反应高效合成1H-吲唑-3-羧酸衍生物

徐长明, 黄金程 - 有机化学, 2021 - sioc-journal.cn
摘要报道了邻氨基苯乙酰胺和邻氨基苯乙酸酯在重氮化试剂作用下直接转化为对应的1H-吲唑-3-
羧酸衍生物. 该反应操作简单, 反应条件温和, 反应迅速, 产率高, 底物范围广, 为1H-吲唑-3 …

Highly Efficient Synthesis of 1H-Indazole-3-carboxylic Acid Derivatives via Diazotization Reaction

X Changming, H Jincheng - Chinese Journal of Organic Chemistry, 2021 - sioc-journal.cn
Direct conversion of ortho-aminobenzacetamides and ortho-aminobenzacetates to the
corresponding 1H-indazole-3-carboxylic acid derivatives under the action of diazotization …