Recent discovery of indoleamine-2, 3-dioxygenase 1 inhibitors targeting cancer immunotherapy

T Weng, X Qiu, J Wang, Z Li, J Bian - European Journal of Medicinal …, 2018 - Elsevier
There has been great attention on indoleamine-2, 3-dioxygenase 1 (IDO1) around cancer
immunotherapy because of its role in enabling cancers to evade the immune system. The …

Design and Synthesis of some new 2, 4, 6-trisubstituted quinazoline EGFR inhibitors as targeted anticancer agents

HA Allam, EE Aly, AK Farouk, AM El Kerdawy… - Bioorganic …, 2020 - Elsevier
The present study describes the synthesis of 6-bromo-2-(pyridin-3-yl)-4-substituted
quinazolines starting from 4-chloro derivative VI via the reaction with either phenolic …

Heme-containing enzymes and inhibitors for tryptophan metabolism

D Yan, YW Lin, X Tan - Metallomics, 2017 - academic.oup.com
Iron-containing enzymes such as heme enzymes play crucial roles in biological systems.
Three distinct heme-containing dioxygenase enzymes, tryptophan 2, 3-dioxygenase (TDO) …

Design, synthesis and biological evaluation of indole-2-carboxylic acid derivatives as IDO1/TDO dual inhibitors

G Cui, F Lai, X Wang, X Chen, B Xu - European Journal of Medicinal …, 2020 - Elsevier
Abstract Indoleamine 2, 3-dioxygenase 1 (IDO1) and tryptophan 2, 3-dioxygenase (TDO) are
involved in the key steps of tryptophan metabolism and are potential new targets for tumor …

Electrochemical Oxidation of Indoles to Access Tryptanthrins at Room Temperature

Z Guo, Y Liu, H Li, J Wu, M Xie… - Advanced Synthesis & …, 2024 - Wiley Online Library
An electrooxidative reconstruction of the indole core under ambient conditions is reported,
resulting in the construction of tryptanthrins. This electrochemical strategy simplifies …

Novel tryptanthrin hybrids bearing aminothiazoles as potential EGFR inhibitors: Design, synthesis, biological screening, molecular docking studies, and ADME/T …

R Palabindela, R Guda, G Ramesh… - Journal of …, 2022 - Wiley Online Library
A variety of novel tryptanthrin aminothiazole analogues 3a‐h and 5a‐h possessing a
biologically active thiazole moiety were synthesized by the reaction of tryptanthrin …

Visible Light‐Induced Radical‐Radical Coupling: One‐Pot Synthesis of 6‐Benzyl‐6‐hydroxyindolo[2,1‐b]quinazolin‐12(6H)‐ones from Isatins and Potassium …

LQ Huang, CL Dong, YH He… - Advanced Synthesis & …, 2022 - Wiley Online Library
A method for one‐pot synthesis of 6‐benzyl‐6‐hydroxyindolo [2, 1‐b] quinazolin‐12 (6H)‐
ones from isatins and potassium benzyl trifluoroborates was developed. Bioactive …

[HTML][HTML] EGFR, HER2 target based molecular docking analysis, in vitro screening of 2, 4, 5-trisubstituted imidazole derivatives as potential anti-oxidant and cytotoxic …

R Guda, G Kumar, R Korra, S Balaji, G Dayakar… - … of Photochemistry and …, 2017 - Elsevier
In our endeavor towards the development of potent molecules for cancer diseases, we have
designed and synthesized a series of 2, 4, 5-trisubstituted imidazole derivatives (B1–B24) …

Synthesis, structural, spectroscopic, anti-cancer and molecular docking studies on novel 2-[(Anthracene-9-ylmethylene) amino]-2-methylpropane-1, 3-diol using XRD …

P Pavitha, J Prashanth, G Ramu, G Ramesh… - Journal of Molecular …, 2017 - Elsevier
Abstract The novel titled compound 2-[(Anthracene-9-ylmethylene) amino]-2-methylpropane-
1, 3-diol (AMD) has been synthesized by slow evaporation technique from mixed solvent …

Expeditious Approach to Indoloquinazolinones via Double Annulations of o-Aminoacetophenones and Isocyanates

Y Ding, H Yan, R Chen, X Xiao, Z Wang… - The Journal of …, 2020 - ACS Publications
A novel procedure for a one-pot cascade reaction of o-aminoacetophenones and
aryl/aliphatic isocyanates catalyzed/oxidized by the [Pd]/[Ag] system was developed. The …