Design, synthesis, and structure-activity relationships of evodiamine-based topoisomerase (Top)/histone deacetylase (HDAC) dual inhibitors

F Zhu, X Meng, H Liang, C Sheng, G Dong, D Liu… - Bioorganic …, 2022 - Elsevier
On the basis of synergistic effect between topoisomerase (Top) and histone deacetylase
(HDAC) inhibitors, a series of novel evodiamine-based Top/HDAC dual inhibitors were …

Evodiamine and its role in chronic diseases

Q Tan, J Zhang - Drug Discovery from Mother Nature, 2016 - Springer
Evodiamine (EVO) is a major alkaloid compound extracted from the dry unripened fruit
Evodiae fructus (Evodia rutaecarpa Benth., Rutaceae). EVO has a variety of …

[HTML][HTML] EM23, A Natural Sesquiterpene Lactone from Elephantopus mollis, Induces Apoptosis in Human Myeloid Leukemia Cells through Thioredoxin- and Reactive …

H Li, M Li, G Wang, F Shao, W Chen, C Xia… - Frontiers in …, 2016 - frontiersin.org
Elephantopus mollis (EM) is a traditional herbal medicine with multiple pharmacological
activities. However, the efficacy of EM in treating human leukemia is currently unknown. In …

N (14)-substituted evodiamine derivatives as dual topoisomerase 1/tubulin-Inhibiting anti-gastrointestinal tumor agents

J Deng, L Long, X Peng, W Jiang, Y Peng… - European journal of …, 2023 - Elsevier
Gastrointestinal tumor is an important factor threatening human health. Natural product-
based drug discovery is a popular paradigm for expanding the chemical space and …

Biomimetic oxidative coupling cyclization enabling rapid construction of isochromanoindolenines

J Ye, Y Lin, Q Liu, D Xu, F Wu, B Liu, Y Gao… - Organic letters, 2018 - ACS Publications
Herein, we report a biomimetic oxidative coupling cyclization strategy for the highly efficient
functionalization of tetrahydrocarbolines (THCs). This process enables rapid access to …

Discovery of novel tubulin inhibitors targeting the colchicine binding site via virtual screening, structural optimization and antitumor evaluation

W Liu, H Jia, M Guan, M Cui, Z Lan, Y He, Z Guo… - Bioorganic …, 2022 - Elsevier
The colchicine binding site of tubulin is a promising target for discovering novel antitumor
agents which exert the antiangiogenic effect and are not susceptible to multidrug resistance …

Design, synthesis and bioactivity evaluation of novel N-phenyl-substituted evodiamine derivatives as potent anti-tumor agents

X Hao, J Deng, H Zhang, Z Liang, F Lei, Y Wang… - Bioorganic & Medicinal …, 2022 - Elsevier
Natural products are important sources for the development of therapeutic medicine, among
which evodia fruit has a wide range of medicinal properties in traditional Chinese medicine …

A concise synthesis and biological study of evodiamine and its analogues

JD Deng, S Lei, Y Jiang, HH Zhang, XL Hu… - Chemical …, 2019 - pubs.rsc.org
Efficient access to evodiamine and its analogues is presented via Lewis acid catalysis. In
this reaction, three chemical bonds and two heterocyclic-fused rings are constructed in one …

Metal–free Decarboxylative Amination: An Alternative Approach Towards Regioselective Synthesis of β‐Carboline N‐fused Imidazoles

D Singh, V Kumar, N Devi, CC Malakar… - Advanced Synthesis …, 2017 - Wiley Online Library
Due to significant activity profile and natural abundance of β‐carboline containing alkaloids,
β‐carboline N‐fused imidazole derivatives were designed and iodine assisted efficient …

Antiproliferative activity and apoptosis inducing effects of nitric oxide donating derivatives of evodiamine

N Zhao, K Tian, K Cheng, T Han, X Hu, D Li, Z Li… - Bioorganic & Medicinal …, 2016 - Elsevier
The first series of nitric oxide donating derivatives of evodiamine were designed and
prepared. NO releasing ability of all target derivatives was evaluated in BGC-823, Bel-7402 …