Evodiamine: a review of its pharmacology, toxicity, pharmacokinetics and preparation researches

Q Sun, L Xie, J Song, X Li - Journal of Ethnopharmacology, 2020 - Elsevier
Ethnopharmacological relevance Evodia rutaecarpa, a well-known herb medicine in China,
is extensively applied in traditional Chinese medicine (TCM). The plant has the effects of …

Design, synthesis and biological evaluation of novel 5, 6, 7-trimethoxy-N-aryl-2-styrylquinolin-4-amines as potential anticancer agents and tubulin polymerization …

S Mirzaei, F Eisvand, F Hadizadeh, F Mosaffa… - Bioorganic …, 2020 - Elsevier
A new series of styrylquinolines was designed and synthesized as anticancer agents and
tubulin polymerization inhibitors. The in vitro anticancer activity of the synthesized quinolines …

Silver-catalyzed cascade cyclization reaction of isocyanides with sulfoxonium ylides: synthesis of 3-aminofurans and 4-aminoquinolines

YX Liang, M Yang, BW He, YL Zhao - Organic Letters, 2020 - ACS Publications
A silver-catalyzed cascade cyclization reaction of isocyanides with sulfoxonium ylides has
been developed for the first time. This reaction provides a new and efficient method for the …

[HTML][HTML] Evodiamine-inspired dual inhibitors of histone deacetylase 1 (HDAC1) and topoisomerase 2 (TOP2) with potent antitumor activity

Y Huang, S Chen, S Wu, G Dong, C Sheng - Acta Pharmaceutica Sinica B, 2020 - Elsevier
A great challenge in multi-targeting drug discovery is to identify drug-like lead compounds
with therapeutic advantages over single target inhibitors and drug combinations. Inspired by …

CF3SO2Na-Mediated, UV-Light-Induced Friedel–Crafts Alkylation of Indoles with Ketones/Aldehydes and Bioactivities of Products

T Yang, H Lu, Y Shu, Y Ou, L Hong, CT Au, R Qiu - Organic letters, 2020 - ACS Publications
A concise, one-step route to produce 3, 3′-diindolylmethanes (DIMs) from simple indoles
and ketones or aldehydes is reported. The key step is the ready formation of indole …

Discovery of evodiamine derivatives as highly selective PDE5 inhibitors targeting a unique allosteric pocket

T Zhang, Z Lai, S Yuan, YY Huang… - Journal of medicinal …, 2020 - ACS Publications
Clinical use of phosphodiesterase-5 (PDE5) inhibitors is limited by several side effects due
to weak isoform selectivity. Herein, a unique allosteric pocket of PDE5 is identified by …

[HTML][HTML] Evodiamine attenuates experimental colitis injury via activating autophagy and inhibiting NLRP3 inflammasome assembly

W Ding, Z Ding, Y Wang, Y Zhu, Q Gao… - Frontiers in …, 2020 - frontiersin.org
Autophagy and NLRP3 inflammasome were associated with the process of colitis. Drugs
targeting NLRP3 inflammasome and autophagy to treat colitis are absent, and they are …

Natural product Evodiamine with borate trigger unit: discovery of potent antitumor agents against colon cancer

X Li, S Wu, G Dong, S Chen, Z Ma, D Liu… - ACS Medicinal …, 2020 - ACS Publications
In order to improve the antitumor potency of the natural product evodiamine, novel boron-
containing evodiamine derivatives were designed by incorporating boronic acid and …

Iodine Catalysed Synthesis of Luminescent β‐Carboline Tethered Thiazolo[4,5‐c]carbazole and Naphtho[2,1‐d]thiazole Derivatives and Estimation of their Light …

M Singh, P Awasthi, V Singh - European Journal of Organic …, 2020 - Wiley Online Library
A Simple, convenient and highly efficient I2‐catalysed approach has been unfolded towards
the synthesis of highly fluorescent β‐carboline C‐1 (3)‐tethered thiazolo [4, 5‐c] carbazoles …

Recent Advance on the Synthesis of 3, 3'-Bisindolylmethane Derivatives under Transition-Metal-Free Catalytic Conditions

Z Zhenguo, L Xiaoxiao, Z Xinlong, Y Yalin… - Chinese Journal of …, 2020 - sioc-journal.cn
Bisindolylmethanes (3, 3'-BIMs) compounds are important indole alkyloads and their units
are widely found in various natural products, functional materials and synthetic …