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Xenobiotica; the Fate of Foreign Compounds in Biological Systems|September 20, 2023
Two curcumin analogs inhibited the function and protein expression of breast cancer resistance protein: <i>in vitro</i> and <i>in vivo</i> studiesChung-Ping Yu, Yi-Ru Wang, Yu-Chi Hou, et al.
Chemical Biology & Drug Design|May 9, 2024
4,4-Diallyl curcumin bis(2,2-hydroxymethyl)propanoate ameliorates nonalcoholic steatohepatitis in methionine-choline-deficient diet and Western diet mouse modelsLi-Chan Yang, Chih-Chiang Wang, Der-Yen Lee, et al.
Bioorganic & Medicinal Chemistry|June 18, 2018
Synthesis and antitumor activity of bis(hydroxymethyl)propionate analogs of pterostilbene in cisplatin-resistant human oral cancer cellsMin-Tsang Hsieh, Li-Jiau Huang, Tian-Shung Wu, et al.
European Journal of Medicinal Chemistry|March 21, 2017
New bis(hydroxymethyl) alkanoate curcuminoid derivatives exhibit activity against triple-negative breast cancer in vitro and in vivoMin-Tsang Hsieh, Ling-Chu Chang, Hsin-Yi Hung, et al.
Oncology Reports|June 7, 2024
[Corrigendum] Next‑generation sequencing analysis reveals that MTH‑3, a novel curcuminoid derivative, suppresses the invasion of MDA‑MB‑231 triple‑negative breast adenocarcinoma cellsYu-Jen Chiu, Fuu-Jen Tsai, Da-Tian Bau, et al.
Molecules (Basel, Switzerland)|January 26, 2020
Synthesis, Anticancer Activity, and Preliminary Pharmacokinetic Evaluation of 4,4-Disubstituted Curcuminoid 2,2-bis(Hydroxymethyl)Propionate DerivativesDer-Yen Lee, Yu-Chi Hou, Jai-Sing Yang, et al.
Oncology Reports|May 20, 2021
Next‑generation sequencing analysis reveals that MTH‑3, a novel curcuminoid derivative, suppresses the invasion of MDA‑MB‑231 triple‑negative breast adenocarcinoma cellsYu-Jen Chiu, Fuu-Jen Tsai, Da-Tian Bau, et al.
The Journal of Organic Chemistry|March 18, 2016
Stereoselective Synthesis of Spiro Bis-C,C-α-arylglycosides by Tandem Heck Type C-Glycosylation and Friedel-Crafts CyclizationYen-Bo Chen, Shi-Hao Liu, Min-Tsang Hsieh, et al.
Journal of Medicinal Chemistry|July 26, 2019
Synthesis and Structure-Activity Relationship Correlations of Gnidimacrin Derivatives as Potent HIV-1 Inhibitors and HIV Latency Reversing AgentsQingbo Liu, Yung-Yi Cheng, Wei Li, et al.
Chemical Biology & Drug Design|December 30, 2025
Identification and Biological Evaluation of (4H-Thieno[3,2-b]indol-3-yl)methanol as a Tumoricidal Scaffold for an Antineoplastic AgentShi-Hong Zhuang, Yi-Han Chang, Hoang-Thuc Huynh, et al.
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