Yi-Wen Lin

发表

Novel indolizino[8,7-b]indole hybrids as anti-small cell lung cancer agents: Regioselective modulation of topoisomerase II inhibitory and DNA crosslinking activities.

M. Hwang, Tai-Lin Chen, Te-Chang Lee, 2017, European journal of medicinal chemistry.

Doubly ortho-linked quinoxaline/triarylamine hybrid as a bifunctional, dipolar electroluminescent template for optoelectronic applications.

Y. Tao, Chien-Tien Chen, Chin-Hsiung Chien, 2005, Chemical communications.

Site-selective DNA photocleavage involving unusual photoinitiated tautomerization of chiral tridentate vanadyl(V) complexes derived from N-salicylidene alpha-amino acids.

P. Chou, Jen-Kan Yu, Chien-Tien Chen, 2004, Organic letters.

Synthesis and in vitro cytotoxicity of 9-anilinoacridines bearing N-mustard residue on both anilino and acridine rings.

T. Chou, R. Kakadiya, Ching-Huang Chen, 2009, European journal of medicinal chemistry.

A novel hexanuclear iron(III) complex containing three-coordination symmetries with two bridging μ-alkoxo groups, two μ3-oxo and four μ-catecholato bridges

Jian-Wei Lu, Ho‐Hsiang Wei, Yi-Wen Lin, 2008 .

Design and Synthesis of 1,2-Bis(hydroxymethyl)pyrrolo[2,1- a]phthalazine Hybrids as Potent Anticancer Agents that Inhibit Angiogenesis and Induce DNA Interstrand Cross-links.

Tai-Lin Chen, Te-Chang Lee, Han‐Chung Wu, 2019, Journal of medicinal chemistry.

Discovery of Oral Anticancer 1,2-Bis(hydroxymethyl)benzo[g]pyrrolo[2,1-a]phthalazine Hybrids That Inhibit Angiogenesis and Induce DNA Cross-Links.

Tai-Lin Chen, Te-Chang Lee, M. Hou, 2021, Journal of medicinal chemistry.

Potent antitumor 9-anilinoacridines and acridines bearing an alkylating N-mustard residue on the acridine chromophore: synthesis and biological activity.

T. Chou, Leroy F. Liu, Ching-Huang Chen, 2006, Journal of Medicinal Chemistry.

Novel oxidative nitrogen to carbon rearrangement found in the conversion of anilines to benzaldoximes by treating with HCHO/H2O2

R. Kakadiya, Ching-Huang Chen, T. Su, 2008 .

Design, synthesis and antitumour evaluation of pyrrolo[1,2-f]-phenanthridine and dibenzo[f,h]pyrrolo[1,2-b]isoquinoline derivatives.

K. Lai, Te-Chang Lee, Vaikar Navakanth Rao, 2020, European journal of medicinal chemistry.

New analogues of AHMA as potential antitumor agents: synthesis and biological activity.

Shu-Yun Cheng, Jang-Yang Chang, Li-Tzong Chen, 2003, Bioorganic & medicinal chemistry.

Novel Oxidative Nitrogen to Carbon Rearrangement Found in the Conversion of Anilines to Benzaldoximes by Treating with HCHO/H2O2.

R. Kakadiya, Ching-Huang Chen, T. Su, 2008 .

Synthesis of new tetracyclic 7-oxo-pyrido[3,2,1-de]acridine derivatives

Te-Chang Lee, Amit Kumar, R. Kakadiya, 2011 .

Derivatives of 6-cinnamamido-quinoline-4-carboxamide impair lysosome function and induce apoptosis

L. Yih, Yi-Chen Wu, Te-Chang Lee, 2016, Oncotarget.

Potent antitumor N-mustard derivatives of 9-anilinoacridine, synthesis and antitumor evaluation.

T. Chou, Ting-Chao Chou, Ching-Huang Chen, 2004, Bioorganic & medicinal chemistry letters.

Potent antitumor 9-anilinoacridines bearing an alkylating N-mustard residue on the anilino ring: synthesis and biological activity.

Xiuguo Zhang, T. Chou, Leroy F. Liu, 2005, Bioorganic & medicinal chemistry.

A Potent Derivative of Indolizino[6,7-b]Indole for Treatment of Human Non–Small Cell Lung Cancer Cells12

T. Tsai, Te-Chang Lee, S. Tala, 2016, Neoplasia.

A Low-Toxicity DNA-Alkylating N-Mustard-Quinoline Conjugate with Preferential Sequence Specificity Exerts Potent Antitumor Activity Against Colorectal Cancer

Tai-Lin Chen, Te-Chang Lee, Jing-Jer Lin, 2017, Neoplasia.

Design and synthesis of potent antitumor water-soluble phenyl N-mustard-benzenealkylamide conjugates via a bioisostere approach.

T. Tsai, Te-Chang Lee, S. Tala, 2014, European journal of medicinal chemistry.

Synthesis and antitumor activity of 5-(9-acridinylamino)anisidine derivatives.

T. Chou, Jang-Yang Chang, Ching-Huang Chen, 2005, Bioorganic & medicinal chemistry.

Teaghrelins, unique acylated flavonoid tetraglycosides in Chin-shin oolong tea, are putative oral agonists of the ghrelin receptor.

Maw-rong Lee, Chi-I Chang, J. Tzen, 2014, Journal of agricultural and food chemistry.