Tai‐Chi Wang

发表

A New Indole Alkaloid and Anti‐Inflammatory Constituents from Strychnos cathayensis

P. Sung, T. Hwang, Tai-Chi Wang, 2008, Chemistry & biodiversity.

Synthesis and cytotoxic and antiplatelet activities of dibenzofuran- and carbazole-substituted oximes

I.-Li Chen, C. Liao, D. Kuo, 2004 .

Synthesis of Coumarin Derivatives as Inhibitors of Platelet Aggregation

C. Tzeng, Yeh-long Chen, C. Teng, 1996 .

Phthalides from Pittosporum illicioides var. illicioides with inhibitory activity on superoxide generation and elastase release by neutrophils.

T. Hwang, I. Chen, Jih-Jung Chen, 2008, Journal of natural products.

Synthesis and antibacterial activity of 1‐(substituted‐benzyl)‐6‐fluoro‐1,4‐dihydro‐4‐oxoquinoline‐3‐carboxylic acids and their 6,8‐difluoro analogs

C. Tzeng, Yeh-long Chen, J. Sheu, 1998 .

Synthesis, and Antimycobacterial and Cytotoxic Evaluation of Certain Fluoroquinolone Derivatives

C. Tzeng, Yeh-long Chen, S. Hsu, 2003 .

Geiparvarin Analogues: Synthesis and Anticancer Evaluation of α‐Methylidene‐γ‐butyrolactone‐Bearing Coumarins.

C. Tzeng, Yeh-long Chen, N. Chang, 1999 .

Synthesis, antiproliferative, and vasorelaxing evaluations of coumarin α-methylene-γ-butyrolactones

C. Tzeng, Yeh-long Chen, Chih-Ming Lu, 2005 .

Synthesis and Cytotoxic Evaluation of a Series of γ-Substituted γ-Aryloxymethyl-α-methylene-γ-butyrolactones Against Cancer Cells

Yeh-long Chen, Kuan-Han Lee, Chein-Hwa Han, 2000, Pharmaceutical Research.

α-Methylene-γ-butyrolactones : Synthesis and Vasorelaxing Activity Assay of Coumarin, Naphthalene, and Quinoline Derivatives

C. Tzeng, Yeh-long Chen, C. Teng, 1998 .

Synthesis and Evaluation of Coumarin α-Methylene-γ-butyrolactones : A New Class of Platelet Aggregation Inhibitors

C. Tzeng, Yeh-long Chen, C. Teng, 1996 .

Synthesis and Evaluation of α‐Methylidene‐γ‐butyrolactone bearing flavone and xanthone moieties

C. Tzeng, Yeh-long Chen, C. Teng, 1997 .

Synthesis and Evaluation of 2‐{[(2‐Oxo‐1H‐quinolin‐8‐yl)oxy]methyl}‐Substituted α‐Methylidene‐γ‐butyrolactones

C. Tzeng, Yeh-long Chen, C. Teng, 1997 .

Geiparvarin Analogues: Synthesis and Anticancer Evaluation ofα-Methylidene-γ-butyrolactone-Bearing Coumarins

C. Tzeng, Yeh-long Chen, N. Chang, 1999 .

Synthesis and Cytotoxicity Evaluation of Certainα-Methylidene-γ-butyrolactones Bearing Coumarin, Flavone, Xanthone, Carbazole, and Dibenzofuran Moieties

C. Tzeng, Yeh-long Chen, I.-Li Chen, 2000 .

Synthesis and anticancer evaluation of certain 4-anilinofuro[2,3-b]quinoline and 4-anilinofuro[3,2-c]quinoline derivatives.

C. Tzeng, Yeh-long Chen, I.-Li Chen, 2005, European journal of medicinal chemistry.

Discovery of oxime-bearing naphthalene derivatives as a novel structural type of Nrf2 activators.

C. Tzeng, Yeh-long Chen, Ken-Ming Chang, 2015, Bioorganic & medicinal chemistry.

Synthesis, antiproliferative, and antiplatelet activities of oxime- and amide-containing quinolin-2(1H)-one derivatives.

Ken-Ming Chang, I.-Li Chen, Jih-Jung Chen, 2007, Bioorganic & medicinal chemistry.

Synthesis and antimycobacterial evaluation of certain fluoroquinolone derivatives.

C. Tzeng, Yeh-long Chen, Tai-Chi Wang, 2005, Bioorganic & medicinal chemistry.

Novel oxime-bearing coumarin derivatives act as potent Nrf2/ARE activators in vitro and in mouse model.

C. Tzeng, Yeh-long Chen, C. Shih, 2015, European journal of medicinal chemistry.

Synthesis and vasorelaxing evaluation of α-methylidene-γ-butyrolactone bearing quinolin-2(1H)-one and 3,4-dihydroquinolin-2(1H)-one derivatives

D. Kuo, Yue Zhao, Tai‐Chi Wang, 2001 .

α‐Methylidene‐γ‐butyrolactones: Synthesis and evaluation of quinolin‐2(1H)‐one derivatives

C. Tzeng, Yeh-long Chen, C. Teng, 1998 .

Antiplatelet α‐Methylidene‐γ‐butyrolactones: Synthesis and evaluation of quinoline, flavone, and xanthone derivatives

C. Tzeng, Yeh-long Chen, C. Teng, 1996 .

Synthesis, and Cytotoxic and Antiplatelet Activities of Oxime‐ and Methyloxime‐Containing Flavone, Isoflavone, and Xanthone Derivatives

I.-Li Chen, C. Liao, D. Kuo, 2005, Chemistry & biodiversity.

Aluminium Chloride‐Catalyzed Intermolecular vs Intramolecular Friedel‐Crafts Reaction of Acrylanilides and 3‐Chloropropanamides

C. Tzeng, Yeh-long Chen, I.-Li Chen, 2000 .

Synthesis and antiproliferative evaluation of amide-containing flavone and isoflavone derivatives.

Tai-Chi Wang, I.-Li Chen, Jih-Jung Chen, 2008, Bioorganic & medicinal chemistry.

Synthesis, antiproliferative, and antiplatelet activities of oxime- and methyloxime-containing flavone and isoflavone derivatives.

C. Tzeng, Yeh-long Chen, P. Lu, 2005, Bioorganic & medicinal chemistry.

New Labdane-Type Diterpenoids and Anti-Inflammatory Constituents from Hedychium coronarium

P. Sung, T. Hwang, Tai-Chi Wang, 2013, International journal of molecular sciences.

Gmelinoiridoside, a New Iridoid Glycoside from Gmelina philippensis

Yun-Ping Lim, P. Sung, Tsung-Hsien Chang, 2014, Chemistry of Natural Compounds.

A new phragmalin-type limonoid and anti-inflammatory constituents from the fruits of Swietenia macrophylla

P. Sung, Tai-Chi Wang, M. Cheng, 2010 .

Thymol, benzofuranoid, and phenylpropanoid derivatives: anti-inflammatory constituents from Eupatorium cannabinum.

T. Hwang, Jih-Jung Chen, Yun-Chen Tsai, 2011, Journal of natural products.

Synthesis and antiproliferative evaluation of oxime, methyloxime, and amide‐containing quinazolinones

C. Tzeng, Ken-Ming Chang, Li-Chai Chen, 2018 .

Synthesis and Cytotoxic Evaluation of Certain 4‐(Phenylamino)furo[2,3‐b]quinoline and 2‐(Furan‐2‐yl)‐4‐(phenylamino)quinoline Derivatives

C. Tzeng, Yue Zhao, Tai‐Chi Wang, 2005, Chemistry & biodiversity.

Synthesis and antiproliferative activities of N-(naphthalen-2-yl)acetamide and N-(substituted phenyl)acetamide bearing quinolin-2(1H)-one and 3,4-dihydroquinolin-2(1H)-one derivatives.

Jih-Jung Chen, S. Juang, Yu‐Chin Lin, 2013, European journal of medicinal chemistry.

Synthesis, Antiproliferative, and Antiplatelet Activities of Oxime‐Containing 3,4‐Dihydroquinolin‐2(1H)‐One Derivatives

C. Liao, Li-Chai Chen, Jhy-Yih Chen, 2010 .

An intermolecular Michael addition of benzene

C. Tzeng, K. Lee, Tai‐Chi Wang, 1996 .

(+)-(6aR,7R)-7-Hydroxy-N-Butyrylcaaverine, a New Aporphine Alkaloid from the Roots of Illigera luzonensis with Cytotoxic Activity

Yun-Ping Lim, P. Sung, I. Chen, 2015, Chemistry of Natural Compounds.

A New Benzenoid and Anti-Inflammatory Constituent of Capparis acutifolia

Y. Kuo, Yun-Ping Lim, P. Sung, 2017, Chemistry of Natural Compounds.

New Pterosin Sesquiterpenes and Antitubercular Constituents from Pteris ensiformis

P. Sung, I. Chen, M. Cheng, 2013, Chemistry & biodiversity.

New Pterosin Sesquiterpenes and Antitubercular Constituents from Pteris ensiformis.

P. Sung, I. Chen, M. Cheng, 2014 .

The Combi-Targeting Concept: Dissection of the Binary Mechanism of Action of the Combi-Triazene SMA41 in Vitro and Antitumor Activity in Vivo

B. Jean-Claude, J. Mcnamee, A. Tari, 2004, Journal of Pharmacology and Experimental Therapeutics.

α-Methylene-γ-butyrolactones: Synthesis and Vasorelaxing Activity Assay of Coumarin, Naphthalene, and Quinoline Derivatives.

C. Tzeng, C. Teng, Ya-Ling Chang, 1998 .

A New 2H-Pyran-2-One Derivative and Anti-inflammatory Constituents of Alpinia zerumbet

Yun-Ping Lim, P. Sung, Chih-Wen Shu, 2017, Chemistry of Natural Compounds.

A New Benzenoid and Anti-Inflammatory Constituent of Capparis acutifolia

Y. Kuo, Yun-Ping Lim, P. Sung, 2017, Chemistry of Natural Compounds.

A new cytotoxic amide from the stem wood of Hibiscus tiliaceus.

Shi-Yu Huang, C. Duh, I. Chen, 2006, Planta medica.

STUDIES ON THE ALKYLATION OF QUINOLIN-2(1H)-ONE DERIVATIVES

C. Tzeng, Ken-Ming Chang, Jih-Jung Chen, 2015 .

WTC‐01, a novel synthetic oxime‐flavone compound, destabilizes microtubules in human nasopharyngeal carcinoma cells in vitro and in vivo

Chien-Shu Chen, Shih-Hao Wang, S. Juang, 2015, British journal of pharmacology.

Lewis Acid Catalyzed Reaction of Cinnamanilides: Competition of Intramolecular and Intermolecular Friedel-Crafts Reaction

C. Tzeng, K. Lee, Tai‐Chi Wang, 1997 .

Novel Nrf2/ARE activator, trans-Coniferylaldehyde, induces a HO-1-mediated defense mechanism through a dual p38α/MAPKAPK-2 and PK-N3 signaling pathway.

Wei-min Liu, C. Shih, T. Yeh, 2015, Chemical research in toxicology.