C. Kuo

发表

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.

Phenyl Benzenesulfonylhydrazides Exhibit Selective Indoleamine 2,3-Dioxygenase Inhibition with Potent in Vivo Pharmacodynamic Activity and Antitumor Efficacy.

Yi-Hui Peng, Y. Chao, Su-Ying Wu, 2016, Journal of medicinal chemistry.

MiR-30a and miR-379 modulate retinoic acid pathway by targeting DNA methyltransferase 3B in oral cancer

Hsuan-Yu Peng, Jang-Yang Chang, C. Kuo, 2020, Journal of Biomedical Science.

Antimitotic and vascular disrupting agents: 2-hydroxy-3,4,5-trimethoxybenzophenones.

T. Yeh, J. Liou, Jang-Yang Chang, 2014, European journal of medicinal chemistry.

Concise syntheses of 7-anilino-indoline-N-benzenesulfonamides as antimitotic and vascular disrupting agents.

Samir Mehndiratta, J. Liou, Jang-Yang Chang, 2014, Bioorganic & medicinal chemistry.

Furanylazaindoles: potent anticancer agents in vitro and in vivo.

Su-Ying Wu, Jian-Sung Wu, S. Pan, 2013, Journal of medicinal chemistry.

Synthesis and biological evaluation of 1-(4'-Indolyl and 6'-Quinolinyl) indoles as a new class of potent anticancer agents.

H. Hsieh, Su-Ying Wu, Jian-Sung Wu, 2011, European journal of medicinal chemistry.

2‐Amino‐3,4,5‐Trimethoxybenzophenones as Potent Tubulin Polymerization Inhibitors

H. Hsieh, J. Liou, Jang-Yang Chang, 2011, ChemMedChem.

5-Amino-2-aroylquinolines as highly potent tubulin polymerization inhibitors. Part 2. The impact of bridging groups at position C-2.

J. Liou, Jang-Yang Chang, C. Kuo, 2011, Journal of medicinal chemistry.

Concise syntheses of N-aryl-5,6,7-trimethoxyindoles as antimitotic and vascular disrupting agents: application of the copper-mediated Ullmann-type arylation.

J. Liou, Jang-Yang Chang, C. Kuo, 2011, Organic & biomolecular chemistry.

Synthesis and biological evaluation of 7-arylindoline-1-benzenesulfonamides as a novel class of potent anticancer agents

Yi-Ting Chang, Yun-Ching Cheng, J. Liou, 2010 .

5-Amino-2-aroylquinolines as highly potent tubulin polymerization inhibitors.

H. Hsieh, Su-Ying Wu, Yuxiang Chen, 2010, Journal of medicinal chemistry.

Synthesis and Structure–Activity Relationships of 1‐Benzyl‐4,5,6‐trimethoxyindoles as a Novel Class of Potent Antimitotic Agents

H. Hsieh, T. Yeh, J. Liou, 2009, ChemMedChem.

Synthesis and structure-activity relationships of 2-amino-1-aroylnaphthalene and 2-hydroxy-1-aroylnaphthalenes as potent antitubulin agents.

H. Hsieh, Su-Ying Wu, M. Coumar, 2008, Journal of medicinal chemistry.

Melatonin promotes neuroblastoma cell differentiation by activating hyaluronan synthase 3‐induced mitophagy

Y. Ho, C. Wu, Hui-Wen Chang, 2019, Cancer medicine.

MPT0B098, a Novel Microtubule Inhibitor That Destabilizes the Hypoxia-Inducible Factor-1α mRNA through Decreasing Nuclear–Cytoplasmic Translocation of RNA-Binding Protein HuR

J. T. Tseng, Yun-Ching Cheng, J. Liou, 2013, Molecular Cancer Therapeutics.

4-Ketopinoresinol, a novel naturally occurring ARE activator, induces the Nrf2/HO-1 axis and protects against oxidative stress-induced cell injury via activation of PI3K/AKT signaling.

Huang-Hui Chen, Yu-Tsen Chen, C. Kuo, 2012, Free radical biology & medicine.

Surface a -Enolase Promotes Extracellular Matrix Degradation and Tumor Metastasis and Represents a New Therapeutic Target

G. Chang, C. Kuo, Tze-Sing Huang, 2013 .

Combined modalities of resistance in an oxaliplatin-resistant human gastric cancer cell line with enhanced sensitivity to 5-fluorouracil

J. Chang, T. Tsou, C. Kuo, 2007, British Journal of Cancer.

Enhanced B‐Raf‐mediated NRF2 gene transcription and HATs‐mediated NRF2 protein acetylation contributes to ABCC1‐mediated chemoresistance and glutathione‐mediated survival in acquired topoisomerase II poison‐resistant cancer cells

C. Chen, Yung-chi Cheng, Chih-Hsiang Huang, 2017, Free radical biology & medicine.

Targeting cathepsin S induces tumor cell autophagy via the EGFR-ERK signaling pathway.

W. Chang, Jang-Yang Chang, C. Kuo, 2012, Cancer letters.

Application of Suzuki arylation, Sonogashira ethynylation and Rosenmund-von Braun cyanation in the exploration of substitution effects on the anticancer activity of 2-aroylquinolines.

J. Liou, Jang-Yang Chang, C. Kuo, 2012, Organic & biomolecular chemistry.

A Novel Oral Indoline-Sulfonamide Agent, N-[1-(4-Methoxybenzenesulfonyl)-2,3-dihydro-1H-indol-7-yl]-Isonicotinamide (J30), Exhibits Potent Activity against Human Cancer Cells in Vitro and in Vivo through the Disruption of Microtubule

J. Liou, Jang-Yang Chang, C. Kuo, 2007, Journal of Pharmacology and Experimental Therapeutics.

Unique sulfur-aromatic interactions contribute to the binding of potent imidazothiazole indoleamine 2,3-dioxygenase inhibitors.

Yi-Hui Peng, Su-Ying Wu, Jen‐Shin Song, 2020, Journal of medicinal chemistry.

A novel bis-benzylidenecyclopentanone derivative, BPR0Y007, inducing a rapid caspase activation involving upregulation of Fas (CD95/APO-1) and wild-type p53 in human oral epidermoid carcinoma cells.

H. Hsieh, J. Liou, Jang-Yang Chang, 2004, Biochemical pharmacology.

Suppression of allergic reactions by dehulled adlay in association with the balance of TH1/TH2 cell responses.

C. Kuo, Jin-Yuarn Lin, Bi-Fong Lin, 2003, Journal of agricultural and food chemistry.

188 POSTER Combined modalities of resistance in an oxaliplaitin-resistant human gastric cancer cell line with enhanced sensitivity

J. Chang, T. Tsou, C. Kuo, 2006 .

2-Aroylquinoline-5,8-diones as potent anticancer agents displaying tubulin and heat shock protein 90 (HSP90) inhibition.

T. Yeh, J. Liou, Jang-Yang Chang, 2016, Organic & biomolecular chemistry.

Antimitotic and antivascular activity of heteroaroyl-2-hydroxy-3,4,5-trimethoxybenzenes.

J. Liou, Jang-Yang Chang, C. Kuo, 2015, Bioorganic & medicinal chemistry.

Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents

J. Liou, Jang-Yang Chang, C. Kuo, 2011, Molecules.

4-Bromophenylhydrazinyl benzenesulfonylphenylureas as indoleamine 2,3-dioxygenase inhibitors with in vivo target inhibition and anti-tumor efficacy.

Y. Chao, Su-Ying Wu, Jen‐Shin Song, 2018, Bioorganic chemistry.

O6‐methylguanine DNA methyltransferase repairs platinum‐DNA adducts following cisplatin treatment and predicts prognoses of nasopharyngeal carcinoma

Huai-chih Chiang, T. Tsou, Chien-Feng Li, 2015, International journal of cancer.

Survivin counteracts the therapeutic effect of microtubule de-stabilizers by stabilizing tubulin polymers

H. Hsieh, M. Coumar, Huang-Hui Chen, 2009, Molecular Cancer.

Four new 6-nor5(6-->7)abeo-abietane type diterpenes and antitumoral cytotoxic diterpene constituents from the bark of Taiwania cryptomerioides.

Y. Kuo, Chi-I Chang, Jang-Yang Chang, 2005, Planta medica.

2-amino and 2'-aminocombretastatin derivatives as potent antimitotic agents.

J. Liou, Jang-Yang Chang, C. Kuo, 2006, Journal of medicinal chemistry.

Scaffold-hopping strategy: synthesis and biological evaluation of 5,6-fused bicyclic heteroaromatics to identify orally bioavailable anticancer agents.

H. Hsieh, C. Liao, Su-Ying Wu, 2011, Journal of medicinal chemistry.

Cytotoxic steroidal saponins from Agave sisalana.

Y. Kuo, C. Kuo, Tzong-Huei Lee, 2011, Planta medica.

Two new acidic diterpenoids from the heartwood of pinus massoniana LAMB.

Y. Kuo, Chi-I Chang, C. Kuo, 2014 .

Salvinal, a novel microtubule inhibitor isolated from Salvia miltiorrhizae Bunge (Danshen), with antimitotic activity in multidrug-sensitive and -resistant human tumor cells.

Y. Kuo, Jang-Yang Chang, C. Kuo, 2004, Molecular pharmacology.

Synthesis and evaluation of 3-aroylindoles as anticancer agents: metabolite approach.

H. Hsieh, C. Chen, Su-Ying Wu, 2009, Journal of medicinal chemistry.

Generation of ligand-based pharmacophore model and virtual screening for identification of novel tubulin inhibitors with potent anticancer activity.

Ping-Chiang Lyu, Mohane Selvaraj Coumar, Yu-Sheng Chao, 2009, Journal of medicinal chemistry.

4- and 5-aroylindoles as novel classes of potent antitubulin agents.

H. Hsieh, J. Liou, Jang-Yang Chang, 2007, Journal of medicinal chemistry.

Structure–Activity Relationship Studies of 3‐Aroylindoles as Potent Antimitotic Agents

Yi-Wei Chang, Hsing-Pang Hsieh, Uan-Kang Tan, 2006, ChemMedChem.

Discovery of 4-amino and 4-hydroxy-1-aroylindoles as potent tubulin polymerization inhibitors.

H. Hsieh, J. Liou, Jang-Yang Chang, 2008, Journal of medicinal chemistry.

Design and synthesis of alpha-ketoamides as cathepsin S inhibitors with potential applications against tumor invasion and angiogenesis.

P. Lyu, H. Hsieh, M. D. Chang, 2010, Journal of medicinal chemistry.

Tamoxifen accelerates proteasomal degradation of O6‐methylguanine DNA methyltransferase in human cancer cells

Jang-Yang Chang, Ching-Chuan Kuo, Jang-Yang Chang, 2007, International journal of cancer.

Cytotoxic triterpenes from the aerial roots of Ficus microcarpa.

Y. Kuo, Y. Chiang, Jang-Yang Chang, 2005, Phytochemistry.

Antimutagenic constituents of adlay (Coix lachryma-jobi L. var. ma-yuen Stapf) with potential cancer chemopreventive activity.

Y. Kuo, Huang-Hui Chen, Jang-Yang Chang, 2011, Journal of agricultural and food chemistry.

Effects of drying and extrusion on colour, chemical composition, antioxidant activities and mitogenic response of spleen lymphocytes of sweet potatoes

C. Kuo, M. Shih, W. Chiang, 2009 .

Two New Labdane‐Type Diterpene Acids from the Wood of Cunninghamia konishii

Y. Kuo, Chi-I Chang, C. Kuo, 2015 .

Diterpenoids from the Wood of Cunninghamia konishii

Y. Kuo, P. Sung, C. Kuo, 2013 .

Two New Lignans from the Wood of Cunninghamia konishii

Sheng-Yang Wang, Y. Kuo, Chi-I Chang, 2013 .

Chamaecypanone C, a novel skeleton microtubule inhibitor, with anticancer activity by trigger caspase 8-Fas/FasL dependent apoptotic pathway in human cancer cells.

Chi-Hung Lin, Y. Kuo, T. Chao, 2010, Biochemical pharmacology.

D-501036, a novel selenophene-based triheterocycle derivative, exhibits potent in vitro and in vivo antitumoral activity which involves DNA damage and ataxia telangiectasia–mutated nuclear protein kinase activation

Jang-Yang Chang, C. Kuo, C. Ashendel, 2007, Molecular Cancer Therapeutics.

Pilot Study: Nutritional and Preclinical Safety Investigation of Fermented Hispidin-Enriched Sanghuangporus sanghuang Mycelia: A Promising Functional Food Material to Improve Sleep

C. Kuo, Tsung-Ju Li, Chin-Chu Chen, 2022, Frontiers in Nutrition.

Cytotoxic and novel skeleton compounds from the heartwood of Chamaecyparis obtusa var. formosana.

Y. Kuo, N. Yang, Jang-Yang Chang, 2007 .

Arecoline arrests cells at prometaphase by deregulating mitotic spindle assembly and spindle assembly checkpoint: implication for carcinogenesis.

Ka-Wo Lee, Y. Jong, Chang-Shen Lin, 2010, Oral oncology.

2,2'-Diphenyl-1-picrylhydrazyl radical-scavenging active components from adlay (Coix lachryma-jobi L. var. ma-yuen Stapf) hulls.

Y. Kuo, Jang-Yang Chang, C. Kuo, 2002, Journal of agricultural and food chemistry.

Two new chromones and a new coumarin from the fruit of Cnidium monnieri (L.) Cusson

Guan-Jhong Huang, Y. Kuo, C. Kuo, 2021, Natural product research.

Discovery and development of a novel N-(3-bromophenyl)-{[(phenylcarbamoyl)amino]methyl}-N-hydroxythiophene-2-carboximidamide indoleamine 2,3-dioxygenase inhibitor using knowledge-based drug design.

Yi-Hui Peng, Su-Ying Wu, Jen‐Shin Song, 2021, European journal of medicinal chemistry.

Antagonism of free-radical-induced damage of adlay seed and its antiproliferative effect in human histolytic lymphoma U937 monocytic cells.

Y. Kuo, C. Kuo, M. Shih, 2001, Journal of agricultural and food chemistry.

Two new diprenylated flavanones from Derris laxiflora Benth

Y. Kuo, C. Kuo, M. Cheng, 2019, Natural product research.

Adlay (薏苡 yì yĭ; “soft-shelled job's tears”; the seeds of Coix lachryma-jobi L. var. ma-yuen Stapf) is a Potential Cancer Chemopreventive Agent toward Multistage Carcinogenesis Processes

C. Kuo, W. Chiang, Huang‐Hui Chen, 2012, Journal of traditional and complementary medicine.

Three new oleanane-type triterpenes from Ludwigia octovalvis with cytotoxic activity against two human cancer cell lines.

Y. Kuo, Chi-I Chang, Jang-Yang Chang, 2004, Journal of natural products.

Drug repurposing for chronic myeloid leukemia: in silico and in vitro investigation of DrugBank database for allosteric Bcr-Abl inhibitors

H. Hsieh, M. Coumar, V. Singh, 2017, Journal of biomolecular structure & dynamics.

7-Aroyl-aminoindoline-1-sulfonamides as a novel class of potent antitubulin agents.

H. Hsieh, J. Liou, Jang-Yang Chang, 2006, Journal of medicinal chemistry.

BPR0L075, a Novel Synthetic Indole Compound with Antimitotic Activity in Human Cancer Cells, Exerts Effective Antitumoral Activity in Vivo

H. Hsieh, C. Chen, Shiow-Ju Lee, 2004, Cancer Research.

c-MYC-directed NRF2 drives malignant progression of head and neck cancer via glucose-6-phosphate dehydrogenase and transketolase activation

S. Jiang, Y. Chuang, Su-Fang Lin, 2021, Theranostics.

Analgesic and anti-inflammatory bioactivities of eburicoic acid and dehydroeburicoic acid isolated from Antrodia camphorata on the inflammatory mediator expression in mice.

Guan-Jhong Huang, Y. Kuo, W. Hou, 2013, Journal of agricultural and food chemistry.

A novel peroxisome proliferator-activated receptor &agr;/&ggr; agonist, BPR1H0101, inhibits topoisomerase II catalytic activity in human cancer cells

H. Hsieh, S. Chuang, Jang-Yang Chang, 2008, Anti-cancer drugs.

A novel NRF2/ARE inhibitor gossypol induces cytotoxicity and sensitizes chemotherapy responses in chemo-refractory cancer cells

Y. Chuang, Yu-Tsen Chen, Hsin-Huei Chang, 2021, Journal of food and drug analysis.

Gene expression profiling for analysis acquired oxaliplatin resistant factors in human gastric carcinoma TSGH-S3 cells: the role of IL-6 signaling and Nrf2/AKR1C axis identification.

Chi-Ying F. Huang, Miao-Fen Chen, Kuan-Der Lee, 2013, Biochemical pharmacology.

Hypoxia-Induced Downregulation of DUSP-2 Phosphatase Drives Colon Cancer Stemness.

S. Tsai, H. Sun, J. Liou, 2017, Cancer research.

Type-3 Hyaluronan Synthase Attenuates Tumor Cells Invasion in Human Mammary Parenchymal Tissues

Y. Ho, C. Wu, Li‐Ching Chen, 2021, Molecules.

Histone deacetylase inhibition improved cardiac functions with direct antifibrotic activity in heart failure.

Shih-Ann Chen, Yu-Hsun Kao, Yi-Jen Chen, 2013, International journal of cardiology.

ERK Activation Modulates Cancer Stemness and Motility of a Novel Mouse Oral Squamous Cell Carcinoma Cell Line

C. Kuo, Ko-Jiunn Liu, T. Chuang, 2019, Cancers.

MPT0B098, a Microtubule Inhibitor, Suppresses JAK2/STAT3 Signaling Pathway through Modulation of SOCS3 Stability in Oral Squamous Cell Carcinoma

Hsuan-Yu Peng, Shiow-Lian Catherine Jin, J. Liou, 2016, PloS one.

Novel microtubule inhibitor MPT0B098 inhibits hypoxia-induced epithelial-to-mesenchymal transition in head and neck squamous cell carcinoma

J. Liou, Jang-Yang Chang, C. Kuo, 2018, Journal of Biomedical Science.

Heart failure and angiotensin II modulate atrial Pitx2c promotor methylation

Shih‐Ann Chen, Yi‐Jen Chen, C. Kuo, 2013, Clinical and experimental pharmacology & physiology.

Discovery of BPR1K871, a quinazoline based, multi-kinase inhibitor for the treatment of AML and solid tumors: Rational design, synthesis, in vitro and in vivo evaluation

Yung Chang Hsu, C. Chen, J. Hsu, 2016, Oncotarget.

Xanthine Derivatives Reveal an Allosteric Binding Site in Methylenetetrahydrofolate Dehydrogenase 2 (MTHFD2)

Yi-Hui Peng, Su-Ying Wu, T. Hsu, 2021, Journal of medicinal chemistry.

Transcriptional Repression of O6-Methylguanine DNA Methyltransferase Gene Rendering Cells Hypersensitive to N,N′-Bis(2-chloroethyl)-N-nitrosurea in Camptothecin-Resistant Cells

Jang-Yang Chang, C. Kuo, Li‐Tzong Chen, 2008, Molecular Pharmacology.

Arginine deprivation as a new treatment strategy for head and neck cancer.

Jang-Yang Chang, C. Kuo, Jeffrey S. Chang, 2012, Oral oncology.

DNA Repair Enzyme, O6-Methylguanine DNA Methyltransferase, Modulates Cytotoxicity of Camptothecin-Derived Topoisomerase I Inhibitors

Jang-Yang Chang, C. Kuo, Jin-Fen Liu, 2006, Journal of Pharmacology and Experimental Therapeutics.

Desferal regulates hCtr1 and transferrin receptor expression through Sp1 and exhibits synergistic cytotoxicity with platinum drugs in oxaliplatin-resistant human cervical cancer cells in vitro and in vivo

T. Tsou, Jang-Yang Chang, C. Kuo, 2016, Oncotarget.

Design, Synthesis, and Evaluation of Thiazolidine-2,4-dione Derivatives as a Novel Class of Glutaminase Inhibitors.

C. Chen, Szu-Huei Wu, Jen‐Shin Song, 2017, Journal of medicinal chemistry.

Aconitamide, a Novel Alkaloid from the Roots of Aconitum carmichaeli

Y. Kuo, L. Lo, Jing-Jer Lin, 2013 .

Azaindolylsulfonamides, with a more selective inhibitory effect on histone deacetylase 6 activity, exhibit antitumor activity in colorectal cancer HCT116 cells.

S. Pan, T. Yeh, J. Liou, 2014, Journal of medicinal chemistry.

Tea polyphenol epigallocatechin-3-gallate inhibits cell proliferation in a patient-derived triple-negative breast cancer xenograft mouse model via inhibition of proline-dehydrogenase-induced effects

Y. Ho, Hui-Wen Chang, Li‐Ching Chen, 2021, Journal of food and drug analysis.

Identification of a Multitargeted Tyrosine Kinase Inhibitor for the Treatment of Gastrointestinal Stromal Tumors (GISTs) and Acute Myeloid Leukemia (AML).

Yi-Hui Peng, C. Chen, Su-Ying Wu, 2019, Journal of medicinal chemistry.

Identification of a Multitargeted Tyrosine Kinase Inhibitor for the Treatment of Gastrointestinal Stromal Tumors and Acute Myeloid Leukemia.

Yi-Hui Peng, C. Chen, Su-Ying Wu, 2019 .

Synthesis and Structure–Activity Relationship of Salvinal Derivatives as Potent Microtubule Inhibitors

Chi-I Chang, J. Cherng, J. Lung, 2023, International journal of molecular sciences.

Mechanistic basis of a combination D-penicillamine and platinum drugs synergistically inhibits tumor growth in oxaliplatin-resistant human cervical cancer cells in vitro and in vivo.

T. Tsou, Jang-Yang Chang, C. Kuo, 2015, Biochemical pharmacology.

A Novel Synthetic Microtubule Inhibitor, MPT0B214 Exhibits Antitumor Activity in Human Tumor Cells through Mitochondria-Dependent Intrinsic Pathway

J. Liou, Jang-Yang Chang, C. Kuo, 2013, PloS one.

Ubiquitin‐conjugating enzyme E2 B regulates the ubiquitination of O6‐methylguanine‐DNA methyltransferase and BCNU sensitivity in human nasopharyngeal carcinoma cells

Jang-Yang Chang, C. Kuo, S. Hsu, 2018, Biochemical pharmacology.

Novel microtubule inhibitor MPT0B098 inhibits hypoxia-induced epithelial-to-mesenchymal transition in head and neck squamous cell carcinoma

J. Liou, Jang-Yang Chang, C. Kuo, 2018, Journal of Biomedical Science.

C35 terpenoids from the bark of Calocedrus macrolepis var. formosana with activity against human cancer cell lines.

Y. Kuo, Jang-Yang Chang, C. Kuo, 2006, Journal of natural products.

Combination of arsenic trioxide and BCNU synergistically triggers redox-mediated autophagic cell death in human solid tumors.

Jang-Yang Chang, C. Kuo, T. Liu, 2011, Free radical biology & medicine.

Novel Terpenoids from Calocedrus macrolepis var. formosana

Y. Kuo, Jang-Yang Chang, C. Kuo, 2011, Chemistry and Biodiversity.

Labdanecaryophyllic acid, a novel cytotoxic C35 terpenoid from Calocedrus macrolepis var. formosana

Y. Kuo, Jang-Yang Chang, C. Kuo, 2011 .

Cytotoxic C(35) terpenoid cryptotrione from the bark of Cryptomeria japonica.

Sheng-Yang Wang, Y. Kuo, N. Yang, 2010, Organic letters.

Cytotoxic C35 Terpenoid Cryptotrione from the Bark of Cryptomeria japonica.

Sheng-Yang Wang, Y. Kuo, N. Yang, 2010 .

Labdanecaryophyllic Acid, a Novel Cytotoxic C35 Terpenoid from Calocedrus macrolepis var. formosana.

Y. Kuo, Jang-Yang Chang, C. Kuo, 2011 .

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.

Gene expression profiling for analysis acquired oxaliplatin resistant factors in human gastric carcinoma TSGH-S3 cells: the role of IL-6 signaling and Nrf2/AKR1C axis identification.

Chi-Ying F. Huang, Miao-Fen Chen, Kuan-Der Lee, 2013, Biochemical pharmacology.

Chamaecypanone C, a novel skeleton microtubule inhibitor, with anticancer activity by trigger caspase 8-Fas/FasL dependent apoptotic pathway in human cancer cells.

Chi-Hung Lin, Y. Kuo, T. Chao, 2010, Biochemical pharmacology.