Comparison of a Pair of Synthetic Tea-Catechin-Derived Epimers: Synthesis, Antifolate Activity, and Tyrosinase-Mediated Activation in Melanoma

Purification and Kinetic Properties of Human Recombinant Dihydrofolate Reductase Produced in Bombyx mori Chrysalides

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Mechanism of dihydrofolate reductase downregulation in melanoma by 3-O-(3,4,5-trimethoxybenzoyl)-(−)-epicatechin

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Melanoma Activation of 3-O-(3,4,5-Trimethoxybenzoyl)-(−)-Epicatechin to a Potent Irreversible Inhibitor of Dihydrofolate Reductase

(2009) Luís Sánchez-del-Campo et al.   MOLECULAR PHARMACEUTICS

Screening of DHFR-binding drugs by MALDI-TOFMS

(2008) Paul Hannewald et al.   ANALYTICAL AND BIOANALYTICAL CHEMISTRY

Targeting the methionine cycle for melanoma therapy with 3-O-(3,4,5-trimethoxybenzoyl)-(−)-epicatechin

(2008) Luís Sánchez-del-Campo et al.   INTERNATIONAL JOURNAL OF CANCER

Synthesis and Biological Activity of a 3,4,5-Trimethoxybenzoyl Ester Analogue of Epicatechin-3-gallate

(2008) Luís Sánchez-del-Campo et al.   JOURNAL OF MEDICINAL CHEMISTRY

Mechanism of inhibition of wt-dihydrofolate reductase fromE. coliby tea epigallocatechin-gallate

(2008) Michele Spina et al.   PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS

The challenge of developing green tea polyphenols as therapeutic agents

(2008) C. Huo et al.   INFLAMMOPHARMACOLOGY