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Macromolecular chemistry and physics, ISSN 1022-1352, 2018, Volume 219, Issue 10, pp. 1700564 - n/a
3,4‐Dihydroxybenzhydrazide (DHBH) could be considered a structural analogue of dopamine, forming polymers under oxidative conditions in a polydopamine (PDA) fashion... 
synthesis | mass spectrometry | NMR | heteroatom‐containing polymers | FTIR | heteroatom-containing polymers | AMINATION | POLYMER SCIENCE | QUINONE | BEHAVIOR | CHEMISTRY | COFACTOR | Oligomers | Polymerization | Catechin | Hydroxides | Mass spectrometry | Resveratrol | Dopamine | Analogue | Catechol | Polymers | Anchoring | Hydroxyl groups
Journal Article
Bioorganic & medicinal chemistry, ISSN 0968-0896, 2012, Volume 20, Issue 9, pp. 3031 - 3037
AMP-activated protein kinase (AMPK) is a critical monitor of cellular energy status and also controls processes related to tumor development, including cell... 
Cell proliferation | EGCG analogs | Breast cancer | AMP-activated protein kinase | Cancer stem cells | METFORMIN | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | PROTEASOME ACTIVITY | MARKERS CD44 | BREAST-CANCER | CATECHOL-O-METHYLTRANSFERASE | IN-VITRO | INHIBITION | ALDEHYDE DEHYDROGENASE-ACTIVITY | GROWTH | GREEN TEA POLYPHENOL | Naphthalenes - chemical synthesis | Naphthalenes - chemistry | Up-Regulation | AMP-Activated Protein Kinases - metabolism | Neoplastic Stem Cells - drug effects | Antineoplastic Agents - chemical synthesis | Benzoates - chemistry | Down-Regulation | Humans | Catechin - chemical synthesis | Benzoates - chemical synthesis | Antineoplastic Agents - chemistry | Naphthalenes - pharmacology | Signal Transduction - drug effects | Benzoates - pharmacology | Cell Line, Tumor | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Antineoplastic Agents - pharmacology | Catechin - analogs & derivatives | Cell Proliferation - drug effects | TOR Serine-Threonine Kinases | Catechin - pharmacology | Catechin - chemistry | Catechin | Protein kinases | Stem cells | Cancer | Cell survival | epigallocatechin gallate | Capsaicin | Genistein | green tea | Protein biosynthesis | Drug development | Energy balance | epigallocatechin-3-gallate | natural products | Cyclin-dependent kinase inhibitor p21 | Cell cycle | Quercetin | Metformin | Tumors | breast cancer | cancer stem cells | cell proliferation
Journal Article
Tetrahedron, ISSN 0040-4020, 05/2014, Volume 70, Issue 21, pp. 3485 - 3490
The high-yielding synthesis of enantiomerically pure epicatechin gallate analogues where the A and/or B-ring hydroxylation is reduced or altered has been achieved by optimising routes to the catechin stereochemistry... 
Cyclisation | Mitsunobu | (−)-Epicatechin gallate analogues | Asymmetric synthesis | MRSA | (-)-Epicatechin gallate analogues | EGCG ANALOGS | CHEMISTRY, ORGANIC | AUREUS | CATECHINS | Gallates | Catechins | Synthesis (chemistry) | Asymmetry | Modulation | Tetrahedrons | Stereochemistry | Optimization
Journal Article
Molecules (Basel, Switzerland), ISSN 1420-3049, 2018, Volume 23, Issue 5, p. 1160
...molecules Article (−)-Epigallocatechin 3-Gallate Synthetic Analogues Inhibit Fatty Acid Synthase and Show Anticancer Activity in Triple Negative Breast Cancer... 
Polyphenolic FASN inhibitors | FASN inhibition | Synthetic analogues | Anticancer activity | Fatty acid synthase | (−)-epigallocatechin 3-gallate | Apoptosis | Triple-negative breast cancer | CELLS | TRICLOSAN | triple-negative breast cancer | (-)-epigallocatechin 3-gallate | BIOCHEMISTRY & MOLECULAR BIOLOGY | apoptosis | ENOYL-ACP REDUCTASE | OVARIAN-CANCER | CHEMISTRY, MULTIDISCIPLINARY | synthetic analogues | polyphenolic FASN inhibitors | POLYPHENOLS | GREEN TEA CATECHINS | fatty acid synthase | anticancer activity | EPIGALLOCATECHIN GALLATE | BINDING | EXPRESSION | Fatty Acid Synthases - antagonists & inhibitors | Apoptosis - drug effects | Antineoplastic Agents - chemical synthesis | Humans | Catechin - chemical synthesis | Antineoplastic Agents - chemistry | Enzyme Inhibitors - chemical synthesis | Cell Line, Tumor | Female | Catechin - analogs & derivatives | Cell Proliferation - drug effects | Molecular Structure | Catechin - chemistry | Triple Negative Breast Neoplasms - enzymology | Carcinoma | Toxicity | Diesters | Epigallocatechin-3-gallate | Cytotoxicity | Breast cancer | Pharmacology | Lead compounds | Derivatives | Fatty acids | ErbB-2 protein | Fatty-acid synthase | Anticancer properties | Proteins | Tea | Polyphenols | Antitumor activity | Biocompatibility | Inhibition | Green tea | Cancer | Breast | Càncer | Mama
Journal Article
Synthesis, ISSN 0039-7881, 08/2019, Volume 51, Issue 16, pp. 3127 - 3141
Abstract A highly efficient and regioselective self-coupling of C8-methylol catechin derivatives is developed for the synthesis of dimeric flavanol analogues under metal-free and mild conditions... 
paper | PHENOLIC ANTIOXIDANTS | TANNINS | CHEMISTRY, ORGANIC | OLIGOMERIC PROANTHOCYANIDINS | FLAVONOIDS | ALDEHYDES | metal-free | regioselective | BENZYL ALCOHOLS | POLYPHENOLS | GREEN TEA CATECHINS | OOLONG | bis-flavanol | catechin | self-coupling
Journal Article
RSC advances, ISSN 2046-2069, 2017, Volume 7, Issue 29, pp. 17968 - 17979
..., or both. All three quercetin analogues were found to exhibit higher radical-scavenging activity than the parent quercetin... 
SUBSTITUTION | RESVERATROL | VITAMIN-E | DIETARY POLYPHENOLS | HEART-DISEASE | ANTIOXIDANTS | ALCOHOL | ELECTRON-TRANSFER MECHANISM | CATECHIN ANALOG | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY
Journal Article