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C0567 Sigma

(−)-Catechin

≥97% (HPLC), from green tea

Synonym: (−)-trans-3,3′,4′,5,7-Pentahydroxyflavane, (2S,3R)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-1(2H)-benzopyran-3,5,7-triol

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(+)-Catechin

analytical standard

(+)-Catechin
03910590(+)-Catechin

primary pharmaceutical reference standard

(+)-Catechin hydrate

≥96.0% (sum of enantiomers, HPLC)

(−)-Catechin gallate

≥98% (HPLC), from green tea

Safety & Documentation

Safety Information

WGK Germany 
3

Documents

Certificate of Analysis

Certificate of Origin

Protocols & Articles

Peer-Reviewed Papers

References

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Inhibition of Plasmodium falciparum fatty acid biosynthesis: evaluation of FabG, FabZ, and FabI as drug targets for flavonoids. Deniz Tasdemir et al J. Med. Chem. 49, 3345-53, (2006)

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An efficient and economical MTT assay for determining the antioxidant activity of plant natural product extracts and pure compounds. Yunbao Liu et al J. Nat. Prod. 73, 1193-5, (2010)

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Flavonoids as opioid receptor ligands: identification and preliminary structure-activity relationships. Peter L Katavic et al J. Nat. Prod. 70, 1278-82, (2007)

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Potent inhibitor scaffold against Trypanosoma cruzi trans-sialidase. Shingo Arioka et al Bioorg. Med. Chem. 18, 1633-40, (2010)

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Tea catechins inhibit hepatocyte growth factor receptor (MET kinase) activity in human colon cancer cells: kinetic and molecular docking studies. Christine A Larsen et al J. Med. Chem. 52, 6543-5, (2009)

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Sulfonamide chalcone as a new class of alpha-glucosidase inhibitors. Woo Duck Seo et al Bioorg. Med. Chem. Lett. 15, 5514-6, (2005)

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Galactolipids from Bauhinia racemosa as a new class of antifilarial agents against human lymphatic filarial parasite, Brugia malayi. Koneni V Sashidhara et al Eur. J. Med. Chem. 50, 230-5, (2012)

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Catechin gallates are NADP+-competitive inhibitors of glucose-6-phosphate dehydrogenase and other enzymes that employ NADP+ as a coenzyme. Eui Seok Shin et al Bioorg. Med. Chem. 16, 3580-6, (2008)

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Merck 14,1902

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