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Results for "

( ) epigallocatechin gallate

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    6
    TargetMol | All_Pathways
  • Natural Products
    4
    TargetMol | Natural_Products
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    TargetMol | Standard_Products
(-)-Epigallocatechin Gallate
Epigallocatechol Gallate, EGCG
T2988989-51-5
(-)-Epigallocatechin Gallate (EGCG) is a phenolic antioxidant polyphenol flavonoid found in plants such as green and black tea, which inhibits telomerase and DNA methyltransferase, blocks the activation of EGF receptors and HER-2 receptors, inhibits cellular oxidation, and prevents free radical damage to cells.
  • $43
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TargetMol | Citations Cited
MST-312
Telomerase Inhibitor IX
T41290368449-04-1In house
MST-312 (Telomerase Inhibitor IX) is a derivative of green tea epigallocatechin gallate (EGCG). MST-312 is a telomerase inhibitor. MST-312 has research value in cancer, such as multiple myeloma (MM).
  • $30
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(+/-)-Epigallocatechin-[13C3] Gallate (Standard)
TMSM-3871
(+/-)-Epigallocatechin-[13C3] Gallate (Standard) is a reference standard of (+/-)-Epigallocatechin-[13C3] Gallate intended for quantitative analysis, quality control, and related biochemical research applications.
  • $2,590
4-6 weeks
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Eicosapentaenoyl Chloride
EPA Chloride, Eicosapentaenoic acid Chloride
TN1113398770-65-1
Eicosapentaenoyl Chloride (Eicosapentaenoic acid Chloride; EPA Chloride) is a derivative of eicosapentaenoic acid. It has been utilized in the synthesis of fatty acid conjugates to improve the lipophilicity and cellular permeability of bioactive compounds such as (–)-epigallocatechin gallate and salicylic acid.
  • Inquiry Price
10-14 weeks
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(-)-Epigallocatechin-3-(3''-O-methyl) gallate
(-)-EGCG-3''-O-ME
TN160883104-87-4
(-)-Epigallocatechin-3-(3''-O-methyl) gallate ((-)-EGCG-3''-O-ME) is a natural product isolated from tea leaves with potent antioxidant, cytotoxic, and antibacterial properties, and it improves the adhesive stability of etching rinsing adhesives to dentin.
  • $159
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TargetMol | Citations Cited
3-O-trans-p-Coumaroyltormentic acid
TN2977121064-78-6
3-O-(E)-p-coumaroyl tormentic acid may be promising lead compound for developing an effective drug for treatment of leukemia, it induces apoptotic cell death in human leukemia (HL60) via mainly mitochondrial pathway by, at least in part, Topo I inhibition. 3-O-trans-p-coumaroyltormentic acid shows cytotoxicity against four human tumor cell lines (A549, SK-OV-3, SK-MEL-2, and HCT-15) in vitro, the IC50 values of 13.72, 14.29,14.61, 14.04 uM, respectively. 3beta-O-cis-p-Coumaroyltormentic acid, and 3beta-O-trans-p-coumaroyltormentic acid are weakly selective for vancomycin-resistant Enterococcus (VRE) compared with eukaryotic cells, with an MIC of 59.4microg/mL and a 50% inhibitory concentration (IC50) of 72.0microg/mL for monkey kidney epithelial (MA104) cells. A mixture of 3-O-cis-p-coumaroyltormentic acid and 3-O-trans-p-coumaroyltormentic acid shows an inhibitory effect comparable to (-)-epigallocatechin gallate (EGCG) of green tea on the activation of Epstein-Barr virus early antigen (EBV-EA) induced by 12-O-tetradeca--noylphorbol-13-acetate (TPA).
  • $1,918
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