Tamoxifen citrate

(E)-2′-Hydroxychalcone is a chalcone derivative. Chalcone derivatives have exhibited unexpectedly good activity as angiogenesis inhibitors. Experimental results indicate that the flavonoids chalcone, 2-hydroxychalcone, and quercetin present in our

(E)-2′-Hydroxychalcone is a chalcone derivative. Chalcone derivatives have exhibited unexpectedly good activity as angiogenesis inhibitors. Experimental results indicate that the flavonoids chalcone, 2-hydroxychalcone, and quercetin present in our

(E)-2′-Hydroxychalcone is a chalcone derivative. Chalcone derivatives have exhibited unexpectedly good activity as angiogenesis inhibitors. Experimental results indicate that the flavonoids chalcone, 2-hydroxychalcone, and quercetin present in our

(E)-4-Hydroxy tamoxifen O-β-D-glucuronide is a glucuronide of (Z)-4-Hydroxy Tamoxifen (or trans-4-hydroxytamoxifen) .

(E,Z)-Tamoxifen N-β-D-Glucuronide is a metabolite of Tamoxifen.

A synthetic analog of curcumin that activates enzymes which catalyze detoxification reactions through the Keap1-Nrf2-ARE pathway increases NQO1 activity, glutathione reductase activity, and total glutathione levels in vitro at 0.6 &ndash 0.

A synthetic analog of curcumin that activates enzymes which catalyze detoxification reactions through the Keap1-Nrf2-ARE pathway increases NQO1 activity, glutathione reductase activity, and total glutathione levels in vitro at 0.6 &ndash 0.

Product Application：6-Hydroxy-1-indanone can be used in the synthesis of tetracyclic ketones intermediates during the total syntheses of (±)-frondosin C and (±)-8-epi-frondosin C. It can also be used in the synthesis of

[³H]tamoxifen.

[³H]tamoxifen.

Anti-BRCA2 breast cancer 2, early onset, 25ul UN 1687 6.1 PG

ANTI-CYTOKERATIN 8 CLONE TROMA-1 ZOOMAB« RAT MONOCLONAL