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

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

General description Breast cancer anti-estrogen resistance protein 1 (UniProt P56945: also known as Cas scaffolding protein family member 1, Crk-associated substrate, p130Cas) is encoded by the BCAR1 (also known as CAS, CAS1, CASS1, CRKAS) gene

General description Carcinomas arising from epithelial cells lining the mammary glands comprise the overwhelming majority of breast cancer cases (1). Transformation of mammary epithelial cells from their normal non-proliferative condition to an