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 About 7 results found for searched term "Tamoxifen" (0.171 seconds)

Cat.No.  Name Target
M2280 Tamoxifen Citrate (ICI 46474) Estrogen Receptor
ICI 46474; Istubal; Nolvadex
Tamoxifen Citrate is an antagonist of the estrogen receptor by competitive inhibition of estrogen binding.
M7353 Tamoxifen Estrogen Receptor
ICI47699; Z-Tamoxifen; trans-Tamoxifen
Tamoxifen is an orally active, selective estrogen receptor partial agonist/antagonist. Tamoxifen is a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity. Tamoxifen also potent inhibits infectious EBOV Zaire and Marburg (MARV) with IC50 of 0.1 µM and 1.8 µM, respectively.
M7776 N-Desmethyltamoxifen HCl Others
N-Desmethyltamoxifen HCl is the primary metabolite of tamoxifen.
M7839 (E/Z)-4-Hydroxytamoxifen Estrogen Receptor
Afimoxifene
(E/Z)-4-Hydroxytamoxifen is the racemate of (Z)-4-Hydroxytamoxifen and (E)-4-Hydroxytamoxifen and a modulator of the estrogen receptor (ER).
M10252 4-Hydroxytamoxifen Estrogen Receptor
(Z)-4-Hydroxytamoxifen; trans-4-Hydroxytamoxifen; (Z)-Afimoxifene
4-Hydroxytamoxifen ((Z)-4-Hydroxytamoxifen) is an orally active, selective estrogen receptor modulator (SERM).
M14627 Droloxifene Estrogen Receptor
3-Hydroxytamoxifen
Droloxifene, a Tamoxifen derivative, is an orally active and selective estrogen receptor modulator.
M29903 N-Desmethyltamoxifen  PKC
N-Desmethyltamoxifen is the major metabolite of tamoxifen in humans. N-Desmethyltamoxifen, a poor antiestrogen, is a ten-fold more potent protein kinase C (PKC) inhibitor than Tamoxifen. N-Desmethyltamoxifen is also a potent regulator of ceramide metabolism in human AML cells, limiting ceramide glycosylation, hydrolysis, and sphingosine phosphorylation.



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