4-Hydroxytamoxifen

4-Hydroxytamoxifen

Catalog Number:
FC01365952APE
Mfr. No.:
APE-B6167
Price:
$231
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          Background

          IC50: 27 and 18 μM for MCF-7 and MDA-MB-231 cell proliferation
          4-Hydroxytamoxifen is an estrogen receptor modulator.
          Estrogen receptor can be selectively stimulated or inhibited, providing promising therapeutic opportunities for auto-immune diseases, prostate and breast cancer, as well as depression.
          In vitro: Previous study was conducted to evaluate the effects of tamoxifen and its active metabolite 4-hydroxytamoxifen on isolated rat cardiac myocyte mechanical function and calcium handling. Results showed that myocytes treated with 4-hydroxytamoxifen had similarly to tamoxifen-treated cells to both calcium handling and contractility [1].
          In vivo: Previous animal study compared the extent of DNA adduct formation in SD rats treated with seven tamoxifen or 4-hydroxytamoxifen. Results showed that the liver weights and microsomal rates were not changed by tamoxifen or 4-hydroxytamoxifen treatment. Moreover, the uterine weights were significantly decreased and uterine peroxidase activity was marginally decreased in tamoxifen or 4-hydroxytamoxifen treated rats. In addition, hepatic DNA adduct levels in rats treated with 4-hydroxytamoxifen did not differ from control rats. Similaryly, the adduct levels in uterus DNA from rats treated with tamoxifen or 4-hydroxytamoxifen were not different from those in control rats [2].
          Clinical trial: Previous clinical study showed that the antiproliferative effect of 4-hydroxytamoxifen gel to breast skin was similar to that of oral tamoxifen, but the effects on endocrine and coagulation parameters decreased [3].

          [1] Asp ML,Martindale JJ,Metzger JM. Direct, differential effects of tamoxifen, 4-hydroxytamoxifen, and raloxifene on cardiac myocyte contractility and calcium handling. PLoS One.2013 Oct 24;8(10):e78768.
          [2] Beland FA,McDaniel LP,Marques MM. Comparison of the DNA adducts formed by tamoxifen and 4-hydroxytamoxifen in vivo. Carcinogenesis.1999 Mar;20(3):471-7.
          [3] Lee O et al. A randomized phase II presurgical trial of transdermal 4-hydroxytamoxifen gel versus oral tamoxifen in women with ductal carcinoma in situ of the breast. Clin Cancer Res.2014 Jul 15;20(14):3672-82.

      • Properties
        • Categories
          estrogen receptor modulator
          Alternative Name
          4-(1-(4-(2-(dimethylamino)ethoxy)phenyl)-2-phenylbut-1-en-1-yl)phenol
          CAS Number
          68392-35-8
          Molecular Formula
          C26H29NO2
          Molecular Weight
          387.51
          Appearance
          A solid
          Purity
          98.00%
          Solubility
          ≥42 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O
          Storage
          Store at -20°C
          SMILES
          OC1=CC=C(C(C2=CC=C(OCCN(C)C)C=C2)=C(CC)C3=CC=CC=C3)C=C1

          * For Research Use Only

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