来曲唑-d4（CGS 20267-d4）是氘标记的来曲唑。 Letrozole (CGS 20267) 是一种有效的、选择性的、可逆的和口服活性的芳香酶非甾体抑制剂，IC50 为 11.5 nM。来曲唑选择性抑制雌激素的生物合成，可用于乳腺癌的研究。
货号:ajcx22814
CAS:1133712-96-5
分子式:C17H7D4N5
分子量：289.3
溶解度:DMF: 16 mg/ml,DMF:PBS (pH 7.2) (1:9): 0.1 mg/ml,DMSO: 16 mg/ml
纯度：98%
存储：Store at -20°C
库存：现货

Background:

Letrozole-d₄is intended for use as an internal standard for the quantification of letrozole by GC- or LC-MS. Letrozole is a potent, cell-permeable inhibitor of aromatase (IC₅₀= 2 nM).¹It inhibits proliferation of estrogen receptor-positive (ER⁺) MCF-7 cells when used alone at concentrations ranging from 0.1 to 100 nM and when used at a concentration of 10 nM in combination with testosterone or 4-androstene-3,17-dione.²It also reduces matrix metalloproteinase-2 (MMP-2) and MMP-9 levels in MCF-7 cells when used at a concentration of 10 nM. Letrozole (10 µg per day) reduces tumor growth in an MCF-7Ca ovariectomized-mouse xenograft model.³Formulations containing letrozole have been used in the treatment of postmenopausal breast cancer.⁴

1.Mayhoub, A.S., Marler, L., Kondratyuk, T.P., et al.Optimization of the aromatase inhibitory activities of pyridylthiazole analogues of resveratrolBioorg. Med. Chem.20(7)2427-2434(2012) 2.Mitropoulou, T.N., Tzanakakis, G.N., Kletsas, D., et al.Letrozole as a potent inhibitor of cell proliferation and expression of metalloproteinases (MMP-2 and MMP-9) by human epithelial breast cancer cellsInt. J. Cancer104(2)155-160(2003) 3.Long, B.J., Jelovac, D., Handratta, V., et al.Therapeutic strategies using the aromatase inhibitor letrozole and tamoxifen in a breast cancer modelJ. Natl. Cancer Inst.96(6)456-465(2004) 4.Cohen, M.H., Johnson, J.R., Li, N., et al.Approval summary: Letrozole in the treatment of postmenopausal women with advanced breast cancerClin Cancer Res.8(3)665-669(2002)