Larotaxel (Synonyms: XRP9881) |
Catalog No.GC36424 |
Larotaxel(XRP9881)은 탁산 내성 유방암에 대한 전임상 활성을 가진 탁산 유사체입니다. 라로탁셀(XRP9881)은 튜불린 조립을 촉진하고 미세소관을 안정화하여 세포 독성 효과를 발휘하여 궁극적으로 세포 사멸에 의한 세포 사멸을 초래합니다. 그것은 혈액 뇌 장벽을 통과하는 능력을 나타내며 Docetaxel보다 P-당단백질 1에 대한 친화도가 훨씬 낮습니다.
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Cas No.: 156294-36-9
Sample solution is provided at 25 µL, 10mM.
Larotaxel (XRP9881) is a taxane analogue with preclinical activity against taxane-resistant breast cancer. Larotaxel (XRP9881) exerts its cytotoxic effect by promoting tubulin assembly and stabilizing microtubules, ultimately leading to cell death by apoptosis. It presents the ability to cross the blood brain barrier and has a much lower affinity for P-glycoprotein 1 than Docetaxel[1][2][3].
[1]. DiÉras V, et al. Phase II multicenter study of larotaxel (XRP9881), a novel taxoid, in patients with metastatic breast cancer who previously received taxane-based therapy. Ann Oncol. 2008 Jul;19(7):1255-60. [2]. Morris PG, et al. Novel anti-tubulin cytotoxic agents for breast cancer. Expert Rev Anticancer Ther. 2009 Feb;9(2):175-85. [3]. Zatloukal P, et al. Randomized multicenter phase II study of larotaxel (XRP9881) in combination with cisplatin or gemcitabine as first-line chemotherapy in nonirradiable stage IIIB or stage IV non-small cell lung cancer. J Thorac Oncol. 2008 Aug;3(8):894-901.
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