Larotaxel (Synonyms: XRP9881) |
カタログ番号GC36424 |
ラロタキセル (XRP9881) は、タキサン耐性乳がんに対する前臨床活性を持つタキサン類似体です。ラロタキセル (XRP9881) は、チューブリン アセンブリを促進し、微小管を安定化することによって細胞毒性効果を発揮し、最終的にアポトーシスによる細胞死を引き起こします。これは、血液脳関門を通過する能力を示し、ドセタキセルよりも P 糖タンパク質 1 に対する親和性がはるかに低くなります。
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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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