
ATM-3507
CAS No. 1861449-70-8
ATM-3507 ( ATM3507 | ATM 3507 )
产品货号. M12876 CAS No. 1861449-70-8
ATM-3507 (ATM3507) 是 Tpm3.1 原肌球蛋白亚型的小分子抑制剂,在 5 uM 浓度下可破坏 SK-N-SH 细胞中含有 Tpm3.1 的微丝。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥2357 | 有现货 |
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50MG | ¥12636 | 有现货 |
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100MG | ¥19116 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称ATM-3507
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述ATM-3507 (ATM3507) 是 Tpm3.1 原肌球蛋白亚型的小分子抑制剂,在 5 uM 浓度下可破坏 SK-N-SH 细胞中含有 Tpm3.1 的微丝。
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产品描述ATM-3507 (ATM3507) is a small molecule inhibitor of Tpm3.1 tropomyosin isoform, disrupts Tpm3.1-containing microfilaments in SK-N-SH cells at 5 uM; shows cancer cell cytotoxicity comparable with the first-in-class tool compound TR100, also shows a strong synergistic effect when TR100 or ATM-3507 were combined with antimicrotubule agents in both in vitro and in vivo neuroblastoma models.
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体外实验The cell lines differ in their relative expression of Tpm3.1 as well as in the expression of other isoforms. After determing the IC50 concentrations for TR100 and ATM-3507 (CHLA-20: 4.99±0.45 μM, CHP-134: 3.83±0.67 μM, CHLA-90: 6.84±2.37 μM, SK-N-BE(2): 5.00±0.42 μM) in each of the neuroblastoma cell lines, combinations of tropomyosin inhibitors plus Vincristine are tested at levels of each drug alone that kill less than 50% of the neuroblastoma cells. The combinations of both tropomyosin inhibitors plus Vincristine are completely cytotoxic in CHLA-20 cells. All 4 cell lines show some degree of synergy as determined by the Chou–Talalay method. The effect is not limited to the vinca alkaloids as a similar combination efficacy using paclitaxel plus TR100 or ATM-3507.
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体内实验The maximal tolerance dose (MTD) for TR100 and ATM-3507 is 60 and 150 mg/kg, respectively. It is found that a significant inhibition of tumor growth and prolongation of animal survival using either combination compared with each monotherapy. The median survival of mice increased from 18 days for mice treated with ATM-3507 to more than 49 days for mice treated with the combination. It is also found that twice weekly intravenous administration of ATM-3507 also show combination efficacy. The impact of each treatment or the combination on body weight is minimal. Drug levels are measured following the intravenous administration of ATM-3507 at 30 mg/kg in Balb/c mice (n=3 per time point). The mean half-life of ATM-3507 is 5.01 hrs for the terminal elimination phase. The mean AUC0-t in the plasma is 14,548 ng/h/mL. The Cmax of ATM-3507 is 5,758 ng/mL and the the t1/2 is 5.01 h. The observed plasma clearance and volume of distribution at steady state of ATM-3507 is 33.8 mL/min/kg and 7.23 L/kg, respectively.
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同义词ATM3507 | ATM 3507
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通路Cytoskeleton/Cell Adhesion Molecules
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靶点Microtubule/Tubulin
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受体Microtubule/Tubulin
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研究领域Cancer
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适应症——
化学信息
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CAS Number1861449-70-8
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分子量611.806
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分子式C37H46FN5O2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 33.33 mg/mL (54.48 mM)
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SMILESO=C(C1=CC=CC(OC2=CC3=C(N(CCCN4CCN(C)CC4)C(C)=C3C)C=C2)=C1)N5CCN(CCC6=CC=C(F)C=C6)CC5
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化学全称(3-((2,3-dimethyl-1-(3-(4-methylpiperazin-1-yl)propyl)-1H-indol-5-yl)oxy)phenyl)(4-(4-fluorophenethyl)piperazin-1-yl)methanone
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Currier MA, et al. Mol Cancer Ther. 2017 Aug;16(8):1555-1565.
2. Mitchell CB, et al. Cytoskeleton (Hoboken). 2018 Jul;75(7):307-317.
产品手册




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