Motixafortide BKT140 (4-fluorobenzoyl; BL-8040; TF14016),99.03%
产品编号:Bellancom-P0171| CAS NO:664334-36-5| 分子式:C97H144FN33O19S2| 分子量:2159.52
Motixafortide (BL-8040) 通过改变的miR-15a/16-1的表达,下调ERK、BCL-2、MCL-1和cyclin-D1,诱导AML胚的凋亡。Motixafortide 在体外诱导 AML 细胞凋亡。这种细胞凋亡是由 miR-15a/miR-16-1 的上调介导的,导致靶基因 BCL-2、MCL-1 和细胞周期蛋白-D1 的下调。miR-15a/miR-16-1 的过表达直接诱导白血病细胞死亡。Motixafortide (BL-8040) 与FLT3抑制剂协同诱导AML细胞死亡。这种联合治疗延长了荷瘤小鼠的存活时间,并减少了体内最小残留疾病。
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Motixafortide BKT140 (4-fluorobenzoyl; BL-8040; TF14016)
产品介绍 | Motixafortide (BKT140 4-fluorobenzoyl) 是一种新型的CXCR4拮抗剂,IC50约为1 nM。 | ||||||||||||||||
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生物活性 | Motixafortide (BKT140 4-fluorobenzoyl) is a novel CXCR4 antagonist with an IC50 vakue of ~1 nM. | ||||||||||||||||
体外研究 |
Motixafortide (BKT140) displays selective toxicity toward AmL and MM cells. Treatment with Motixafortide (BKT140) can overcome IL-6 dependent proliferation and survival of ARH77 MM cells. Motixafortide (BKT140) specifically triggers CXCR4-dependent cell death in leukemia and MM cells. Motixafortide (BKT140) stimulates apoptotic cell death in leukemia and MM cells. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 |
Subcutaneous injections of Motixafortide (BKT140) significantly reduces, in a dose-dependent manner, the growth of human acute myeloid leukemia and multiple myeloma xenografts. Tumors from animals treated with Motixafortide (BKT140) are smaller in size and weights, had larger necrotic areas and high apoptotic scores. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 |
Subcutaneous injections of Motixafortide (BKT140) significantly reduces, in a dose-dependent manner, the growth of human acute myeloid leukemia and multiple myeloma xenografts. Tumors from animals treated with Motixafortide (BKT140) are smaller in size and weights, had larger necrotic areas and high apoptotic scores. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
性状 | Solid | ||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : ≥ 100 mg/mL (46.31 mM) H2O : 50 mg/mL (23.15 mM; Need ultrasonic) * "≥" means soluble, but saturation unknown. 配制储备液
*
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
*以上所有助溶剂都可在 西域 网站选购。
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运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
Sealed storage, away from moisture
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
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