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LDN193189 (DM-3189) 是一种 BMP I 型受体的选择性抑制剂,可以抑制 ALK2 和 ALK3 (IC50=5/30 nM),对 ALK4、ALK5 和 ALK7 的活性较弱。LDN193189 可以用于进行性骨化性纤维发育不良的研究。
别名 LDN-193189, LDN 193189, DM-3189
LDN193189 (DM-3189) 是一种 BMP I 型受体的选择性抑制剂,可以抑制 ALK2 和 ALK3 (IC50=5/30 nM),对 ALK4、ALK5 和 ALK7 的活性较弱。LDN193189 可以用于进行性骨化性纤维发育不良的研究。

| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 398 | 现货 | |
| 2 mg | ¥ 578 | 现货 | |
| 5 mg | ¥ 788 | 现货 | |
| 10 mg | ¥ 1,330 | 现货 | |
| 25 mg | ¥ 2,430 | 现货 | |
| 50 mg | ¥ 3,930 | 现货 | |
| 100 mg | ¥ 5,590 | 现货 | |
| 200 mg | ¥ 7,690 | 现货 |
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| 产品描述 | LDN193189 (DM-3189) is a selective inhibitor of the BMP type I receptor that inhibits ALK2 and ALK3 (IC50=5/30 nM), with less activity against ALK4, ALK5, and ALK7. LDN193189 can be used in studies of progressive ossifying fibrous dysplasia. |
| 靶点活性 | ALK3:30 nM (C2C12 cells), BMPR1A:30 nM, ALK2:5 nM (C2C12 cells) |
| 体外活性 | 方法:肺动脉平滑肌细胞 PASMCs 用 LDN193189 (2-32000 nM) 预处理 10 min,再用 BMP4 (10 ng/mL) 或 TGF-β (0.5 ng/mL) 处理 30 min,使用 Western Blot 检测靶点蛋白表达水平。 |
| 体内活性 | 方法:为研究 ALK2 激酶抑制对体内异位钙化的影响,将 LDN193189 (3 mg/kg) 腹腔注射给 caALK2 转基因和野生型小鼠,每 12 h 一次,持续 60 天。 |
| 细胞实验 | C2C12 cells were seeded into 96-well plates at 2,000 cells per well in DMEM supplemented with 2% FBS. We treated the wells in quadruplicate with BMP ligands and LDN-193189 or vehicle. We collected the cells after 6 d in culture in 50 μl Tris-buffered saline and 1% Triton X-100. We added the lysates to p-nitro-phenylphosphate reagent in 96-well plates for 1 h and then evaluated alkaline phosphatase activity (absorbance at 405 nm). We measured cell viability and quantity by Cell Titer Aqueous One (absorbance at 490 nm), using replicate wells treated identically to those used for alkaline phosphatase measurements [1]. |
| 动物实验 | In the first experiment, SCID mice were implanted with MDA-PCa-118b tumors. After 7 days when tumors reached measurable sizes, mice were injected with LDN-193189 (3 mg/kg) or with vehicle intraperitoneally twice a day. Tumor sizes and body weights were measured weekly. Mice were injected with calcein at three days and one day prior to sacrifice. Blood was collected and tumors were weighed. A portion of the tumors were fixed in formaldehyde for micro-computed tomography, using EVS CT, or further decalcified for bone histomorphometric analysis, using the OsteoMeasure Analysis System, or flash frozen for RNA preparation. Osteocalcin in the mouse serum was determined by ELISA. In the second experiment, PCa-118b tumors were first digested with Accumax, and the isolated cells were plated overnight, digested by Accutase, resuspended in Matrigel in 1:1 ratio, and injected into SCID mice (1 × 10^6 cells/mouse) subcutaneously. Mice were treated with LDN-193189 five days post-injection [3]. |
| 别名 | LDN-193189, LDN 193189, DM-3189 |
| 分子量 | 406.48 |
| 分子式 | C25H22N6 |
| CAS No. | 1062368-24-4 |
| Smiles | C1CN(CCN1)c1ccc(cc1)-c1cnc2c(cnn2c1)-c1ccnc2ccccc12 |
| 密度 | 1.33 g/cm3 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. 实际储存温度请以COA为准 | ||||||||||
| 溶解度信息 | H2O: Insoluble DMSO: 1 mg/mL (2.46 mM), when pH is adjusted to 2 with HCl. Sonication and heating are recommended. 0.01M HCl: 1.67 mg/mL (4.11 mM), Sonication is recommended. | ||||||||||
溶液配制表 | |||||||||||
DMSO/0.01M HCl
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。 | |||||||||||
对于不同动物的给药剂量换算,您也可以参考 更多