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LPA2 antagonist 2 纯度: 95.03%
LPA2 antagonist 2 是一种选择性 LPA2 拮抗剂,IC50 为 28.3 nM,Ki 为 21.1 nM,比 LPA3 (IC50 为 13.85 μM) 选择性高 480 倍以上。
LPA2 antagonist 2 Chemical Structure
CAS No. : 36840-10-5
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥2930 | In-stock | |
1 mg | ¥1200 | In-stock | |
5 mg | ¥3500 | In-stock | |
10 mg | ¥5500 | In-stock | |
50 mg | 询价 | ||
100 mg | 询价 |
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LPA2 antagonist 2 相关产品
•相关化合物库:
- Covalent Screening Library Plus
- Bioactive Compound Library Plus
- GPCR/G Protein Compound Library
- Immunology/Inflammation Compound Library
- Anti-Cancer Compound Library
- Covalent Screening Library
生物活性 |
LPA2 antagonist 2 (H2L 5226501) is a selective LPA2 antagonist with an IC50 of 28.3 nM and a Ki of 21.1 nM. LPA2 antagonist 2 is >480-fold more selective than LPA3 (IC50 of 13.85 μM)[1]. |
IC50 & Target |
IC50: 28.3 nM (LPA2); 13.85 μM (LPA3)[1] |
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体外研究 (In Vitro) |
Lysophosphatidic acid (LPA) is a phospholipid mediator that elicits a host of biological effects including cell proliferation, survival, motility and differentiation. LPA has been shown to regulate cancer cell invasion, metastasis, and resistance to both chemotherapeutics and radiation. LPA2 antagonist 2 (H2L 5226501) inhibits LPA1 with an Imax of 59.0% at 30 µM[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. |
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分子量 |
380.35 |
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Formula |
C20H16N2O6 |
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CAS 号 |
36840-10-5 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 83.33 mg/mL (219.09 mM; Need ultrasonic) 配制储备液
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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。 |
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参考文献 |
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