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L-798106 (Synonyms: CM9; GW671021) 纯度: 99.85%
L-798106 是强效且高度选择性的前列腺素类 EP3 受体拮抗剂 (Ki=0.3 nM),它在 EP4,EP1 和 EP2 受体上也具有微摩尔活性,针对 EP4,EP1,EP2 的 Ki 值分别为 916 nM,>5000 nM 和 >5000 nM。
L-798106 Chemical Structure
CAS No. : 244101-02-8
规格 | 价格 | 是否有货 | 数量 |
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Free Sample (0.1-0.5 mg) | Apply now | ||
10 mM * 1 mL in DMSO | ¥1841 | In-stock | |
5 mg | ¥1560 | In-stock | |
10 mg | ¥2496 | In-stock | |
25 mg | ¥5460 | In-stock | |
50 mg | ¥8775 | In-stock | |
100 mg | ¥14040 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
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L-798106 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
- Angiogenesis Related Compound Library
生物活性 |
L-798106 is potent and highly selective prostanoid EP3 receptor antagonist (Ki=0.3 nM), it also has micromolar activities at the EP4, EP1 and EP2 receptors with Ki values of 916 nM, >5000 nM and >5000 nM at EP4, EP1 and EP2, respectively[1]. |
IC50 & Target |
Ki values: 0.3 nM (EP3 receptor); 916 nM (EP4 receptor); > 5000 nM (EP1/2 receptor)[1] |
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分子量 |
536.44 |
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Formula |
C27H22BrNO4S |
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CAS 号 |
244101-02-8 |
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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 : 10 mg/mL (18.64 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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