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- 文献和实验
- 技术资料
- 保存条件:
-20°C, sealed storage, away from moisture
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1004312-94-0
- 规格:
1 mg/5 mg/10 mg
| 规格: | 1 mg | 产品价格: | ¥1525.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥3200.0 |
| 规格: | 10 mg | 产品价格: | ¥5122.0 |
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CHF5407
CAS No. : 1004312-94-0
MCE 国际站:CHF5407
产品活性:CHF5407 是一种选择性,长效和竞争性毒蕈碱 M3 受体拮抗剂。CHF5407 对人毒蕈碱 M1 (hM1),M2 (hM2) 和 M3 (hM3) 受体显示纳摩尔亲和力。CHF5407 表现出延长的抗支气管痉挛活性。
研究领域:GPCR/G Protein | Neuronal Signaling
作用靶点:mAChR
In Vitro: CHF5407 has a very slow dissociation from M3 receptors (hM3; t1/2=166 min) and markedly short-acting at M2 receptors (hM2; t1/2=31 min).
CHF5407 produces a potent (pIC50=9.0-9.6) and long-lasting (up to 24 h) inhibition of M3 receptor-mediated contractile responses to carbachol in the guinea pig isolated trachea and human isolated bronchus.
In Vivo: CHF5407 (0.1, 0.3, 1 nmol/kg; intratracheally; 100 ul; sigle dose) exerted a dose-dependent and potent inhibition of ACh-induced (20 g/kg; i.v.) bronchospasm, with an ED50 value of 0.15 nmol/kg in guinea pigs (450-550 g).
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文献和实验. Normalized relative fluorescence levels were calculated by 2^mean (of log2 transformed, loess normalized values). Change factors (CHF) were calculated as fold change on the linear scale minus 1 as previously described (2 ). Raw data, non-normalized
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