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  3. PF-3774076

PF-3774076是一种中枢神经系统(CNS)渗透性强、效力高、选择性好的人类α1A-肾上腺素受体部分激动剂。它在多种结合和功能测定中表现出良好的效力和选择性。PF-3774076通过中枢机制以剂量依赖性方式增加麻醉雌性犬的尿道峰值压力。PF-3774076在体内可同时影响尿道的近端和远端部分。这些特性表明,PF-3774076作为一种CNS渗透性α1A受体部分激动剂可能在抑制压力性尿失禁(SUI)方面具有显著益处。然而,尽管PF-3774076对α1A受体具有部分激动作用和选择性,但在心血管功能的体内模型中,它未能提供足够的安全性差异。这可能是由于同时激活了外周和中枢的α1A受体。这些数据表明,虽然中枢性α1A部分激动剂可能在SUI抑制中有显著益处,但这类试剂可能难以实现理想的尿道选择性而不影响心血管功能。

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PF-3774076 Chemical Structure

PF-3774076 Chemical Structure

CAS No. : 1171824-96-6

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  • 生物活性

  • 纯度 & 产品资料

生物活性

PF-3774076 is a highly central nervous system (CNS) penetrant, potent, and selective human α1A-adrenoceptor partial agonist. It exhibits good potency and selectivity in multiple binding and functional assays. PF-3774076 increases peak urethral pressure in anesthetized female dogs in a dose-dependent manner via a central mechanism. PF-3774076 affects both the proximal and distal portions of the urethra in vivo. These properties suggest that PF-3774076 may have significant benefit in the treatment of stress urinary incontinence (SUI) as a CNS-penetrant α1A receptor partial agonist. However, despite its partial agonism and selectivity for α1A receptors, PF-3774076 failed to provide adequate safety differences in in vivo models of cardiovascular function. This may be due to the simultaneous activation of both peripheral and central α1A receptors. These data suggest that while central α1A partial agonists may have significant benefit in the treatment of SUI, this class of agents may have difficulty achieving the desired urethral selectivity without affecting cardiovascular function.

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
CHO EC50
> 10000 nM
Compound: 1
Agonist activity at human adrenergic Alpha-1B receptor expressed in CHO cells assessed as calcium mobilization by FLIPR
Agonist activity at human adrenergic Alpha-1B receptor expressed in CHO cells assessed as calcium mobilization by FLIPR
[PMID: 19414260]
CHO EC50
> 7000 nM
Compound: 1
Agonist activity at human adrenergic Alpha-1D receptor expressed in CHO cells assessed as calcium mobilization by FLIPR
Agonist activity at human adrenergic Alpha-1D receptor expressed in CHO cells assessed as calcium mobilization by FLIPR
[PMID: 19414260]
CHO EC50
27 nM
Compound: 2
Agonist activity at human cloned adrenergic alpha1A receptor expressed in CHO cells assessed as calcium mobilization by FLIPR
Agonist activity at human cloned adrenergic alpha1A receptor expressed in CHO cells assessed as calcium mobilization by FLIPR
[PMID: 19394220]
CHO EC50
31 nM
Compound: 1
Agonist activity at human adrenergic alpha1A receptor expressed in CHO cells assessed as calcium mobilization by FLIPR
Agonist activity at human adrenergic alpha1A receptor expressed in CHO cells assessed as calcium mobilization by FLIPR
[PMID: 19414260]
CHO EC50
31 nM
Compound: 14
Agonist activity at human cloned adrenergic alpha1A receptor expressed in CHO cells by calcium mobilization-based fluorescence assay
Agonist activity at human cloned adrenergic alpha1A receptor expressed in CHO cells by calcium mobilization-based fluorescence assay
[PMID: 18980842]
分子量

262.73

Formula

C14H15ClN2O

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料

PF-3774076 相关分类

  • 摩尔计算器

  • 稀释计算器

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
PF-3774076
目录号:
HY-137055
需求量: