1. Membrane Transporter/Ion Channel
  2. P2X Receptor
  3. Ro-51

Ro-51 是一种高效、选择性的 P2X3/P2X2/3 双重拮抗剂,对 P2X3 和 P2X2/3 作用的IC50 值分别为 2 nM 和 5 nM。Ro-51 可以用于痛觉研究。

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Ro-51 Chemical Structure

Ro-51 Chemical Structure

CAS No. : 1050670-85-3

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规格 价格 是否有货 数量
5 mg ¥3832
3 - 4 周
10 mg ¥6134
3 - 4 周
50 mg   询价  
100 mg   询价  

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Customer Review

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Ro-51 is a potent and selective dual P2X3/P2X2/3 antagonist, with IC50 of 2 nM and 5 nM for P2X3 and P2X2/3, respectively. Ro-51 can be used for the research for pain[1][2].

IC50 & Target

IC50: 2 nM (P2X3), 5 nM (P2X2/3)[1]

体外研究
(In Vitro)

Ro-51 has highly selective for P2X 3 and P2X 2/3 exhibiting no antagonistic activity at other P2X receptor family members tested (P2X 1 , P2X 2 , P2X 4 , P2X 5 , and P2X 7 ) at concentrations up to 10 μM[1].
RO51 also shows a significant drop in potency on human P2X3 receptors (IC50 = 110.5 and 0.04 nM, respectively for human and rat P2X3)[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Ro-51 suffers rapid clearance, short half-lives, and high protein binding in rat[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Rat[1]
Dosage: 2 mg/kg (Pharmacokinetic Analysis)
Administration: Oral administration
Result: AUC= 237 ng/h/mL, T 1/2 =1.52 h
分子量

474.29

Formula

C17H23IN4O4

CAS 号
Unlabeled CAS

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
参考文献
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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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Ro-51
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HY-14485
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