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  3. ST 198

ST 198 是 D3R 拮抗剂,具有口服活性。 ST 198 可以在对 D3R 有选择性的剂量下阻断尼古丁诱导的 CPP 的表达。 ST 198 可用于神经系统疾病的研究。

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ST 198 Chemical Structure

ST 198 Chemical Structure

CAS No. : 854924-64-4

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

ST 198 is an orally active D3R antagonist. ST 198 can block the expression of nicotine-induced CPP at doses selective for D3R. ST 198 can be used for the research of neurological disease[1].

体外研究
(In Vitro)

ST 198 可以在对 D3R 具有选择性的剂量下阻断尼古丁诱导的 CPP 的表达[1]

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

体内研究
(In Vivo)

ST 198 (p.o.; 3, 30, 100 mg/kg) 抑制尼古丁 CPPs 的表达[1]

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

Animal Model: Rats[1].
Dosage: 3, 30, 100 mg/kg
Administration: p.o
Result: Displayed nicotine-induced CPP.
分子量

334.45

Formula

C22H26N2O

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
参考文献
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  • 稀释计算器

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

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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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ST 198
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HY-111280
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