L-(-)-α-Methyldopa
CAS No. 555-30-6
L-(-)-α-Methyldopa ( Methyldopa | MK-351 | NSC 169916 )
产品货号. M15017 CAS No. 555-30-6
甲基多巴是一种α-肾上腺素能激动剂(对α2-肾上腺素能受体有选择性)精神活性化合物,用作交感神经药或抗高血压药。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 50MG | ¥129 | 有现货 |
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| 100MG | ¥165 | 有现货 |
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| 200MG | ¥223 | 有现货 |
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| 500MG | ¥354 | 有现货 |
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| 1G | ¥509 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥167 | 有现货 |
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生物学信息
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产品名称L-(-)-α-Methyldopa
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述甲基多巴是一种α-肾上腺素能激动剂(对α2-肾上腺素能受体有选择性)精神活性化合物,用作交感神经药或抗高血压药。
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产品描述Methyldopa is an alpha-adrenergic agonist (selective for α2-adrenergic receptors) psychoactive drug used as a sympatholytic or antihypertensive.(In Vivo):Methyldopa hydrate (L-(-)-α-Methyldopa hydrate; 200 mg/kg; i.p.) decreases the hyperglycemic response in the first 2 hr after Dieldrin treatment.
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体外实验——
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体内实验Methyldopa (L-(-)-α-Methyldopa; 200 mg/kg; i.p.) decreases the hyperglycemic response in the first 2 hr after Dieldrin treatment. Animal Model:60-day-old male rats Dosage:200 mg/kg Administration:I.p.Result: Decreased the plasma concentration of glucose in Dieldrin-exposed rats by 24% during the 30 min following its administration.
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同义词Methyldopa | MK-351 | NSC 169916
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通路GPCR/G Protein
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靶点Dopamine Receptor
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受体DOPA decarboxylase
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研究领域Cardiovascular Disease
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适应症——
化学信息
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CAS Number555-30-6
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分子量211.21
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分子式C10H13NO4
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纯度>98% (HPLC)
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溶解度Ethanol: <1 mg/mL (<1 mM); Water: <1 mg/mL (<1 mM); DMSO: <1 mg/mL (<1 mM)
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SMILESO=C(O)[C@@](C)(N)CC1=CC=C(O)C(O)=C1
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化学全称(S)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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左舒必利是舒必利的 (S)-对映体,是 D2 受体 a 拮抗剂。
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Benperidol
Benperidol (Anquil) is a butanone analog with antipsychotic and stabilizing properties, and has been shown to be effective in blocking D2 receptors.Benperidol can be used in positron emission tomography (PET) scanning to measure D(2) dopamine receptor binding in vivo.Benperidol has been shown to be effective in blocking D2 receptors in vivo.Benperidol has been shown to be effective in blocking D2 receptors in vivo.
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