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> 产品中心 > 抑制剂 & 激动剂 > Membrane Transporter/Ion Chann > Monoamine Transporter

Reserpine

Cat. No.:YN360932

  • CAS No. :50-55-5

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    • 参考文献
    • 产品名称: Reserpine
      CAS No.: 50-55-5
      Chemical Name: (3β,16β,17α,18β,20α)-11,17-dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-yohimban-16-carboxylic acid, methyl ester
      Synonyms:利血平
      分子量:608.68
      分子式:C₃₃H₄₀N₂O₉
      SMILES:O=C([C@H]([C@@H](OC)[C@H](OC(C1=CC(OC)=C(OC)C(OC)=C1)=O)C[C@]2([H])CN3CC4)[C@@]2([H])C[C@]3([H])C5=C4C(C=CC(OC)=C6)=C6N5)OC
      存储:Please store the product under the recommended conditions in theCertificate of Analysis.
      运输:Room temperature in continental US; may vary elsewhere.
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      Purity: 98%
    • 产品描述: Reserpine 是囊泡单胺转运蛋白 2 (VMAT2) 的抑制剂。
      IC50和靶点:
      In Vitro:
      In Vivo:
      Clinical Trial:
      Solvent & Solubility:
    • Schuldiner, S., Liu, Y., and Edwards, R.H.Reserpine binding to a vesicular amine transporter expressed in Chinese hamster ovary fibroblastsJ. Biol. Chem.268(1),29-34(1993)

      Erickson, J.D., Schäfer, M.K.H., Bonner, T.I., et al.Distinct pharmacological properties and distribution in neurons and endocrine cells of two isoforms of the human vesicular monoamine transporterProc. Natl. Acad. Sci. USA93(10),5166-5171(1996)

      Hu, X.T., Wachtel, S.R., Galloway, M.P., et al.Lesions of the nigrostriatal dopamine projection increase the inhibitory effects of D1 and D2 dopamine agonists on caudate-putamen neurons and relieve D2 receptors from the necessity of D1 receptor stimulationJ. Neurosci.10(7),2318-2329(1990)

      Stanwood, G.D., Lucki, I., and McGonigle, P.Differential regulation of dopamine D2 and D3 receptors by chronic drug treatmentsJ. Pharmacol. Exp. Ther.295(3),1232-1240(2000)

      Matsumoto, K., Mizowaki, M., Suchitra, T., et al.Central antinociceptive effects of mitragynine in mice: Contribution of descending noradrenergic and serotonergic systemsEur. J. Pharmacol.317(1),75-81(1996)

      Wang, E.j., Lew, K., Barecki, M., et al.Quantitative distinctions of active site molecular recognition by P-glycoprotein and cytochrome P450 3A4Chem. Res. Toxicol.14(12),1596-1603(2001)

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