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Rauwolscine hydrochloride

CAS No. 6211-32-1

Rauwolscine hydrochloride ( α-Yohimbine hydrochloride | Isoyohimbine hydrochloride )

产品货号. M18915 CAS No. 6211-32-1

Rauwolscine 是一种天然生物碱,是一种特异性、可逆的 α2-肾上腺素受体拮抗剂 (Ki: 12 nM)。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
50MG ¥405 有现货
100MG 获取报价 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Rauwolscine hydrochloride
  • 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
  • 产品简述
    Rauwolscine 是一种天然生物碱,是一种特异性、可逆的 α2-肾上腺素受体拮抗剂 (Ki: 12 nM)。
  • 产品描述
    Rauwolscine, a natural alkaloid, is a specific and reversible α2-adrenergic receptor antagonist (Ki: 12 nM). It is a stereoisomer of yohimbine, which potently antagonizes both α1- and α2-adrenergic receptors. Rauwolscine also acts as a receptor antagonist at the serotonin 5-HT2B receptor (Ki: 14.3 nM) and as a weak partial agonist at 5-HT1A (IC50: 1.3 μM). The α2-adrenergic receptor has diverse physiological functions and antagonists like rauwolscine have numerous applications, including the modulation of mood and behavior.(In Vitro):[3H]Rauwolscine binding to α2 adrenergic receptor is reversible, stcreospccific, and saturable. [3H]Rauwolscine specifically labels both the high and low affinity states of the α2 adrenergic receptor in brain membranes. [3H]Rauwolscine also behaves as a 5-HT1A receptor agonist and this conclusion is compatible with earlier functional studies, indicating that rauwolscine (as well as yohimbine) has agonistic properties at the level of 5-HT autoreceptors. When using [3H]5-HT as a radioligand, rauwolscine is determined to have relatively high affinity for the human receptor (Ki human=14.3 nM, Ki rat=35.8 nM). Saturation studies shows that the affinity of [3H]Rauwolscine is similar in mouse, rat, rabbit, dog (2.33-3.03 nM) except man where it is significantly higher (0.98 nM) .
  • 体外实验
    [3H]Rauwolscine binding to α2 adrenergic receptor is reversible, stcreospccific, and saturable. [3H]Rauwolscine specifically labels both the high and low affinity states of the α2 adrenergic receptor in brain membranes. [3H]Rauwolscine also behaves as a 5-HT1A receptor agonist and this conclusion is compatible with earlier functional studies, indicating that rauwolscine (as well as yohimbine) has agonistic properties at the level of 5-HT autoreceptors. When using [3H]5-HT as a radioligand, rauwolscine is determined to have relatively high affinity for the human receptor (Ki human=14.3 nM, Ki rat=35.8 nM). Saturation studies shows that the affinity of [3H]Rauwolscine is similar in mouse, rat, rabbit, dog (2.33-3.03 nM) except man where it is significantly higher (0.98 nM) .
  • 体内实验
    ——
  • 同义词
    α-Yohimbine hydrochloride | Isoyohimbine hydrochloride
  • 通路
    Cytoskeleton/Cell Adhesion Molecules
  • 靶点
    Microtubule/Tubulin
  • 受体
    α2 adrenergic receptor
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    6211-32-1
  • 分子量
    390.9
  • 分子式
    C21H27ClN2O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : 6 mg/mL 15.35 mM; H2O : 5 mg/mL 12.79 mM
  • SMILES
    Cl.[H][C@]12CC[C@H](O)[C@@H](C(=O)OC)[C@@]1([H])C[C@]1([H])N(CCc3c1[nH]c1ccccc31)C2
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Perry B D, U'Prichard D C. [3H] Rauwolscine (α-yohimbine): a specific antagonist radioligand for brain α2-adrenergic receptors[J]. European journal of pharmacology, 1981, 76(4): 461-464.
产品手册
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