Yohimbine hydrochloride, 99%
Yohimbine hydrochloride, 99%
Yohimbine hydrochloride, 99%
Yohimbine hydrochloride, 99%
Thermo Scientific Chemicals

Yohimbine hydrochloride, 99%

Yohimbine hydrochloride, CAS # 65-19-0, is an α2-adrenergic receptor antagonist, which blocks the central α2-adrenegic receptors in the brain. | CAS: 65-19-0 | C21H27ClN2O3 | 390.91 g/mol
数量:
5 g
25 g
パッケージ:
Glass bottle
製品番号(カタログ番号) 141030050
価格(JPY)
-
見積もりを依頼する
数量:
5 g
パッケージ:
Glass bottle
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化学物質識別子
CAS65-19-0
IUPAC Namehydrogen methyl (1S,15R,18S,19R,20S)-18-hydroxy-3,13-diazapentacyclo[11.8.0.0²,¹⁰.0⁴,⁹.0¹⁵,²⁰]henicosa-2(10),4,6,8-tetraene-19-carboxylate chloride
Molecular FormulaC21H27ClN2O3
InChI KeyPIPZGJSEDRMUAW-VJDCAHTMSA-N
SMILES[H+].[Cl-].COC(=O)[C@H]1[C@@H](O)CC[C@H]2CN3CCC4=C(NC5=CC=CC=C45)[C@@H]3C[C@H]12
さらに表示
Appearance (Color)White to light yellow
Appearance (Form)Powder
Infrared spectrumConforms
Titration with HClO4>=98.5 %
Specific optical rotation+99° to +105° (20°C, 589 nm) (c=1, H2O)
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

General Description

  • Yohimbine hydrochloride is an indole alkaloid derived from the tree bark
  • It is an antagonist of α2-adrenergic receptors in the brain, reducing the effects of xylazine, which is an α2-adrenergic agonist

Applications

  • Yohimbine hydrochloride blocks the central α2-adrenegic receptors in the brain
  • It can reduce or eradicate effects of xylazine, which is an α2-adrenergic agonist
  • It can have an antidiuretic effect
RUO – Research Use Only

General References:

  1. Zhang, W. and Roomans, G.M. A yohimbine-dependent, UK14,304 induced ion transient in HT29 cells studied by X-ray microanalysis. Scanning microscopy, 1996, 10 (1), 293-299.
  2. Susan, X. Jiang et. al. Reversible inhibition of intracellular calcium influx through NMDA receptors by imidazoline I2receptor antagonists. European Journal of Pharmacology. 2010, 629,(1), 12-19.