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Submit ReviewRauwolscine hydrochloride
Description: α2 antagonist
Alternative Names: α-Yohimbine hydrochloride, Corynanthidine
Chemical Name: 17α-Hydroxy-20α-yohimban-16β-carboxylic acid,methyl ester hydrochloride
Purity: ≥95% (HPLC)
Biological Activity for Rauwolscine hydrochloride
Rauwolscine hydrochloride is a standard α2-adrenergic antagonist (Ki values are 3.5, 4.6, and 0.6 nM at cloned human α2A, α2B, and α2C-adrenoceptors respectively). Partial agonist at 5-HT1A receptors.
Diastereomer also avilable.
Technical Data for Rauwolscine hydrochloride
| M. Wt | 390.91 |
| Formula | C21H26N2O3.HCl |
| Storage | Store at RT |
| Purity | ≥95% (HPLC) |
| CAS Number | 6211-32-1 |
| PubChem ID | 197067 |
| InChI Key | PIPZGJSEDRMUAW-ZKKXXTDSSA-N |
| Smiles | [H][C@]12C4=C(C(C=CC=C5)=C5N4)CCN1C[C@]3([H])[C@]([C@H]([C@](OC)=O)[C@@H](O)CC3)([H])C2.Cl |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Solubility Data for Rauwolscine hydrochloride
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| water | 5 with gentle warming | ||
| DMSO | 9.77 | 25 with gentle warming |
Preparing Stock Solutions for Rauwolscine hydrochloride
The following data is based on the product molecular weight 390.91. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.25 mM | 10.23 mL | 51.16 mL | 102.33 mL |
| 1.25 mM | 2.05 mL | 10.23 mL | 20.47 mL |
| 2.5 mM | 1.02 mL | 5.12 mL | 10.23 mL |
| 12.5 mM | 0.2 mL | 1.02 mL | 2.05 mL |
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Product Datasheets for Rauwolscine hydrochloride
References for Rauwolscine hydrochloride
References are publications that support the biological activity of the product.
Arthur et al (1993) Partial agonist properties of rauwolscine and yohimbine for the inhibition of adenylyl cyclase by recombinant human 5-HT1A receptors. Biochem.Pharmacol. 45 2337 PMID: 8517875
Hieble et al (1995) β- and γ-Adrenoceptors: from the gene to the clinic. 1. Molecular biology and adrenoceptor subclassification. J.Med.Chem. 38 3415 PMID: 7658428
Uhlen et al (1998) [3H]RS79948-197 binding to human, rat, guinea pig and pig α2A-, α2B-, and α2C-adrenoceptors. Comparison with MK912, RX821002, rauwolscine and yohimbine. Eur.J.Pharmacol. 343 93 PMID: 9551719
If you know of a relevant reference for Rauwolscine hydrochloride, please let us know.
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Keywords: Rauwolscine hydrochloride, Rauwolscine hydrochloride supplier, α2-adrenoceptor, alpha2-adrenoceptor, antagonists, α2-Adrenergic, alpha2-Adrenergic, a2-adrenoceptor, a2-adrenergic, Receptors, alpha-Yohimbine, hydrochloride, a-Yohimbine, Corynanthidine, Adrenergic, Alpha-2, 0891, Tocris Bioscience
2 Citations for Rauwolscine hydrochloride
Citations are publications that use Tocris products. Selected citations for Rauwolscine hydrochloride include:
Cardin and Schmidt (2004) Noradrenergic inputs mediate state dependence of auditory responses in the avian song system. J Neurosci 24 7745 PMID: 15342742
Moura et al (2006) Alpha2-adrenoceptor subtypes involved in the regulation of catecholamine release from the adrenal medulla of mice. Br J Pharmacol 149 1049 PMID: 17075569
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