4 Results for "

Rauwolscine

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "Rauwolscine" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-12710
CAS No.: 131-03-3
Purity:  98.27%
Synonyms: α-Yohimbine; Corynanthidine; Isoyohimbine
Rauwolscine is a selective α2-adrenoceptor antagonist that inhibits tumor growth and induces apoptosis .
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Cat. No.: HY-12710A
CAS No.: 6211-32-1
Synonyms: α-Yohimbine hydrochloride; Corynanthidine hydrochloride; Isoyohimbine hydrochloride
Rauwolscine hydrochloride is a potent and specific α2 adrenergic receptor antagonist with a Ki of 12 nM.
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Cat. No.: HY-106838A
CAS No.: 67384-25-2
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease

Org 6906 is a monoamine reuptake inhibitor that promotes monoaminergic neurotransmission by inhibiting the reuptake of noradrenaline, dopamine, and serotonin. Org 6906 is also an α2 Adrenergic Receptor antagonist, with a pKi value of 6.3 (using the selective α2 adrenergic receptor ligand [ 3H]rauwolscine as a ligand). Org 6906 exhibits antidepressant activity and can be used in research related to neurological disorders .
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Cat. No.: HY-136693
CAS No.: 98719-20-1
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease

L-654284 is an α2-adrenergic receptor antagonist with significant selectivity. L-654284 competes with the binding of 3H-clonidine and 3H-rauwolscine in vitro and shows Ki values of 0.8 nM and 1.1 nM, respectively. L-654284 can block the protrusion effect of clonidine in isolated vas deferens in rats, with a pA2 value of 9.1. L-654284 exhibits remarkable selectivity for α2 and α1 adrenergic receptors, and exhibits a Ki of 110 nM in inhibiting 3H-prazosin binding. L-654284 can significantly increase the turnover rate of norepinephrine in rat cerebral cortex in vivo, showing α2-adrenergic receptor blocking activity in the central nervous system .
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