| Name | (R)-Terazosin |
| Description | (R)-Terazosin is an active R-enantiomer of Terazosin and a potent antagonist of α1-adrenoceptor [(α1a, α1b, and α1d-adrenoceptor] with Ki values of 6.51 nM, 1.01 nM, and 1.97 nM, respectively). |
| In vitro | (R)-Terazosin exhibits low affinity for α2a, α2B, and α2c-adrenoceptors (Ki of 3.85 μM, 0.33 μM, and 0.37 μM, respectively). It may serve as a useful probe for exploring the functional roles of adrenoceptor subtypes in various tissues. |
| In vivo | (R)-Terazosin demonstrates antagonism at rat atrial α2B receptor (pEC30: 5.69) and at rat vas deferens α1A and α2A receptors (pA2: 7.5 and 5.31, respectively). |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 5 mg/mL (12.91 mM), Sonication is recommended. DMSO : 55 mg/mL (141.96 mM), Sonication is recommended.
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| Keywords | α2-adrenoceptor | α1d-adrenoceptor | α1b-adrenoceptor | α1B-adrenergic receptor | α1-adrenoceptor | α1a-adrenoceptor | α1A-adrenergic receptor | Terazosin | subtypes | prove | Low | Inhibitor | inhibit | Beta Receptor | affinity | AdrenergicReceptor | Adrenergic Receptor | (R)-Terazosin | (R)Terazosin | (R) Terazosin |
| Inhibitors Related | Trifluoperazine dihydrochloride | Mirtazapine | Octopamine hydrochloride | Gemfibrozil | Buflomedil hydrochloride | Dexmedetomidine hydrochloride | Isoprenaline hydrochloride | D-Mannitol | Mianserin hydrochloride | Trazodone hydrochloride | Atenolol | Doxepin hydrochloride |
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