Item no. |
HY-B0354A-25mg |
Manufacturer |
MedChem Express
|
CASRN |
64887-14-5 |
Amount |
25 mg |
Quantity options |
100 mg
10 mM/1 mL
10 mg
25 mg
500 mg
50 mg
5 mg
|
Category |
|
Type |
Inhibitors |
Specific against |
other |
Purity |
99.97 |
Citations |
[1]Gross, G., G. Hanft, and N. Kolassa, Urapidil and some analogues with hypotensive properties show high affinities for 5-hydroxytryptamine (5-HT) binding sites of the 5-HT1A subtype and for alpha 1-adrenoceptor binding sites. Naunyn Schmiedebergs Arch Pharmacol, 1987. 336(6): p. 597-601. [2]Buch, J., Urapidil, a dual-acting antihypertensive agent: Current usage considerations. Adv Ther, 2010. 27(7): p. 426-43. [3]Vanhaesebrouck S, et al. Neonatal transient respiratory depression after maternal urapidil infusion for hypertension. Eur J Pediatr. 2009 Feb;168(2):221-3. |
Smiles |
O=C1N(C)C(C=C(NCCCN2CCN(C3=CC=CC=C3OC)CC2)N1C)=O.Cl |
ECLASS 10.1 |
32160490 |
ECLASS 11.0 |
32160490 |
UNSPSC |
12000000 |
Alias |
64887-14-5 |
Shipping condition |
Room temperature |
Available |
|
Manufacturer - Type |
Reference compound |
Manufacturer - Applications |
COVID-19-immunoregulation |
Manufacturer - Targets |
5-HT Receptor; Adrenergic Receptor |
Shipping Temperature |
Room Temperature |
Storage Conditions |
4°C (Powder, sealed storage, away from moisture) |
Molecular Weight |
423.94 |
Product Description |
Urapidil hydrochloride is an orally active α1-adrenoceptor antagonist and 5-HT1A receptor agonist with a pIC50 of 6.13 and 4.38 against α1- and α2-adrenoceptor, respectively. Urapidil hydrochloride shows antihypertensive effect[1][2]. |
Manufacturer - Research Area |
Cardiovascular Disease; Endocrinology |
Solubility |
DMSO : 14.29 mg/mL (ultrasonic; warming; heat to 60°C)|H2O : 100 mg/mL (ultrasonic) |
Manufacturer - Pathway |
GPCR/G Protein; Neuronal Signaling |
Isoform |
5-HT1 Receptor; α adrenergic receptor |
Clinical information |
Launched |
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All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.