GLPBio

Astemizole

Catalog No.: GC16945Purity:>99.50%Synonyms: NSC 329963
Astemizol (R 43512), ein Antihistaminikum der zweiten Generation zur Linderung allergischer Symptome mit langer Wirkdauer, ist ein Histamin-H1-Rezeptor-Antagonist mit einem IC50 von 4 nM.

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Astemizole
Cas No.: 68844-77-9
10mM (in 1mL DMSO)In Stock
$38.00
1
1mgIn Stock
$17.00
1
5mgIn Stock
$35.00
1
10mgIn Stock
$50.00
1
25mgIn Stock
$77.00
1
50mgIn Stock
$115.00
1
100mgIn Stock
$162.00
1

Zitate (Citations)

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    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    31, 1291–1307 (2021)

Beschreibung (Description)

Astemizole is a potent anti-histamine compound that antagonizes the histamine H1-receptor with an IC50 value of 4nM [1]. Astemizole can inhibit the KCa1.1 potassium ion channel in osteosarcoma cells, with an IC50 value of 0.135μM [2]. Astemizole has been widely used as an anti-cancer agent, inhibiting the growth of various tumor cells[3].

In vitro, Astemizole treatment for 6 days significantly inhibited cell death in BT-474 cells, with an IC50 value of 1.72μM[4]. 1µM of Astemizole was pre-treated for 12 hours, which significantly restored the viability of human umbilical vein endothelial cells (HUVECs) under oxidative stress and eliminated the intracellular reactive oxygen species (ROS) induced by H2O2[5]. Treatment with 5µM Astemizole for 96 hours can target the expression of Eag1 protein, induce apoptosis in HeLa cells, and inhibit cell proliferation[6].

In vivo, Astemizole treatment for 7 days (20mg/kg/day; p.o.) can effectively reverse the leakage of albumin across the blood-retinal barrier in experimental diabetes[7]. Oral administration of 50mg/kg of Astemizole daily for 12 weeks significantly inhibited the occurrence of hepatocellular carcinoma (HCC) in rats induced by diethylnitrosamine[8].

References:
[1] Laduron P M, Janssen P F, Gommeren W, et al. In vitro and in vivo binding characteristics of a new long-acting histamine H1 antagonist, astemizole[J]. Molecular Pharmacology, 1982, 21(2): 294-300.
[2] Mészáros B, Csoti A, Szanto T G, et al. The hEag1 K+ Channel Inhibitor Astemizole Stimulates Ca2+ Deposition in SaOS-2 and MG-63 Osteosarcoma Cultures[J]. International journal of molecular sciences, 2022, 23(18): 10533.
[3] Garcia-Quiroz J, Camacho J. Astemizole: an old anti-histamine as a new promising anti-cancer drug[J]. Anti-Cancer Agents in Medicinal Chemistry-Anti-Cancer Agents), 2011, 11(3): 307-314.
[4] García-Quiroz J, González-González M E, Díaz L, et al. Astemizole, an inhibitor of ether-à-go-go-1 potassium channel, increases the activity of the tyrosine kinase inhibitor gefitinib in breast cancer cells[J]. Revista de investigación clínica, 2019, 71(3): 186-194.
[5] Tian J N, Shi X D, Wang X K, et al. Astemizole protects against human umbilical vein endothelial cell injury induced by hydrogen peroxide via the p53 signaling pathway[J]. Molecular Medicine Reports, 2017, 15(6): 4286-4290.
[6] de Guadalupe Chávez-López M, Hernández-Gallegos E, Vázquez-Sánchez A Y, et al. Antiproliferative and proapoptotic effects of astemizole on cervical cancer cells[J]. International Journal of Gynecological Cancer, 2014, 24(5): 824-828.
[7] Hollis T M, Sill H W, Butler C, et al. Astemizole reduces blood-retinal barrier leakage in experimental diabetes[J]. Journal of diabetes and its complications, 1992, 6(4): 230-235.
[8] de Guadalupe Chavez-Lopez M, Pérez-Carreón J I, Zuñiga-García V, et al. Astemizole-based anticancer therapy for hepatocellular carcinoma (HCC), and Eag1 channels as potential early-stage markers of HCC[J]. Tumor Biology, 2015, 36(8): 6149-6158.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

BT-474 cells

Preparation Method

BT-474 cells were maintained in Hybri-Care medium supplemented with 1.5g/l sodium bicarbonate, 100units/ml penicillin plus 100µg/ml streptomycin, and heat-inactivated FBS to a final concentration of 10% in humidified atmosphere with 5% CO2 at 37°C. Cells were seeded in 96-well plates at a density of 1000 cells per well. After 24h, cells were incubated in the presence of different concentrations of Astemizole (0, 0.5, 1, 1.5, 2.0, 2.5μM), or the vehicle alone (DMSO) during 6 days. Cell proliferation was measured.

Reaction Conditions

0, 0.5, 1, 1.5, 2.0, 2.5μM; 6 days

Applications

Astemizole treatment reduced the cell viability of BT-474 cells in a dose-dependent manner.
Animal experiment [2]:

Animal models

Male Wistar rats

Preparation Method

Male Wistar rats weighing 200g received intraperitoneal injections of Diethylnitrosamine (50mg/kg) once a week for 12 weeks. Oral administration of Astemizole (50mg/kg) was given daily for 12 weeks. The control group received PBS. Mice were weighed weekly. At the end of treatments, mice were sacrificed by decapitation. Livers were rapidly removed weighed, and photographed.

Dosage form

50mg/kg/day for 12 weeks; p.o.

Applications

Astemizole treatment prevented diethylnitrosamine-induced rat HCC development in rats.

References:
[1] García-Quiroz J, González-González M E, Díaz L, et al. Astemizole, an inhibitor of ether-à-go-go-1 potassium channel, increases the activity of the tyrosine kinase inhibitor gefitinib in breast cancer cells[J]. Revista de investigación clínica, 2019, 71(3): 186-194.
[2] de Guadalupe Chavez-Lopez M, Pérez-Carreón J I, Zuñiga-García V, et al. Astemizole-based anticancer therapy for hepatocellular carcinoma (HCC), and Eag1 channels as potential early-stage markers of HCC[J]. Tumor Biology, 2015, 36(8): 6149-6158.

Produktdokumente (Product Documents)

Purity:>99.50%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
68844-77-9
Synonyme
NSC 329963
Chemischer Name
1-(4-fluorobenzyl)-N-(1-(4-methoxyphenethyl)piperidin-4-yl)-1H-benzo[d]imidazol-2-amine
SMILES
FC1=CC=C(C=C1)CN2C(NC3CCN(CCC(C=C4)=CC=C4OC)CC3)=NC5=CC=CC=C25
Summenformel
C28H31FN4O
Molekulargewicht
458.57
Löslichkeit
≥ 11.5mg/mL in DMSO with gentle warming
Lagerung
Store at -20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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