GLPBio

Ebselen

Catalog No.: GC10331Purity:99.97%
Ebselen (SPI-1005), ein Glutathionperoxidase-Mimetikum, ist ein potenter Blocker des spannungsabhÄngigen Calciumkanals (VDCC).

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


Ebselen
Cas No.: 60940-34-3
10mM (in 1mL DMSO)In Stock
$38.00
1
5mgIn Stock
$34.00
1
10mgIn Stock
$49.00
1
25mgIn Stock
$80.00
1
50mgIn Stock
$98.00
1
100mgIn Stock
$168.00
1

Zitate (Citations)

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    641, 529–536 (2025)
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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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    Science
    388(6745) (2025)
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    387(6734) (2025)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

Beschreibung (Description)

Ebselen is a selenoorganic compound with glutathione peroxidase-like activity and is an anti-inflammatory and antioxidant agent[1]. Ebselen is an inhibitor of inositol monophosphatase (IMPase) with an IC50 of 1.5μM[2]. Ebselen is a potent scavenger of hydrogen peroxide and hydroperoxides, including membrane-bound phospholipid and cholesterol ester hydroperoxides[3]. Ebselen can penetrate the blood-brain barrier and has anti-inflammatory, antioxidant and anti-cancer activities[4].

In vitro, Ebselen (0-100μM) treatment of U266 and RPMI8226 cells for 24h reduced cell viability in a concentration-dependent manner, induced cell apoptosis, increased the generation of intracellular ROS, and induced the translocation of Bax protein from the cytosol to the mitochondria[5]. Ebselen (5-10μM) treatment of V79 cells reduced hydrogen peroxide-induced DNA damage[6]. Ebselen (10-20μM) inhibited the growth of A549 lung cancer cells, Calu-6 lung cancer cells and primary normal human lung fibroblasts (HPF) cells, with IC50 values of approximately 12.5μM, 10μM and 20μM, respectively[7].

In vivo, Ebselen (10mg/kg) was intraperitoneally injected into rats with spinal cord injury (SCI), which reduced the levels of malondialdehyde (MDA) and protein carbonyl (PC) in spinal cord tissue and prevented the inhibition of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and catalase (CAT) enzyme activities in tissues induced by SCI[8].

References:
[1] Nakamura Y, Feng Q, Kumagai T, et al. Ebselen, a glutathione peroxidase mimetic seleno-organic compound, as a multifunctional antioxidant: implication for inflammation-associated carcinogenesis[J]. Journal of Biological Chemistry, 2002, 277(4): 2687-2694.
[2] Ramli F F, Cowen P J, Godlewska B R. The potential use of ebselen in treatment-resistant depression[J]. Pharmaceuticals, 2022, 15(4): 485.
[3] Santofimia-Castaño P, Izquierdo-Alvarez A, de la Casa-Resino I, et al. Ebselen alters cellular oxidative status and induces endoplasmic reticulum stress in rat hippocampal astrocytes[J]. Toxicology, 2016, 357: 74-84.
[4] Ali F, Alom S, Ali S R, et al. Ebselen: A Review on its Synthesis, Derivatives, Anticancer Efficacy and Utility in Combating SARS-COV-2[J]. Mini Reviews in Medicinal Chemistry, 2024, 24(12): 1203-1225.
[5] Zhang L, Zhou L, Du J, et al. Induction of apoptosis in human multiple myeloma cell lines by ebselen via enhancing the endogenous reactive oxygen species production[J]. BioMed Research International, 2014, 2014(1): 696107.
[6] Miorelli S T, Rosa R M, Moura D J, et al. Antioxidant and anti-mutagenic effects of ebselen in yeast and in cultured mammalian V79 cells[J]. Mutagenesis, 2008, 23(2): 93-99.
[7] Park W H. Ebselen Inhibits the Growth of Lung Cancer Cells via Cell Cycle Arrest and Cell Death Accompanied by Glutathione Depletion[J]. Molecules, 2023, 28(18): 6472.
[8] Kalayci M, Coskun O, Cagavi F, et al. Neuroprotective effects of ebselen on experimental spinal cord injury in rats[J]. Neurochemical Research, 2005, 30: 403-410.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

U266、RPMI8226 cells

Preparation Method

Cells were treated with 0 (control), 10, 20, 30, 40, 50, and 100μM Ebselen for 24h, respectively. Concentration dependent changes of cell viability determined by CCK-8 assay in cells.

Reaction Conditions

0, 10, 20, 30, 40, 50, 100μM; 24h

Applications

Ebselen induced a decrease in cell viability in a concentration-dependent manner.

Animal experiment [2]:

Animal models

Wistar albino rats

Preparation Method

Rats were allotted in six experimental groups: A (control), B (only laminic tomy), C (Trauma; laminectomy+spinal trauma), D (Placebo group; laminectomy+spinal trauma+serum physiology), E (Methylprednisolone group; laminectomy+spinal trauma+Methylprednisolone treated), F (Ebselen group; laminectomy+spinal trauma+Ebselen treated), each containing six rats. Group A, B and C were not treated by any drug. Group D received 1 mL serum physiology, group E received 30mg/kg Methylprednisolone intraperitoneally (i.p.) and group F received 10mg/kg Ebselen i.p. just after the trauma. Rats were examined neurologically at 24h after trauma and spinal cord tissue samples were harvested for both biochemical and histopathological evaluation.

Dosage form

10mg/kg; i.p.

Applications

Ebselen treatment reduced malondialdehyde (MDA) and protein carbonyl (PC) levels in spinal cord tissue and prevented SCI-induced inhibition of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) enzyme activities in the tissue.

References:
[1]Zhang L, Zhou L, Du J, et al. Induction of apoptosis in human multiple myeloma cell lines by ebselen via enhancing the endogenous reactive oxygen species production[J]. BioMed Research International, 2014, 2014(1): 696107.
[2]Kalayci M, Coskun O, Cagavi F, et al. Neuroprotective effects of ebselen on experimental spinal cord injury in rats[J]. Neurochemical Research, 2005, 30: 403-410.

Produktdokumente (Product Documents)

Purity:99.97%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
60940-34-3
Chemischer Name
2-phenylbenzo[d][1,2]selenazol-3(2H)-one
SMILES
O=C1C2=CC=CC=C2[Se]N1C3=CC=CC=C3
Summenformel
C13H9NOSe
Molekulargewicht
274.18
Löslichkeit
≤5mg/ml in ethanol;5mg/ml in DMSO;5mg/ml in dimethyl formamide
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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