GLPBio

Zebularine

Catalog No.: GC12153Purity:>98.00%
Zebularine, a cytidine lacking the 4-amino group, is a DNMT inhibitor that inhibits DNA methylation.

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Zebularine
Cas No.: 3690-10-6
10mM (in 1mL DMSO)In Stock
$27.00
1
5mgIn Stock
$25.00
1
10mgIn Stock
$40.00
1
50mgIn Stock
$154.00
1
100mgIn Stock
$231.00
1

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Beschreibung (Description)

Zebularine, a cytidine lacking the 4-amino group, is a DNMT inhibitor that inhibits DNA methylation[1]. Zebularine can cause DNA demethylation and enhance cGAS-STING pathway activity, leading to accumulation of DNA fragments in the cytoplasm[2]. Zebularine has been widely used in cell models to inhibit tumor growth and alter cancer cell gene expression[3].

In vitro, Zebularine treatment for 24 hours significantly inhibited the viability of HCCLM3, MHCC97H, and MHCC97L cells with IC50 values of 56.75µM, 59.72µM, and 64.93µM, respectively[4]. Treatment of MDA-MB-231 cells with 200µM Zebularine for 96 hours significantly inhibited cell proliferation, induced S-phase arrest, and resulted in decreased expression of cyclins B and D[5]. Treatment of A549 cells with 100µM Zebularine for 72h induced apoptosis, accompanied by loss of mitochondrial membrane potential, decrease of Bcl-2, increase of Bax and p53, and activation of caspase-3 and caspase-8[6].

In vivo, Zebularine treatment via oral administration at a dose of 100mg/kg every four days for 20 days significantly inhibited tumor growth in the BGC823 cell xenograft mouse model[7]. Daily intraperitoneal injection of Zebularine (225mg/kg) for 7 days reduced the fibrotic lesion area and inflammatory response in the kidney in a mouse model of unilateral ureteral obstruction (UUO)[8].

References:
[1] Champion C, Guianvarc'h D, Sénamaud-Beaufort C, et al. Mechanistic insights on the inhibition of c5 DNA methyltransferases by zebularine[J]. PloS one, 2010, 5(8): e12388.
[2] Lai J, Fu Y, Tian S, et al. Zebularine elevates STING expression and enhances cGAMP cancer immunotherapy in mice[J]. Molecular Therapy, 2021, 29(5): 1758-1771.
[3] Cheng J C, Yoo C B, Weisenberger D J, et al. Preferential response of cancer cells to zebularine[J]. Cancer cell, 2004, 6(2): 151-158.
[4] Sanaei M, Kavoosi F. Effect of zebularine on apoptotic pathways in hepatocellular carcinoma cell lines[J]. International Journal of Preventive Medicine, 2023, 14(1): 63.
[5] Billam M, Sobolewski M D, Davidson N E. Effects of a novel DNA methyltransferase inhibitor zebularine on human breast cancer cells[J]. Breast cancer research and treatment, 2010, 120(3): 581-592.
[6] You B R, Park W H. Zebularine inhibits the growth of A549 lung cancer cells via cell cycle arrest and apoptosis[J]. Molecular Carcinogenesis, 2014, 53(11): 847-857.
[7] Tan W, Zhou W, Yu H, et al. The DNA methyltransferase inhibitor zebularine induces mitochondria-mediated apoptosis in gastric cancer cells in vitro and in vivo[J]. Biochemical and biophysical research communications, 2013, 430(1): 250-255.
[8] Koh E S, Kim S, Son M, et al. The protective effect of zebularine, an inhibitor of DNA methyltransferase, on renal tubulointerstitial inflammation and fibrosis[J]. International Journal of Molecular Sciences, 2022, 23(22): 14045.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

HCCLM3 cells

Preparation Method

HCCLM3 cells were cultured in DMEM medium supplemented with 10% fetal bovine serum and antibiotics (0.1mg/ml streptomycin and 100U/ml penicillin) at 37°C and 5% CO2 for 24 hours. Subsequently, all HCCLM3 cells were seeded in 96-well plates (3×105 cells per well). After 1 day, the medium was removed, and medium containing different concentrations of Zebularine (0, 10, 25, 50, 75, and 100μM) was added, while the control group was treated with 0.05% DMSO. After 24 hours of treatment with Zebularine, MTT solution (5mg/ml) was added to each well and incubated at 37°C for 4 hours. Subsequently, absorbance was measured at a wavelength of 570nm using a microplate reader.

Reaction Conditions

0, 10, 25, 50, 75, and 100μM; 24h

Applications

Zebularine treatment inhibited the cell viability of HCCLM3 cells in a dose-dependent manner.
Animal experiment [2]:

Animal models

Female BALB/c nude mice

Preparation Method

BGC823 cells were injected into the flank of BALB/c nude mice (female, 4-6 weeks of age) and maintained under specific pathogen-free (SPF) conditions. Mice were randomly divided into two groups: a control group and an experimental group (100mg/kg; p.o). Each group contained five nude mice (at least six tumors per group; 1-2 nude mice per group were randomly sacrificed and used to establish the time course of expression). When tumor volume reached 100-150mm3, nude mice were treated by gavage with Zebularine (dissolved in 0.45% saline) every 4 days for 20 days. The control group was given 0.45% normal saline by gavage every 4 days for 20 days. Tumor growth was monitored by measuring tumor volume (TV), which was calculated using the formula: TV (mm3) = width2(mm2)×length(mm)/2.

Dosage form

100mg/kg; every four days for 20 days; p.o.

Applications

Zebularine treatment significantly reduced tumor xenograft growth in mice.

References:
[1] Sanaei M, Kavoosi F. Effect of zebularine on apoptotic pathways in hepatocellular carcinoma cell lines[J]. International Journal of Preventive Medicine, 2023, 14(1): 63.
[2] Tan W, Zhou W, Yu H, et al. The DNA methyltransferase inhibitor zebularine induces mitochondria-mediated apoptosis in gastric cancer cells in vitro and in vivo[J]. Biochemical and biophysical research communications, 2013, 430(1): 250-255.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
3690-10-6
Chemischer Name
1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one
SMILES
C1=CN(C(=O)N=C1)C2C(C(C(O2)CO)O)O
Summenformel
C9H12N2O5
Molekulargewicht
228.2
Löslichkeit
DMF: 5 mg/ml,DMSO: 14 mg/ml,Ethanol: 0.25 mg/ml,PBS (pH 7.2): 10 mg/ml
Lagerung
Store at 2-8°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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