GLPBio

Adenosine Dialdehyde (ADOX)

Catalog No.: GC16509Purity:>95.00%
Adox, un analogue nucléosidique purique, est un puissant inhibiteur de la S-adénosylhomocystéine hydrolase (SAHH) (Ki = 3,3 nM). L'adénosine dialdéhyde présente une puissante activité anti-tumorale in vivo et peut être utilisée pour la recherche sur le cancer.

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Adenosine Dialdehyde (ADOX)
Cas No.: 34240-05-6
10mM (in 1mL DMSO)In Stock
$42.00
1
1mgIn Stock
$19.00
1
5mgIn Stock
$42.00
1
10mgIn Stock
$55.00
1
25mgIn Stock
$96.00
1
50mgIn Stock
$148.00
1
100mgIn Stock
$222.00
1
200mgIn Stock
$333.00
1
500mgIn Stock
$543.00
1

Citations

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    Nature
    641, 529–536 (2025)
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    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)

Description

Adenosine Dialdehyde (ADOX) is an adenosine analog, acts as an inhibitor of S-adenosylhomocysteine hydrolase (SAHH)[1]. SAHH is an enzyme that regulates cellular methylation process, resulting in broad inhibition of methylation reactions. Adenosine Dialdehyde as an SAHH inhibitor, can effectively arrest the cell cycle at the G2 phase and induce apoptosis in HeLa, HCT116 cells[1]. Adenosine Dialdehyde is a potent anti-cancer drug with broad inhibiting proliferative effects and anti-invasive and anti-migratory properties[1].

In vitro, Adenosine Dialdehyde (0.01, 0.1, 1, 10 and 100μM; 72h) significantly inhibited the proliferation of MCF-7, MDA-MB-231, H292 cells in a dose dependent manner[2].

In vivo, Adenosine Dialdehyde (1.5-2.5mg/kg; 7d; s.c.) significantly increased the mean life span of A/J mice bearing C1300 murine neuroblastoma tumor[3]. Adenosine Dialdehyde (10μmol/kg; 32d; q1w; i.p.) suppressed prostate cancer growth in NCr-nu/nu mice inoculated with LNCaP cells[4].

References:
[1] Nguyen T T, Hemmer J, Kiemer A K, et al. Biodynamers as prodrugs with controlled uptake and activity [J]. Journal of controlled release, 2026, 390: 114538.
[2] Ghemrawi R, Al Qassem A, Ramadan A, et al. DNA and protein methyltransferases inhibition by adenosine dialdehyde reduces the proliferation and migration of breast and lung cancer cells by downregulating autophagy [J]. PLoS One, 2023, 18(7): e0288791.
[3] Bostrom B, Hogenkamp H P, Mirkin B L. Inhibitory effect of adenosine dialdehyde on in situ murine neuroblastoma growth [J]. Cancer Research, 1988, 48(21): 5933-5936.
[4] Shiota M, Takeuchi A, Yokomizo A, et al. Methyltransferase inhibitor adenosine dialdehyde suppresses androgen receptor expression and prostate cancer growth [J]. The Journal of urology, 2012, 188(1): 300-306.

Protocole (Protocol)

Cell experiment [1]:

Cell lines

H292 cells

Preparation Method

H292 cells (5×104 cells/well) were seeded in a 96-well plate and treated with different concentrations (0.01, 0.1, 1, 10 and 100μM) of Adenosine Dialdehyde (DMSO as control) for 72h. The colorimetric MTT metabolic activity assay was used to assess cell proliferation.

Reaction Conditions

0.01, 0.1, 1, 10 and 100μM; 72h

Applications

Adenosine Dialdehyde significantly inhibited the proliferation of H292 cells in a dose dependent manner.
Animal experiment [2]:

Animal models

Male NCr-nu/nu mice

Preparation Method

LNCaP cells (1.0×107) were inoculated subcutaneously in the lateral flank of 10 mice. At 5 days the mice were randomly divided into 2 groups of 5 each and administered vehicle or 10μmol/kg Adenosine Dialdehyde by intraperitoneal injection. Vehicle or Adenosine Dialdehyde was administered intraperitoneally once per week. Inoculated tumor size was determined every 2 to 3 days using calipers.

Dosage form

10μmol/kg; 32d; q1w; i.p.

Applications

Adenosine Dialdehyde suppressed prostate cancer growth in vivo in the mouse xenograft model.

[1] Ghemrawi R, Al Qassem A, Ramadan A, et al. DNA and protein methyltransferases inhibition by adenosine dialdehyde reduces the proliferation and migration of breast and lung cancer cells by downregulating autophagy [J]. PLoS One, 2023, 18(7): e0288791.
[2]Shiota M, Takeuchi A, Yokomizo A, et al. Methyltransferase inhibitor adenosine dialdehyde suppresses androgen receptor expression and prostate cancer growth [J]. The Journal of urology, 2012, 188(1): 300-306.

Documents produit (Product Documents)

Purity:>95.00%Appearance:A solid

Propriétés chimiques (Chemical Properties)

N° CAS
34240-05-6
Nom chimique
2-(1-(6-amino-9H-purin-9-yl)-2-oxoethoxy)-3-hydroxypropanal
SMILES
O=C(C(OC(CO)C([H])=O)N1C=NC2=C1N=CN=C2N)[H]
Formule moléculaire
C10H11N5O4
Masse moléculaire
265.23
Solubilité
10mg/mL in DMSO, or in DMF
Conservation
Store at -20°C
Conseils généraux
Choisissez un solvant adapté selon les données de solubilité du produit. Après préparation, répartissez la solution mère en aliquotes afin d’éviter les cycles répétés de congélation-décongélation.
Utilisez les solutions mères dans les 6 mois si elles sont conservées à -80°C, ou dans le mois si elles sont conservées à -20°C.
Pour améliorer la solubilité, réchauffez le tube à 37°C et soniquez-le pendant une durée appropriée.
Conditions d’expédition
Les échantillons d’évaluation sont expédiés avec des blocs réfrigérants. Les autres formats sont expédiés à température ambiante ou, sur demande, avec des blocs réfrigérants.

Calculateurs (Calculators)Molarité / Dilution / Masse moléculaire / Conversion d’unités / Formulation in vivo / Solubilité

g/mol

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