GLPBio

Adenosine Dialdehyde (ADOX)

Catalog No.: GC16509Purity:>95.00%
퓨린 뉴클레오시드 유사체인 Adox는 S-아데노실호모시스테인 가수분해효소(SAHH)(Ki=3.3nM)의 강력한 억제제입니다. 아데노신 디알데히드는 생체 내에서 강력한 항종양 활성을 나타내며 암 연구에 사용될 수 있습니다.

제품은 연구용으로만 사용됩니다. 인체에 사용할 수 없으며 환자에게 판매하지 않습니다.


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

인용 문헌 (Citations)

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제품 설명 (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.

실험 프로토콜 (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.

제품 문서 (Product Documents)

Purity:>95.00%Appearance:A solid

화학적 특성 (Chemical Properties)

CAS 번호
34240-05-6
화학명
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]
분자식
C10H11N5O4
분자량
265.23
용해도
10mg/mL in DMSO, or in DMF
보관
Store at -20°C
일반 주의사항
제품의 용해도 데이터에 따라 적절한 용매를 선택하십시오. 조제 후에는 반복적인 동결·해동을 피할 수 있도록 저장 용액을 소분하십시오.
저장 용액은 -80°C 보관 시 6개월 이내, -20°C 보관 시 1개월 이내에 사용하십시오.
용해도를 높이려면 튜브를 37°C로 데운 뒤 적절한 시간 동안 초음파 처리하십시오.
배송 조건
평가용 샘플은 아이스팩과 함께 배송됩니다. 그 외 용량은 실온 배송되며, 요청 시 아이스팩과 함께 배송할 수 있습니다.

계산 도구 (Calculators)몰 농도 / 희석 / 분자량 / 단위 변환 / 생체 내 제형 / 용해도

g/mol

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