Adenosine dialdehyde

Modify Date: 2025-08-27 19:08:02

Adenosine dialdehyde Structure
Adenosine dialdehyde structure
Common Name Adenosine dialdehyde
CAS Number 34240-05-6 Molecular Weight 265.22500
Density N/A Boiling Point N/A
Molecular Formula C10H11N5O4 Melting Point N/A
MSDS Chinese USA Flash Point N/A

 Use of Adenosine dialdehyde


Adenosine Dialdehyde is a purine nucleoside analogue and is an irreversible inhibitor of S-adenosylhomocysteine hydrolase (SAH) (IC50=40 nM). Adenosine Dialdehyde exhibits potent anti-tumor activity in vivo and can be used for the cancer research[1][2].

 Names

Name Adenosine, periodate oxidized
Synonym More Synonyms

 Adenosine dialdehyde Biological Activity

Description Adenosine Dialdehyde is a purine nucleoside analogue and is an irreversible inhibitor of S-adenosylhomocysteine hydrolase (SAH) (IC50=40 nM). Adenosine Dialdehyde exhibits potent anti-tumor activity in vivo and can be used for the cancer research[1][2].
Related Catalog
In Vitro Adenosine dialdehyde suppresses MNB cell replication in tissue culture with concentra tions of 1.5 μM with producing 50% inhibition[1].
In Vivo Adenosine dialdehyde (subcutaneous injection; 1.5-2.5 mg/kg; infused over a 7-day period ( minipump infusion)) significantly increases the mean life span of tumor bearing mice from 20.9 days in diluent treated controls to 35.3 days in AD treated animals[2]. Adenosine dialdehyde (subcutaneous injection; 1.5-2.5 mg/kg; two 7-day periods interspersed by a 7-day drug free interval( minipump infusion))increases mean life span 80% in diluent treated controls (controls, 21.3 days; AD treated 38.4 days) in mice[2]. Adenosine dialdehyde (subcutaneous injection; 2-3 mg/kg; infused over a 7-day period ( minipump infusion)) does not exhibit any hematopoietic toxicity in mice, and it can significantly suppress murine neuroblastoma tumor growth with little systemic toxicity[2]. Animal Model: Adult male A/J mice, weighing 20 to 25 g with MNB cells[2] Dosage: 1.5-2.5 mg/kg Administration: Subcutaneous injection; 1.5-2.5 mg/kg; two 7-day periods interspersed by a 7-day drug free interval (minipump infusion) Result: Significantly suppressed murine neuroblastoma tumor growth. Prolongs the life span of tumor bearing mice. Did not suppress hematopoiesis when administered by steady state infusion[2].
References

[1]. G V Madhavan, et al. Synthesis and antiviral evaluation of 6'-substituted aristeromycins: potential mechanism-based inhibitors of S-adenosylhomocysteine hydrolase. J Med Chem

[2]. B Bostrom, et al. Inhibitory effect of adenosine dialdehyde on in situ murine neuroblastoma growth.Cancer Res. 1988 Nov 1;48(21):5933-6.

 Chemical & Physical Properties

Molecular Formula C10H11N5O4
Molecular Weight 265.22500
Exact Mass 265.08100
PSA 133.22000
Storage condition -20℃

 Safety Information

Personal Protective Equipment Eyeshields;Faceshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Risk Phrases 36/37/38
Safety Phrases 26-36
RIDADR NONH for all modes of transport
HS Code 2933990090

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles32

More Articles
Elasticity assessment of electrospun nanofibrous vascular grafts: a comparison with femoral ovine arteries.

Mater. Sci. Eng. C. Mater. Biol. Appl. 45 , 446-54, (2014)

Development of successful small-diameter vascular grafts constitutes a real challenge to biomaterial engineering. In most cases these grafts fail in-vivo due to the presence of a mechanical mismatch b...

Efflux of glutathione and glutathione complexes from human erythrocytes in response to vanadate.

Blood Cells Mol. Dis. 50(1) , 1-7, (2013)

The main objective of the present study was to investigate if vanadate is extruded from the cells in a glutathione dependent manner resulting in the appearance of extracellular glutathione and complex...

Involvement of Src and the actin cytoskeleton in the antitumorigenic action of adenosine dialdehyde.

Biochem. Pharmacol. 85(8) , 1042-56, (2013)

Transmethylation is an important reaction that transfers a methyl group in S-adenosylmethionine (SAM) to substrates such as DNA, RNA, and proteins. It is known that transmethylation plays critical rol...

 Synonyms

ADENOSINE, PERIODATE OXIDIZED
α-adenosine 2',3'-dialdehyde
ADENOSINE, PERIODATE OXIDISED
Adenosine Dialdehyde
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here



Get all suppliers and price by the below link:

Adenosine dialdehyde suppliers

Adenosine dialdehyde price