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Merck

D8296

3-Deazaadenosine

Synonym(s):

4-Amino-1-(β-D-ribofuranosyl)-1H-imidazo(4,5)-pyridine

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About This Item

Empirical Formula (Hill Notation):
C11H14N4O4
CAS Number:
6736-58-9
Molecular Weight:
266.25
NACRES:
NA.77
PubChem Substance ID:
24278391
UNSPSC Code:
51111800
MDL number:
MFCD00153951
Form:
powder
Quality level:
200

Key Documents

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form

powder

Quality Level

200

storage temp.

2-8°C

SMILES string

Nc1nccc2n(cnc12)[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O

InChI

1S/C11H14N4O4/c12-10-7-5(1-2-13-10)15(4-14-7)11-9(18)8(17)6(3-16)19-11/h1-2,4,6,8-9,11,16-18H,3H2,(H2,12,13)/t6-,8-,9-,11-/m1/s1

InChI key

DBZQFUNLCALWDY-PNHWDRBUSA-N

Gene Information

rat ... Adora1(29290), Adora2a(25369), Adora3(25370)

Related Categories

Application

3-Deazaadenosine has been used as a methylation inhibitor:
  • to study the effect of m6A modification on suppressor of cytokine signaling 2 (SOCS2) expression in colon cancer cells
  • to study its effects on the expression of influenza A virus (IAV) proteins in human lung epithelial cell line
  • to evaluate its effects on the replication of SV40 virus in BSC40 cells

Biochem/physiol Actions

3-Deazaadenosine (DZA), an analog of adenosine, acts as a blocker of S-adenosylhomocysteine (SAH)-hydrolase, a regulator of cellular methyltransferase activity. It has been observed in inhibiting some of the factors involved in atherosclerosis and restenosis. DZA inhibits lymphocyte-mediated tumor cell lysis, macrophage phagocytosis, microfilament disorganization, monocyte, and neutrophil chemotaxis. It also inhibits histamine release by basophils, superoxide anion generation, and macrophage lysosomal secretion. DZA possesses anti-inflammatory, anti-human immunodeficiency virus (HIV) properties and inhibitory effects of cytokine expression that include interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), and nuclear factor-κB (NF-κB) transcription activity.
Possesses antiviral activity inhibitor of leukocyte adhesion to TNF-treated endothelial cells.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

D8296-10MG: + D8296-5MG-PW: + D8296-BULK: + D8296-10MG-PW: + D8296-5MG: + D8296-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
0000477755
0000477755
0000410679
0000410679
0000379922

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Cynthia J DeLong et al.
The Journal of biological chemistry, 277(19), 17217-17225 (2002-02-28)
Despite being widely hypothesized, the actual contribution of choline as a methyl source for phosphatidylethanolamine (PE) methylation has never been demonstrated, mainly due to the inability of conventional methods to distinguish the products from that of the CDP-choline pathway. Using
Mary C Long et al.
The Journal of antimicrobial chemotherapy, 59(1), 118-121 (2006-11-07)
Analyse a series of halogenated 3-deaza-adenosine analogues for efficacy against Mycobacterium tuberculosis H37Ra and determine if adenosine (Ado) kinase plays a role in the mechanism of action of these compounds. The MIC as determined by microdilution broth assay provided a
Juliane K Soukup et al.
Biochemistry, 41(33), 10426-10438 (2002-08-14)
The A-minor motifs appear to be the most ubiquitous helix packing elements within RNA tertiary structures. These motifs have been identified throughout the ribosome and almost every other tertiary-folded RNA for which structural information is available. These motifs utilize the
C H Jurgensen et al.
Journal of immunology (Baltimore, Md. : 1950), 144(2), 653-661 (1990-01-15)
Previous reports demonstrate that cultured human umbilical vein endothelial cells (HEC) treated with TNF and other inflammatory mediators show an increased capacity to adhere human neutrophils. This increase is associated with the up-regulation of intercellular adhesion molecule 1 (ICAM-1) and
3-Deaza-adenosine and inhibition of HIV.
C W Flexner et al.
Lancet (London, England), 339(8790), 438-438 (1992-02-15)
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