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Deoxyadenosines

Known as: Adenylyldeoxyribonucleosides, Deoxyadenosines [Chemical/Ingredient], Adenine Deoxyribonucleosides 
Adenosine molecules which can be substituted in any position, but are lacking one hydroxyl group in the ribose part of the molecule.
National Institutes of Health

Papers overview

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2011
2011
The discovery of imidazole/amine-functionalized DNAzymes that efficiently cleave RNA independently of divalent metal cations (M(2… 
2009
2009
It is known that there are several codes residing simultaneously on the DNA double helix. The two best-characterized codes are… 
2005
2005
[reaction: see text] An efficient route to deoxyadenosine derivatives labeled on both the amino group and nitrogen 1 is uncovered… 
2003
2003
Novel deoxyadenosine derivatives tethering a phenyl or naphthyl group by means of an amido linker have been synthesized, and… 
1998
1998
In reactions between styrene oxide and the ring nitrogen at the 1-position of deoxyadenosine, the epoxide is opened at both the… 
1996
1996
We isolated and sequenced a genomic clone (CatA) encoding CAT-A catalase, a homologue of the maize catalase isozyme 3 (CAT-3… 
1990
1990
Several 2-substituted deoxyadenosine derivatives were synthesized and screened for cytotoxicity toward hematopoietic cells in… 
1984
1984
Three kinds of substituted phthaloyl groups and a succinyl group were introduced onto the N6-amino function of deoxyadenosine… 
1982
1982
The reaction of the racemic mixture of 7 beta, 8 alpha-dihydroxy-9 alpha, 10 alpha-epoxy-7,8,9,10-tetrahydrobenzo [a] pyrene (B[a…