| Weight | 251.246 g/mol |
|---|---|
| Formula | C10H13N5O3 |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
2'-deoxyadenosine
deoxyadenosine · 2-deoxyadenosine
16373-93-6, 958-09-8, 40627-14-3
Score:
#1297 in Biochemistry
,
#3178 in Biology
,
#3976 in Chemistry
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- The Role of Adenosine and 2'-Deoxyadenosine in Mammalian Cells (Annual Review of Biochemistry, 1978)
- Mechanism of deoxyadenosine and 2-chlorodeoxyadenosine toxicity to nondividing human lymphocytes. (Journal of Clinical Investigation, 1985)
- Synthesis of 2'-deoxytubercidin, 2'-deoxyadenosine, and related 2'-deoxynucleosides via a novel direct stereospecific sodium salt glycosylation procedure (Journal of the American Chemical Society, 1984)
- Deoxyadenosine triphosphate as a potentially toxic metabolite in adenosine deaminase deficiency (Proceedings of the National Academy of Sciences of the United States of America, 1978)
- Induction of apoptotic cell death in chronic lymphocytic leukemia by 2-chloro-2'-deoxyadenosine and 9--D-arabinosyl-2-fluoroadenine (Blood, 1993)
- Deoxyadenosine analogs induce programmed cell death in chronic lymphocytic leukemia cells by damaging the DNA and by directly affecting the mitochondria. (Blood, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - deoxyadenosine
- 2-deoxyadenosine
-
SMILESC1C(C(OC1N2C=NC3=C2N=CN=C3N)CO)O
-
InChIKeyOLXZPDWKRNYJJZ-UHFFFAOYSA-N
- Pubchem - 2'-deoxyadenosine
- Wikipedia - 2'-deoxyadenosine
Deoxyadenosine (symbol dA or dAdo) is a deoxyribonucleoside. It is a derivative of the nucleoside adenosine, differing from the latter by the replacement of a hydroxyl group (-OH) by hydrogen (-H) at the 2' position of its ribose sugar moiety. Deoxyadenosine is the DNA nucleoside A, which pairs with deoxythymidine (T) in double-stranded DNA.
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