Weight | 235.247 g/mol |
---|---|
Formula | C10H13N5O2 |
Hydrogen Acceptors | 7 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
2',3'-Dideoxyadenosine (4097-22-7)
Dideoxyadenosine · 2',3' Dideoxyadenosine · ddA (Antiviral)
Score:
#424 in Microbiology
,
#1438 in Biochemistry
,
#3411 in Biology
,
#4258 in Chemistry
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- Sigma-Aldrich - 2',3'-Dideoxyadenosine168.00 - 603.00 USD
- Fisher Scientific - Search for 2',3'-Dideoxyadenosine
- TCI - 2',3'-Dideoxyadenosine228.00 USD
- Electrochemical oxidation of 2',3' -dideoxyadenosine at pyrolytic graphite electrode (Electrochimica Acta, 2008)
- Pharmacokinetics of 2, 3dideoxyadenosine and 2, 3dideoxyinosine in patients with severe human immunodeficiency virus infection (Clinical Pharmacology & Therapeutics, 1990)
- Metabolic pathways for the activation of the antiretroviral agent 2',3'-dideoxyadenosine in human lymphoid cells (Journal of Biological Chemistry, 1988)
- Metabolism and anti-human immunodeficiency virus-1 activity of 2-halo-2',3'-dideoxyadenosine derivatives. (Journal of Biological Chemistry, 1988)
- cycloSal-Pronucleotides of 2',3'-dideoxyadenosine and 2', 3'-dideoxy-2',3'-didehydroadenosine: synthesis and antiviral evaluation of a highly efficient nucleotide delivery system. (Journal of Medicinal Chemistry, 1999)
- Preparation of 1-(2,3-dideoxy-.beta.-D-glycero-pent-2-enofuranosyl)thymine (d4T) and 2',3'-dideoxyadenosine (ddA): general methods for the synthesis of 2',3'-olefinic and 2',3'-dideoxy nucleoside analogs active against HIV (Journal of Organic Chemistry, 1989)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Dideoxyadenosine
- 2',3' Dideoxyadenosine
- ddA (Antiviral)
-
SMILESC1CC(OC1CO)N2C=NC3=C2N=CN=C3N
-
InChIKeyWVXRAFOPTSTNLL-UHFFFAOYSA-N
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