| Weight | 267.245 g/mol |
|---|---|
| Formula | C10H13N5O4 |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
9-Arabinofuranosyladenine (5536-17-4, 2006-02-2)
Score:
#188 in Microbiology
,
#685 in Biochemistry
,
#1918 in Biology
,
#2323 in Chemistry
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- Sigma-Aldrich - Search for 9-Arabinofuranosyladenine
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- Inhibition of Mammalian DNA Polymerase by the 5-Triphosphate of 1--d-Arabinofuranosylcytosine and the 5-Triphosphate of 9--d-Arabinofuranosyladenine (Cancer Research, 1968)
- The Antiviral Activity of 9--D-Arabinofuranosyladenine (ARA-A) (Chemotherapy, 1968)
- Synthesis and biologic activity of 2'-fluoro-2-halo derivatives of 9-beta-D-arabinofuranosyladenine. (Journal of Medicinal Chemistry, 1992)
- Mode of Action of 9--d-Arabinofuranosyladenine on the Synthesis of DNA, RNA, and Protein in Vivo and in Vitro (Cancer Research, 1975)
- Biologic activity of 9--d-arabinofuranosyl-2-fluoroadenine, a metabolically stable analog of 9--d-arabinofuranosyladenine (Biochemical Pharmacology, 1977)
- Syntheses with Partially Benzylated Sugars. III.1 A Simple Pathway to a cis- Nucleoside, 9--D-Arabinofuranosyladenine (Spongoadenosine) (Journal of Organic Chemistry, 1963)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=NC2=C(C(=N1)N)N=CN2C3C(C(C(O3)CO)O)O
-
InChIKeyOIRDTQYFTABQOQ-UHFFFAOYSA-N
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