Abstract
Carbocyclic analogs of arabinofuranosylguanine (VII) and 2,6‐diamino‐9‐β‐arabinofuranosylpurine (VIII) and the corresponding 8‐azapurine analogs, 5‐amino‐7‐hydroxy‐3‐[2α,3β‐dihydroxy‐4α‐(hydroxymethyl)cyclopent‐1α‐yl]‐v‐triazolo[4,5‐d]pyrimidine (X) and 5,7‐diamino‐3‐[2α,3β‐dihydroxy‐4α‐(hydroxymethyl)cyclopent‐1α‐yl]‐v‐triazolo[4,5‐d]pyrimidine (XI), were prepared. Carbocyclic nucleoside analogs VII and × exhibited significant cytotoxicity against P‐388 mouse leukemia cells in culture. In vitro testing against herpes simplex type 1 (strain HF) indicated that only VIII exhibited significant antiviral activity.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1019-1021 |
| Number of pages | 3 |
| Journal | Journal of Pharmaceutical Sciences |
| Volume | 69 |
| Issue number | 9 |
| DOIs | |
| State | Published - Sep 1980 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Antitumor activity—carbocyclic analogs of arabinosylpurine nucleosides, synthesis and testing
- Antiviral activity—carbocyclic analogs of arabinosylpurine nucleosides, synthesis and testing
- Arabinosylpurine nucleosides—Carbocyclic analogs, synthesis and evaluation for antitumor and antiviral activity
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