A 2,6-diaminopurine that is an analogue of abacavir in which the cyclopropylamino group at position 6 of the purine moiety is replaced by a 3-fluoroazetidin-1-yl group. One of a series of synthesised abacavir analogues with antiviral activity found to stimulate IFN-γ secretion in abacavir-responsive clones.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
CHEBI:38001| Molecular formula | C14H17FN6O |
|---|---|
| Charge | 0 |
| Average mass | 304.329 Da |
| Monoisotopic mass | 304.14479 Da |
| Source | ChEBI |
| InChIKey | AJAFGTUGXORIBL-SCZZXKLOSA-N |
Nc1nc(N2CC(F)C2)c2ncn([C@H]3C=C[C@@H](CO)C3)c2n1
InChI=1S/C14H17FN6O/c15-9-4-20(5-9)12-11-13(19-14(16)18-12)21(7-17-11)10-2-1-8(3-10)6-22/h1-2,7-10,22H,3-6H2,(H2,16,18,19)/t8-,10+/m1/s1
CHEBI:22587| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:149434 |
6-de(cyclopropylamino)-6-(3-fluoroazetidin-1-yl)abacavir | antibioticmech:chebi-b76b330d35 |
2026-08-30 |
Seeded from data/raw/ inventories (CHEBI)
Re-seeded from updated data/raw/ inventories
Re-seeded from updated data/raw/ inventories