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 -methylazetidin-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 | C15H20N6O |
|---|---|
| Charge | 0 |
| Average mass | 300.366 Da |
| Monoisotopic mass | 300.16986 Da |
| Source | ChEBI |
| InChIKey | OQWZETPYVIVWBB-ZOCYIJKUSA-N |
CC1CCN1c1nc(N)nc2c1ncn2[C@H]1C=C[C@@H](CO)C1
InChI=1S/C15H20N6O/c1-9-4-5-20(9)13-12-14(19-15(16)18-13)21(8-17-12)11-3-2-10(6-11)7-22/h2-3,8-11,22H,4-7H2,1H3,(H2,16,18,19)/t9?,10-,11+/m1/s1
CHEBI:22587| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:149426 |
6-de(cyclopropylamino)-6-(2-methylazetidin-1-yl)abacavir | antibioticmech:chebi-57e56dbf9b |
2026-08-30 |
Seeded from data/raw/ inventories (CHEBI)
Re-seeded from updated data/raw/ inventories
Re-seeded from updated data/raw/ inventories