159326-68-8, 吡咯并[2,1-F][1,2,4]三嗪-4-胺, Cas:159326-68-8

159326-68-8, PYRROLO[1,2-F][1,2,4]TRIAZIN-4-AMINE;
IFLAB-BB F2108-0125;
Pyrrolo[2,1-f][1,2,4]triazin-4-amine;
Pyrrolo[1,2-f][1,2,4]tria...;
4-AMino-pyrrolo[2,1-f][1,2,4]triazin;
4-AMinopyrrolo[2,1-f][1,2,4]triazine;
Pyrrolo[2,1-f][1,2,4]triazin-4-aMin;
4-pyrrolo[2,1-f][1,2,4]triazinamine,
Cas:159326-68-8
C6H6N4 / 134.14
MFCD08234647

PYRROLO[1,2-F][1,2,4]TRIAZIN-4-AMINE;IFLAB-BB F2108-0125;

Pyrrolo[2,1-f][1,2,4]triazin-4-amine;Pyrrolo[1,2-f][1,2,4]tria...;4-AMino-pyrrolo[2,1-f][1,2,4]triazin;4-AMinopyrrolo[2,1-f][1,2,4]triazine;Pyrrolo[2,1-f][1,2,4]triazin-4-aMin;4-pyrrolo[2,1-f][1,2,4]triazinamine

Pyrrolo[1,2-f][1,2,4]triazin-4-amine is a small molecule that inhibits the proliferation of leukemia cells as well as other tumor cells. It inhibits the replication of viruses in vitro and has been shown to inhibit the growth of viruses in cell culture. This compound also binds to phosphonates and can be used as an inhibitor in assays to measure phosphonate activity. Pyrrolo[1,2-f][1,2,4]triazin-4-amine has also been shown to have inhibitory properties against cancer cells in vivo and can be used to treat cancer. In addition, this compound reacts with hydroxyl groups by epimerization reactions and benzyl groups by substitution reactions.

IUPAC Name	pyrrolo[2,1-f][1,2,4]triazin-4-amine
Molecular Formula	C6H6N4
Molecular Weight	134.14 g/mol
InChI	InChI=1S/C6H6N4/c7-6-5-2-1-3-10(5)9-4-8-6/h1-4H,(H2,7,8,9)
InChI Key	VSPXQZSDPSOPRO-UHFFFAOYSA-N
SMILES	C1=CN2C(=C1)C(=NC=N2)N
Canonical SMILES	C1=CN2C(=C1)C(=NC=N2)N