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159326-68-8, Pyrrolo[2,1-f][1,2,4]triazin-4-amine

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 Namepyrrolo[2,1-f][1,2,4]triazin-4-amine
Molecular FormulaC6H6N4
Molecular Weight134.14 g/mol
InChIInChI=1S/C6H6N4/c7-6-5-2-1-3-10(5)9-4-8-6/h1-4H,(H2,7,8,9)
InChI KeyVSPXQZSDPSOPRO-UHFFFAOYSA-N
SMILESC1=CN2C(=C1)C(=NC=N2)N
Canonical SMILESC1=CN2C(=C1)C(=NC=N2)N

Remdesivir,瑞德西韦中间体

55094-52-5 ,2,3,5-三苄氧基-D-核糖酸-1,4-内酯,现货 CAS:55094-52-5

55094-52-5.png

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