Bioactivity:

BAY-707 is well-tolerated in mice, but shows a clear lack of in vitro or in vivo anticancer efficacy[1] and it is a substrate-competitive, highly potent and selective inhibitor of MTH1(NUDT1) with an IC50 of 2.3 nM. BAY-707 has a good pharmacokinetic (PK)

CAS nr:

2109805-96-9

Purity:

98%

Molecular Weight:

288,34

SMILES:

O=C(NCC)C(N1)=CC2=C1N=CC=C2N3CCOC[C@@H]3C

Formula:

C15H20N4O2

Pathway:

Others

Target:

Others