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 About 9 results found for searched term "MTH1" (0.126 seconds)

Cat.No.  Name Target
M42496 MTHFD2-IN-1 Dehydrogenase
MTHFD2-IN-1 is a potent methylenetetrahydrofolate dehydrogenase (MTHFD2) inhibitor.
M2350 (S)-crizotinib MTH1
(S)-crizotinib, the (S)-enantiomer of crizotinib, is a potent MTH1 (NUDT1) inhibitor with IC50 of 72 nM.
M4357 3-Isomangostin DNA/RNA Synthesis
3 - Isomangostin from Garciniamangostana. L. Extracted from shell, 3-isomangostin is an effective MutT homolog 1 (MTH1) inhibitor with IC50 value of 52 nM. 3-Isomangostin can be used to develop anticancer agents.
M8899 TH588 MTH1
TH588 is a first-in-class, potent, selective MTH1 (NUDT1) inhibitor with an IC50 value of 5 nM.
M13654 TH287 DNA/RNA Synthesis
TH287 is a potent and selective inhibitor of MTH1, with an IC50 of 0.8 nM.
M14724 LY 345899 Dehydrogenase
LY 345899 is a Folate analog and is a methylene tetrahydrofolate dehydrogenase (MTHFD1; DC301) and MTHFD2 inbhibitor with IC50 values of 96 nM and 663 nM, respectively and a Ki of 18 nM for MTHFD1.
M29249 BAY-707  DNA/RNA Synthesis
BAY-707 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) profile to other MTH1 compounds and is well-tolerated in mice, but shows a clear lack of in vitro or in vivo anticancer efficacy.
M29453 TH5427 hydrochloride  DNA/RNA Synthesis
TH5427 hydrochloride is a potent, selective NUDT5 inhibitor (IC50=29 nM). TH5427 hydrochloride shows an apparent 690-fold selectivity for NUDT5 over MTH1. TH5427 hydrochloride blocks progestin-dependent, PAR-derived nuclear ATP synthesis and subsequent chromatin remodeling, gene regulation and proliferation in breast cancer cells.
M29534 DS44960156  Dehydrogenase
DS44960156 is a selective Methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) inhibitor, with IC50 values of 1.6 μM and >30 μM for MTHFD2 and MTHFD1, respectively.



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