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Cat. No. Product Name Information
PC-61921

NSC 19630

WRN helicase inhibitor

NSC 19630 (MIRA-1) is a potent, selective Werner syndrome helicase (WRN helicase) with IC50 of 20 uM.
PC-61920

NSC 617145

WRN inhibitor

NSC 617145 is a novel small-molecule, selective inhibitor of WRN helicase with IC50 of 230 nM.
PC-61900

Rev1-IN-5

Rev1 inhibitor

Rev1-IN-5 is a small molecule inhibitor of the C-terminal domain of Rev1 and the Rev1-interacting region protein-protein interaction (Rev1-CT/RIR PPI) with IC50 of 2.5 uM.
PC-61067

BAY-707

MTH1 inhibitor

BAY-707 is a highly potent, selective and substrate-competitive inhibitor of MTH1 (NUDT1) with IC50 of 2.3 nM.
PC-42079

HUHS-015

PCA-1/ALKBH3 inhibitor

HUHS-015 (HUHS015) is a potent, orally active prostate cancer antigen-1 (PCA-1/ALKBH3) inhibitor with IC50 of 0.67 uM.
PC-43226

TH-588

MTH1 inhibitor

TH-588 is a potent and selective inhibitor of MTH1 (NUDT1) protein with IC50 of 5 nM.
PC-45104

TH-287

MTH1 inhibitor

TH-287 is a potent and selective inhibitor of MTH1 (NUDT1) protein with IC50 of 0.8 nM.
PC-22774

HDGFRP2 PWWP domain inhibitor BBP

HDGFRP2 PWWP inhibitor

BBP is a small molecule inhibitor of the hepatoma-derived growth factor-related protein 2 (HDGFRP2) PWWP domain, dually targets both HDGFRP2 and PSIP1 PWWP domains, engage with the aromatic cage of the HDGFRP2 PWWP domain.
PC-22697

MUS81 inhibitor 24

MUS81 inhibitor

MUS81 inhibitor 24 is a small molecule inhibitor of DNA repair endonuclease Mus81 with IC50 of 0.27 uM and SPR Kd of 1.1 uM (MUS81-EME1).
PC-22696

MUS81 inhibitor 23

MUS81 inhibitor

MUS81 inhibitor 23 is a small molecule inhibitor of DNA repair endonuclease Mus81 with IC50 of 0.32 uM and SPR Kd of 0.67 uM (MUS81-EME1).
PC-22445

SNM1A inhibitor 19

SNM1A inhibitor

SNM1A inhibitor 19 is a cell-active small molecule inhibitor of SNM1A DNA repair nuclease with IC50 of 44 uM, sensitises cancer cells to cisplatin and delays resolution of cisplatin-induced DNA damage.
PC-22110

GSK_WRN4

WRN helicase inhibitor

GSK_WRN4 (WRNi, GSK-WRN4) is a potent and highly selective WRN helicase covalent inhibitor with biochemical pIC50 of 7.6, covalently targets WRN Cys727 residue.

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