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Cat. No. Product Name Information
PC-73255

A83B4C63

PNKP inhibitor

A83B4C63 is a potent small molecule DNA repair protein, polynucleotide kinase 3′-phosphatase (PNKP) inhibitor with Kd of 80 nM.
PC-72920

T2AA

PCNA inhibitor

T2AA (T2 amino alcohol) is a small molecule proliferating cell nuclear antigen (PCNA) inhibitor, inhibits interaction of PCNA/PIP-box peptide with IC50 of 1 uM.
PC-72682

BLM inhibitor 2

BLM helicase inhibitor

BLM inhibitor 2 is a specific inhibitor of BLM (Bloom syndrome protein) ATPase-coupled DNA helicase activity (IC50=2.2 uM) via the allosteric binding site.
PC-72026

AZ13792138

NUDT1 inhibitor

AZ13792138 is a highly potent, selective inhibitor of MTH1 (NUDT1) with Kd/IC50 of 0.4/0.5 nM.
PC-72025

SU0383

OGG1-MTH1 inhibitor

SU0383 (SU 0383) is a potent, dual inhibitor of repair enzyme OGG1 and NUDT1 (MTH1) with IC50 of 34 nM and 490 nM, respectively.
PC-35806

TH5487

OGG1 inhibitor

TH5487 (TH-5487, TH 5487) is a potent, selective, active-site inhibitor of 8-oxoguanine DNA glycosylase 1 (OGG1) with IC50 of 342 nM, prevents OGG1 from binding to its DNA substrate.
PC-35301

AOH1160

PCNA inhibitor

AOH1160 (AOH-1160) is a potent, first-in-class, orally available small molecule inhibitor of Proliferating cell nuclear antigen (PCNA).
PC-35266

A12B4C3

hPNKP inhibitor

A12B4C3 is a potent, specific human polynucleotide kinase/phosphatase (hPNKP) inhibitor, inhibits hPNKP phosphatase activity with IC50 of 60 nM.
PC-35174

MLAF50

REV1 UBM2 inhibitor

MLAF50 is the first small-molecule inhibitor of the REV1 UBM2-Ubiquitin interaction, directly binds to REV1 UBM2 with Kd of 37 uM in SPR assays.
PC-42991

ML216

BLM helicase inhibitor

ML216 (CID49852229) is a potent, selective inhibitor of DNA unwinding activity of BLM (Bloom's syndrome protein) with IC50 of 2.98 and 0.97 uM for full length BLM and BLM636-1298, respectively.
PC-63192

IACS-4619

MTH1 inhibitor

IACS-4619 is a potent, selective aminopyrimidine MTH1 (MutT homolog 1) inhibitor with IC50 of 0.2 nM.
PC-62970

IBR2

RAD51 inhibitor

IBR2 is a novel small molecule RAD51 inhibitor that specifically binds to RAD51 and disrupts the BRC repeats of BRCA2/RAD51 interaction with IC50 of 0.11 uM.

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