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Cat. No. Product Name Information
PC-42295

Beaucage reagent

A potent DNA cleavage agent.
PC-43227

TH-588 hydrochloride

A potent and selective inhibitor of MTH1 protein with IC50 of 5 nM.
PC-45105

TH-287 hydrochloride

A potent and selective inhibitor of MTH1 protein with IC50 of 0.8 nM.
PC-45350

Actinomycin D

A chemotherapy agent that has the ability to inhibit transcription.
PC-22070

RTx-161

DNA Polθ inhibitor

RTx-161 (RTx161) is a potent, selective, allosteric DNA Polymerase θ (Polθ) inhibitor with IC50 of 4.1 nM, exhibits preferential killing of HR-deficient cells.
PC-21698

Fraisinib

GARS1 inhibitor

Fraisinib is a specific and effective inhibitor of glycyl-tRNA synthetase 1 (GARS1), suppresses the synthesis of Ap4A by GARS1 and displays strong anti-tumoral potential.
PC-20939

RBI2

Ribosome biogenesis inhibitor

RBI2 (Ribosome biogenesis inhibitor 2) is a small molecule inhibitor of ribosome biogenesis inhibitor, potently inhibits pre-rRNA levels in A375 with IC50 of 169 nM.
PC-20598

DNA polymerase theta inhibitor

POLθ inhibitor

DNA polymerase theta inhibitor (POLθi) is a small-molecule DNA polymerase theta (POLθ) inhibitor, binds to an allosteric pocket in the thumb subdomain of POLθ, inhibits its polymerase activity.
PC-49362

ART812

Polθ inhibitor

ART812 (ART-812) is a selective small molecule DNA polymerase theta (Polθ) in vivo probe, recapitulates the phenotype of Polθ loss and is efficacious in a model of PARP inhibitor resistant TNBC in vivo.
PC-38801

Congo red

DNA Pol γ inhibitor

Congo red (Zinc 03830554) is a high-affinity small molecule targeting mitochondrial DNA polymerase gamma (Pol γ), selectively kills MLH1 deficient cancer cells.
PC-38616

Lurbinectedin

DNA covalent binder

Lurbinectedin (PM01183) is a marine-derived DNA minor groove covalent binder with potent in vitro and in vivo anti-tumour activity, inhibits RMG1 and RMG2 cell growth with IC50 of 1.25 nM and 1.16 nM, respectively.
PC-38571

L189

DNA ligase inhibitor

L189 is a small moelcule DNA ligase I, III and IV inhibitor with IC50 of 5, 9 and 5 uM, blocks DNA ligase I DNA binding activity with Ki of 5 uM.

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