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Cat. No. Product Name Information
PC-70241

Saframycin A

Saframycin A is a heterocyclic quinone antibiotic that inhibits RNA synthesis in vivo and in vitro.
PC-70029

Minnelide

RNA polymerase II inhibitor

Minnelide is a water-soluble prodrug of triptolide, an inhibitor of RNA polymerase II-mediated transcription, also is a selective inhibitor of CIC::DUX4 sarcoma (CDS).
PC-45353

Bleomycin sulfate

An anticancer agent that acts by induction of DNA strand breaks.
PC-45751

COH29

Ribonucleotide reductase inhibitor

COH29 is a small-molecule inhibitor of ribonucleotide reductase (RNR) that binds to RRM2, interfering with RRM1-RRM2 interactions with IC50 of 16 uM.
PC-42295

Beaucage reagent

A potent DNA cleavage agent.
PC-45350

Actinomycin D

Transcription inhibitor

Actinomycin D is a chemotherapy agent that has the ability to inhibit transcription, binds to DNA at the transcription initiation complex and preventing elongation of RNA chain by RNA polymerase, inhibits DNA repair with IC50 of 0.42 uM.
PC-28440

RP-3467

Polθ inhibitor

RP-3467 is a potent, selective inhibitor of DNA polymerase theta (Polθ) helicase domain with EC50 of <0.25 nM, shows no discernible inhibitory activity against other DNA repair-related ATPases WRN, BLM, and FANCM.
PC-26796

ART615

ART558 negative control

ART615 is the related isomer of ART558 and ART558 negative control compound.
PC-26687

Polθ ATPase inhibitor XL-20

DNA Polθ inhibitor

XL-20 is a potent, selective orally bioavailable selenium-containing DNA polymerase theta (Polθ) inhibitor with IC50 of 4.3 nM for Polθ ATPase.
PC-26267

RP-4029

DNA Polθ inhibitor

RP-4029 is a potent, selective and covalent inhibitor of DNA polymerase θ (Polθ) with IC50 of 0.013 nM and 6.6 nM for human and mouse Polθ respectively, forms a covalent adduct with Cys2411 of human Polθ.
PC-26252

SY-589

DNA Polθ inhibitor

SY-589 is a highly potent, selective and orally bioavailable DNA polymerase theta (Polθ) helicase inhibitor with ATPase inhibitory IC50 of 2.29 nM in ADP-Glo assays, inhibits microhomology-mediated end joining (MMEJ) pathway.
PC-25301

NVL inhibitor MM17

NVL inhibitor

NVL inhibitor MM17 is a small molecule inhibitor of 60S ribosomal subunit assembly factor NVL with IC50 of 0.38 uM, inhibits HCT116 growth in a dose-dependent manner with IC50 of 0.54 uM.

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