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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T12019 | Methylproamine | Others | |
Methylproamine is a DNA-binding radioprotector , acts by repair of transient radiation-induced oxidative species on DNA. | |||
TN1637 | Eurycomalactone | Anti-infection , NF-κB | |
Eurycomalactone is a natural product isolated from Eurycoma longifolia Jack., acts as a potent NF-κB inhibitor( IC50 of 0.5 μM). Eurycomalactone inhibits protein synthesis, depletes cyclin D1, but does not affect TNFα-in... | |||
T9168 | NSC 617145 | NSC617145,NSC-617145 | DNA/RNA Synthesis |
NSC 617145 (NSC617145) is an inhibitor of WRN helicase that inhibits the ATPase, but not exonuclease, activity of WRN helicase in a concentration-dependent manner. | |||
T24925 | UNC-2170 | UNC2170 Maleate,UNC-2170 Maleate,UNC 2170 Maleate | Others |
UNC-2170 (UNC2170 Maleate) is the methyl-lysine binding protein, 53BP1 ligand. | |||
T14858 | Calicheamicin | Calicheamicin γ1 | Others |
Calicheamicin (Calicheamicin γ1) is an antitumor antibiotic and is a DNA synthesis inhibitor. It also is a cytotoxic agent that causes double-strand DNA breaks. | |||
T9760 | IC 86621 | DNA-PK | |
IC 86621 is a selective and reversible ATP-competitive inhibitor of DNA-PK with an IC50 of 120 nM. IC 86621 increases DNA double-strand break(DSB)-induced antitumor activity with an EC50 of 68 µM for DNA-PK mediated cell... | |||
T6228 | Irinotecan | CPT-11,Topotecin,(+)-Irinotecan | Topoisomerase , Autophagy |
Irinotecan (CPT-11), a derivative of camptothecin, is an inhibitor of DNA topoisomerase I (Topo I). Irinotecan has antitumor activity by preventing DNA strand reattachment through binding to the Topo I complex, resulting... | |||
T11600 | IBR2 | Isoquinoline | DNA/RNA Synthesis |
IBR2 (Isoquinoline) is a potent and specific RAD51 inhibitor known for its ability to suppress RAD51-mediated DNA double-strand break repair. By interfering with RAD51 multimerization, accelerating proteasome-mediated RA... | |||
T63228 | Simmiparib | SMOCL-9112 | Apoptosis , PARP |
Simmiparib (SMOCL-9112) is a novel and potent PARP1 and PARP2 inhibitor, a derivative of Olaparib.Simmiparib induces DNA double-strand breaks (DSBs) and cell cycle arrest in homologous recombination repair (HR)-deficient... | |||
T11067 | VX-984 | M9831 | DNA-PK |
VX-984 (M9831) is an oral, selective DNA-PK inhibitor that can cross the blood-brain barrier. VX-984 inhibited the conjugation of non-homologous terminal NHEJ and acted on DSBs to break DNA double strand. VX-984 is commo... | |||
T3157 | COH29 | RNR Inhibitor COH29 | DNA/RNA Synthesis |
COH29 (RNR Inhibitor COH29) is an orally available, aromatically substituted thiazole and inhibitor of the human ribonucleotide reductase (RNR), with potential antineoplastic activity. Upon oral administration, the RNR i... | |||
TD0003 | CelGreen nucleic acid gel stain *10,000× concentrate in water* | Others | |
CelGreen nucleic acid gel stain 10,000× concentrate in water is a fluorescent dye with a unique involvement that binds to all dsDNA double helix sulcus regions. | |||
T16283 | Neocarzinostatin | 5-HT Receptor | |
Neocarzinostatin is an effective DNA-damaging, anti-tumor antibiotic. It recognizes double-stranded DNA bulge and induces DNA double strand breaks (DSBs). Neocarzinostatin leads to apoptosis. Neocarzinostatin has potenti... | |||
T21303 | Etoposide Phosphate | Eposin Etopophos Vepesid VP16 | |
Etoposide phosphate is a phosphate salt of Etoposide, which binds to the enzyme topoisomerase II, then induces double-strand DNA breaks and inhibits DNA repair, leading to decreased DNA synthesis and tumor cell prolifera... | |||
T19149 | 5-BrdUTP sodium salt | 5-Bromo-2'-deoxyuridine 5'-triphosphate sodium salt | Others |
5-BrdUTP sodium salt is a TdT substrate that can be used to label the DNA double-strand breaks. | |||
T68985 | Amonafide L-malate | ||
Amonafide L-malate is the malate salt of amonafide, an imide derivative of naphthalic acid, with potential antineoplastic activity. Amonafide intercalates into DNA and inhibits topoisomerase II, resulting in DNA double-s... | |||
T60621 | PFM03 | ||
PFM03 is an inhibitor of MRE11 Endonuclease that regulates DNA double-strand break repair (DSBR) by nonhomologous end-joining (NHEJ) [1]. | |||
T68672 | Amsacrine lactate | ||
Amsacrine lactate is an aminoacridine derivative with potential antineoplastic activity. Although its mechanism of action is incompletely defined, amsacrine may intercalate into DNA and inhibit topoisomerase II, resultin... | |||
T68673 | Amsacrine gluconate | ||
Amsacrine gluconate is an aminoacridine derivative with potential antineoplastic activity. Although its mechanism of action is incompletely defined, amsacrine may intercalate into DNA and inhibit topoisomerase II, result... | |||
T68671 | Amsacrine Isothionate | ||
Amsacrine Isothionate is an aminoacridine derivative with potential antineoplastic activity. Although its mechanism of action is incompletely defined, amsacrine may intercalate into DNA and inhibit topoisomerase II, resu... |