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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T9271 | RAD51-IN-1 | DNA/RNA Synthesis | |
Rad51-in-1 is a derivative of B02 and an effective inhibitor of Rad51. | |||
T4656 | RAD51 Inhibitor B02 | B02 | Apoptosis , DNA/RNA Synthesis |
RAD51 Inhibitor B02 (B02) (B02) is an inhibitor of human RAD51 with an IC50 of 27.4 μM. | |||
T39824 | RAD51-IN-3 | RAD51-IN-3 | |
RAD51-IN-3 is a Rad51 inhibitor. | |||
T12682 | Emzadirib | CYT-0851,RAD51-IN-2 | DNA/RNA Synthesis |
Emzadirib (RAD51-IN-2) is a potent RAD51 inhibitor with potential anticancer activity for the study of DNA damage repair. | |||
T2276 | RI-1 | RI1,RAD51 inhibitor 1 | DNA/RNA Synthesis |
RI-1 (RAD51 inhibitor 1) is a RAD51 inhibitor (IC50: 5-30 μM). | |||
T63892 | RAD51-IN-5 | ||
RAD51-IN-5 is a potent inhibitor of RAD51. RAD51-IN-5 has shown potential for the study of mitochondrial deficiency disorders. | |||
T61469 | RAD51-IN-8 | ||
RAD51-IN-8, a new RAD51 binder, is a RAD51-BRCA2 inhibitor that inhibits the RAD51 BRCA2 protein protein interaction in the micromolar range. RAD51-IN-8 also is a protein protein interaction (PPI) inhibitor. RAD51-IN-8 h... | |||
T63728 | RAD51-IN-7 | ||
RAD51-IN-7 is a potent inhibitor of RAD51, a eukaryotic gene. RAD51-IN-7 has shown research potential for mitochondrial deficiency disorders. | |||
T63883 | RAD51-IN-6 | ||
RAD51-IN-6 is a potent inhibitor of RAD51, which is a eukaryotic gene. RAD51-IN-6 has shown potential for the study of mitochondrial deficiency disorders. | |||
T73107 | RAD51-IN-4 | ||
RAD51-IN-4 is a potent RAD51 inhibitor, targeting a eukaryote gene critical for studies on conditions associated with mitochondrial defects. | |||
T2628 | RI-2 | DNA/RNA Synthesis | |
RI-2 is an optimized RAD51 inhibitor with an IC50 of 44.17 μM in the standard DNA binding assay; specifically inhibits HR(Homologous recombination) repair in human cells. | |||
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... | |||
T6972 | RS-1 | DNA/RNA Synthesis | |
RS-1 is a RAD51 activator. RS-1 also increases CRISPR/Cas9-mediated knock-in efficiencies. | |||
T8873 | Bractoppin | Others , DNA/RNA Synthesis | |
Bractoppin is a drug-like inhibitor of phosphopeptide recognition by the human BRCA1 tandem (t)BRCT domain (IC50 = 0.074 μM), which selectively inhibits substrate binding with nanomolar potency in vitro. Structure-activi... | |||
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. | |||
T2516 | Amuvatinib | MP470,HPK 56 | Apoptosis , FLT , c-Met/HGFR , c-RET , DNA/RNA Synthesis , PDGFR , c-Kit |
Amuvatinib (MP470) is an orally bioavailable synthetic carbothioamide with potential antineoplastic activity. | |||
T60006 | Aromatase inhibitor 23 | Others | |
Aromatase inhibitor 23 is an inhibitor that target protein-protein interactions in RAD51 family of recombinases. | |||
T10936 | D-I03 | DI03 | DNA/RNA Synthesis |
D-I03 is a selective RAD52 inhibitor with a Kd of 25.8 µM. D-I03 specifically inhibits RAD52-dependent single-chain annealing (SSA) and D-loop formation, with IC50 of 5 µM and 8 µM, respectively. D-I03 inhibited the grow... | |||
T6960L | PU-H71 HCl | PU-H71 HCl(873436-91-0 Free base),Zelavespib HCl | HSP , DNA/RNA Synthesis |
PU-H71 HCl (Zelavespib HCl) is a novel Hsp90 inhibitor, a novel purine-based analog, and a radiosensitizer that may be a promising agent for CIRT. PU-H71 HCL shows antitumor activity in many preclinical models of maligna... | |||
T63717 | CAM833 | ||
CAM833 is a potent orthosteric inhibitor of the interaction between BRCA2 and RAD51 and also inhibits RAD51 oligomerization and is able to act on the ChimRAD51 protein (Kd: 366 nM). |