20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T25175 | BRD 9757 | BRD9757,N-Hydroxy-1-cyclopentene-1-carboxamide,BRD-9757 | HDAC |
BRD 9757 (N-Hydroxy-1-cyclopentene-1-carboxamide) is a selective inhibitor of HDAC6 (IC50 = 30 nM). | |||
T10602L | BRD 4354 | HDAC | |
BRD 4354 is an inhibitor of HDAC5 and HDAC9. For HDAC5 and HDAC9, the IC50s values are 0.85 and 1.88 μM, respectively. | |||
T10603 | BRD-6929 | HIV Protease , HDAC | |
BRD-6929 is a selective, brain-penetrant HDAC1 and HDAC2 inhibitor (IC50: 1 and 8 nM). BRD-6929 (Cpd-60) shows high-affinity to HDAC1 and HDAC2 (Kis: 0.2 and 1.5 nM) [2]. BRD-6929 potentiates the efficacy of gnidimacrin... | |||
T26894 | BRD0209 | BRD-0209,BRD 0209 | GSK-3 |
BRD0209 is a highly selective and potent GSK3 inhibitor. | |||
T30577 | BRD0418 | BRD 0418,BRD-0418 | Others |
BRD0418 acts as an upregulator of TRIB1 expression by leading to reprogramming of hepatic lipoprotein metabolism from adipogenesis to clearance it. | |||
T26901 | BRD-9526 | BRD 9526 | |
BRD-9526 is a potent and selective inhibitor of Sonic Hedgehog (Shh). | |||
T23820 | BRD32048 | BRD-32048,BRD 32048 | DNA/RNA Synthesis |
BRD32048 is the ETV1 transcription factor oncoprotein inhibitor. | |||
T2292 | FPH2 | BRD-9424 | Others |
FPH2 (BRD-9424) (BRD-9424) is a small molecule promoting differentiation of iPS-derived hepatocytes. | |||
T6506 | FPH1 | BRD-6125 | Others |
FPH1 (BRD-6125) (BRD-6125) can promote the expansion of iPS-derived hepatocytes. | |||
T35872 | BRD-8000.3 | ||
BRD-8000.3 is a narrow-spectrum, bactericidal antimycobacterial agent known for its specific inhibition of EfpA. It exhibits potent activity against wild-type strains and proves to be a valuable tool in tuberculosis rese... | |||
T10602 | BRD 4354 ditrifluoroacetate | BRD 4354 ditrifluoroacetate (315698-07-8 free base) | HDAC |
BRD 4354 (ditrifluoroacetate) is a moderately potent inhibitor of HDAC5 and HDAC9 (IC50s: 0.85 and 1.88 μM). | |||
T70600 | BRD-7880 | ||
BRD-7880 is a potent and highly specific inhibitor of aurora kinases B and C. | |||
T10605 | BRD-K98645985 | Others | |
BRD-K98645985 is a BAF transcriptional repression inhibitor (EC50: ~2.37 µM). It binds ARID1A-specific BAF complexes, potently reverses HIV-1 latency and prevents nucleosomal positioning. | |||
T69692 | BRD-K25923209 | ||
BRD-K25923209 is a novel inhibitor of BAF transcriptional repression. | |||
T2102 | FH1 | BRD-K4477,NSC 12407 | Others |
FH1 (NSC-12407) (BRD-K4477), a small molecule, enhances the functions of hepatocytes and promotes differentiation hepatocytes derived by iPS. | |||
T41198 | BRD PHOTAC-I-3 | ||
BRD PHOTAC-I-3 is a photoswitchable BET bromodomain degrader (PHOTAC, PHOtochemically TArgeting Chimera). BRD PHOTAC-I-3 comprises a ligand for an E3 ligase, a photoswitch, and the BET bromodomain targeting ligand (+)-JQ... | |||
T16905 | SNIPER(BRD)-1 | Others | |
SNIPER(BRD)-1 is a chemical compound composed of a derivative of the IAP antagonist LCL-161 and the BET inhibitor (+)-JQ-1, linked together. It promotes the degradation of BRD4 through the ubiquitin-proteasome pathway an... | |||
T10604 | BRD-IN-3 | Others | |
BRD-IN-3 is a highly potent PCAF bromodomain (BRD) inhibitor (IC50: 7 nM). It also exhibits activity against GCN5 and FALZ. | |||
T61361 | BRD-8899 | ||
BRD-8899 is a STK33 inhibitor, with an IC 50 of 11 nM [1]. | |||
T2353 | BRD7116 | BRD7716 | DNA gyrase , Antibacterial |
BRD7116 competitively binds to bacterial DNA gyrase, with cell-non-autonomous anti-leukemia activity. |