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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T1983 | CAY10603 | HDAC6 Inhibitor,BML-281 | HDAC |
CAY10603 (BML-281) is a potent and selective inhibitor of HDAC6. | |||
T10255 | AES-135 | HDAC | |
AES-135 is a potent HDAC inhibitor, inhibits HDAC3, HDAC6, HDAC11 (IC50s: 654, 190, and 636 nM) with anti-tumor activity. | |||
T3661 | Citarinostat | ACY241,HDAC-IN-2 | HDAC |
ACY-241, also known as Citarinostat (ACY241), is a potent, selective and orally available histone deacetylase (HDAC) inhibitor, with potential antineoplastic activity. Upon oral administration, ACY-241 inhibits the activ... | |||
T6481 | Droxinostat | NS 41080 | Apoptosis , HDAC |
Droxinostat (NS 41080) is a selective inhibitor of HDAC, mostly for HDACs 6 and 8 with IC50 of 2.47 μM and 1.46 μM, greater than 8-fold selective against HDAC3 and no inhibition to HDAC1, 2, 4, 5, 7, 9, and 10. | |||
T10777 | CG347B | HDAC | |
CG347B is a selective inhibitor of HDAC6. | |||
T69735 | ITF3756 | HDAC | |
ITF3756 is a selective HDAC6 inhibitor. | |||
T7385 | WT-161 | Apoptosis , HDAC | |
WT161 is a potent and selective inhibitor of HDAC6 (IC50:0.40 nM). | |||
T2489 | Ricolinostat | ACY-1215,Rocilinostat | Apoptosis , HDAC |
Ricolinostat (Rocilinostat) is an orally bioavailable, specific inhibitor of histone deacetylase 6 (HDAC6) with potential antineoplastic activity. | |||
T1819 | Nexturastat A | HDAC | |
Nexturastat A is an effective and specific HDAC6 inhibitor (IC50: 5 nM). Its selectivity is >190-fold than other HDACs. | |||
T16129 | MPI_5a | HDAC | |
MPI_5a is an effective and selective inhibitor of HDAC6 (IC50=36 nM). MPI_5a weakly inhibits other HDAC isoforms and it also inhibits acyl-tubulin accumulation in cells (IC50: 210 nM). | |||
T16936 | SS-208 | HDAC | |
SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes. | |||
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). | |||
T5332 | TH34 | HDAC | |
TH34 is an HDAC6/8/10 inhibitor (IC50s: 4.6/1.9/7.7 μM). It shows high selectivity over HDAC1/2/3. | |||
T6161 | Tubastatin A Hydrochloride | TSA HCl,Tubastatin A HCl | Apoptosis , HDAC , Autophagy |
Tubastatin A Hydrochloride (TSA HCl) is an effective and specific HDAC6 inhibitor (IC50: 15 nM). It has selectivity (>1000-fold) against all other isozymes except HDAC8 (>57-fold). | |||
T2430 | HPOB | Apoptosis , HDAC | |
HPOB is an effective and specific HDAC6 inhibitor (IC50: 56 nM), >30-fold selectivity over other HDACs. | |||
T60082 | HDAC-IN-40 | HDAC | |
HDAC-IN-40 is a potent alkoxyamide-based HDAC inhibitor with Ki of 60 nM and 30 nM for HDAC2 and HDAC6, respectively. HDAC-IN-40 had antitumor effects | |||
T6421 | BRD73954 | HDAC | |
BRD73954, an effective and specific HDAC inhibitor, which is with IC50 of 36 nM and 120 nM for HDAC6 and HDAC8, respectively. | |||
T6327 | Tubacin | Virus Protease , HDAC | |
Tubacin is a highly potent and selective, reversible, cell-permeable HDAC6 inhibitor with an IC50 of 4 nM, approximately 350-fold selectivity over HDAC1. | |||
T10244 | ACY-1083 | HDAC | |
ACY-1083 is a selective and brain-penetrating HDAC6 inhibitor (IC50: 3 nM) and effectively reverses chemotherapy-induced peripheral neuropathy. | |||
T4370 | Resminostat hydrochloride | 4SC-201 hydrochloride,RAS2410 hydrochloride | HDAC |
Resminostat hydrochloride (RAS2410 hydrochloride) is an effective inhibitor of HDAC1/HDAC3/HDAC6 (IC50: 42.5/50.1/71.8 nM), respectively, and shows less potent activities against HDAC8 (IC50: 877 nM). |