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Search Results for " hdac6 inhibitor "

20

Compounds

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).
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