sales@targetmol.com (US) / info@targetmol.com    Tel: (781) 999-4286 / (781) 999-5354
Home > HDAC
HDAC
Cat.No. Product Name Information Area
T7082 HDAC8-IN-1 MDK-7933 (HDAC8-IN-1) is a HDAC8 inhibitor with an IC50 of 27.2 nM in cancer cell lin...
T3983 TMP 195 TMP195 is a selective class IIa histone deacetylase (HDAC) inhibitor. Others
T3516 Minomustine EDO-S101 is a pan HDAC inhibitor with IC50 values of 9, 9 and 25 nM for HDAC1, HDAC2 ... Others
T3509 ACY-738 ACY-738 demonstrates inhibitory activity against recombinant HDAC6 (IC50: 1.7 nM), wi... Others
T3937 Methyl L-histidinate dihydrochloride Inhibition of histidine decarboxylase in Sprague-Dawley rat stomach assessed as decre...
T3878 Raddeanin(Anemodeanin) A Raddeanin A has moderate inhibitory activity against histone deacetylases (HDACs). Ra... Others
T3499 Remodelin Remodelin is an effective and specific inhibitor of the acetyl-transferase protein NA... Cancer
T6980 Scriptaid Scriptaid is an inhibitor of HDAC,and has a greater effect on acetylated H4 than H3. Others
T3661 ACY-241 ACY-241, also known as Citarinostat, is a potent, selective and orally available hist... Cancer
T6865 Quisinostat (JNJ-26481585) 2HCl Quisinostat (JNJ-26481585) 2HCl is a novel second-generation HDAC inhibitor with high... Others
T6270 Trichostatin A (TSA) Trichostatin A is a natural derivative of dienohydroxamic acid isolated from species ... Cancer
T1558 Resveratrol Resveratrol is a polyphenolic phytoalexin with antioxidant and potential chemoprevent... Cancer
T3205 UF010 UF010 is a potent and selective HADC inhibitor with IC50 ~0.06 μM, 0.1 μM, 0.5 μM and... Cancer
T3204 BML-210 BML-210 is a new-type HDAC inhibitor. Cancer
T3199 PTACH PTACH (NCH-51) is a SAHA-based inhibitor of human HDAC. It can potently inhibit the g... Cancer
T3193 Pimelic diphenylamide 106 Pimelic diphenylamide 106 is a slow, tight-binding inhibitor of class I HDAC (with IC... Cancer
T6639 RG2833 (RGFP109) RG2833 (RGFP109), a brain-penetrant HDAC inhibitor, is with IC50 of 60 nM and 50 nM ... Cancer
T6421 BRD73954 BRD73954, an effective and specific HDAC inhibitor, which is with IC50 of 36 nM and 1... Cancer
T6362 4SC-202 free base 4SC-202 is a selective class I HDAC inhibitor with IC50 of 1.20 μM, 1.12 μM, and 0.57... Cancer
T6637 Resminostat Resminostat is an orally bioavailable inhibitor of histone deacetylases (HDACs) with ... Cancer
T6481 Droxinostat Droxinostat is a selective inhibitor of HDAC, mostly for HDACs 6 and 8 with IC50 of 2... Cancer
T6695 Tasquinimod Tasquinimod is a quinoline-3-carboxamide linomide analog with antiangiogenic and pote... Cancer
T6233 Entinostat (MS-275) Entinostat (MS-275) is an effective inhibitor of HDAC1 and HDAC3. The IC50 of Entinos... Cancer
T6161 Tubastatin A hydrochloride Tubastatin A HCl is an effective and specific HDAC6 inhibitor (IC50: 15 nM). It has s... Others
T6061 LMK-235 LMK-235 is a potent HDAC inhibitor, and is used in cancer research. Cancer
T6055 Quisinostat (JNJ-26481585) Quisinostat (JNJ-26481585) is a novel second-generation HDAC inhibitor with highest p... Cancer
T6006 Romidepsin (FK228, Depsipeptide)hot Romidepsin is an intravenously administered histone deacetylase inhibitor and antineo... Cancer
T3108 CUDC-101 CUDC-101 is a potent inhibitor of HDAC, EGFR and HER2 with IC50s of 4.4, 2.4 and 15.7... Cancer
T2512 Mocetinostat Mocetinostat (MGCD0103) is an orally available, Class 1-selective and small molecule ... Cancer
T2489 Rocilinostat (ACY-1215) Ricolinostat is an orally bioavailable, specific inhibitor of histone deacetylase 6 (... Cancer
1