| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V53007 | 5-Phenylpentan-2-one (phenylbutyric acid; phenylbutyric acid) | 2235-83-8 | 5-Phenylpentan-2-one is a potent inhibitor of histone deacetylase enzymes (HDACs). |
|
V5095 | BML-210 (CAY10433) | 537034-17-6 | BML-210 (also known as BML210; CAY-10433) is novel and potent HDAC inhibitor (IC50 value: 5 μM) with anticancer activity. |
|
V52089 | FNDR-20123 free base | 1267502-34-0 | FNDR-20123 free base is an effective, safe and first-in-class anti-malarial HDAC inhibitor (antagonist) with IC50 of 31 nM and 3 nM against Plasmodium and human HDAC respectively. |
|
V51996 | HDAC-IN-56 | 2814571-89-4 | HDAC-IN-56 ((S)-17b) is an orally bioactive class I histone deacetylase HDAC inhibitor (antagonist) with IC50s of 56.0±6.0 and 90.0 for HDAC1, HDAC2, HDAC3 and HDAC4-11, respectively. |
|
V75833 | HDAC6-IN-26 | 2991427-19-9 | HDAC6-IN-26 (compound 23) is a potent inhibitor of HDAC6. |
|
V12132 | KA2507 monohydrochloride | 2972712-63-1 | KA2507 HCl is a highly efficient and selective HDAC6 inhibitor (IC50=2.5 nM) without obvious toxicity. |
|
V31449 | SS-208 | 2245942-72-5 | SS-208 is a selective HDAC6 inhibitor (antagonist) with IC50 of 12 nM. |
|
V35169 | Triciferol | 957214-00-5 | Triciferol is a multi-ligand with combined VDR agonist and HDAC antagonist effects. |
|
V4130 | Tinostamustine | 1236199-60-2 | Tinostamustine (also known as EDO-S101; EDO-S 101;Minomustine)is a novel, potent, fisrt-in-class alkylating agent and pan histone-deacetylase (HDAC)inhibitor with anticancer activity. |
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