Table 1 |.
Inhibitor | Drug target | Stage of development | Animal models tested | Refs |
---|---|---|---|---|
DNMT inhibitors | ||||
Decitabine (also known as 5-aza-2- deoxycytidine; marketed as Dacogen by Eisai) | DNMTs | Approved in 2006 | Stroke | 76,77 |
Zebularine | DNMTs | Preclinical | Stroke | 132 |
HDAC inhibitors | ||||
Valproic acid | Class I and II HDACs | Approved in 1986 | AD, HD, stroke and global ischaemia | 133–139 |
Phenylbutyrate | Class I and II HDACs | Approved in1996 | AD and HD | 140–143 |
Suberoylanilide hydroxamic acid (also known as vorinostat; marketed as Zolinza by Merck) | Class I and II HDACs | Approved in 2006 | AD, HD and stroke | 133, 144–147 |
Nicotinamide (sirtuin inhibitor) | Class III HDACs | Phase III | AD and HD | 94,95 |
Entinostat (also known as MS-275) | Class I HDACs | Phase II | AD and stroke | 80,148 |
Trichostatin A | Class I and II HDACs | Preclinical | HD, stroke and global ischaemia | 28,149,150 |
AGK2 (sirtuin 2 inhibitor) | Class III HDACs | Preclinical | HD and PD | 151,152 |
Sodium butyrate | Class I and II HDACs | Preclinical | AD, HD, stroke, brain atrophy and the bi-transgenic CK-p25 mouse model of neurodegeneration | 26,133,140, 153–156 |
AD, Alzheimer disease; CK-p25, mouse model in which p25 is conditionally expressed under the control of the promoter of the gene that encodes calcium/calmodulin-dependent protein kinase II; DNMT, DNA methyltransferase; HD, Huntington disease; HDAC, histone deacetylase; PD, Parkinson disease.