2-Aminobenzamides compound M122 |
Especially inhibit HDAC1 HDAC2 |
High potency and selectivity |
HeLa, etc. |
[21] |
2-Oxo-1,3-thiazolidine derivatives |
Class II HDACIs |
Good bioactivities, oral bioavailability |
Cervical cancer |
[22] |
TSA |
Except for class III HDACs |
Acetylated HIF-1α at lysine 674 |
HeLa cells |
[50,51] |
Vorinostat (SAHA) |
Pan-HDAC inhibitor |
Reduce E6 and E7 activity |
HPV infections |
[52,53] |
Oxamflatin |
HDAC inhibitor |
Induces E-cadherin Expression |
HeLa cells |
[54] |
Valproic acid (VPA) |
HDAC inhibitor |
Re-expression of E-cadherin |
HeLa and TC1 cell lines |
[55] |
OH-VPA |
HDAC inhibitor |
Antioxidant |
HeLa cells |
[56] |
Genistein |
HDAC families |
Time-dependent |
HeLa cells |
[57] |
Caffeic acid |
HDAC inhibitor |
Induction of apoptosis |
Colon and cervical cancer cells |
[58] |
Mocetinostat and entinostat |
Class I HDACIs |
Pan-gynecologic cancer inhibitors |
Ovarian, cervical cells, etc. |
[59] |
Scriptaid (SCR) |
HDAC-8 inhibitor |
Inhibit HDAC-8 effectively than TSA |
HeLa cells, etc. |
[60] |
Isatin-based compounds |
HDACIs |
Inhibit proliferation |
HeLa cells |
[61] |