trapoxin a has been researched along with hc toxin in 3 studies
| Studies (trapoxin a) | Trials (trapoxin a) | Recent Studies (post-2010) (trapoxin a) | Studies (hc toxin) | Trials (hc toxin) | Recent Studies (post-2010) (hc toxin) |
|---|---|---|---|---|---|
| 8 | 0 | 1 | 41 | 0 | 7 |
| 8 | 0 | 1 | 7 | 0 | 1 |
| Protein | Taxonomy | trapoxin a (IC50) | hc toxin (IC50) |
|---|---|---|---|
| Histone deacetylase 3 | Homo sapiens (human) | 0.43 | |
| Histone deacetylase 4 | Homo sapiens (human) | 0.43 | |
| Histone deacetylase 1 | Homo sapiens (human) | 0.43 | |
| Histone deacetylase 7 | Homo sapiens (human) | 0.43 | |
| Histone deacetylase 2 | Homo sapiens (human) | 0.43 | |
| HD2 type histone deacetylase HDA106 | Zea mays | 0.11 | |
| Polyamine deacetylase HDAC10 | Homo sapiens (human) | 0.43 | |
| Histone deacetylase 11 | Homo sapiens (human) | 0.43 | |
| Histone deacetylase 8 | Homo sapiens (human) | 0.43 | |
| Histone deacetylase 6 | Homo sapiens (human) | 0.43 | |
| Histone deacetylase 9 | Homo sapiens (human) | 0.43 | |
| Histone deacetylase 5 | Homo sapiens (human) | 0.43 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hoque, MA; Islam, MN; Islam, MS; Ito, A; Kato, T; Nishino, N; Yoshida, M | 1 |
| Brosch, G; Esposito, M; Loidl, P; Mai, A; Massa, S; Ragno, R; Sbardella, G | 1 |
| Altucci, L; Brosch, G; Loidl, P; Mai, A; Massa, S; Nebbioso, A; Pezzi, R; Rotili, D; Scognamiglio, A; Simeoni, S | 1 |
3 other study(ies) available for trapoxin a and hc toxin
| Article | Year |
|---|---|
Bicyclic tetrapeptides as potent HDAC inhibitors: effect of aliphatic loop position and hydrophobicity on inhibitory activity.
Topics: Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Hydrophobic and Hydrophilic Interactions; Intercellular Signaling Peptides and Proteins; Oligopeptides; Peptides; Peptides, Cyclic; Protein Binding | 2014 |
3-(4-aroyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a new class of synthetic histone deacetylase inhibitors.
Topics: Drug Design; Enzyme Inhibitors; Histone Deacetylase Inhibitors; Histone Deacetylases; Models, Molecular; Molecular Conformation; Pyrroles | 2001 |
Class II (IIa)-selective histone deacetylase inhibitors. 1. Synthesis and biological evaluation of novel (aryloxopropenyl)pyrrolyl hydroxyamides.
Topics: Amides; Antineoplastic Agents; Apoptosis; Cell Cycle; Cell Differentiation; Drug Screening Assays, Antitumor; Histone Deacetylase 1; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Propane; Pyrroles; Repressor Proteins; Structure-Activity Relationship; U937 Cells; Zea mays | 2005 |