- Производитель:
- Sigma-Aldrich
NACRES: | NA.41 |
- CI-994
Molecular Formula: C15H15N3O2
Molecular Weight: 269.3
- Panobinostat (LBH589)
Molecular Formula: C21H23N3O2
Molecular Weight: 349.43
- SAHA
Molecular Formula: C14H20N2O3
Molecular Weight: 264.3
- SBHA
Molecular Formula: C8H16N2O4
Molecular Weight: 204.22
- Scriptaid
Molecular Formula: C18H18N2O4
Molecular Weight: 326.35
- Trichostatin A
Molecular Formula: C17H22N2O3
Molecular Weight: 302.4
- Tubacin
Molecular Formula: C41H43N3O7S
Molecular Weight: 721.86
- CI-994 - Cell-permeable. A histone deacetylase (HDAC) inhibitor: Ki values are 0.41, 0.75, >100 and >100 µM for HDAC1, HDAC3, HDAC6 and HDAC8, respectively. Displays significant antitumor activity in vitro and in vivo against a broad spectrum of murine and human tumor models.
- Panobinostat (LBH589) - Highly potent inhibitor of both histone deacetylase 1 (HDAC1) activity and tumour cell proliferation in vitro. The IC50 values of HDAC isozymes HDAC1-IP Ac-H4, HDAC8, MALunselective, B61HDAC1 and B12HDAC6 are 0.23±0.06, 283±29, 75±4, 47±5 and 89±12 nM, respectively. And to A2780 proliferation, IC50 value is 4.6±1.8 nM.
- SAHA - Potent, reversible inhibitor of histone deacetylase 1 (HDAC1) and 3 (HDAC3). Induces cell growth arrest at both G1 and G2 phases. Induces apoptosis.
- SBHA - Competitive histone deacetylase (HDAC) inhibitor that has been shown to inhibit HDAC1 (IC50 = 0.25 µM) and HDAC3 (IC50 = 0.30 µM). SBHA causes cell differentiation, cell cycle arrest, or apoptosis. SBHA also enhances cytotoxicity induced by Oxaliplatin in the colorectal cancer cell lines.
- Scriptaid - A relatively non-toxic Inhibitor of histone deacetylase (HDAC). Facilitates transcriptional activation (TGF-/Smad4) in both stable and transient receptor assays in a concentration-dependent manner. At ~2 µg/ml (6-8 µM) concentrations, results in a greater than 100-fold increase in histone acetylation in PANC-1 cells.
- Trichostatin A - Potent, reversible inhibitor of histone deacetylase. Mediates the activation of O6-methylguanine-DNA methyltransferase (MGMT). May be involved in cell cycle progression of several cell types, induces cell growth arrest at both G1 and G2/M phases. In some cases induces apoptosis.
- Tubacin - Tubacin (Tubulin acetylation inducer) is a highly potent, selective, reversible, and cell-permeable inhibitor of histone deacetylase 6 (HDAC6, IC50 = 4 nM). Displays 1000-fold more selectivity for HDAC6 over other HDACs. It inhibits -tubulin deacetylation in mammalian cells. Unlike trichostatin A (TSA), which is a broad spectrum HDAC inhibitor, tubacin is specific for the tubulin deacetylase activity of HDAC6. Tubacin causes increased acetylation of -tubulin, accumulation of polyubiquitinated proteins, and apoptosis. It does not affect global histone deacetylation, gene-expression profiling, or cell cycle progression mediated -tubulin deacetylation in mammalian cells.
Quality Level | 100 |
shipped in | wet ice |
storage temp. | −20°C |
pictograms | GHS05,GHS06,GHS08 |
signalword | Danger |
hcodes | H301 + H331 - H312 - H315 - H317 - H318 - H335 - H341 - H360 - H373 |
pcodes | P201 - P261 - P280 - P301 + P310 - P305 + P351 + P338 - P311 |
Target Organs | Respiratory system |
RIDADR | UN 3316 9 |
Flash Point F | 188.6 °F - closed cup |
Flash Point C | 87 °C - closed cup |
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