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TMP269

Cat. No. M3643

All AbMole products are for research use only, cannot be used for human consumption.

TMP269 Structure
Size Price Availability Quantity
10mM*1mL in DMSO USD 120 In stock
2mg USD 65 In stock
5mg USD 110 In stock
10mg USD 175 In stock
25mg USD 330 In stock
50mg USD 530 In stock
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Quality Control & Documentation
Biological Activity

TMP269 is a novel and selective class IIa histone deacetylase inhibitor with IC50s of 126/80/36/9 nM for HDAC 4/5/7/9, respectively; 20-400 fold selectivity over class1 HDACs. TMP269 showes no effect at the acetylation level of histone H3-K9, no signifcant effects (2-fold) in gene expression on T-cells and no cytotoxicity in T cell expansion assay. TMP269 prevents cell cycle progression, DNA synthesis, and proliferation induced in response to G protein-coupled receptor/PKD1 activation.In addition, TMP269 significantly promotes reprogramming.

Customer Product Validations & Biological Datas
Source Breast Cancer Res Treat (2014). Figure 1. TMP269
Method qPCR
Cell Lines MDAMB-231 cells
Concentrations 100 nM
Incubation Time 24 h
Results Quantitation of the CV assay dose response (10nM–10μM) in MDA-MB-231 cells demonstrated a similar effect on cell proliferation by LBH589 as previously observed, while SAHA and TMP269 were much less effective
Protocol (for reference only)
Cell Experiment
Cell lines Human CD4+ T cells
Preparation method Isolating human CD4+ T cells from whole blood via negative selection according to manufacturer's instructions (RosetteSep Human CD4+ T cell enrichment kit), re-suspended in T-cell culture medium (10% FBS, 2 mM L-glutamine, 1 mM pyruvate, 10 mM HEPES, 10 U/10 mg penicillin/streptomycin, 0.5% DMSO in RPMI) and plating at 50,000 cells/well with IL-2 (10 BRMP units/mL) and 100,000 human T-expander Dynabeads for 72 h. Determination of mitochondrial function or cell viability is done according to manufacturer’s instructions (Cell Proliferation Assay Kit I (MTT)) and is represented as a percent of control (no inhibitor) wells.
Concentrations 10 μM
Incubation time 72 hours
Animal Experiment
Animal models
Formulation
Dosages
Administration
Chemical Information
Molecular Weight 514.52
Formula C25H21F3N4O3S
CAS Number 1314890-29-3
Solubility (25°C) DMSO
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Sinnett-Smith J, et al. Am J Physiol Cell Physiol. Protein kinase D1 mediates class IIa histone deacetylase phosphorylation and nuclear extrusion in intestinal epithelial cells: role in mitogenic signaling.

[2] Lobera M, et al. Nat Chem Biol. Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding group.

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Keywords: TMP269 supplier, HDAC, inhibitors, activators

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