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| Product Name | MS-275 |
| Description |
HDAC inhibitor |
| Purity | >98.5 |
| CAS No. | 209783-80-2 |
| Molecular Formula | C21H20N4O3 |
| Molecular Weight | 376.41 |
| Field of Use | Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only. |
Properties
| Storage Temperature | -20ºC |
| Shipping Temperature | Shipped Ambient |
| Product Type | Inhibitor |
| Solubility | Soluble in DMSO or methanol. |
| Source | Synthetic |
| Appearance | Off white solid |
| SMILES | C2=C(C(=O)NC1=C(N)C=CC=C1)C=CC(=C2)CNC(OCC3=CN=CC=C3)=O |
| InChI | InChI=1S/C21H20N4O3/c22-18-5-1-2-6-19(18)25-20(26)17-9-7-15(8-10-17)13-24-21(27)28-14-16-4-3-11-23-12-16/h1-12H,13-14,22H2,(H,24,27)(H,25,26) |
| InChIKey | INVTYAOGFAGBOE-UHFFFAOYSA-N |
| Safety Phrases |
Classification: D1B Toxic Material Causing Immediate and SeriousToxic Effects, Toxic by ingestion, D2A Very Toxic Material Causing Other Toxic Effects, Teratogen, D2B Toxic Material Causing Other Toxic Effects, Reproductive hazard, Moderate skin irritant, Moderate eye irritant Safety Phrases: S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. Hazard statements: H301 Toxic if swallowed. H315 Causes skin irritation. H319 Causes serious eye irritation. H335 May cause respiratory irritation. H360 May damage fertility or the unborn child. Precautionary statements: P201 Obtain special instructions before use. P261 Avoid breathing dust/ fume/ gas/ mist/ vapours/ spray. P301 + P310 IF SWALLOWED: Immediately call a POISON CENTER or doctor/ physician. P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P308 + P313 IF exposed or concerned: Get medical advice/ attention. |
| Cite This Product | MS 275 (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-416) |
Biological Description
| Alternative Names | 3-pyridinylmethyl [[4-[[(2-aminophenyl)amino]carbonyl]phenyl]methyl]carbamate, N-(2-Aminophenyl)-4-[N-(pyridine-3ylmethoxycarbonyl)aminomethyl]benzamide |
| Research Areas | Cancer, Cell Signaling |
| PubChem ID | 4261 |
| Scientific Background | MS 275 (Entinostat) is a selective inhibitor of class I histone deacetylases (HDACs), which regulate chromatin structure and gene expression. In neuroscience, MS 275 is used to study epigenetic mechanisms underlying neurodevelopment, synaptic plasticity, and neurodegeneration. HDAC inhibition by MS 275 promotes histone acetylation, leading to transcriptional activation of neuroprotective genes. It has shown promise in models of Alzheimer's and Huntington's disease by enhancing cognitive function and reducing neuroinflammation. MS 275 is a valuable tool for exploring epigenetic therapies aimed at restoring neuronal health and function. |
| References | 1. Camphausen K., Burgan W., Cerra M., Oswald K.A., Trepel J.B., Lee M.J., et al. (2004) Cancer Res. 316-21. |
Product Images
Chemical structure of MS 275 (SIH-416), a HDAC inhibitor. CAS #: 209783-80-2. Molecular Formula: C21H20N4O3. Molecular Weight: 376.41 g/mol.
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