Product Name | C-646 |
Description |
HAT inhibitor |
Purity | >98% (TLC); NMR (Conforms) |
CAS No. | 328968-36-1 |
Molecular Formula | C24H19N3O6 |
Molecular Weight | 445.4 |
Field of Use | Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only. |
Storage Temperature | -20ºC |
Shipping Temperature | Shipped Ambient |
Product Type | Inhibitor |
Solubility | Soluble in 10 mg/ml DMSO |
Source | Synthetic |
Appearance | Orange Solid |
SMILES | CC1=CC(=C(C=C1C)[N+](=O)[O-])C2=CC=C(O2)/C=C/3C(=NN(C3=O)C4=CC=C(C=C4)C(=O)O)C |
InChI | InChI=1S/C24H19N3O6/c1-13-10-20(21(27(31)32)11-14(13)2)22-9-8-18(33-22)12-19-15(3)25-26(23(19)28)17-6-4-16(5-7-17)24(29)30/h4-12H,1-3H3,(H,29,30)/b19-12+ |
InChIKey | HEKJYZZSCQBJGB-XDHOZWIPSA-N |
Safety Phrases |
Classification: Caution – Substance not yet fully tested. Safety Phrases: S22 - Do not breathe dust S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection S24/25- Avoid contact with skin and eyes |
Cite This Product | C-646 (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-350) |
Alternative Names | 4-[4-[[5-(4,5-Dimethyl-2-nitrophenyl)-2-furanyl]methylene]- 4,5-dihydro-3-methyl-5-oxo-1Hpyrazol- 1-yl]benzoic acid |
Research Areas | Cell Signaling |
PubChem ID | 1285940 |
Scientific Background | Potent and selective inhibitor of the histone acetyl transferase p300/CBP (Ki=400 nM ). Induces apoptosis in prostate cancer cells. Enhances fear extinction memory and synaptic plasticity in mice. Promotes tau deacetylation reducing levels of pathogenic p-tau. Cell permeable. |
References |
1. Bowers E.M., et al. (2010) Chem. Biol. 17: 471. 2. Santer F.R., et al. (2011) Mol. Cancer Ther. 10: 1644. 3. Marek R., et al. (2011) J. Neurosci. 31: 7486. 4. Min S.W., et al. (2010) Neuron 67: 953. |
Reviews
There are no reviews yet.