NSC59984 is a novel and potenl p53 activator with potential anticancer activity. It works by causing the degradation of mutant p53 protein and the activation of p73.
Physicochemical Properties
Molecular Formula | C12H15N3O4 | |
Molecular Weight | 265.27 | |
Exact Mass | 265.106 | |
Elemental Analysis | C, 54.33; H, 5.70; N, 15.84; O, 24.12 | |
CAS # | 803647-40-7 | |
Related CAS # |
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PubChem CID | 5356520 | |
Appearance | Light yellow to yellow solid powder | |
Density | 1.3±0.1 g/cm3 | |
Boiling Point | 451.8±45.0 °C at 760 mmHg | |
Flash Point | 227.1±28.7 °C | |
Vapour Pressure | 0.0±1.1 mmHg at 25°C | |
Index of Refraction | 1.596 | |
LogP | 0.82 | |
Hydrogen Bond Donor Count | 0 | |
Hydrogen Bond Acceptor Count | 5 | |
Rotatable Bond Count | 2 | |
Heavy Atom Count | 19 | |
Complexity | 372 | |
Defined Atom Stereocenter Count | 0 | |
SMILES | O=C(N1CCN(C)CC1)C=CC1=CC=C([N+](=O)[O-])O1 |
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InChi Key | QKTRIGNWBRHBFV-DUXPYHPUSA-N | |
InChi Code | InChI=1S/C12H15N3O4/c1-13-6-8-14(9-7-13)11(16)4-2-10-3-5-12(19-10)15(17)18/h2-5H,6-9H2,1H3/b4-2+ | |
Chemical Name | (E)-1-(4-methylpiperazin-1-yl)-3-(5-nitrofuran-2-yl)prop-2-en-1-one | |
Synonyms | NSC59984; NSC 59984; NSC-59984 | |
HS Tariff Code | 2934.99.9001 | |
Storage |
Powder-20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
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Shipping Condition | Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs) |
Biological Activity
Targets | p53 | |||
ln Vitro | NSC59984 specifically induces p73-dependent cell death and restores p53 pathway signaling in mutant p53-expressing human colorectal cancer cells. Additionally, NSC59984 causes cell death in a panel of cancer cell lines with various p53 mutations while causing little to no genotoxicity in healthy cells. [1] | |||
ln Vivo | NSC59984 (45 mg/kg, i.p.) significantly inhibits tumor growth in nude mice with DLD-1 xenograft tumors in a p73-dependent manner. [1] | |||
Cell Assay | Cells are seeded at 5,000 cells per well on 96-well plates. The manufacturer's recommended procedure is followed when mixing cells with an equal volume of CellTiter-Glo reagents, and the IVIS imager is used to measure the bioluminescence. | |||
Animal Protocol |
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References |
[1]. Small-Molecule NSC59984 Restores p53 Pathway Signaling and Antitumor Effects against Colorectal Cancer via p73 Activation and Degradation of Mutant p53. Cancer Res. 2015 Sep 15;75(18):3842-52. [2]. Small-Molecule NSC59984 Restores p53 Pathway Signaling and Antitumor Effects againstColorectal Cancer via p73 Activation and Degradation of Mutant p53. Cancer Res. 2015 Sep 15;75(18):3842-52. |
Solubility Data
Solubility (In Vitro) |
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Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 2.5 mg/mL (9.42 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 2: ≥ 2.5 mg/mL (9.42 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly. Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.  (Please use freshly prepared in vivo formulations for optimal results.) |
Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
1 mM | 3.7697 mL | 18.8487 mL | 37.6974 mL | |
5 mM | 0.7539 mL | 3.7697 mL | 7.5395 mL | |
10 mM | 0.3770 mL | 1.8849 mL | 3.7697 mL |