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Peroxynitrite decomposition catalysts and methods of use thereof

a technology of peroxynitrite and catalyst, which is applied in the field of substituting porphyrin, porphyrazine, texaphyrin, or corrolemetal complex, can solve problems such as damage to biological targets, and achieve the effects of high catalytic activity, enhanced lifetime in the blood pool, and high stability

Inactive Publication Date: 2006-09-07
THE TRUSTEES FOR PRINCETON UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0006] The invention is based in part on the discovery of novel substituted metallic complexes that are effective peroxynitrite decomposition catalysts. Preferred catalysts have one or more of the properties of high catalytic activity, high stability and enhanced lifetime in the blood pool, advantageous tissue distribution, and low toxicity. The peroxynitrite decomposition catalysts can be used to treat a variety of conditions and diseases, including those known to involve the accumulation of the oxidant peroxynitrite.

Problems solved by technology

These oxidizing intermediates can damage biological targets.

Method used

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  • Peroxynitrite decomposition catalysts and methods of use thereof
  • Peroxynitrite decomposition catalysts and methods of use thereof
  • Peroxynitrite decomposition catalysts and methods of use thereof

Examples

Experimental program
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Effect test

example 1

Synthesis of Tetrakis(allyl-2-pyridyl)porphyrin (VIII)

[0086] In an oven-dried flask under argon, 100 mg tetrakis(2-pyridyl)porphyrin (2-PyP) was dissolved in 5 mL allyl bromide, and reaction was heated at 100° C. for 16 hours. The reaction mixture was heated at 100° C. for 8 hours. Two methods were used to monitor the completion of the reaction. First, the shift of the porphyrin Soret band from λmax=412 nm (methanol) to λmax=418 nm (methanol) was monitored. A second method involved partition of an aliquot of the reaction mixture between H2O and CHCl3 whereby a complete reaction showed no color in the CHCl3 layer. Upon completion of the reaction, the allyl bromide was distilled off under high vacuum, and the residue was triturated with ethyl ether (Et2O). Chromatography was performed on Sephadex LH-20 (column dimensions were 2×20 cm) using methanol as the eluent and fractions that showed porphyrin with λmax=418 nm were retained. Compound VIII was produced as a shiny purple solid, in...

example ii

Synthesis of Compound (IX): Tetrakis(acetamido-2-pyridyl)porphyrin

[0087] In an oven-dried flask under argon, 50 mg 2-PyP was added to 1.0 g bromoacetamide and 2.5 mL dry DMF. The reaction mixture was heated at 100° C. for 8 hours. The reaction was monitored as above. Compound IX was isolated by dropping the completed reaction mixture into Et2O and precipitating the resulting solid from methanol / Et2O. The solid was filtered and washed well with CHCl3 and Et2O. Chromatography on Sephadex LH-20 (column dimensions 2×15 cm) using methanol as the eluent and by collecting the fastest-running red band produced (IX) in 75% yield. Absorbance data included the following: UV-Vis: λmax (run) (log10ε0) 418(5.20) 512(4.27) 587(4.01). ES-MS: Molecular ion at 850 (M-4 Br).

example iii

Synthesis of Compound (X): Tetrakis (ethylaceto-2-pyridyl)porphyrin

[0088] To an oven-dried flask under argon was added 10 mg 2-PyP, 1 mL ethyl bromoacetate, and 2 mL dry DMF. The reaction mixture was heated at 100° C. for 6 hours. The reaction was monitored by the shift in the porphyrin Soret band from λmax=412 nm (methanol) to λmax=420 nm (methanol), and, by, partition of an aliquot of the reaction mixture between H2O and CHCl3 where a complete reaction showed no color in the CHCl3 layer. When the reaction mixture was cooled to room temperature, some of the desired porphyrin precipitated out of solution. The remainder of product was precipitated from the reaction mixture by addition of Et2O, and precipitate was filtered and washed well with CHCl3 and Et2O. The brown solid was precipitated from methanol / Et2O and filtered to give compound (X), as purple crystals, in 75% yield. Absorbance data included the following: UV-vis: λmax (nm) (log10ε0) 420(5.29) 512(4.46) 555(4.30) 585(4.28)...

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Abstract

This invention provides a novel class of substituted macrocyclic metallic complexes. The complexes are useful as peroxynitrite decomposition catalysts. Pharmaceutical compositions, and methods of making and using the compounds, or a pharmaceutically acceptable salt, hydrate, prodrug, or mixture thereof are also described.

Description

RELATED APPLICATIONS [0001] This application claims priority to U.S. Ser. No. 60 / 137,308, filed Jun. 3, 1999; U.S. Ser. No. 09 / 587,382, filed Jun. 1, 2000. The contents of this application are incorporated herein by reference in their entirety.FIELD OF THE INVENTION [0002] The invention relates in general to substituted metallic complexes and more particularly to substituted porphyrin-, porphyrazine-, texaphyrin-, salen-, or corrole-metal complexes. BACKGROUND OF THE INVENTION [0003] The peroxynitrite ion (ONOO−) is a potent oxidant formed by the combination of nitric oxide (NO) and the superoxide anion (O2)−. NO has been shown to be generated by numerous cell types, such as macrophages, neutrophils, hepatocytes and endothelial cells. The direct combination of NO with O2 produces the peroxynitrite ion (ONOO−), which decomposes rapidly under physiological conditions to oxidizing intermediates. These oxidizing intermediates can damage biological targets. [0004] Pathological consequenc...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/555C07D487/22C07F15/06C07F15/04C07F15/02A61K31/409A61P9/10A61P21/04A61P25/00A61P25/14A61P25/28A61P29/00A61P35/00A61P37/00A61P39/00A61P43/00C07F9/00C07F13/00
CPCC07D487/22C07F9/005C07F13/005C07F15/025C07F15/045A61P9/10A61P21/04A61P25/00A61P25/14A61P25/28A61P29/00A61P35/00A61P37/00A61P39/00A61P43/00
Inventor GROVES, JOHN T.MOELLER, SUZANNE M.
Owner THE TRUSTEES FOR PRINCETON UNIV
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