Iridium containing hydrosilylation catalysts and compositions containing the catalysts
US-9221041-B2 · Dec 29, 2015 · US
US9944668B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9944668-B2 |
| Application number | US-201414759114-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 7, 2014 |
| Priority date | Jan 7, 2013 |
| Publication date | Apr 17, 2018 |
| Grant date | Apr 17, 2018 |
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Manganese coordination complexes with utility as magnetic resonance probes and as biological reductant sensors are disclosed. In one embodiment, ligands can stabilize both the Mn 2+ and Mn 3+ oxidation states. In the presence of a reductant such as glutathione, low relaxivity Mn III -HBET is rapidly converted to high relaxivity Mn II -HBET with a 3-fold increase in relaxivity, and concomitant increase in magnetic resonance signal. In another embodiment, ligands were designed to chelate Mn(ll) in a thermodynamically stable and kinetically inert fashion while allowing for direct interaction of Mn(ll) with water. In yet another embodiment, high molecular weight multimers containing six Mn(ll) chelators were prepared. The high molecular weight results in slower tumbling of the molecules in solution and can strongly enhance the Mn(ll) relaxivity.
Opening claim text (preview).
What is claimed is: 1. A contrast agent for magnetic resonance imaging, the contrast agent comprising a compound of Formula (IX): 2. The contrast agent of claim 1 , wherein the Mn is a positron emitting manganese isotope. 3. A pharmaceutical composition, comprising the contrast agent of claim 1 and a pharmaceutically acceptable carrier. 4. The pharmaceutical composition of claim 3 , further comprising an additional pharmaceutically active ingredient. 5. A method of diagnostic imaging, comprising administering to a subject a contrast agent comprising a compound of Formula (IX): 6. The method of claim 5 , wherein the diagnostic technique is selected from among the group consisting of magnetic resonance imaging (MM), positron emission tomography (PET), and concurrent Mill and PET. 7. The method of claim 5 , wherein the Mn is a positron emitting manganese isotope. 8. The method of claim 5 , wherein the contrast agent is administered directly to a tissue being diagnostically imaged, to a body fluid that contacts a tissue being diagnostically imaged, or to a body location from which the contrast agent can diffuse or be transported to a tissue being diagnostically imaged. 9. The method of claim 5 , wherein the contrast agent is administered intravenously, intramuscularly, subcutaneously, intracerebrally, or intrathecally.
Compounds without a metal-carbon linkage · CPC title
involving electronic [EMR] or nuclear [NMR] magnetic resonance, e.g. magnetic resonance imaging · CPC title
the complex-forming compound being acyclic, e.g. DTPA · CPC title
Organic compounds · CPC title
having six-membered rings with one nitrogen as the only ring hetero atom · CPC title
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