US2006141054A1PendingUtilityA1
Metal coordinated compositions
Est. expiryOct 25, 2024(expired)· nominal 20-yr term from priority
Inventors:Thomas Piccariello
A61P 9/12A61P 3/10A61P 5/14A61P 7/06A61P 37/06A61P 7/02A61P 43/00A61P 7/10A61P 25/12A61P 27/02A61P 25/06A61P 25/16A61P 25/18A61P 29/00A61P 25/10A61P 35/00A61P 31/12A61P 31/04A61P 25/24A61P 25/22A61P 25/00A61P 25/04A61P 11/06A61P 17/06A61K 47/55A61K 47/52A61P 11/08C07F 3/02A61K 47/552C07F 3/003A61K 47/547C07H 21/02A61P 19/00A61P 13/04A61P 1/08A61P 1/04C07F 3/06
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Claims
Abstract
A metal coordination complex of a biologically active moiety and a metal is disclosed. The complex confers to the biologically active moiety an improved performance which can include potency, stability, absorbability, targeted delivery, and combinations thereof.
Claims
exact text as granted — not AI-modified1 . A metal coordination complex of a biologically active moiety and a metal, wherein
the biologically active moiety is selected from the group consisting of thyronine, tetracycline antibiotics, dimethylbiguanide, hydrochlorothiazide, acycloguanosine, hydrocodone, oxycodone, and their derivatives, and the metal is selected from the group consisting of aluminum, bismuth, calcium, iron, magnesium, silicon, and zinc.
2 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of thyronine and its derivatives.
3 . A complex according to claim 2 , wherein the complex is bis(triiodothyroninato)zinc.
4 . A complex according to claim 2 , wherein the complex is bis(triiodothyroninato)magnesium.
5 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of tetracycline antibiotics and their derivatives.
6 . A complex according to claim 4 , wherein the complex is bis(tetracyclinato)magnesium.
7 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of oxycodone and its derivatives.
8 . A complex according to claim 7 , wherein the complex is (oxycodone)magnesium.
9 . A complex according to claim 7 , wherein the complex is (oxycodone)zinc.
10 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of hydrocodone and its derivatives.
11 . A complex according to claim 10 , wherein the complex is his (hydrocodonato)magnesium.
12 . A complex according to claim 10 , wherein the complex is his (hydrocodonato)zinc.
13 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of penicillin and its derivatives.
14 . A complex according to claim 13 wherein the complex is his bis(penicillinato)zinc.
15 . A complex according to claim 13 wherein the complex is his bis(penicillinato)magnesium.
16 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of dimethylbiguanide and its derivatives.
17 . A complex according to claim 16 wherein the complex is bis(dimethylbiguanido)zinc.
18 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of hydrochlorothiazide and its derivatives.
19 . A complex according to claim 18 wherein the complex is bis(hydrochlorothiazido)zinc.
20 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of acycloguanosine and its derivatives.
21 . A complex according to claim 19 wherein the complex is bis(acycloguanosinato)magnesium.
22 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of furosemide and its derivatives.
23 . A complex according to claim 22 wherein the complex is bis(furosemidato)zinc.
24 . A complex according to claim 22 wherein the complex is bis(furosemidato)magnesium.
25 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of DOPA and its derivatives.
26 . A complex according to claim 25 wherein the complex is bis(DOPA)zinc.
27 . A complex according to claim 25 wherein the complex is bis(DOPA)magnesium.
28 . A complex according to claim 1 wherein the biologically active moiety is selected from the group consisting of alendronate and its derivatives.
29 . A complex according to claim 28 wherein the complex is bis(alendronato)zinc.
30 . A complex according to claim 28 wherein the complex is bis(alendronato)magnesium.
31 . A metal coordination complex of a biologically active moiety and a metal, wherein the biologically active moiety contains a β-diketone, ketophenol or β-ketoalcohol, functional group and
the metal is selected from the group consisting of aluminum, bismuth, calcium, iron, magnesium, silicon, and zinc.
32 . A metal coordination complex of a biologically active moiety and a metal, wherein
the biologically active moiety contains an alcohol and an azole functional group, and the metal is selected from the group consisting of aluminum, bismuth, calcium, iron, magnesium, silicon, and zinc.
33 . A metal coordination complex of a biologically active moiety and a metal, wherein
the biologically active moiety contains a guanide or a diamine functional group, and the metal is selected from the group consisting of aluminum, bismuth, calcium, iron, magnesium, silicon, and zinc.
34 . A method of modulating the properties of a biologically active moiety comprising
forming a metal coordination complex with the biologically active moiety and a metal is selected from the group consisting of aluminum, bismuth, calcium, iron, magnesium, silicon, and zinc, wherein the biologically active moiety is selected from the group consisting of thyronine, tetracycline antibiotics, hydrocodone, oxycodone, and their derivatives, and the metal is selected from the group consisting of aluminum, bismuth, calcium, iron, magnesium, silicon, and zinc.
35 . A method of claim 34 further comprising
adding an adjuvant selected from the group consisting of peptides, carbohydrates or lipids that confer desired performance parameters to the biologically active agent.
36 . The method of claim 34 , wherein the properties to be modulated are selected from the group consisting of potency, stability, absorbability, targeted delivery, and combinations thereof.Cited by (0)
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