Patent US4845090A successfully refreshed from Google Patents.
US4845090A
Expired / Lapsed
US
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Nitroxyl compound and diagnostic media based thereon useful for enhancing NMR imaging
Assignee: Bayer Pharma AG
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Filing: 1985-09-24
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Granted: 1989-07-04
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Expires: 2005-09-24
Abstract
Abstract Diagnostic media suitable for NMR diagnoses contain compounds of Formula I ##STR1## wherein is a single bond or a double bond, X is the grouping --(CH 2 ) n -- or, if is a single bond, also the grouping --NHCO(CH 2 ) n -- wherein n means 0 to 4, m means the numbers 0, 1, or 2, R 1 is an alkyl residue substituted by hydroxy groups, acyloxy groups and/or alkylidenedioxy groups, R 2 has the same meanings as R 1 or is a hydrogen atom or an alkyl residue, R 3 and R 4 are alkyl residues, and R 5 and R 6 are alkyl residues optionally substituted by hydroxy groups.
Inventors
- 👤 Heinz Gries
- 👤 Ulrich Niedballa
- 👤 Hanns-Joachim Weinmann
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-10 02:22
CPC Classifications
C; C07; C07D; C07D405/00; C07D405/02; C07D405/12; A; A61; A61K; A61K49/00; A61K49/06; A61K49/20; C07D207/00; C07D207/02; C07D207/04; C07D207/10; C07D207/16; C07D207/18; C07D207/22; C07D207/46; C07D211/00; C07D211/92; C07D211/94; G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/53; G01N33/531; G01N33/532; G01N33/58; G01N33/60; Y; Y10; Y10T; Y10T436/00; Y10T436/24
Claims Analysis
Total Claims: 36
Claim 1
Independent Claim
134 words
A pharmaceutical diagnostic medium comprising an effective amount for NMR diagnosis of a compound of the formula ##STR10## wherein B is a pharmacologically acceptable protein, sugar, or lipid residue, or ##STR11## is a single or double bond, X is --(CH 2 ) n -- or, when is a single bond, also --NHCO(CH 2 ) n -- wherein n is an integer 0 to 4, m is 0, 1, or 2, R 1 is C 2-8 -alkyl substituted by hydroxy, C 2-6 -alkanoyloxy or C 1-6 -alkylidenedioxy, R 2 independently is one of the R 1 groups, hydrogen or C 1-4 -alkyl, R 3 and R 4 independently are C 1-4 -alkyl, and R 5 and R 6 independently are C 1-4 -alkyl or C 1-4 -alkyl substituted by hydroxy, and a pharmacologically acceptable carrier.
Claim 2
Dependent Claim
134 words
A pharmaceutical diagnostic medium comprising an effective amount for NMR diagnosis of a compound of the formula ##STR10## wherein B is a pharmacologically acceptable protein, sugar, or lipid residue, or ##STR11## is a single or double bond, X is --(CH 2 ) n -- or, when is a single bond, also --NHCO(CH 2 ) n -- wherein n is an integer 0 to 4, m is 0, 1, or 2, R 1 is C 2-8 -alkyl substituted by hydroxy, C 2-6 -alkanoyloxy or C 1-6 -alkylidenedioxy, R 2 independently is one of the R 1 groups, hydrogen or C 1-4 -alkyl, R 3 and R 4 independently are C 1-4 -alkyl, and R 5 and R 6 independently are C 1-4 -alkyl or C 1-4 -alkyl substituted by hydroxy, and a pharmacologically acceptable carrier.
Claim 3
Dependent Claim
12 words
A diagnostic medium of claim 1, wherein B is a protein residue.
Claim 4
Dependent Claim
12 words
A diagnostic medium of claim 1, wherein m is 0 or 1.
Claim 5
Dependent Claim
20 words
A diagnostic medium of claim 1, wherein when X is --(CH 2 ) n --, n is 0 or 1.
Claim 6
Dependent Claim
21 words
A diagnostic medium of claim 1, wherein when X is --NHCO(CH 2 ) n --, n is 2, 3, or 4.
Claim 7
Dependent Claim
20 words
A diagnostic medium of claim 1, wherein said compound is the conjugate of beef serum albumin and 2,2,5,5-tetramethyl pyrrolidine-1-oxyl-3-carboxylic acid.
Claim 8
Dependent Claim
196 words
A compound of the formula ##STR12## wherein B is a pharmacologically acceptable protein, sugar, or lipid residue, or ##STR13## is a single or double bond, X is --(CH 2 )n-- or, when is a single bond, also --NHCO(CH 2 ) n -- wherein n is an integer 0 to 4, m is 0, 1, or 2, R 1 is C 2-8 -alkyl substituted by polyhydroxy, C 2-6 -alkanoyloxy or C 2-6 -alkylidenedioxy, R 2 independently is one of the R 1 groups, hydrogen or C 1-4 -alkyl, R 3 and R 4 independently are C 1-4 -alkyl, and R 5 and R 6 independently are C 1-4 -alkyl or C 1-4 -alkyl substituted by hydroxy, with the provisos that when R 3 -R 6 are each methyl or ethyl, is a double bond, m is 0, X is --(CH 2 ) n --, n is 0 or 1, B is --NR 1 R 2 and R 2 is H or methyl, then R 1 is not, 2,3-dihydroxypropyl or 1,1-dimethyl-2-hydroxyethyl; and when R 5 and R 6 are each alkyl, is a double bond and m and n are 0, then B is not a sugar residue.
Claim 9
Dependent Claim
196 words
A compound of the formula ##STR12## wherein B is a pharmacologically acceptable protein, sugar, or lipid residue, or ##STR13## is a single or double bond, X is --(CH 2 )n-- or, when is a single bond, also --NHCO(CH 2 ) n -- wherein n is an integer 0 to 4, m is 0, 1, or 2, R 1 is C 2-8 -alkyl substituted by polyhydroxy, C 2-6 -alkanoyloxy or C 2-6 -alkylidenedioxy, R 2 independently is one of the R 1 groups, hydrogen or C 1-4 -alkyl, R 3 and R 4 independently are C 1-4 -alkyl, and R 5 and R 6 independently are C 1-4 -alkyl or C 1-4 -alkyl substituted by hydroxy, with the provisos that when R 3 -R 6 are each methyl or ethyl, is a double bond, m is 0, X is --(CH 2 ) n --, n is 0 or 1, B is --NR 1 R 2 and R 2 is H or methyl, then R 1 is not, 2,3-dihydroxypropyl or 1,1-dimethyl-2-hydroxyethyl; and when R 5 and R 6 are each alkyl, is a double bond and m and n are 0, then B is not a sugar residue.
Claim 10
Dependent Claim
15 words
The conjugate of beef serum albumin and 2,2,5,5-tetramethyl pyrrolidine-1-oxyl-3-carboxylic acid, a compound of claim 7.
Claim 11
Dependent Claim
11 words
A compound of claim 7, wherein B is a protein residue.
Claim 12
Dependent Claim
11 words
A compound of claim 7, wherein m is 0 or 1.
Claim 13
Dependent Claim
19 words
A compound of claim 7, wherein when X is --(CH 2 ) n --, n is 0 or 1.
Claim 14
Dependent Claim
20 words
A compound of claim 7, wherein when X is --NHCO(CH 2 ) n --, n is 2, 3 or 4.
Claim 15
Dependent Claim
21 words
A diagnostic medium comprising an effective amount for NMR diagnosis of a compound of claim 7 and a pharmacologically acceptable carrier.
Claim 16
Dependent Claim
15 words
A diagnostic medium of claim 13, wherein the compound is a clathrate in a liposome.
Claim 17
Dependent Claim
12 words
A compound of claim 7, wherein B is albumin or an antibody.
Claim 18
Dependent Claim
14 words
A compound of claim 7, wherein B is an immunoglobulin or a monoclonal antibody.
Claim 19
Dependent Claim
10 words
A diagnostic medium of claim 1, wherein m is 2.
Claim 20
Dependent Claim
24 words
A diagnostic medium of claim 1, wherein B is NR 1 R 2 and R 1 is C 2-6 -alkanoyloxy or C 1-6 -alkylidenedioxy.
Claim 21
Dependent Claim
19 words
A diagnostic medium of claim 1, wherein R 5 or R 6 is C 1-4 -alkyl substituted by hydroxy.
Claim 22
Dependent Claim
26 words
A diagnostic medium of claim 1, wherein B is NR 1 R 2 and R 5 or R 6 is C 1-4 -alkyl substituted by hydroxy.
Claim 23
Dependent Claim
18 words
A diagnostic medium of claim 20, wherein X is --(CH 2 ) n -- and n is 0.
Claim 24
Dependent Claim
12 words
A diagnostic medium of claim 1, wherein B is a sugar residue.
Claim 25
Dependent Claim
12 words
A diagnostic medium of claim 1, wherein B is a lipid residue.
Claim 26
Dependent Claim
14 words
A diagnostic medium of claim 1, wherein B is --NR 1 R 2 .
Claim 27
Dependent Claim
13 words
A diagnostic medium of claim 1, wherein said compound is 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid (2-hydroxyethyl)amide.
Claim 28
Dependent Claim
13 words
A diagnostic medium of claim 1, wherein said compound is 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid (2,3-dihydroxypropyl)amide.
Claim 29
Dependent Claim
39 words
2,2,5,5-Tetramethylpyrrolidine-1-oxyl-3-carboxylic acid [2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethyl]-amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid (1,3-dihydroxyprop-2-yl)amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid (2,2-dimethyl-1,3-dioxolan-4-ylmethyl)amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid [N-(2,2-dimethyl-1,3-dioxolan-4-ylmethyl)-N-methyl]amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid N-(2,3-dihydroxypropyl)-N-methylamide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid (2,3,4-trihydroxybutyl)amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid [N-(2,3,4,5,6-pentahydroxyhexyl)-N-methyl]-amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid (2,3-dihydroxypropyl)amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid bis(2-hydroxyethyl)amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid [N-(2,2-dimethyl-1,3-dioxolan-4-ylmethyl)-N-methyl]amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid N-(2,3-dihydroxypropyl)-N-methylamide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid [2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethyl]amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid (2,3,4-trihydroxybutyl)amide,
Claim 30
Dependent Claim
39 words
2,2,5,5-Tetramethylpyrrolidine-1-oxyl-3-carboxylic acid [2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethyl]-amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid (1,3-dihydroxyprop-2-yl)amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid (2,2-dimethyl-1,3-dioxolan-4-ylmethyl)amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid [N-(2,2-dimethyl-1,3-dioxolan-4-ylmethyl)-N-methyl]amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid N-(2,3-dihydroxypropyl)-N-methylamide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid (2,3,4-trihydroxybutyl)amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid [N-(2,3,4,5,6-pentahydroxyhexyl)-N-methyl]-amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid (2,3-dihydroxypropyl)amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid bis(2-hydroxyethyl)amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid [N-(2,2-dimethyl-1,3-dioxolan-4-ylmethyl)-N-methyl]amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid N-(2,3-dihydroxypropyl)-N-methylamide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid [2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethyl]amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid (2,3,4-trihydroxybutyl)amide,
Claim 31
Dependent Claim
43 words
2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid (5-hydroxy-2,2-dimethyl-1,3-dioxepan-6-yl)amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid (1,3,4-trihydroxybut-2-yl)amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid (5-hydroxy-2,2-dimethyl-1,3-dioxepan-6-yl)amide, 2,2,5,5-tetramethylpyrrolidine-1-oxyl-3-carboxylic acid (1,3,4-trihydroxybut-2-yl)amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid [N-(2,3,4,5,6-pentahydroxyhexyl)-N-methyl]-amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid (1,3-dihydroxyprop-2-yl)amide, 2,2,5,5-tetramethyl-3-pyrroline-1-oxyl-3-carboxylic acid (5-hydroxy-2,2-dimethyl-1,3-dioxepan-6-yl)amide, succinic acid N-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethyl]-N'-(2,2,6,6-tetramethyl-1-oxylpiperidin-4-yl) diamide, succinic acid [N-(2,2,6,6-tetramethyl-1-oxylpiperidin-4-yl)-N'-(2,3,4-trihydroxybutyl)] diamide, (1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)-acetic acid [N-(2,3,4,5,6-pentahydroxyhexyl)-N-methyl]amide, or succinic acid [N-(1-oxyl-2,2,5,5-tetramethylpyrrolidin-3-yl)-N'-(2,3,4,5,6-pentahydroxyhexyl)] diamide, each a compound of claim 7.
Claim 32
Dependent Claim
11 words
A compound of claim 7, wherein B is a sugar residue.
Claim 33
Dependent Claim
11 words
A compound of claim 7, wherein B is a lipid residue.
Claim 34
Dependent Claim
13 words
A compound of claim 7, wherein B is --NR 1 R 2 .
Claim 35
Dependent Claim
14 words
A diagnostic medium of claim 24, wherein R 1 is alkyl substituted by hydroxy.
Claim 36
Dependent Claim
13 words
A compound of claim 30, wherein R 1 is alkyl substituted by hydroxy.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1992-07-03 | 1993-01-02 | 1993-07-04 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1996-07-03 | 1997-01-02 | 1997-07-04 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2000-07-03 | 2001-01-02 | 2001-07-04 | $7700.00 | Window Closed / Lapsed |