← Back to Patent Explorer
US4574079A Expired / Lapsed US ⏱️ 0.0 years remaining

Radiolabeled angiotensin converting enzyme inhibitors for radiolabeling mammalian organ sites

Assignee: Boston University
•
Filing: 1983-05-27
•
Granted: 1986-03-04
•
Expires: 2003-05-27
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract Radiolabeled angiotensin converting enzyme inhibitors having the general formula: ##STR1## wherein X is a radiolabeling substituent, preferably a radiolabeling halogen substituent such as 123 I, 125 I, 131 I, 75 Br or 77 Br, Y is hydroxy, alkoxy containing from 1 to 6 carbon atoms, phenoxy, benzyloxy, or amino, R 1 is hydrogen or methyl, R 2 is hydrogen, an ester moiety hydrolyzable under mammalian in vivo conditions, such as alkyl of 1 or 2 carbon atoms, phenyl or benzyl, or an ionically bonded anion of a physiologically acceptable non-toxic salt, and m is an integer of from 1 to 6, are useful as in vivo radioimaging compounds for mammalian sites.

Inventors

  • 👤 Haralambos P. Gavras
  • 👤 James W. Ryan
  • 👤 Alfred Chung

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-07 21:42
CPC Classifications
C; C07; C07K; C07K5/00; C07K5/02; C07K5/022; C07K5/0222; A; A61; A61K; A61K51/00; A61K51/02; A61K51/04; A61K51/041; A61K51/044; A61K51/0468; A61K51/047; A61K2123/00

Claims Analysis

Total Claims: 15
Claim 1
Independent Claim 73 words
A radiolabeled angiotensin converting enzyme (ACE) inhibitor having the general formula: ##STR17## wherein X is a radiolabeling substituent, Y is hydroxy, alkoxy containing from 1 to 6 carbon atoms, phenoxy, benzyloxy or amino, R 1 is hydrogen or methyl, R 2 is hydrogen, an ester moiety hydrolyzable under mammalian in vivo conditions or an ionically bonded anion of a physiologically acceptable non-toxic salt, and m is an integer of from 1 to 6.
Claim 2
Dependent Claim 73 words
A radiolabeled angiotensin converting enzyme (ACE) inhibitor having the general formula: ##STR17## wherein X is a radiolabeling substituent, Y is hydroxy, alkoxy containing from 1 to 6 carbon atoms, phenoxy, benzyloxy or amino, R 1 is hydrogen or methyl, R 2 is hydrogen, an ester moiety hydrolyzable under mammalian in vivo conditions or an ionically bonded anion of a physiologically acceptable non-toxic salt, and m is an integer of from 1 to 6.
Claim 3
Dependent Claim 16 words
A radiolabeled ACE inhibitor as described in claim 1 wherein X is a radiolabeling halogen substituent.
Claim 4
Dependent Claim 23 words
A radiolabeled ACE inhibitor as described in claim 2 wherein X is 123 I, 125 I, 131 I, 75 Br or 77 Br.
Claim 5
Dependent Claim 16 words
A radiolabeled ACE inhibitor as described in claim 2 wherein X is a radiolabeling iodine substituent.
Claim 6
Dependent Claim 56 words
A radiolabeled ACE inhibitor having the general formula: ##STR18## wherein X' is a radiolabeling iodine substituent, R 1 is hydrogen or methyl, R 2 is hydrogen, an ester moiety hydrolyzable under mammalian in vivo conditions or an ionically bonded anion of a physiologically acceptable non-toxic salt, and m is an integer of from 1 to 6.
Claim 7
Dependent Claim 56 words
A radiolabeled ACE inhibitor having the general formula: ##STR18## wherein X' is a radiolabeling iodine substituent, R 1 is hydrogen or methyl, R 2 is hydrogen, an ester moiety hydrolyzable under mammalian in vivo conditions or an ionically bonded anion of a physiologically acceptable non-toxic salt, and m is an integer of from 1 to 6.
Claim 8
Dependent Claim 3 words
N-[L-1-carboxy-2-(4-hydroxy-3- 123 iodophenyl)ethyl]-Ala-L-Pro.
Claim 9
Dependent Claim 3 words
N-[L-1-carboxy-2-(4-hydroxy-3- 123 iodophenyl)ethyl]-Ala-L-Pro.
Claim 10
Dependent Claim 3 words
N-[L-1-carboxy-2-(4-hydroxy-3- 125 iodophenyl)ethyl]-Ala-L-Pro.
Claim 11
Dependent Claim 3 words
N-[L-1-carboxy-2-(4-hydroxy-3- 125 iodophenyl)ethyl]-Ala-L-Pro.
Claim 12
Dependent Claim 3 words
N-[L-1-carboxy-2-(4-hydroxy-3- 131 iodophenyl)ethyl]-Ala-L-Pro.
Claim 13
Dependent Claim 3 words
N-[L-1-carboxy-2-(4-hydroxy-3- 131 iodophenyl)ethyl]-Ala-L-Pro.
Claim 14
Dependent Claim 58 words
A method of radioimaging a mammalian site which comprises administering into a blood vessel in the mammal a dose of from about 0.01 mg to about 15 mg, per kilogram of body weight, of a radiolabeled angiotensin converting enzyme (ACE) inhibitor as described in claim 1, and then scanning the mammal to produce an image of the site.
Claim 15
Dependent Claim 57 words
A method as described in claim 9 wherein said mammal is a human being, said radiolabeled ACE inhibitor is N-[L-1-carboxy-2-(4-hydroxy-3- 123 iodophenyl)ethyl]-Ala-L-Pro or N-[L-1-carboxy-2-(4-hydroxy-3- 131 iodophenyl)ethyl]-Ala-L-Pro, administered in a dose of from about 0.05 mg to about 5 mg per kilogram of body weight, and the total radioactivity from said dose is less than about 100 μCi.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-03-03 1989-09-02 1990-03-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1993-03-03 1993-09-02 1994-03-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1997-03-03 1997-09-02 1998-03-04 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag