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US5219878A Expired / Lapsed US ⏱️ 0.0 years remaining

Tetrapyrrole hydroxyalkylamide photochemotherapeutic agents

Assignee: Queen's University
•
Filing: 1991-12-16
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Granted: 1993-06-15
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Expires: 2011-12-16
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Abstract

Abstract This invention relates to new preparations which are valuable for photodetection and photochemotherapy of tumors and malignant tissues. The active compounds of these therapeutic preparations are mono-, di- or polyamides of an amino alcohol and a cyclic tetrapyrrole containing at least one carboxyl group. The general structure of these active compounds is (ZNHCO)nX wherein Z is the amino alcohol molecule less the amino group, X is the tetrapyrrole molecule less a carboxyl group, and "n" is an integer from 1 to 8.

Inventors

  • 👤 Michel M. Ringuet
  • 👤 James C. Kennedy
  • 👤 Roy H. Pottier

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-28 15:03
CPC Classifications
C; C07; C07D; C07D487/00; C07D487/22; A; A61; A61K; A61K41/00; A61K41/0057; A61K41/0071

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 115 words
A therapeutic composition for the detection and treatment of tumors and malignant tissue sensitive thereto, comprising a therapeutically effective quantity of mono-, di- or polyamides of an amino alcohol and a cyclic tetrapyrrole, the general structure of which is: (ZNHCO).sub.n X wherein: Z is the amino alcohol molecule less the amino group and is selected from mono-, di-, and polyhydroxyalkyl residues with the provisio that Z does not include a carboxyl group; X is selected from substituted tetrapyrroles in which the substituent is at least one of the group consisting of methyl, ethyl, vinyl, hydroxyethyl, alkoxyethyl, methylcarboxy, ethylcarboxy, Z-substituted propylamide, phenyl and (ZNHCO) n -substituted phenylamide, and n is an integer from 1 to 8.
Claim 2
Dependent Claim 115 words
A therapeutic composition for the detection and treatment of tumors and malignant tissue sensitive thereto, comprising a therapeutically effective quantity of mono-, di- or polyamides of an amino alcohol and a cyclic tetrapyrrole, the general structure of which is: (ZNHCO).sub.n X wherein: Z is the amino alcohol molecule less the amino group and is selected from mono-, di-, and polyhydroxyalkyl residues with the provisio that Z does not include a carboxyl group; X is selected from substituted tetrapyrroles in which the substituent is at least one of the group consisting of methyl, ethyl, vinyl, hydroxyethyl, alkoxyethyl, methylcarboxy, ethylcarboxy, Z-substituted propylamide, phenyl and (ZNHCO) n -substituted phenylamide, and n is an integer from 1 to 8.
Claim 3
Dependent Claim 268 words
A therapeutic composition as claimed in claim 1 wherein the tetrapyrrole compound is of the formula: ##STR3## or the corresponding di- or tetrahydropyrroles and wherein R 2 is H, CO 2 H or CH 2 CH 2 CO 2 H R 3 is H, CH 3 or CH 2 CO 2 H R 5 is H, C 6 H 5 , C 6 H 4 CH 3 or C 6 H 4 CO 2 H R 7 is H, CH 2 CH 3 , CH═CH 2 , CH 2 CH 2 CO 2 H, CH(OH)CH 3 or CH(OR)CH 3 R 8 is H, CH 3 , CH 2 CO 2 H R 10 is H, C 6 H 5 , C 6 H 4 CH 3 or C 6 H 4 CO 2 H R 12 is H, CH 2 CH 3 , CH═CH 2 , CH 2 CH 2 CO 2 H, CH(OH)CH 3 or CH(OR)CH 3 R 13 is H, CH 3 or CH 2 CO 2 H R 15 is H, CH 6 H 5 , C 6 H 4 CH 3 or C 6 H 4 CO 2 H R 17 is H, CH 3 , CH 2 CO 2 H or CH 2 CH 2 CO 2 H R 18 is H, CH 3 , CH 2 CO 2 H or CH 2 CH 2 CO 2 H R 2 0 is H, CH 2 CO 2 H, C 6 H 5 , C 6 H 4 CH 3 or C 6 H 4 CO 2 H and a pharmaceutically acceptable carrier therefor.
Claim 4
Dependent Claim 19 words
A composition as claimed in claim 2 wherein said amino alcohol is selected from 2-aminoethanol, 2-amino-1,3-propanediol, 2-amino-2-(hydroxymethyl)-1,3-propanediol and D-glucosamine.
Claim 5
Dependent Claim 48 words
A composition as claimed in claim 2 wherein said tetrapyrrole is selected from coproporphyrin I and III, deuteroporphyrin IX, hematoporphyrin IX, hematoporphyrin IX di(alkylether), mesoporphyrin IX, protoporphyrin IX, uroporphyrin IX, chlorin e 6 , pentacarboxyporphyrin I and III, hexacarboxyporphyrin I and III, heptacarboxyporphyrin I, meso-tetracarboxyphenylporphin, meso-tricarboxyphenyl-phenylporphin, meso-dicarboxyphenyl-diphenylporphin, meso-carboxyphenyl-triphenylporphin.
Claim 6
Dependent Claim 64 words
A composition as claimed in claim 3 wherein said tetrapyrrole is selected from coproporphyrin I, coproporphyrin III, deuteroporphyrin IX, hematoporphyrin IX, hematoporphyrin IX di(alkylether), hematoporphyrin IX di(methylether), hematoporphyrin IX di(ethylether), hematoporphyrin IX di(propylether), hematoporphyrin IX di(butylether), hematoporphyrin IX di(isobutylether), mesoporphyrin IX, protoporphyrin IX, uroporphyrin IX, chlorin e 6 , pentacarboxyporphyrin I, pentacarboxyporphyrin III, hexacarboxyporphyrin I, hexacarboxyporphyrin III, heptacarboxyporphyrin I, meso-tetracarboxyphenylporphin, meso-tricarboxyphenyl-phenylporphin, meso-dicarboxyphenyl-diphenylporphin, and meso-carboxyphenyltriphenylporphin.
Claim 7
Dependent Claim 112 words
A composition as claimed in claim 2 wherein said amide is selected from mesoporphyrin IX di(ethanolamide), mesoporphyrin IX di(bis(hydroxymethyl)methanamide), mesoporphyrin IX di(tris(hydroxymethyl)methanamide), deuteroporphyrin IX di(ethanolamide), deuteroporphyrin IX di(bis(hydroxymethyl)methanamide), deuteroporphyrin IX di(tris(hydroxymethyl)methanamide), hematoporphyrin IX di(ethanolamide), hematoporphyrin IX di(bis(hydroxymethyl)methanamide), hematoporphyrin IX di(tris(hydroxymethyl)methanamide), hematoporphyrin di(alkylether) di(ethanolamide), hematoporphyrin IX di(alkylether) di(bis(hydroxymethyl)methanamide), hematoporphyrin IX di(alkylether) di(tris(hydroxymethyl)methanamide), hematoporphyrin IX di(methylether) di(ethanolamide), hematoporphyrin IX di(methylether) di(bis(hydroxymethyl)methanamide), hematoporphyrin IX di(methylether) di(tris(hydroxymethyl)methanamide), hematoporphyrin IX di(ethylether) di(ethanolamide), hematoporphyrin IX di(ethylether) di(bis(hydroxymethyl)methanamide), hematoporphyrin IX di(ethylether) di(tris(hydroxymethyl)methanamide, hematoporphyrin IX (dipropylether) di(ethanolamide), hematoporphyrin IX (dipropylether) di(bis(hydroxymethyl)methanamide, hematoporphyrin IX (dipropylether) di(tris(hydroxymethyl)methanamide), hematoporphyrin IX (dibutylether) di(ethanolamide), hematoporphyrin IX (dibutylether) di(bis(hydroxymethyl)methanamide), hematoporphyrin IX (dibutylether) di(tris(hydroxymethyl)methanamide, hematoporphyrin IX (diisobutylether) di(ethanolamide), hematoporphyrin IX (diisobutylether) di(bis(hydroxymethyl)methanamide and hematoporphyrin IX (diisobutylether) di(tris(hydroxymethyl)methanamide.
Claim 8
Dependent Claim 54 words
A method for detecting malignant tissue abnormalities in a patient comprising administering to said patient an effective amount of a tetrapyrrole derivative of an amino alcohol as claimed in claim 1, exposing said tissue abnormality to at least one of Ultra violet and visible light and detecting the presence of said abnormality by fluorescence.
Claim 9
Dependent Claim 21 words
A method as claimed in claim 7 wherein said tetrapyrrole derivative is selected from a composition as claimed in claim 2.
Claim 10
Dependent Claim 46 words
A method for treating malignant tissue abnormalities in a patient comprising administering to said patient an effective amount of a tetrapyrrole derivative of an amino alcohol as claimed in claim 1, and exposing said tissue abnormalty to light within the photoactivating spectrum of said tetrapyrrole derivative.
Claim 11
Dependent Claim 21 words
A method as claimed in claim 9 wherein said tetrapyrrole derivative is selected from a composition as claimed in claim 2.

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1996-06-14 1996-12-14 1997-06-15 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2000-06-14 2000-12-14 2001-06-15 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2004-06-14 2004-12-14 2005-06-15 $7700.00 Window Closed / Lapsed

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