The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jan. 07, 2025

Filed:

Jan. 31, 2023
Applicant:

Biolitec Untergehmensbeteiligungs Ii Ag, Vienna, AT;

Inventors:

Benjamin Florian Hohlfeld, Berlin, DE;

Arno Wiehe, Berlin, DE;

Burkhard Gitter, Jena, DE;

Dorika Steen, Jena, DE;

Gerhard Wieland, Jena, DE;

Volker Albrecht, Nuthetal, DE;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C07F 15/00 (2006.01); A61K 41/00 (2020.01); A61K 47/54 (2017.01); A61P 31/04 (2006.01); A61P 35/00 (2006.01); C07F 17/02 (2006.01);
U.S. Cl.
CPC ...
C07F 15/0033 (2013.01); A61K 41/0057 (2013.01); A61K 47/549 (2017.08); A61P 31/04 (2018.01); A61P 35/00 (2018.01); C07F 17/02 (2013.01);
Abstract

Biologically active compounds and their methods of preparation are provided that may be used as photosensitizers for diagnostic and therapeutic applications, particularly for PDT of cancer, infections and other hyperproliferative diseases, fluorescence diagnosis and PDT treatment of non-tumorous indications such as arthritis, inflammatory diseases, viral or bacterial infections, dermatological, otorhinolaryngology disorders, ophthalmological or urological disorders. As the compounds exhibit also toxicity against targets (tumor cells, bacteria inflammation-related cells) without light these biologically active compounds may also be used for the light-independent treatment of such indications. Embodiments also include methods to synthesize iridium(III) complex structures incorporating a substituted 2,3,5,6-tetrafluorophenyl-dipyrromethene (2,3,5,6-tetratfluorophenyldipyrrin) unit or a substituted 3-nitrophenyl-dipyrromethene (3-nitrophenyl-dipyrrin) unit. Amphiphilic compounds with increased anti-tumour and anti-bacterial efficacy are also provided. Specifically, this is achieved by substitution with bromine atoms and sugar moieties.


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