IP Library Granted Patent US 8,344,133
Granted Patent B2
US 8,344,133 · App. 12/819,801 · Granted Jan 1, 2013

Neoglycorandomization and digitoxin analogs

Assignee: Wisconsin Alumni Research Foundation
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Quick Facts
Patent No.
US 8,344,133
App. No.
12/819,801
Granted
Jan 1, 2013
Kind
B2
Abstract

The present invention provides methods of producing compounds with enhanced desirable properties and diminished side effects as well as the compounds produced by the methods. In preferred embodiments, methods of the present invention use a universal chemical glycosylation method that employs reducing sugars and requires no protection or activation. In a preferred embodiment, the invention provides neoglycoside digitoxin analogs that include compounds with significantly enhanced cytotoxic potency toward human cancer cells and tumor-specificity, but are less potent Na + /K + -ATPase inhibitors in a human cell line than digitoxin.

Claims (14)

1. A neoglycoside produced by the reaction of (a) an aglycon having a secondary alkoxylamine selected from the group consisting of a cardiac glycoside aglycon, an indolocarbazole, an anthracyline, a macrolide; and (b) a reducing sugar selected from the group consisting of an L-sugar, a D-sugar, a deoxy-sugar, a dideoxy-sugar, a glucose epimer, a substituted sugar, a uronic acid, and an oligosaccharide; wherein the reducing sugar is linked to the aglycon according to the structure:

and wherein the moiety represented by

is the reducing sugar.

2. The neoglycoside of claim 1 wherein the reducing sugar is selected from the group consisting of L-ribose, D-ribose, L-fucose, D-fucose, 2-deoxy-D-galactose, 3-deoxy-D-glucose, 6-deoxy-D-glucose, 2-deoxy-2-fluoro-D-glucose, 6-deoxy-6-fluoro-D-glucose, L-lyxose, D-lyxose, L-rhamnose, L-allose, D-allose, L-altrose, D-altrose, L-galactose, D-galactose, L-xylose, D-xylose, D-gulose, L-mannose, D-mannose, L-idose, D-idose, L-mycarose, 6-keto-D-galactose, L-arabinose, D-arabinose, N-acetyl-D-galactosaminose, melibiose, lactose, maltose, D-galacturonose, L-talose, D-talose, 6-deoxy-6-azo-D-mannose, L-glucose, and D-glucose.

3. The neoglycoside of claim 1 wherein the aglycon is

4. A composition comprising the neoglycoside of claim 1 , or a salt thereof, combined with a pharmaceutically acceptable carrier.

5. A neoglycoside of the formula:

where R 1 , R 2 , R 3 , and R 4 are independently selected from —H, —OH, —N 3 , —NH 2 , —CH 3 , —CH 2 OH, —CN 3 , —CH 2 NH, —CH 2 SH, —CNH 2 , —CH 2 N 3 , —COOH, —COCH 3 , —CXH 2 , —CX 2 H, and where X is Cl, Br, F, or I and the aglycon is a cardiac glycoside aglycon, an indolocarbazole, an anthracyline, or a macrolide.

6. The neoglycoside of claim 5 wherein the aglycon is

7. A composition comprising the neoglycoside of claim 5 , or a salt thereof, combined with a pharmaceutically acceptable carrier.

8. A neoglycoside having the chemical formula:

wherein R is selected from the group consisting of L-ribose (5β), D-ribose (6β), L-fucose (7β), D-fucose (8β), 2-deoxy-D-galactose (9β), 3-deoxy-D-glucose (10β), 6-deoxy-D-glucose (11β), 2-deoxy-2-fluoro-D-glucose (12β), 6-deoxy-6-fluoro-D-glucose (13β), L-lyxose (14β), D-lyxose (15β), L-rhamnose (16β), L-allose (17β), D-allose (18β), L-altrose (19β), D-altrose (20β), L-galactose (21β), D-galactose (22β), L-xylose (23β), D-xylose (24β), D-gulose (25β), L-mannose (26β), D-mannose (27β), L-idose (28β), D-idose (29β), L-mycarose (30β), 6-keto-D-galactose (31β), L-arabinose (32β), D-arabinose (33β), N-acetyl-D-galactosaminose (34β), melibiose (35β), lactose (36β), maltose (37β), D-galacturonose (38β), L-talose (39β), D-talose (40β), 6-deoxy-6-azido-D-mannose (41β), L-glucose (42β), D-glucose (4β), 0-D-glucose (43β), and H (3β); or

wherein R is selected from the group consisting of H(3a), L-ribose (5α), D-ribose (6α), L-fucose (7α), D-fucose (8α), 2-deoxy-D-galactose (9α), 3-deoxy-D-glucose (10α), 6-deoxy-D -glucose (11α), 2-deoxy-2-fluoro-D-glucose (12α), 6-deoxy-6-fluoro-D-glucose (13α), L-lyxose (14α), D-lyxose (15α), L-rhamnose (16α), L-allose (17α), D-allose (18α), L-altrose (19α), D-altrose (20α), L-galactose (21α), D-galactose (22α), L-xylose (23α), D-xylose (24α), D-gulose (25α), L-mannose (26α), D-mannose (27α), L-idose (28α), D-idose (29α), L-mycarose (30α), 6-keto-D-galactose (31α), L-arabinose (32α), D-arabinose (33α), N-acetyl-D-galactosaminose (34α), melibiose (35α), lactose (36α), maltose (37α), D-galacturonose (38α), L-talose (39α), D-talose (40α), 6-deoxy-6-azido-D-mannose (41α), L-glucose (42α) and D-glucose (4α).

9. A composition comprising the neoglycos of claim 8 , or a salt thereof, combined with a pharmaceutically acceptable carrier.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 6, 2013
From: THORSON, JON S.; LANGENHAN, JOSEPH M.
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 029763/0440 →
CONFIRMATORY LICENSE Recorded Jun 24, 2010
From: UNIVERSITY OF WISCONSIN MADISON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024585/0435 →
Continuity (3)
Division 11166881 · Jun 24, 2005
Provisional Application 60521721 · Jun 24, 2004
Related Publication 20100256078A1 · Oct 7, 2010