IP Library Granted Patent US 10,376,531
Granted Patent B2
US 10,376,531 · App. 16/023,232 · Granted Aug 13, 2019

Substituted-6,8-dioxabicyclo[3.2.1]octane-2,3-diol compounds as targeting agents of ASGPR

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Quick Facts
Patent No.
US 10,376,531
App. No.
16/023,232
Granted
Aug 13, 2019
Kind
B2
Abstract

Compounds of Formula (A) are described herein and the uses thereof for the treatment of diseases, conditions and/or disorders mediated by pharmaceutical compositions and the uses thereof as asialoglycoprotein receptor (ASGPR) targeting agents.

Claims (29)

1. A compound of Formula (A)

wherein

R 1 is —Z—X—Y wherein X is a linker of any of structures L1or L2

each Q is independently absent or is C(O), C(O)—NR 4 , NR 4 —C(O),O—C(O)—NR 4 , NR 4 —C(O)—O, —CH 2 —, or —O—, wherein at least two carbon atoms separate the —O— from any other heteroatom group;

each T is independently absent or is alkylene, wherein one or more —CH 2 — groups of the alkylene, may each independently be replaced with a —O—, wherein the —O— are separated by at least 2 carbon atoms;

Y is an amino acid sequence, a nucleic acid sequence, or an oligomer, and

Z is absent;

each n is independently 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, or 40, wherein if n is greater than 1, each T and each Q of each (T-Q-T-Q) is independently selected;

R 2 is —N(R 3 )—C(O)—R 3 or —N(R 3 )—C(O)—OR 3 ; and

each R 3 is independently H, —(C 1 -C 5 )alkyl, halo-substituted (C 1 -C 5 )alkyl, or (C 3 -C 6 )cycloalkyl,

each R 4 is independently —H, —(C 1 -C 20 )alkyl, or (C 3 -C 6 )cycloalkyl wherein one to six —CH 2 — groups of the alkyl or cycloalkyl separated by at least two carbon atoms may be replaced with —O—, —S—, or —N(H)—, and wherein the alkyl and cycloalkyl may be substituted with one to six halo atoms; and

or a pharmaceutically acceptable salt thereof.

2. A compound of Formula (A)

wherein

R 1 is —Z—X—Y, —Z—Y, or —X—Y wherein X is a linker of any of structures L1, L2, L9 or L10

each Q is independently absent or is C(O), C(O)—NR 4 , NR 4 —C(O),O—C(O)—NR 4 , NR 4 —C(O)—O, —CH 2 —, or —O—, wherein at least two carbon atoms separate the —O— from any other heteroatom group;

each T is independently absent or is alkylene, wherein one or more —CH 2 — groups of the alkylene, may each independently be replaced with a —O—, wherein the —O— are separated by at least 2 carbon atoms;

Y is an amino acid sequence, a nucleic acid sequence, or an oligomer, and

Z is absent;

each n is independently 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,11,12,13,14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, or 40, wherein if n is greater than 1, each T and each Q of each (T-Q-T-Q) is independently selected;

R 2 is —N(R 3 )—C(O)—R 3 or —N(R 3 )—C(O)—OR 3 , and

each R 3 is independently —H, —(C 1 -C 5 )alkyl, halo-substituted (C 1 -C 5 )alkyl, or (C 3 -C 6 )cycloalkyl,

each R 4 is independently-H, —(C 1 -C 20 )alkyl, or (C 3 -C 6 )cycloalkyl wherein one to six —CH 2 — groups of the alkyl or cycloalkyl separated by at least two carbon atoms may be replaced with —O—, —S—, or —N(H)—, and wherein the alkyl and cycloalkyl may be substituted with one to six halo atoms; and

or a pharmaceutically acceptable salt thereof.

3. The compound of claim 1 or 2 or a pharmaceutically acceptable salt thereof, wherein R 1 is —X—Y and R 2 is —NH—C(O)—CH 3 .

4. The compound of claim 1 or 2 or a pharmaceutically acceptable salt thereof, wherein the compound of Formula (A) is capable of binding to a receptor present on a hepatocyte.

5. The compound of claim 4 or a pharmaceutically acceptable salt thereof, wherein the receptor present on a hepatocyte is an asialoglycoprotein receptor.

6. A pharmaceutical composition comprising (i) a compound of claim 5 ; or a pharmaceutically acceptable salt thereof; and (ii) a pharmaceutically acceptable excipient, diluent, or carrier.

7. The composition of claim 6 wherein said compound or said therapeutically acceptable salt thereof is present in a therapeutically effective amount.

Assignments (1)
ASSIGNEE ADDRESS CORRECTION Recorded Mar 20, 2023
From: PFIZER INC.
To: PFIZER INC.
Reel/Frame 063119/0087 →
Cited By (2)
US 12,622,972 US 12,667,620