IP Library Granted Patent US 10,869,929
Granted Patent B2
US 10,869,929 · App. 16/072,347 · Granted Dec 22, 2020

Phosphonate linkers and their use to facilitate cellular retention of compounds

Inventors: Robert M. Garbaccio (Lansdale, PA); Jeffrey C. Kern (Gilbertsville, PA); James J. Mulhearn (Elkins Park, PA); Philip E. Brandish (Needham, MA)
Assignee: MERCK SHARP & DOHME CORP.
A61K47/548A61K47/6803A61K47/6849A61K47/6889C07F9/3839C07F9/40A61P29/00A61P35/00
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Quick Facts
Patent No.
US 10,869,929
App. No.
16/072,347
Granted
Dec 22, 2020
Kind
B2
Abstract

Phosphonate linkers and their use for delivering compounds with passive cell permeability into a cell wherein the phosphonate group facilitates cellular retention of the compound are described.

Claims (14)

1. A compound of the formula

wherein

V is selected from O and S;

W is selected from a bivalent, straight or branched, saturated or unsaturated, optionally substituted C1-30 hydrocarbon chain wherein one or more methylene units are optionally and independently replaced by —O—, —S—, —N(R)—, —C(O)—, C(O)O—, OC(O)—, —N(R)C(O)—, —C(O)N(R)—, —S(O)—, —S(O) 2 —, —N(R)SO 2 —, SO 2 N(R)—, a heterocyclic group, an aryl group, or a heteroaryl group;

X is selected from a covalent bond; a carbon atom; a heteroatom; an optionally substituted group selected from the group consisting of acyl, aliphatic, heteroaliphatic, aryl, heteroaryl, and heterocyclic; or nucleoside;

Y is selected from a covalent bond or a bivalent, straight or branched, saturated or unsaturated, optionally substituted C1-30 hydrocarbon chain wherein one or more methylene units are optionally and independently replaced by —O—, —S—, —N(R)—, —C(O)—, C(O)O—, OC(O)—, —N(R)C(O)—, —C(O)N(R)—, —S(O)—, —S(O) 2 —, —N(R)SO 2 —, SO 2 N(R)—, a heterocyclic group, an aryl group, or a heteroaryl group;

Z is a reactive functional group selected from the group consisting of N-hydroxysuccinimide, para-nitrophenyl carbonate, para-nitrophenyl carbamate, azide, hydrazine, pentafluorophenyl, haloacetamide, maleimide, hydroxylamine, cycloalkyne, heterocycloalkyne, alkyne, diene, and heterocyclic azadience, wherein halo is iodine (I), bromine (Br), fluorine (F), or chlorine (Cl) and hetero is N, O, or S;

D is a therapeutic agent linked to W via a covalent linkage formed via a reaction with a primary amine, a secondary amine, a hydroxyl, a sulfhydryl, a carboxyl, an aldehyde, or a ketone group of the therapeutic agent;

Each occurrence of R is independently hydrogen, an acyl, arylalkyl, aliphatic, aryl, heteroaryl, or heteroaliphatic group; and

n is 1, 2, 3, or 4.

2. The compound of claim 1 , wherein the therapeutic agent is an anti-inflammatory agent.

3. The compound of claim 2 , wherein the anti-inflammatory agent is a glucocorticoid receptor agonist.

4. The compound of claim 2 wherein the anti-inflammatory agent is Cortisol, cortisone acetate, beclometasone, prednisone, prednisolone, methylprednisolone, betamethasone, trimcinolone, budesonide, dexamethasone, fluticasone, or mometasone.

5. The compound of claim 1 , wherein the therapeutic agent is a cytotoxic agent.

Assignments (2)
MERGER Recorded Aug 8, 2022
From: MERCK SHARP & DOHME CORP.
To: MERCK SHARP & DOHME LLC
Reel/Frame 061102/0145 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2019
From: GARBACCIO, ROBERT M.; KERN, JEFFREY C.; MULHEARN, JAMES; BRANDISH, PHILIP E.
To: MERCK SHARP & DOHME CORP.
Reel/Frame 048216/0051 →