IP Library Granted Patent US 10,550,190
Granted Patent B2
US 10,550,190 · App. 15/301,564 · Granted Feb 4, 2020

Phosphate based linkers for intracellular delivery of drug conjugates

Inventors: Robert M. Garbaccio (Lansdale, PA); Jeffrey Kern (Gilbertsville, PA); Philip E. Brandish (Needham, MA); Sanjiv Shah (Wakefield, MA); Linda Liang (Mountain View, CA); Ying Sun (San Diego, CA); Jianing Wang (San Diego, CA); Nick Knudsen (Escondido, CA); Andrew Beck (San Diego, CA); Anthony Manibusan (San Diego, CA); Dennis Gately (San Diego, CA)
Assignees: Merck Sharp & Dohme Corp.; Ambrx, Inc.
C07K16/2866
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Quick Facts
Patent No.
US 10,550,190
App. No.
15/301,564
Granted
Feb 4, 2020
Kind
B2
Abstract

Phosphate-based linkers with tunable stability for intracellular delivery of drug conjugates are described. The phosphate-based linkers comprise a monophosphate, diphosphate, triphosphate, or tetraphosphate group (phosphate group) and a linker arm comprising a tuning element and optionally a spacer. A payload is covalently linked to the phosphate group at the distal end of the linker arm and the functional group at the proximal end of the linker arm is covalently linked to a cell-specific targeting ligand such as an antibody. These phosphate-based linkers have a differentiated and tunable stability in blood vs. an intracellular environment (e.g. lysosomal compartment).

Claims (14)

1. A compound comprising the formula

wherein

V is selected from O and S;

W is selected from O, N, and CH 2 ;

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; a carbon atom linked to a trimethylammonium group by a C1-C5 hydrocarbon chain; nucleoside, protease sensitive group, cathepsin B sensitive group, or glycosidase sensitive group;

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 of Y 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;

T is an NR, O, or S;

Z is a cyclooctyne;

D is an anti-inflammatory agent;

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

n is 1, 2, 3, or 4.

2. The compound of claim 1 , wherein the anti-inflammatory agent is a glucocorticoid receptor agonist.

3. The compound of claim 1 , wherein the anti-inflammatory agent is Cortisol, cortisone acetate, beclometasone, prednisone, prednisolone, methylprednisolone, betamethasone, trimcinolone, budesonide, dexamethasone, fluticasone, fluticasone propionate, fluticasone furoate, compound 15-5, or mometasone.

4. The compound of claim 1 , wherein the compound has a structure selected from the group consisting of

Assignments (3)
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 Apr 7, 2017
From: SUN, YING; WANG, JIANING; KNUDSEN, NICK; BECK, ANDREW; MANIBUSAN, ANTHONY; GATELY, DENNIS
To: AMBRX, INC.
Reel/Frame 041929/0913 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 10, 2016
From: GARBACCIO, ROBERT M.; KERN, JEFFREY; BRANDISH, PHILIP E.; SHAH, SANJIV; LIANG, LINDA
To: MERCK SHARP & DOHME CORP.
Reel/Frame 039977/0454 →
Continuity (3)
Provisional Application 62112222 · Feb 5, 2015
Provisional Application 61975407 · Apr 4, 2014
Related Publication 20170182181A1 · Jun 29, 2017
Cited By (1)
US 12,465,614