IP Library Granted Patent US 9,403,858
Granted Patent B2
US 9,403,858 · App. 14/944,610 · Granted Aug 2, 2016

Platinum compounds, compositions, and uses thereof

Inventors: Mark T. Bilodeau (Concord, MA); Benoît Moreau (Newton, MA); Adam H. Brockman (Arlington, MA)
Assignee: Placon Therapeutics, Inc.
C07F15/00A61K31/282A61K33/24
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Quick Facts
Patent No.
US 9,403,858
App. No.
14/944,610
Granted
Aug 2, 2016
Kind
B2
Abstract

The present teachings relate to compounds and compositions for treatment of cancers. In some embodiments, the composition comprises a platinum (IV) complex having at least one reacting group for reacting with a functional group on a protein, engineered protein, antibody, antibody fragment, peptide, agonist, antagonist, aptamer or ligand which may be capable of recognizing a selected target cell population, and/or derivatives/analogs/mimics thereof.

Claims (18)

1. A compound of Formula IIb:

or a pharmaceutically acceptable salt thereof, wherein:

X and Y are independently selected from NH, alkyl and aryl;

R 1 and R 2 each is Cl, or R 1 and R 2 are joined to form an oxalate;

R 3 is hydrogen, alkyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl, wherein each of the alkyl, alkenyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl groups optionally is substituted with one or more groups, each independently selected from halogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl, and heterocyclyl, wherein each of the carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl, or heterocyclyl is optionally substituted with one or more groups, each independently selected from halogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl, and heterocyclyl,

and

Z is alternatively absent, alkyl, aryl, cycloalkyl, heterocyclyl, aryl, and heteroaryl, wherein each of the alkyl, alkenyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl groups optionally is substituted with one or more groups, each independently selected from halogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl, heterocyclyl, or alkylidene hydrazine, wherein each of the carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl, heterocyclyl or alkylidene hydrazine is optionally substituted with one or more groups, each independently selected from halogen, cyano, nitro, hydroxyl, carboxyl, carbamoyl, ether, alkoxy, aryloxy, amino, amide, carbamate, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, heteroaryl, and heterocyclyl.

2. The compound of claim 1 , wherein the compound conjugates with a functional group on a protein, engineered protein, antibody, antibody fragment, peptide, agonist, antagonist, aptamer or ligand which may be capable of recognizing a selected target cell population, and/or derivative/analogy/mimics thereof.

3. The compound of claim 2 , wherein the conjugation between the compound and the functional group takes place in vivo.

4. The compound of claim 2 , wherein the conjugation between the compound and the functional group is performed prior to administration in vivo.

5. The compound of claim 2 , wherein the compound conjugates with a functional group on a protein which is albumin.

6. The compound of claim 1 , wherein R 1 and R 2 each is Cl.

7. The compound of claim 1 , wherein R 1 and R 2 are joined to form an oxalate.

8. The compound of claim 1 , wherein R 3 is alkyl.

9. The compound of claim 1 , wherein R 3 is methyl or ethyl.

10. A compound selected from:

11. A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.

12. A pharmaceutical composition comprising any compound of claim 10 and a pharmaceutically acceptable carrier.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 29, 2020
From: PLACON THERAPEUTICS, INC.
To: XLINK THERAPEUTICS, INC.
Reel/Frame 054215/0859 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 28, 2016
From: BLEND THERAPEUTICS, INC.
To: PLACON THERAPEUTICS, INC.
Reel/Frame 037610/0876 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 5, 2016
From: BILODEAU, MARK T.; MOREAU, BENOÎT; BROCKMAN, ADAM H.
To: BLEND THERAPEUTICS, INC.
Reel/Frame 037411/0507 →
Continuity (7)
Continuation PCTUS2015037071 · Jun 23, 2015
Provisional Application 62015714 · Jun 23, 2014
Provisional Application 62034124 · Aug 6, 2014
Provisional Application 62035126 · Aug 8, 2014
Provisional Application 62035739 · Aug 11, 2014
Provisional Application 62150045 · Apr 20, 2015
Related Publication 20160068557A1 · Mar 10, 2016