IP Library Granted Patent US 12,528,775
Granted Patent B2
US 12,528,775 · App. 17/935,539 · Granted Jan 20, 2026

Oxygenated and amino- or ammonium-containing phosphonic acid derivatives and their medical use

Inventors: Georg Schlechtingen (Dresden, DE); Hans-Joachim Knolker (Dresden, DE); Tim Friedrichson (Dresden, DE); Gary Jennings (Dresden, DE); Tobias Braxmeier (Kuppenheim, DE)
Assignee: GRI Bio, Inc.
C07D223/04A61P29/00A61P37/00C07D207/02C07D221/00
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Quick Facts
Patent No.
US 12,528,775
App. No.
17/935,539
Granted
Jan 20, 2026
Kind
B2
Abstract

The present invention relates to oxygenated amino and ammonium-containing sulfonic acid, phosphonic acid and carboxylic acid derivatives, in particular the compounds of formula 1, 2, 3, 4, 5 or 6, and their medical use, including their use in the treatment, prevention or amelioration of an inflammatory, autoimmune and/or allergic disorder, or a proliferative, neoplastic or dysplastic disease or disorder.

Claims (43)

1 . A compound of formula 1 or a pharmaceutically acceptable salt, solvate or prodrug thereof,

wherein:

R 1 is a C 10-20 hydrocarbon group;

R 2 and R 3 are mutually linked to form a pyrrolidine ring, a piperidine ring or an azepane ring together with the nitrogen atom X to which they are attached, wherein said pyrrolidine ring, said piperidine ring or said azepane ring is optionally substituted with one or more groups independently selected from —OH, —O(C 1-3 alkyl), —O—C(O)—(C 1-3 alkyl), C 1-3 alkyl, —NH 2 , —NH(C 1-3 alkyl) or —N(C 1-3 alkyl)(C 1-3 alkyl);

R 4 is a C 3-6 alkylene group which is substituted with one or more groups independently selected from —OH, —O(C 1-3 alkyl), —O—C(O)—(C 1-3 alkyl), —O—C(O)—O(C 1-3 alkyl), —O—C(O)—NH 2 , —O—C(O)—NH(C 1-3 alkyl), —O—C(O)—N(C 1-3 alkyl)(C 1-3 alkyl), —O(CH 2 ) 2 OH or —O(CH 2 ) 3 OH;

R 5 is —PO 3 H − , —PO 3 2− , —PO 3 H 2 , —PO 2 (OC 1-3 alkyl), —PO 2 H(OC 1-3 alkyl), or —PO(OC 1-3 alkyl) 2 ; and

X is N + .

2 . The compound according to claim 1 , wherein R 5 is —PO 3 2− , PO 3 H − , or —PO 3 H 2 .

3 . The compound according to claim 1 , wherein R 4 is —CH 2 —CH(—R 41 )—CH 2 — and R 41 is selected from —OH, —O(C 1-3 alkyl), —O—C(O)—(C 1-3 alkyl), —O—C(O)—O(C 1-3 alkyl), O—C(O)—NH 2 , —O—C(O)—NH(C 1-3 alkyl), —O—C(O)—N(C 1-3 alkyl)(C 1-3 alkyl), O(CH 2 ) 2 OH, or —O(CH 2 ) 3 OH.

4 . The compound according to claim 1 , wherein R 1 is a linear C 10-20 alkyl group, a linear C 10-20 alkenyl group, or a linear C 10-20 alkynyl group.

5 . The compound according to claim 1 , wherein R 1 is —(CH 2 ) 11 —CH 3 , —(CH 2 ) 13 —CH 3 , or —(CH 2 ) 15 —CH 3 .

6 . The compound of claim 1 , wherein the compound is a compound of formula 2

wherein:

R 1 is a C 10-20 hydrocarbon group;

R 4 is a C 3-6 alkylene group which is substituted with one or more groups independently selected from —OH, —O(C 1-3 alkyl), —O—C(O)—(C 1-3 alkyl), —O—C(O)—O(C 1-3 alkyl), —O—C(O)—NH 2 , —O—C(O)—NH(C 1-3 alkyl), —O—C(O)—N(C 1-3 alkyl)(C 1-3 alkyl), —O(CH 2 ) 2 OH or —O(CH 2 ) 3 OH;

R 5 is —PO 3 H − , —PO 3 2− , —PO 3 H 2 , —PO 2 (OC 1-3 alkyl), —PO 2 H(OC 1-3 alkyl), or —PO(OC 1-3 alkyl) 2 ;

n is 1 and m is 0, 1, 2, or 3; and

each R 6 is independently selected from —OH, —O(C 1-3 alkyl), —O—C(O)—(C 1-3 alkyl), C 1-3 alkyl, —NH 2 , —NH(C 1-3 alkyl) or —N(C 1-3 alkyl)(C 1-3 alkyl).

7 . The compound of claim 1 , wherein the compound is a compound of the following formula 2

wherein:

R 1 is a C 10-20 hydrocarbon group;

R 4 is a C 3-6 alkylene group which is substituted with one or more groups independently selected from —OH, —O(C 1-3 alkyl), —O—C(O)—(C 1-3 alkyl), —O—C(O)—O(C 1-3 alkyl), —O—C(O)—NH 2 , —O—C(O)—NH(C 1-3 alkyl), —O—C(O)—N(C 1-3 alkyl)(C 1-3 alkyl), —O(CH 2 ) 2 OH or —O(CH 2 ) 3 OH;

R 5 is —PO 3 H − , —PO 3 2− , —PO 3 H 2 , —PO 2 (OC 1-3 alkyl), —PO 2 H(OC 1-3 alkyl), or —PO(OC 1-3 alkyl) 2 ;

n is 2 and m is 0, 1, 2, or 3 and

each R 6 is independently selected from —OH, —O(C 1-3 alkyl), —O—C(O)—(C 1-3 alkyl), C 1-3 alkyl, —NH 2 , —NH(C 1-3 alkyl) or —N(C 1-3 alkyl)(C 1-3 alkyl).

8 . The compound of claim 1 , wherein the compound is a compound of the following formula 2

wherein:

R 1 is a C 10-20 hydrocarbon group;

R 4 is a C 3-6 alkylene group which is substituted with one or more groups independently selected from —OH, —O(C 1-3 alkyl), —O—C(O)—(C 1-3 alkyl), —O—C(O)—O(C 1-3 alkyl), —O—C(O)—NH 2 , —O—C(O)—NH(C 1-3 alkyl), —O—C(O)—N(C 1-3 alkyl)(C 1-3 alkyl), —O(CH 2 ) 2 OH or —O(CH 2 ) 3 OH;

R 5 is —PO 3 H − , —PO 3 2− , —PO 3 H 2 , —PO 2 (OC 1-3 alkyl), —PO 2 H(OC 1-3 alkyl), or —PO(OC 1-3 alkyl) 2 ;

n is 3 and m is 0, 1, 2, or 3; and

each R 6 is independently selected from —OH, —O(C 1-3 alkyl), —O—C(O)—(C 1-3 alkyl), C 1-3 alkyl, —NH 2 , —NH(C 1-3 alkyl) or —N(C 1-3 alkyl)(C 1-3 alkyl).

9 . A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable excipient.

10 . A method of treating or ameliorating a disorder in a subject in need thereof, the method comprising administering the compound of claim 1 to the subject, wherein said disorder is selected from: psoriasis, atopic dermatitis, contact dermatitis, xerotic eczema, seborrheic dermatitis, neurodermitis, dyshidrosis, discoid eczema, venous eczema, dermatitis herpetiformis, autoeczematization, dermatomyositis, hyper-IgE syndrome, Wiskott-Aldrich syndrome, anaphylaxis, food allergy, allergic reactions to venomous stings, acute urticarias, chronic urticarias, physical urticarias including aquagenic urticaria, cholinergic urticaria, cold urticaria, delayed pressure urticaria, dermatographic urticaria, heat urticaria, solar urticaria, vibration urticaria, adrenergic urticaria, urticaria angioedema, inflammatory bowel disease, Crohn's disease, ulcerative colitis, collagenous colitis, lymphocytic colitis, diversion colitis, Behget's syndrome, indeterminate colitis, celiac disease, irritable bowel syndrome, post-operative ileus, eosinophilic gastroenteropathy, gastritis, chronic allergic rhinitis, seasonal allergic rhinitis, allergic conjunctivitis, chemical conjunctivitis, neonatal conjunctivitis, Sjogren syndrome, open-angle glaucoma, dry eye disease, diabetic macular edema, chronic obstructive pulmonary disease, allergic asthma, allergic bronchopulmonary aspergillosis, hypersensitivity pneumonitis, lung fibrosis, rheumatoid arthritis, juvenile rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus, scleroderma, reactive arthritis, polymyalgia rheumatica, Guillain-Barre syndrome, Hashimoto's thyroiditis, Grave's disease, temporal arteritis, primary biliary cirrhosis, sclerosing cholangitis, autoimmune hepatitis, alopecia areata, a graft-versus-host disease, a host-versus-graft disease, or a transplant rejection.

11 . The method of claim 10 , wherein said disorder is selected from psoriasis, atopic dermatitis, contact dermatitis, xerotic eczema, seborrheic dermatitis, neurodermitis, dyshidrosis, discoid eczema, venous eczema, dermatitis herpetiformis, autoeczematization, dermatomyositis, hyper-IgE syndrome, Wiskott-Aldrich syndrome, anaphylaxis, food allergy, or allergic reactions to venomous stings.

12 . The method of claim 10 , wherein said disorder is selected from acute urticarias, chronic urticarias, physical urticarias including aquagenic urticaria, cholinergic urticaria, cold urticaria, delayed pressure urticaria, dermatographic urticaria, heat urticaria, solar urticaria, vibration urticaria, adrenergic urticaria, or urticaria angioedema.

13 . The method of claim 10 , wherein said disorder is selected from inflammatory bowel disease, Crohn's disease, ulcerative colitis, collagenous colitis, lymphocytic colitis, diversion colitis, Behget's syndrome, indeterminate colitis, celiac disease, irritable bowel syndrome, post-operative ileus, eosinophilic gastroenteropathy, or gastritis.

14 . The method of claim 10 , wherein said disorder is selected from chronic allergic rhinitis, seasonal allergic rhinitis, allergic conjunctivitis, chemical conjunctivitis, neonatal conjunctivitis, Sjogren syndrome, open-angle glaucoma, dry eye disease, or diabetic macular edema.

15 . The method of claim 10 , wherein said disorder is selected from chronic obstructive pulmonary disease, allergic asthma, allergic bronchopulmonary aspergillosis, hypersensitivity pneumonitis, or lung fibrosis.

16 . The method of claim 10 , wherein said disorder is selected from rheumatoid arthritis, juvenile rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus, scleroderma, reactive arthritis, or polymyalgia rheumatica.

17 . The method of claim 10 , wherein said disorder is selected from Guillain-Barre syndrome, Hashimoto's thyroiditis, Grave's disease, temporal arteritis, primary biliary cirrhosis, sclerosing cholangitis, autoimmune hepatitis, or alopecia areata.

18 . The method of claim 10 , wherein said disorder is selected from a graft-versus-host disease, a host-versus-graft disease or a transplant rejection.

19 . A method of treating or ameliorating a disorder in a subject in need thereof, the method comprising administering the pharmaceutical composition of claim 10 to the subject, wherein said disorder is selected from: psoriasis, atopic dermatitis, contact dermatitis, xerotic eczema, seborrheic dermatitis, neurodermitis, dyshidrosis, discoid eczema, venous eczema, dermatitis herpetiformis, autoeczematization, dermatomyositis, hyper-IgE syndrome, Wiskott-Aldrich syndrome, anaphylaxis, food allergy, allergic reactions to venomous stings, acute urticarias, chronic urticarias, physical urticarias including aquagenic urticaria, cholinergic urticaria, cold urticaria, delayed pressure urticaria, dermatographic urticaria, heat urticaria, solar urticaria, vibration urticaria, adrenergic urticaria, urticaria angioedema, inflammatory bowel disease, Crohn's disease, ulcerative colitis, collagenous colitis, lymphocytic colitis, diversion colitis, Behcee s syndrome, indeterminate colitis, celiac disease, irritable bowel syndrome, post-operative ileus, eosinophilic gastroenteropathy, gastritis, chronic allergic rhinitis, seasonal allergic rhinitis, allergic conjunctivitis, chemical conjunctivitis, neonatal conjunctivitis, Sjogren syndrome, open-angle glaucoma, dry eye disease, diabetic macular edema, chronic obstructive pulmonary disease, allergic asthma, allergic bronchopulmonary aspergillosis, hypersensitivity pneumonitis, lung fibrosis, rheumatoid arthritis, juvenile rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus, scleroderma, reactive arthritis, polymyalgia rheumatica, Guillain-Barre syndrome, Hashimoto's thyroiditis, Grave's disease, temporal arteritis, primary biliary cirrhosis, sclerosing cholangitis, autoimmune hepatitis, alopecia areata, a graft-versus-host disease, a host-versus-graft disease, or a transplant rejection.

Assignments (3)
SECURITY INTEREST Recorded Dec 15, 2022
From: GRI BIO, INC.
To: ALTIUM GROWTH FUND, LP
Reel/Frame 062108/0599 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 14, 2022
From: SCHLECHTINGEN, GEORG; KNOLKER, HANS-JOACHIM; FRIEDRICHSON, TIM; JENNINGS, GARY; BRAXMEIER, TOBIAS
To: GLYCOREGIMMUNE, INC.
Reel/Frame 061430/0519 →
CHANGE OF NAME Recorded Oct 14, 2022
From: GLYCOREGIMMUNE, INC.
To: GRI BIO, INC.
Reel/Frame 061571/0566 →
Priority Claims (1)
EP 11167731 · May 26, 2011 · regional
Continuity (4)
Continuation 17080636 · Oct 26, 2020
Continuation 15694303 · Sep 1, 2017
Continuation 14403168
Related Publication 20230265052A1 · Aug 24, 2023
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