IP Library › Granted Patent US 9,371,286
Granted Patent B2
US 9,371,286 · App. 14/232,598 · Granted Jun 21, 2016

Pharmaceutical composition with enhanced efficacy for inhibiting angiogenesis

Inventors: Ho Jeong Kwon (Seoul, KR); Gyoon Hee Han (Gyeonggi-do, KR); Hye Jin Jung (Seoul, KR); Jeong Jea Seo (Seoul, KR)
Assignee: INDUSTRY-ACADEMIC COOPERATION FOUNDATION, YONSEI UNIVERSITY
C07D215/38C07C311/20C07C311/21C07C2101/14
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Quick Facts
Patent No.
US 9,371,286
App. No.
14/232,598
Granted
Jun 21, 2016
Kind
B2
Abstract

The present invention relates to a pharmaceutical composition for inhibiting angiogenesis and a novel sulfonyl amide derivative compound which can be useful for the prevention or treatment of angiogenesis-related diseases or disorders. Since the compound used as an active ingredient in the pharmaceutical composition of the invention is specifically bound to UQCRB and inhibits biological functions thereof, apoptosis is not induced and angiogenic responses are inhibited. Therefore, the compound used as an active ingredient in the pharmaceutical composition of the invention can be useful as an effective and safe angiogenesis inhibitory agent.

Claims (18)

1. A pharmaceutical composition comprising a compound represented by Chemical Formula 1:

wherein

R 1 is selected from the group consisting of

naphthalyl, and naphthalyl substituted with C 1 -C 6 alkyl;

R 2 is selected from the group consisting of

hydroxynaphthalyl, and 4-(2-hydroxyethyl)cyclohexyl;

A 1 is C 1 -C 6 alkyl or phenyl; and

B 1 , B 2 , B 4 , and B 5 are each independently selected from the group consisting of H—, halo, hydroxyl, nitro, and C 1 -C 6 alkyl, and B 3 is selected from the group consisting of H—, halo hydroxyl, and C 1 -C 6 alkyl.

2. The pharmaceutical composition of claim 1 , wherein A 1 is methyl, ethyl, phenyl, or tert-butyl.

3. The pharmaceutical composition of claim 1 , wherein B 1 is H—, chloro, fluoro, hydroxyl, nitro, or methyl.

4. The pharmaceutical composition of claim 1 , wherein the hydroxy naphthalyl is 7-hydroxy naphthalyl.

5. The pharmaceutical composition of claim 1 , wherein the compound is selected from the group consisting of:

6. The pharmaceutical composition of claim 5 , wherein the composition is selected from the group consisting of the compounds represented by Chemical Formulas 5, 6, 12, 17, 21, 23, and 24.

7. A method of treating a disease or disorder selected from the group consisting of cancer, diabetic retinopathy, retinopathy of prematurity, neovascular glaucoma and, proliferative retinopathy, the method comprising:

administering an appropriate dose of the pharmaceutical composition of claim 1 to a subject in need thereof.

8. The method of claim 7 , wherein the disease or disorder is a cancer, diabetic retinopathy, or proliferative retinopathy.

9. The method of claim 8 , wherein the proliferative retinopathy is age-related macular degeneration.

10. A compound selected from the group consisting of compounds represented by Chemical Formulas 2, 3, 4, 11, 12, 13, 15, 16, 17, 18, 19, 20, 22, 23, 24, 26, and 29:

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 9, 2024
From: NEXTGEN BIOSCIENCE CO.
To: INDUSTRY-ACADEMIC COOPERATION FOUNDATION YONSEI UNIVERSITY
Reel/Frame 066427/0777 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2019
From: INDUSTRY-ACADEMIC COOPERATION FOUNDATION YONSEI UNIVERSITY
To: NEXTGEN BIOSCIENCE CO.
Reel/Frame 049037/0249 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 6, 2014
From: KWON, HO JEONG; HAN, GYOON HEE; JUNG, HYE JIN
To: INDUSTRY-ACADEMIC COOPERATION FOUNDATION, YONSEI UNIVERSITY
Reel/Frame 033246/0751 →
Priority Claims (1)
KR 10-2011-0023211 · Mar 16, 2011 · national
Continuity (1)
Related Publication 20140315947A1 · Oct 23, 2014