IP Library Granted Patent US 12709606
Granted Patent B2
US 12709606 · App. 18/228,672 · Granted Aug 18, 2026

Acid secretion inhibitor and use thereof

Inventors: Hong Chul Yoon (Gyeonggi-do, KR); Joon Tae Park (Gyeonggi-do, KR); Jung Woo Lee (Gyeonggi-do, KR); Kyung Mi An (Gyeonggi-do, KR); A Rang Im (Gyeonggi-do, KR); Woo Jin Jeon (Gyeonggi-do, KR); Jae Ho Heo (Gyeonggi-do, KR); Chang Hee Hong (Gyeonggi-do, KR); Jung Eun Park (Gyeonggi-do, KR); Te Ik Sohn (Gyeonggi-do, KR); Da Hae Hong (Gyeonggi-do, KR); Jung Ho Kim (Gyeonggi-do, KR); Jae Eui Shin (Gyeonggi-do, KR); Yeong Ran Yoo (Gyeonggi-do, KR); Min Whan Chang (Gyeonggi-do, KR); In Gyu Je (Gyeonggi-do, KR); Su Yeon Kang (Gyeonggi-do, KR); Yoon Sung Song (Gyeonggi-do, KR); Joo Yun Lee (Gyeonggi-do, KR)
Assignee: ILDONG PHARMACEUTICAL CO., LTD.
C07D401/12A61P1/04A61P29/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12709606
App. No.
18/228,672
Granted
Aug 18, 2026
Kind
B2
Abstract

The present invention provides a novel compound represented by Chemical Formula 2, or a pharmaceutically acceptable salt thereof. The novel compound according to the present invention exhibits an excellent acid secretion inhibitory effect.

Claims (38)

1 . A method of treating gastrointestinal ulcers, gastrointestinal inflammatory diseases, or gastric acid-related diseases, the method comprising administering to a subject in need a therapeutically effective amount of a compound represented by the following Chemical Formula 2 or a pharmaceutically acceptable salt thereof:

in the Chemical Formula 2,

X 1 is F;

X 2 is hydrogen or F;

R 1 is methyl; and

R 2 is methoxy, ethoxy, methyl or ethyl.

2 . The method of claim 1 , wherein R 2 is methoxy or methyl.

3 . The method of claim 1 , wherein R 1 is methyl, and R 2 is methoxy or methyl.

4 . The method of claim 1 , wherein

X 1 is F;

X 2 is F;

R 1 is methyl; and

R 2 is methoxy or methyl.

5 . The method of claim 1 , wherein

X 1 is F;

X 2 is hydrogen;

R 1 is methyl; and

R 2 is methoxy or methyl.

6 . The method of claim 1 , wherein

X 1 is F;

X 2 is hydrogen or F;

R 1 is methyl; and

R 2 is methoxy.

7 . The method of claim 1 , wherein

X 1 is F;

X 2 is hydrogen or F;

R 1 is methyl; and

R 2 is methyl.

8 . The method of claim 1 , wherein the compound represented by Chemical Formula 2 is any one selected from the group consisting of the following compounds:

1-(5-(2-fluorophenyl)-4-methoxy-1-((6-methoxypyridin-3-yl) sulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine;

1-(5-(2,4-difluorophenyl)-4-methoxy-1-((6-methoxypyridin-3-yl) sulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine;

1-(5-(2,4-difluorophenyl)-4-methoxy-1-((6-methylpyridin-3-yl) sulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine; and

1-(5-(2-fluorophenyl)-4-methoxy-1-((6-methylpyridin-3-yl) sulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine.

9 . The method of claim 1 , wherein the gastrointestinal ulcer, gastrointestinal inflammatory disease or gastric acid-related disease is any one or more selected from the group consisting of peptic ulcer, gastric ulcer, duodenal ulcer, NSAID-induced ulcer, acute stress ulcer, Zollinger-Ellison syndrome, Helicobacter pylori infection, gastritis, erosive esophagitis, non-erosive esophagitis, reflux esophagitis, inflammatory bowel disease, symptomatic gastroesophageal reflux disease (symptomatic GERD), functional dyspepsia, gastric cancer, gastric MALT lymphoma, hyperacidity, and upper gastrointestinal hemorrhage due to invasive stress.

10 . The method of claim 1 , wherein the administering is oral administrating.

11 . The method of claim 1 , wherein a daily dosage of the compound is from about 0.001 to about 100 mg/kg.

12 . The method of claim 1 , wherein the compound inhibits the proton pump.

13 . The method of claim 1 , wherein the compound inhibits gastric acid secretion.