PE20231652A1 - Nuevo inhibidor de la secrecion de acido y uso del mismo - Google Patents
Nuevo inhibidor de la secrecion de acido y uso del mismoInfo
- Publication number
- PE20231652A1 PE20231652A1 PE2022002955A PE2022002955A PE20231652A1 PE 20231652 A1 PE20231652 A1 PE 20231652A1 PE 2022002955 A PE2022002955 A PE 2022002955A PE 2022002955 A PE2022002955 A PE 2022002955A PE 20231652 A1 PE20231652 A1 PE 20231652A1
- Authority
- PE
- Peru
- Prior art keywords
- compound
- acid secretion
- same
- new inhibitor
- alkyl
- Prior art date
Links
- 230000009858 acid secretion Effects 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- UDMABANYJMEZDH-UHFFFAOYSA-N 1-[5-(2-fluorophenyl)-4-methoxy-1-(6-methoxypyridin-3-yl)sulfonylpyrrol-3-yl]-N-methylmethanamine Chemical compound CNCC(C(OC)=C1C(C=CC=C2)=C2F)=CN1S(C(C=N1)=CC=C1OC)(=O)=O UDMABANYJMEZDH-UHFFFAOYSA-N 0.000 abstract 1
- 208000018522 Gastrointestinal disease Diseases 0.000 abstract 1
- 206010061459 Gastrointestinal ulcer Diseases 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 210000004211 gastric acid Anatomy 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Nutrition Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Referido a un compuesto de formula II, o una sal farmaceuticamente aceptable del mismo, en donde X1 es F; X2 es H o F; R1 es metilo o etilo; y R2 es -O(alquilo C1-C4) o -(alquilo C1-C4). En donde un compuesto seleccionado es 1-(5-(2-fluorofenil)-4-metoxi-1-((6-metoxipiridin-3-il)sulfonil)-1H-pirrol-3-il)-N-metilmetanamina. Este compuesto es inhibidor de la secrecion de acido. Tambien se refiere a una composicion farmaceutica que comprende dicho compuesto o una sal farmaceuticamente aceptable del mismo y su uso en la prevencion o tratamiento de ulceras gastrointestinales o enfermedades relacionadas con el acido gastrico.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR20200073900 | 2020-06-17 | ||
PCT/KR2021/007572 WO2021256861A1 (ko) | 2020-06-17 | 2021-06-16 | 신규한 산 분비 억제제 및 이의 용도 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20231652A1 true PE20231652A1 (es) | 2023-10-17 |
Family
ID=79176045
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2022002955A PE20231652A1 (es) | 2020-06-17 | 2021-06-16 | Nuevo inhibidor de la secrecion de acido y uso del mismo |
Country Status (16)
Country | Link |
---|---|
US (2) | US11767311B2 (es) |
EP (1) | EP4148050A4 (es) |
JP (1) | JP7404561B2 (es) |
KR (2) | KR20210156235A (es) |
CN (1) | CN115884968B (es) |
AU (1) | AU2021293694B2 (es) |
BR (1) | BR112022025613A2 (es) |
CA (1) | CA3182882A1 (es) |
CL (1) | CL2022003601A1 (es) |
CO (1) | CO2023000396A2 (es) |
DO (1) | DOP2022000291A (es) |
EC (1) | ECSP23002606A (es) |
MX (1) | MX2022016515A (es) |
PE (1) | PE20231652A1 (es) |
TW (1) | TWI797645B (es) |
WO (1) | WO2021256861A1 (es) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20210156235A (ko) | 2020-06-17 | 2021-12-24 | 일동제약(주) | 신규한 산 분비 억제제 및 이의 용도 |
KR20230091056A (ko) * | 2021-12-15 | 2023-06-22 | 일동제약(주) | 1-설포닐 피롤 유도체의 신규 염, 이의 제조 방법 및 이를 포함하는 약학 조성물 |
WO2023113474A1 (ko) * | 2021-12-15 | 2023-06-22 | 일동제약(주) | 1-설포닐 피롤 유도체의 신규 염, 이의 제조 방법 및 이를 포함하는 약학 조성물 |
KR20230102353A (ko) * | 2021-12-30 | 2023-07-07 | 주식회사 대웅제약 | 삼중음성유방암의 예방 또는 치료용 약학적 조성물 |
CN114539219A (zh) * | 2022-03-17 | 2022-05-27 | 日照正济药业有限公司 | 一种富马酸伏诺拉生的制备方法 |
WO2023211843A1 (en) * | 2022-04-25 | 2023-11-02 | Daewoong Pharmaceutical Co., Ltd. | Potassium-competitive acid blockers for the treatment of pathological hypersecretory conditions |
TW202411216A (zh) * | 2022-05-23 | 2024-03-16 | 南韓商日東製藥股份有限公司 | 6-甲氧基吡啶-3-基衍生物之製造方法 |
TW202411215A (zh) * | 2022-05-23 | 2024-03-16 | 南韓商日東製藥股份有限公司 | 6-甲氧基吡啶-3-基衍生物之製造方法 |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE437642T1 (de) * | 2002-06-14 | 2009-08-15 | Takeda Pharmaceutical | Prodrugs von imidazol-derivaten, zur verwendung als protonenpumpen-hemmer zur behandlung von z.b. peptischen magengeschwüren |
ES2402362T3 (es) * | 2004-09-30 | 2013-05-03 | Takeda Pharmaceutical Company Limited | Inhibidores de la bomba de protones |
SI2327692T1 (sl) * | 2005-08-30 | 2012-11-30 | Tekeda Pharmaceutical Company Ltd | heterociklilsulfonil aminometil hetero arilno substituirani H pirolni derivati kot inhibitorji izločanja kisline |
WO2007114338A1 (ja) * | 2006-03-31 | 2007-10-11 | Takeda Pharmaceutical Company Limited | 酸分泌抑制薬 |
US8933105B2 (en) * | 2007-02-28 | 2015-01-13 | Takeda Pharmaceutical Company Limited | Pyrrole compounds |
US8969387B2 (en) * | 2008-08-27 | 2015-03-03 | Takeda Pharmaceutical Company Limited | Pyrrole compounds |
US8895588B2 (en) * | 2009-03-26 | 2014-11-25 | Takeda Pharmaceutical Company Limited | Pyrazole compound |
SG11201408511QA (en) * | 2012-06-27 | 2015-01-29 | Takeda Pharmaceutical | Liquid preparations of amines and organic acids stabilized by salts |
CN105143187B (zh) | 2013-02-28 | 2018-04-03 | 武田药品工业株式会社 | 制备磺酰氯化合物的方法 |
CN105693693A (zh) * | 2014-11-27 | 2016-06-22 | 江苏柯菲平医药股份有限公司 | 一种吡咯类胃酸分泌和抑制剂化合物盐的制备 |
CN105985278A (zh) * | 2015-01-27 | 2016-10-05 | 江苏柯菲平医药股份有限公司 | 吡咯磺酰类衍生物、其制备方法及其在医药上的应用 |
KR101613245B1 (ko) * | 2015-04-27 | 2016-04-18 | 주식회사 대웅제약 | 신규의 4-메톡시 피롤 유도체 또는 이의 염 및 이를 포함하는 약학 조성물 |
CN106432191A (zh) * | 2015-08-10 | 2017-02-22 | 陕西合成药业股份有限公司 | 一种新的吡咯类衍生物、其制备方法及其在医药上的应用 |
KR20170113040A (ko) | 2016-03-25 | 2017-10-12 | 주식회사 대웅제약 | 1-(5-(2,4-다이플루오로페닐)-1-((3-플루오로페닐)술포닐)-4-메톡시-1h-피롤-3-일)-n-메틸메탄아민의 신규한 산부가염 |
CN109843869B (zh) * | 2016-09-29 | 2021-07-16 | 江苏吉贝尔药业股份有限公司 | 1-[(吡啶-3-基-磺酰基)-1h-吡咯-3-基]甲胺衍生物及其药物组合物和用途 |
WO2019013310A1 (en) | 2017-07-10 | 2019-01-17 | Takeda Pharmaceutical Company Limited | PREPARATION COMPRISING VONOPRAZAN |
CN110396080B (zh) * | 2018-04-24 | 2022-07-08 | 广东东阳光药业有限公司 | 一种富马酸沃诺拉赞代谢物及其氘代物的制备方法 |
CN108558831B (zh) * | 2018-06-08 | 2021-07-27 | 上海璃道医药科技有限公司 | 取代吡咯-4-烷基胺类化合物及其用途 |
KR20210156235A (ko) | 2020-06-17 | 2021-12-24 | 일동제약(주) | 신규한 산 분비 억제제 및 이의 용도 |
CN111943932B (zh) * | 2020-08-06 | 2023-07-14 | 四川国康药业有限公司 | 一种可以治疗消化性溃疡的3-吡啶磺酰-1-n-杂吡咯衍生物及其制备方法和用途 |
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2021
- 2021-06-16 KR KR1020210078284A patent/KR20210156235A/ko active Search and Examination
- 2021-06-16 CA CA3182882A patent/CA3182882A1/en active Pending
- 2021-06-16 AU AU2021293694A patent/AU2021293694B2/en active Active
- 2021-06-16 WO PCT/KR2021/007572 patent/WO2021256861A1/ko active Application Filing
- 2021-06-16 US US18/011,084 patent/US11767311B2/en active Active
- 2021-06-16 MX MX2022016515A patent/MX2022016515A/es unknown
- 2021-06-16 CN CN202180043522.8A patent/CN115884968B/zh active Active
- 2021-06-16 EP EP21826347.3A patent/EP4148050A4/en active Pending
- 2021-06-16 KR KR1020210078283A patent/KR102432523B1/ko active IP Right Grant
- 2021-06-16 BR BR112022025613A patent/BR112022025613A2/pt unknown
- 2021-06-16 PE PE2022002955A patent/PE20231652A1/es unknown
- 2021-06-16 JP JP2022577797A patent/JP7404561B2/ja active Active
- 2021-06-17 TW TW110122142A patent/TWI797645B/zh active
-
2022
- 2022-12-15 CL CL2022003601A patent/CL2022003601A1/es unknown
- 2022-12-15 DO DO2022000291A patent/DOP2022000291A/es unknown
-
2023
- 2023-01-13 CO CONC2023/0000396A patent/CO2023000396A2/es unknown
- 2023-01-16 EC ECSENADI20232606A patent/ECSP23002606A/es unknown
- 2023-08-01 US US18/228,672 patent/US20230373954A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
CA3182882A1 (en) | 2021-12-23 |
TW202325702A (zh) | 2023-07-01 |
CN115884968B (zh) | 2024-06-21 |
ECSP23002606A (es) | 2023-03-31 |
MX2022016515A (es) | 2023-01-30 |
EP4148050A1 (en) | 2023-03-15 |
TW202214588A (zh) | 2022-04-16 |
KR102432523B1 (ko) | 2022-08-16 |
BR112022025613A2 (pt) | 2023-01-17 |
TWI797645B (zh) | 2023-04-01 |
EP4148050A4 (en) | 2023-10-25 |
JP2023524172A (ja) | 2023-06-08 |
AU2021293694A1 (en) | 2023-01-19 |
AU2021293694B2 (en) | 2023-12-21 |
US20230373954A1 (en) | 2023-11-23 |
CL2022003601A1 (es) | 2023-07-07 |
US20230192650A1 (en) | 2023-06-22 |
WO2021256861A1 (ko) | 2021-12-23 |
KR20210156234A (ko) | 2021-12-24 |
CN115884968A (zh) | 2023-03-31 |
US11767311B2 (en) | 2023-09-26 |
DOP2022000291A (es) | 2023-01-15 |
JP7404561B2 (ja) | 2023-12-25 |
KR20210156235A (ko) | 2021-12-24 |
CO2023000396A2 (es) | 2023-02-27 |
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