PE20181301A1 - Bloqueador del canal de sodio - Google Patents
Bloqueador del canal de sodioInfo
- Publication number
- PE20181301A1 PE20181301A1 PE2018000765A PE2018000765A PE20181301A1 PE 20181301 A1 PE20181301 A1 PE 20181301A1 PE 2018000765 A PE2018000765 A PE 2018000765A PE 2018000765 A PE2018000765 A PE 2018000765A PE 20181301 A1 PE20181301 A1 PE 20181301A1
- Authority
- PE
- Peru
- Prior art keywords
- hydrogen
- alkyl
- alkylene
- sodium channel
- halogen
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- 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
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/50—Nitrogen atoms bound to hetero atoms
- C07D277/52—Nitrogen atoms bound to hetero atoms to sulfur atoms, e.g. sulfonamides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
Referido a un compuesto de Formula (I), en donde R1 es hidrogeno, alquilo C1-4, alcoxilo C1-4, entre otros; R2 y R3 son cada uno independientemente hidrogeno o halogeno; R4 es heteroarilo C5-10, que contiene uno o dos elementos cada uno seleccionado independientemente del grupo que consiste en N, S y O; R5 es -CH2CH2-N(R7)(R8) o -CH2CH2CH2-N(R7)(R8); R6 es hidrogeno o alquilo C1-4; R5 y R6 forman juntos alquileno C3-5, (alquileno C2-4)-N(R9)-(alquileno C2-4), entre otros; R7, R8 y R9 son cada uno independientemente hidrogeno o alquilo C1-4; X1 es C-R´o N, en el que R´ es hidrogeno o halogeno; X2 es CH o N y X3 es N-R´´, en el que R´´ es hidrogeno o alquilo C1-4. Estos compuestos tienen actividad bloqueante de canales de ion sodio. Tambien se refiere a una composicion farmaceutica que contiene dicho compuesto, la cual se utiliza en la prevencion o tratamiento de enfermedades relacionadas con bloqueantes de canales de sodio como, dolor agudo, dolor cronico, migrana, dolor neuropatico, artralgia, entre otros.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20150159637 | 2015-11-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20181301A1 true PE20181301A1 (es) | 2018-08-09 |
Family
ID=58695815
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2018000765A PE20181301A1 (es) | 2015-11-13 | 2016-11-11 | Bloqueador del canal de sodio |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US10227338B2 (es) |
| EP (1) | EP3375782B1 (es) |
| JP (1) | JP6559894B2 (es) |
| KR (1) | KR102245930B1 (es) |
| CN (1) | CN108349963B (es) |
| AU (1) | AU2016351526B2 (es) |
| BR (1) | BR112018009754B1 (es) |
| CA (1) | CA3003119C (es) |
| CL (1) | CL2018001281A1 (es) |
| CO (1) | CO2018005064A2 (es) |
| EC (1) | ECSP18038014A (es) |
| ES (1) | ES2821962T3 (es) |
| HK (1) | HK1251229A1 (es) |
| HR (1) | HRP20201695T1 (es) |
| HU (1) | HUE052569T2 (es) |
| MA (1) | MA43231B1 (es) |
| MX (1) | MX2018005940A (es) |
| MY (1) | MY194015A (es) |
| NZ (1) | NZ742069A (es) |
| PE (1) | PE20181301A1 (es) |
| PH (1) | PH12018500999A1 (es) |
| PL (1) | PL3375782T3 (es) |
| PT (1) | PT3375782T (es) |
| RS (1) | RS60927B1 (es) |
| RU (1) | RU2705578C1 (es) |
| SA (1) | SA518391540B1 (es) |
| SG (1) | SG11201803867TA (es) |
| SI (1) | SI3375782T1 (es) |
| TN (1) | TN2018000157A1 (es) |
| WO (1) | WO2017082688A1 (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20190078587A (ko) * | 2016-10-17 | 2019-07-04 | 제넨테크, 인크. | 치료 화합물 및 그의 사용 방법 |
| CN110885319B (zh) * | 2018-09-10 | 2022-08-12 | 成都康弘药业集团股份有限公司 | 作为钠通道阻滞剂的磺酰胺类化合物及其用途 |
| CN112759559B (zh) * | 2019-11-06 | 2022-08-12 | 成都康弘药业集团股份有限公司 | 作为钠通道阻滞剂的磺酰胺类化合物及其用途 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5591761A (en) * | 1993-05-20 | 1997-01-07 | Texas Biotechnology Corporation | Thiophenyl-, furyl-and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin |
| US5464853A (en) | 1993-05-20 | 1995-11-07 | Immunopharmaceutics, Inc. | N-(5-isoxazolyl)biphenylsulfonamides, N-(3-isoxazolyl)biphenylsulfonamides and derivatives thereof that modulate the activity of endothelin |
| KR100886854B1 (ko) * | 2001-03-12 | 2009-03-05 | 오노 야꾸힝 고교 가부시키가이샤 | Ｎ-페닐아릴설폰아미드 화합물, 이 화합물을 유효성분으로서 함유하는 약제, 이 화합물의 합성 중간체 및이의 제조 방법 |
| JP2006290791A (ja) * | 2005-04-11 | 2006-10-26 | Astellas Pharma Inc | アゾール置換スルホニルベンゼン誘導体 |
| EP1901747A2 (en) * | 2005-05-25 | 2008-03-26 | Ingenium Pharmaceuticals AG | Pyrimidine-based cdk inhibitors for treating pain |
| CA2652669A1 (en) | 2006-06-09 | 2007-12-21 | Merck & Co., Inc. | Benzazepinones as sodium channel blockers |
| US9422235B2 (en) * | 2006-12-19 | 2016-08-23 | Pharmos Corporation | Sulfonamide derivatives with therapeutic indications |
| SA08290245B1 (ar) | 2007-04-23 | 2012-02-12 | استرازينيكا ايه بي | مشتقات كربو كساميد جديدة من -n (8-اريل رباعي هيدرو نفثالين غير متجانس- 2- يل) أو -n (5-اريل كرومان غير متجانس -3-يل) لعلاج الألم |
| JP2008290791A (ja) * | 2007-05-22 | 2008-12-04 | Funai Electric Co Ltd | 画像形成装置 |
| US8124610B2 (en) * | 2007-07-13 | 2012-02-28 | Icagen Inc. | Sodium channel inhibitors |
| BRPI1006128A2 (pt) * | 2009-01-12 | 2016-11-01 | Cagen Inc | derivados de sulfonamida |
| JP2013532184A (ja) * | 2010-07-12 | 2013-08-15 | ファイザー・リミテッド | 電位開口型ナトリウムチャネル阻害剤として有用なｎ−スルホニルベンズアミド誘導体 |
| CN104093716B (zh) * | 2011-10-31 | 2017-06-23 | 克赛农制药股份有限公司 | 联芳醚磺酰胺化合物及其作为治疗剂的用途 |
| WO2013086229A1 (en) | 2011-12-07 | 2013-06-13 | Amgen Inc. | Bicyclic aryl and heteroaryl sodium channel inhibitors |
| EP2791108B1 (en) | 2011-12-15 | 2016-07-27 | Pfizer Limited | Sulfonamide derivatives |
| WO2013093688A1 (en) | 2011-12-19 | 2013-06-27 | Pfizer Limited | Sulfonamide derivatives and use thereof as vgsc inhibitors |
| EA026393B1 (ru) | 2012-05-22 | 2017-04-28 | Дженентек, Инк. | N-замещенные бензамиды и их применение в лечении боли |
| AU2013332648B2 (en) * | 2012-10-15 | 2017-09-07 | In Therapeutics | Sodium channel blockers, preparation method thereof and use thereof |
| WO2015130957A1 (en) * | 2014-02-27 | 2015-09-03 | Zalicus Pharmaceuticals, Ltd. | Heterocyclic inhibitors of the sodium channel |
-
2016
- 2016-11-11 MY MYPI2018000662A patent/MY194015A/en unknown
- 2016-11-11 KR KR1020160150511A patent/KR102245930B1/ko active IP Right Grant
- 2016-11-11 TN TNP/2018/000157A patent/TN2018000157A1/en unknown
- 2016-11-11 PE PE2018000765A patent/PE20181301A1/es unknown
- 2016-11-11 US US15/771,775 patent/US10227338B2/en active Active
- 2016-11-11 WO PCT/KR2016/013029 patent/WO2017082688A1/ko active Application Filing
- 2016-11-11 PL PL16864614.9T patent/PL3375782T3/pl unknown
- 2016-11-11 MA MA43231A patent/MA43231B1/fr unknown
- 2016-11-11 NZ NZ742069A patent/NZ742069A/en unknown
- 2016-11-11 JP JP2018524451A patent/JP6559894B2/ja active Active
- 2016-11-11 MX MX2018005940A patent/MX2018005940A/es active IP Right Grant
- 2016-11-11 CN CN201680066269.7A patent/CN108349963B/zh active Active
- 2016-11-11 SG SG11201803867TA patent/SG11201803867TA/en unknown
- 2016-11-11 BR BR112018009754-3A patent/BR112018009754B1/pt active IP Right Grant
- 2016-11-11 SI SI201630902T patent/SI3375782T1/sl unknown
- 2016-11-11 RU RU2018119954A patent/RU2705578C1/ru active
- 2016-11-11 HU HUE16864614A patent/HUE052569T2/hu unknown
- 2016-11-11 RS RS20201235A patent/RS60927B1/sr unknown
- 2016-11-11 ES ES16864614T patent/ES2821962T3/es active Active
- 2016-11-11 AU AU2016351526A patent/AU2016351526B2/en active Active
- 2016-11-11 EP EP16864614.9A patent/EP3375782B1/en active Active
- 2016-11-11 PT PT168646149T patent/PT3375782T/pt unknown
- 2016-11-11 CA CA3003119A patent/CA3003119C/en active Active
-
2018
- 2018-05-08 PH PH12018500999A patent/PH12018500999A1/en unknown
- 2018-05-09 SA SA518391540A patent/SA518391540B1/ar unknown
- 2018-05-10 CL CL2018001281A patent/CL2018001281A1/es unknown
- 2018-05-11 CO CONC2018/0005064A patent/CO2018005064A2/es unknown
- 2018-05-18 EC ECIEPI201838014A patent/ECSP18038014A/es unknown
- 2018-08-17 HK HK18110615.4A patent/HK1251229A1/zh unknown
-
2020
- 2020-10-20 HR HRP20201695TT patent/HRP20201695T1/hr unknown
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