PE20120126A1 - Nuevas bencenosulfonamidas como bloqueadores de canales de calcio - Google Patents
Nuevas bencenosulfonamidas como bloqueadores de canales de calcioInfo
- Publication number
- PE20120126A1 PE20120126A1 PE2011001348A PE2011001348A PE20120126A1 PE 20120126 A1 PE20120126 A1 PE 20120126A1 PE 2011001348 A PE2011001348 A PE 2011001348A PE 2011001348 A PE2011001348 A PE 2011001348A PE 20120126 A1 PE20120126 A1 PE 20120126A1
- Authority
- PE
- Peru
- Prior art keywords
- benzenosulphonamides
- calcium channel
- channel blockers
- benzenosulfonamide
- ylcarbonyl
- Prior art date
Links
- 229940127291 Calcium channel antagonist Drugs 0.000 title abstract 2
- 239000000480 calcium channel blocker Substances 0.000 title abstract 2
- -1 PYRROLIDINYL Chemical class 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 208000019901 Anxiety disease Diseases 0.000 abstract 1
- WZKSXHQDXQKIQJ-UHFFFAOYSA-N F[C](F)F Chemical group F[C](F)F WZKSXHQDXQKIQJ-UHFFFAOYSA-N 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 230000036506 anxiety Effects 0.000 abstract 1
- 206010015037 epilepsy Diseases 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
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- A61P13/00—Drugs for disorders of the urinary system
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P13/10—Drugs for disorders of the urinary system of the bladder
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
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- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Cardiology (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Urology & Nephrology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Reproductive Health (AREA)
- Endocrinology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Gynecology & Obstetrics (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Pregnancy & Childbirth (AREA)
- Vascular Medicine (AREA)
- Psychology (AREA)
- Immunology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE BENCENOSULFONAMIDAS DE FORMULAS (I) Y (II) DONDE R1 Y R2 SON CADA UNO X E Y, EN DONDE X ES UN COMPUESTO DE FORMULA (i) O (ii) DONDE m Y n SON CADA UNO 1 O 2; G1 ES AZETIDINILO, PIRROLIDINILO, MORFOLINILO, ENTRE OTROS; Y ES NRcAr1, NRcCH(Ar1)2, ENTRE OTROS, EN DONDE Ar1 ES ARILO O HETEROARILO OPCIONALMENTE SUSTITUIDOS CON ALCOXI, ALQUILO, CN, ENTRE OTROS; Rc ES H O ALQUILO; R3, R4, R5 Y R6 SON CADA UNO H, ALCOXI, ALQUILO O HALOGENO. SON COMPUESTOS PREFERIDOS: 3-[(8aR)-HEXAHIDROPIRROLO[1,2-a]PIRAZIN-2(1H)-ILCARBONIL]-N-[4-(TRIFLUOROMETIL)FENIL]BENCENOSULFONAMIDA; N-(2-FLUOROFENIL)-3-[(8aR)-HEXAHIDROPIRROLO[1,2-a]PIRAZIN-2(1H)-ILCARBONIL]BENCENOSULFONAMIDA; N-(3-FLUOROFENIL)-3-[(8aS)-HEXAHIDROPIRROLO[1,2-a]PIRAZIN-2(1H)-ILCARBONIL]BENCENOSULFONAMIDA; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON BLOQUEADORES DE CANALES DE CALCIO SIENDO UTILES EN EL TRATAMIENTO DEL DOLOR, EPILEPSIA, DEPRESION, ANSIEDAD, MIGRANA
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14489909P | 2009-01-15 | 2009-01-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20120126A1 true PE20120126A1 (es) | 2012-03-18 |
Family
ID=41796157
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2011001348A PE20120126A1 (es) | 2009-01-15 | 2010-01-14 | Nuevas bencenosulfonamidas como bloqueadores de canales de calcio |
Country Status (22)
| Country | Link |
|---|---|
| US (3) | US8101614B2 (es) |
| EP (1) | EP2382191B1 (es) |
| JP (1) | JP5619773B2 (es) |
| KR (1) | KR20110110299A (es) |
| CN (1) | CN102282131B (es) |
| AR (1) | AR077440A1 (es) |
| AU (1) | AU2010204753A1 (es) |
| BR (1) | BRPI1005675A2 (es) |
| CA (1) | CA2747752A1 (es) |
| CL (1) | CL2011001714A1 (es) |
| CO (1) | CO6400194A2 (es) |
| DO (1) | DOP2011000217A (es) |
| ES (1) | ES2527467T3 (es) |
| IL (1) | IL213500A0 (es) |
| MX (1) | MX337190B (es) |
| PE (1) | PE20120126A1 (es) |
| RU (1) | RU2011134052A (es) |
| SG (1) | SG172308A1 (es) |
| TW (1) | TW201028421A (es) |
| UY (1) | UY32384A (es) |
| WO (1) | WO2010083264A1 (es) |
| ZA (1) | ZA201104715B (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2527589T3 (es) | 2008-04-24 | 2015-01-27 | Msd K.K. | Inhibidor de la enzima de elongación de ácidos grasos de cadena larga que comprende un derivado de arilsulfonilo como principio activo |
| TW201028421A (en) * | 2009-01-15 | 2010-08-01 | Abbott Lab | Novel benzenesulfonamides as calcium channel blockers |
| TWI464147B (zh) * | 2011-09-15 | 2014-12-11 | Univ Taipei Medical | 吲哚氫胺酸和吲哚啉氫胺酸於治療心臟衰竭或神經損傷的用途 |
| WO2013049174A1 (en) * | 2011-09-29 | 2013-04-04 | Abbvie Inc. | Substituted octahydropyrrolo[1,2-a]pyrazine sulfonamides as calcium channel blockers |
| WO2013049164A1 (en) | 2011-09-29 | 2013-04-04 | Abbvie Inc. | SUBSTITUTED OCTAHYDROPYRROLO[1,2-a]PYRAZINES AS CALCIUM CHANNEL BLOCKERS |
| US20130178477A1 (en) * | 2012-01-05 | 2013-07-11 | Abbvie Inc. | Methods of treating diabetic neuropathy using benzenesulfonamides |
| US9029361B2 (en) | 2012-12-12 | 2015-05-12 | Abbvie Inc. | Agents for treating pain and uses thereof |
| HK1224291A1 (zh) | 2013-09-10 | 2017-08-18 | Board Of Regents Of The University Of Texas System | 靶向截短的腺瘤性結腸息肉(apc)蛋白的治療法 |
| US9700549B2 (en) | 2013-10-03 | 2017-07-11 | David Wise | Compositions and methods for treating pelvic pain and other conditions |
| US10082496B2 (en) | 2014-09-10 | 2018-09-25 | Board Of Regents Of The University Of Texas System | Targeting emopamil binding protein (EBP) with small molecules that induce an abnormal feedback response by lowering endogenous cholesterol biosynthesis |
| ES2936400T3 (es) | 2015-10-22 | 2023-03-16 | Cavion Inc | Métodos para tratar el síndrome Angelman |
| EP3585376A4 (en) | 2017-02-15 | 2020-11-25 | Cavion, Inc. | CALCIUM CHANNELS INHIBITORS |
| SG10202111885PA (en) | 2017-04-26 | 2021-12-30 | Cavion Inc | Methods for improving memory and cognition and for treating memory and cognitive disorders |
| TWI823890B (zh) | 2018-01-10 | 2023-12-01 | 美商克拉治療有限責任公司 | 包含苯基磺醯胺之醫藥組合物及其治療應用 |
| JP7405834B2 (ja) | 2018-08-24 | 2023-12-26 | サンシャイン・レイク・ファーマ・カンパニー・リミテッド | ピリジニルメチレンピペリジン誘導体及びその使用 |
| AU2019355021B2 (en) | 2018-10-03 | 2024-09-12 | Cavion, Inc. | Treating essential tremor using (R)-2-(4-Isopropylphenyl)-N-(1-(5-(2,2,2-Trifluoroethoxy)pyridin-2-yl)ethyl)acetamide |
| US20200131156A1 (en) * | 2018-10-30 | 2020-04-30 | H. Lundbeck A/S | ARYLSULFONYLPYROLECARBOXAMIDE DERIVATIVES AS Kv3 POTASSIUM CHANNEL ACTIVATORS |
| CN114340670A (zh) | 2019-07-11 | 2022-04-12 | 普拉克西斯精密药物股份有限公司 | T-型钙通道调节剂的制剂及其使用方法 |
| CA3146157A1 (en) * | 2019-07-11 | 2021-01-14 | Cura Therapeutics, Llc | Sulfone compounds and pharmaceutical compositions thereof, and their therapeutic applications for the treatment of neurodegenerative diseases |
| CN117229257A (zh) * | 2022-06-06 | 2023-12-15 | 中国药科大学 | 间氨磺酰苯甲酰胺类化合物及制法、药物组合物和应用 |
| WO2025255502A1 (en) | 2024-06-07 | 2025-12-11 | Cavion, Inc. | PYRIDYL AMIDE Cav3 CHANNEL MODULATORS |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60011755T2 (de) | 1999-04-07 | 2005-06-30 | The University Of Virginia Patent Foundation | Calciumkanalblocker als antikrebsmittel |
| TW200503994A (en) * | 2003-01-24 | 2005-02-01 | Novartis Ag | Organic compounds |
| US7223754B2 (en) | 2003-03-10 | 2007-05-29 | Dynogen Pharmaceuticals, Inc. | Thiazolidinone, oxazolidinone, and imidazolone derivatives for treating lower urinary tract and related disorders |
| ATE482747T1 (de) * | 2003-04-11 | 2010-10-15 | High Point Pharmaceuticals Llc | Neue amide derivate und deren pharmazeutische verwendungen |
| CA2527170A1 (en) * | 2003-04-15 | 2004-10-28 | Astrazeneca Ab | Therapeutic compounds |
| JP5140577B2 (ja) * | 2005-03-31 | 2013-02-06 | タケダ カリフォルニア インコーポレイテッド | ヒドロキシステロイドデヒドロゲナーゼ阻害剤 |
| WO2007052843A1 (ja) * | 2005-11-04 | 2007-05-10 | Takeda Pharmaceutical Company Limited | 複素環アミド化合物およびその用途 |
| WO2008043183A1 (en) * | 2006-10-13 | 2008-04-17 | Neuromed Pharmaceuticals Ltd. | Cyclopropyl-piperazine compounds as calcium channel blockers |
| JP5622568B2 (ja) * | 2007-06-03 | 2014-11-12 | バンダービルト ユニバーシティ | ベンズアミドmGluR5の正のアロステリック調節因子ならびにその作製および使用方法 |
| ES2527589T3 (es) | 2008-04-24 | 2015-01-27 | Msd K.K. | Inhibidor de la enzima de elongación de ácidos grasos de cadena larga que comprende un derivado de arilsulfonilo como principio activo |
| TW201028421A (en) * | 2009-01-15 | 2010-08-01 | Abbott Lab | Novel benzenesulfonamides as calcium channel blockers |
-
2009
- 2009-12-31 TW TW098146447A patent/TW201028421A/zh unknown
-
2010
- 2010-01-14 EP EP10701070.4A patent/EP2382191B1/en active Active
- 2010-01-14 RU RU2011134052/04A patent/RU2011134052A/ru not_active Application Discontinuation
- 2010-01-14 AU AU2010204753A patent/AU2010204753A1/en not_active Abandoned
- 2010-01-14 WO PCT/US2010/020964 patent/WO2010083264A1/en not_active Ceased
- 2010-01-14 US US12/687,465 patent/US8101614B2/en not_active Expired - Fee Related
- 2010-01-14 PE PE2011001348A patent/PE20120126A1/es not_active Application Discontinuation
- 2010-01-14 BR BRPI1005675A patent/BRPI1005675A2/pt not_active IP Right Cessation
- 2010-01-14 ES ES10701070.4T patent/ES2527467T3/es active Active
- 2010-01-14 MX MX2011007496A patent/MX337190B/es active IP Right Grant
- 2010-01-14 CN CN201080004675.3A patent/CN102282131B/zh not_active Expired - Fee Related
- 2010-01-14 JP JP2011546319A patent/JP5619773B2/ja not_active Expired - Fee Related
- 2010-01-14 SG SG2011045564A patent/SG172308A1/en unknown
- 2010-01-14 CA CA2747752A patent/CA2747752A1/en active Pending
- 2010-01-14 KR KR1020117018567A patent/KR20110110299A/ko not_active Withdrawn
- 2010-01-15 UY UY0001032384A patent/UY32384A/es not_active Application Discontinuation
- 2010-01-15 AR ARP100100091A patent/AR077440A1/es not_active Application Discontinuation
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2011
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- 2011-06-24 ZA ZA2011/04715A patent/ZA201104715B/en unknown
- 2011-07-07 DO DO2011000217A patent/DOP2011000217A/es unknown
- 2011-07-14 CL CL2011001714A patent/CL2011001714A1/es unknown
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2013
- 2013-02-04 US US13/758,615 patent/US8741899B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| KR20110110299A (ko) | 2011-10-06 |
| AR077440A1 (es) | 2011-08-31 |
| EP2382191A1 (en) | 2011-11-02 |
| US20100197693A1 (en) | 2010-08-05 |
| DOP2011000217A (es) | 2011-07-31 |
| TW201028421A (en) | 2010-08-01 |
| US8404719B2 (en) | 2013-03-26 |
| JP2012515209A (ja) | 2012-07-05 |
| MX2011007496A (es) | 2011-08-04 |
| CO6400194A2 (es) | 2012-03-15 |
| SG172308A1 (en) | 2011-07-28 |
| US8741899B2 (en) | 2014-06-03 |
| ES2527467T3 (es) | 2015-01-26 |
| IL213500A0 (en) | 2011-07-31 |
| JP5619773B2 (ja) | 2014-11-05 |
| US20120083499A1 (en) | 2012-04-05 |
| CN102282131A (zh) | 2011-12-14 |
| RU2011134052A (ru) | 2013-02-20 |
| BRPI1005675A2 (pt) | 2017-06-13 |
| AU2010204753A1 (en) | 2011-08-11 |
| US8101614B2 (en) | 2012-01-24 |
| CN102282131B (zh) | 2015-08-26 |
| EP2382191B1 (en) | 2014-11-12 |
| CA2747752A1 (en) | 2010-07-22 |
| US20130210827A1 (en) | 2013-08-15 |
| MX337190B (es) | 2016-02-16 |
| UY32384A (es) | 2010-08-31 |
| ZA201104715B (en) | 2014-01-29 |
| WO2010083264A1 (en) | 2010-07-22 |
| CL2011001714A1 (es) | 2011-11-11 |
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