BRPI0716491A2 - Composto sulfonamida ou sal do mesmo 3/00 c07c 311/21 c07c 311/29 c07d 207/27 c07d 207/325 c07d 209/08 c07d 213/40 c07d 213/68 c07d 213/70 c07d 213/79 c07d 213/89 c07d 215/12 c07d 217/06 c07d 231/12 c07d 237/08 c07d 239/26 c07d 241/12 c07d 249/08 c07d 263/32 c07d 263/58 c07d 277/20 c07d 277/28 c07d 277/36 c07d 295/12 c07d 307/52 c07d 307/81 c07d 333/20 c07d 333/34 c07d 333/38 c07d 333/40 c07d 333/58 c07k 7/00 - Google Patents
Composto sulfonamida ou sal do mesmo 3/00 c07c 311/21 c07c 311/29 c07d 207/27 c07d 207/325 c07d 209/08 c07d 213/40 c07d 213/68 c07d 213/70 c07d 213/79 c07d 213/89 c07d 215/12 c07d 217/06 c07d 231/12 c07d 237/08 c07d 239/26 c07d 241/12 c07d 249/08 c07d 263/32 c07d 263/58 c07d 277/20 c07d 277/28 c07d 277/36 c07d 295/12 c07d 307/52 c07d 307/81 c07d 333/20 c07d 333/34 c07d 333/38 c07d 333/40 c07d 333/58 c07k 7/00Info
- Publication number
- BRPI0716491A2 BRPI0716491A2 BRPI0716491-2A2A BRPI0716491A BRPI0716491A2 BR PI0716491 A2 BRPI0716491 A2 BR PI0716491A2 BR PI0716491 A BRPI0716491 A BR PI0716491A BR PI0716491 A2 BRPI0716491 A2 BR PI0716491A2
- Authority
- BR
- Brazil
- Prior art keywords
- salt
- same
- sulfonamide compound
- sulfonamide
- compound
- Prior art date
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Classifications
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
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- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
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- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
- A61K31/198—Alpha-aminoacids, e.g. alanine, edetic acids [EDTA]
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- A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
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- A61K31/235—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group
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- A61K31/24—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group having an amino or nitro group
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- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
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- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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- A61K31/4015—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 having oxo groups directly attached to the heterocyclic ring, e.g. piracetam, ethosuximide
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- A61K31/403—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 condensed with carbocyclic rings, e.g. carbazole
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- 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)
- Peptides Or Proteins (AREA)
- Pyrane Compounds (AREA)
- Pyrrole Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006218923 | 2006-08-10 | ||
PCT/JP2007/065613 WO2008018544A1 (fr) | 2006-08-10 | 2007-08-09 | Composé de sulfonamide ou son sel |
Publications (1)
Publication Number | Publication Date |
---|---|
BRPI0716491A2 true BRPI0716491A2 (pt) | 2014-03-11 |
Family
ID=39033073
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0716491-2A2A BRPI0716491A2 (pt) | 2006-08-10 | 2007-08-09 | Composto sulfonamida ou sal do mesmo 3/00 c07c 311/21 c07c 311/29 c07d 207/27 c07d 207/325 c07d 209/08 c07d 213/40 c07d 213/68 c07d 213/70 c07d 213/79 c07d 213/89 c07d 215/12 c07d 217/06 c07d 231/12 c07d 237/08 c07d 239/26 c07d 241/12 c07d 249/08 c07d 263/32 c07d 263/58 c07d 277/20 c07d 277/28 c07d 277/36 c07d 295/12 c07d 307/52 c07d 307/81 c07d 333/20 c07d 333/34 c07d 333/38 c07d 333/40 c07d 333/58 c07k 7/00 |
Country Status (18)
Country | Link |
---|---|
US (1) | US7973078B2 (pt) |
EP (1) | EP2050446B1 (pt) |
JP (1) | JP5029970B2 (pt) |
KR (1) | KR101352217B1 (pt) |
CN (1) | CN101500554B (pt) |
AU (1) | AU2007282465C1 (pt) |
BR (1) | BRPI0716491A2 (pt) |
CA (1) | CA2660424C (pt) |
ES (1) | ES2467097T3 (pt) |
IL (1) | IL196656A (pt) |
MX (1) | MX2009001512A (pt) |
NO (1) | NO20091058L (pt) |
PL (1) | PL2050446T3 (pt) |
PT (1) | PT2050446E (pt) |
RU (1) | RU2425029C2 (pt) |
TW (1) | TW200817319A (pt) |
WO (1) | WO2008018544A1 (pt) |
ZA (1) | ZA200900549B (pt) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008099907A1 (ja) * | 2007-02-16 | 2008-08-21 | Ono Pharmaceutical Co., Ltd. | 尿排出障害治療剤 |
EP2280601A4 (en) * | 2008-02-21 | 2012-08-29 | Sequoia Pharmaceuticals Inc | AMINO ACID HEMMER OF CYTOCHROM P450 |
CA2797694A1 (en) | 2010-04-29 | 2011-11-03 | The United States Of America, As Represented By The Secretary, Departmen T Of Health And Human Services | Activators of human pyruvate kinase |
US9657013B2 (en) | 2012-02-29 | 2017-05-23 | Baruch S. Blumberg Institute | Inhibitors of hepatitis B virus covalently closed circular DNA formation and their method of use |
WO2014049047A1 (en) | 2012-09-27 | 2014-04-03 | F. Hoffmann-La Roche Ag | Substituted sulfonamide compounds |
US9624208B2 (en) | 2012-10-26 | 2017-04-18 | Merck Sharp & Dohme Corp. | Benzoxazolinone compounds with selective activity in voltage-gated sodium channels |
EP2774919A1 (en) * | 2013-03-06 | 2014-09-10 | Pharmeste S.R.L. In Liquidazione | Novel sulfonamide TRPA1 receptor antagonists |
WO2018086530A1 (zh) * | 2016-11-08 | 2018-05-17 | 正大天晴药业集团股份有限公司 | 作为cccDNA抑制剂的磺酰胺类化合物 |
WO2020199683A1 (zh) * | 2019-04-04 | 2020-10-08 | 上海海雁医药科技有限公司 | 氮杂环取代的磺酰基苯甲酰胺衍生物、其制法与医药上的用途 |
CN110698420B (zh) * | 2019-10-25 | 2022-10-14 | 上海阿拉丁生化科技股份有限公司 | 一种2-噁唑甲胺杂环化合物的制备方法 |
Family Cites Families (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU715604B2 (en) | 1996-04-03 | 2000-02-03 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
TW523506B (en) | 1996-12-18 | 2003-03-11 | Ono Pharmaceutical Co | Sulfonamide or carbamide derivatives and drugs containing the same as active ingredients |
ZA984040B (en) * | 1997-05-15 | 1998-11-20 | Ono Pharmaceutical Co | Benzenesulfonamide compounds |
US6211197B1 (en) * | 1998-10-07 | 2001-04-03 | Merck Frosst Canada & Co. | Prostaglandin receptor ligands |
AU1707700A (en) | 1998-10-29 | 2000-05-22 | Bristol-Myers Squibb Company | Novel inhibitors of impdh enzyme |
AU773273B2 (en) | 1999-02-26 | 2004-05-20 | Bristol-Myers Squibb Company | Novel sulfonamide compounds and uses thereof |
AU4431400A (en) | 1999-05-12 | 2000-12-05 | Japan As Represented By President Of National Cancer Center | Anticancer agents containing ep1 antagonists as the active ingredient |
EP1196386A2 (en) | 1999-07-06 | 2002-04-17 | Vertex Pharmaceuticals Incorporated | N-substituted glycine derivatives |
CZ2002518A3 (cs) | 1999-08-13 | 2002-05-15 | Biogen, Inc. | Inhibitory buněčné adheze a farmaceutické prostředky, které je obsahují |
AU2001288623A1 (en) | 2000-09-05 | 2002-03-22 | Tularik, Inc. | Fxr modulators |
DE60141849D1 (de) | 2000-10-17 | 2010-05-27 | Merck Serono Sa Coinsins | Pharmazeutisch aktive sulfonamid-derivate |
MXPA03008134A (es) | 2001-03-12 | 2004-03-10 | Ono Pharmaceutical Co | Compuesto de n-fenilarilsulfonamida, medicamento que contiene el compuesto como ingrediente activo, intermediario para el compuesto y procedimientos para su produccion. |
SE0100873D0 (sv) * | 2001-03-13 | 2001-03-13 | Astrazeneca Ab | Method of treatment |
KR20030081520A (ko) * | 2001-03-14 | 2003-10-17 | 오노 야꾸힝 고교 가부시키가이샤 | Ep1 안타고니스트를 유효 성분으로서 함유하는 울병의치료제 |
EP1447096A1 (en) | 2001-11-19 | 2004-08-18 | Ono Pharmaceutical Co., Ltd. | Remedies for urinary frequency |
WO2004033418A2 (en) | 2002-10-11 | 2004-04-22 | Actelion Pharmaceuticals Ltd. | Sulfonylamino-acetic derivatives and their use as orexin receptor antagonists |
US20050020646A1 (en) | 2003-06-25 | 2005-01-27 | Pfizer Inc. | Treatment of BPH |
EP1642594A1 (en) | 2003-06-27 | 2006-04-05 | Ono Pharmaceutical Co., Ltd. | Remedy for urinary tract diseases |
JP2005206492A (ja) | 2004-01-21 | 2005-08-04 | Sankyo Co Ltd | スルホンアミド化合物 |
US7504431B2 (en) | 2004-04-16 | 2009-03-17 | Bristol-Myers Squibb Company | Sulfonyl amide inhibitors of calcium channel function |
DE102005013967A1 (de) | 2004-11-05 | 2006-10-05 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Bradykinin-B1-Antagonisten, Verfahren zu deren Herstellung sowie deren Verwendung als Arzneimittel |
-
2007
- 2007-08-07 TW TW096129052A patent/TW200817319A/zh unknown
- 2007-08-09 CN CN2007800297302A patent/CN101500554B/zh not_active Expired - Fee Related
- 2007-08-09 ZA ZA200900549A patent/ZA200900549B/xx unknown
- 2007-08-09 KR KR1020087031380A patent/KR101352217B1/ko not_active IP Right Cessation
- 2007-08-09 AU AU2007282465A patent/AU2007282465C1/en not_active Ceased
- 2007-08-09 ES ES07792264.9T patent/ES2467097T3/es active Active
- 2007-08-09 BR BRPI0716491-2A2A patent/BRPI0716491A2/pt not_active IP Right Cessation
- 2007-08-09 EP EP07792264.9A patent/EP2050446B1/en active Active
- 2007-08-09 CA CA2660424A patent/CA2660424C/en not_active Expired - Fee Related
- 2007-08-09 RU RU2009108275/04A patent/RU2425029C2/ru not_active IP Right Cessation
- 2007-08-09 PL PL07792264T patent/PL2050446T3/pl unknown
- 2007-08-09 JP JP2008528874A patent/JP5029970B2/ja not_active Expired - Fee Related
- 2007-08-09 WO PCT/JP2007/065613 patent/WO2008018544A1/ja active Application Filing
- 2007-08-09 US US12/297,445 patent/US7973078B2/en not_active Expired - Fee Related
- 2007-08-09 MX MX2009001512A patent/MX2009001512A/es active IP Right Grant
- 2007-08-09 PT PT77922649T patent/PT2050446E/pt unknown
-
2009
- 2009-01-22 IL IL196656A patent/IL196656A/en not_active IP Right Cessation
- 2009-03-09 NO NO20091058A patent/NO20091058L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CA2660424C (en) | 2014-01-07 |
CN101500554B (zh) | 2012-06-27 |
JPWO2008018544A1 (ja) | 2010-01-07 |
ES2467097T3 (es) | 2014-06-11 |
NO20091058L (no) | 2009-04-24 |
CN101500554A (zh) | 2009-08-05 |
KR20090048401A (ko) | 2009-05-13 |
US7973078B2 (en) | 2011-07-05 |
MX2009001512A (es) | 2009-02-18 |
WO2008018544A1 (fr) | 2008-02-14 |
TW200817319A (en) | 2008-04-16 |
KR101352217B1 (ko) | 2014-01-15 |
JP5029970B2 (ja) | 2012-09-19 |
EP2050446A1 (en) | 2009-04-22 |
EP2050446A4 (en) | 2011-02-16 |
ZA200900549B (en) | 2010-03-31 |
PT2050446E (pt) | 2014-07-18 |
IL196656A (en) | 2013-11-28 |
EP2050446B1 (en) | 2014-05-07 |
US20090312328A1 (en) | 2009-12-17 |
AU2007282465B2 (en) | 2011-12-01 |
PL2050446T3 (pl) | 2014-10-31 |
CA2660424A1 (en) | 2008-02-14 |
AU2007282465C1 (en) | 2012-05-10 |
RU2009108275A (ru) | 2010-09-20 |
RU2425029C2 (ru) | 2011-07-27 |
IL196656A0 (en) | 2009-11-18 |
AU2007282465A1 (en) | 2008-02-14 |
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