WO2012017166A3 - Traitement d'une pathologie liee a un effet excessif du tnf par un compose de benzene sulfonamide - Google Patents
Traitement d'une pathologie liee a un effet excessif du tnf par un compose de benzene sulfonamide Download PDFInfo
- Publication number
- WO2012017166A3 WO2012017166A3 PCT/FR2011/051742 FR2011051742W WO2012017166A3 WO 2012017166 A3 WO2012017166 A3 WO 2012017166A3 FR 2011051742 W FR2011051742 W FR 2011051742W WO 2012017166 A3 WO2012017166 A3 WO 2012017166A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- tnf
- pathological condition
- benzenesulfonamide
- compound treatment
- excessive effect
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
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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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—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
- 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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- A—HUMAN NECESSITIES
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
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- A—HUMAN NECESSITIES
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- 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
- A61K31/403—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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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/502—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
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- 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
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- 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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- C07D207/36—Oxygen or sulfur atoms
- C07D207/38—2-Pyrrolones
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- C07D237/30—Phthalazines
- C07D237/34—Phthalazines with nitrogen atoms directly attached to carbon atoms of the nitrogen-containing ring, e.g. hydrazine radicals
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- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
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- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring 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 atoms of the carbocyclic ring
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- Animal Behavior & Ethology (AREA)
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Abstract
ou l'un de ses sels d'addition avec les acides pharmaceutiquement acceptables, pour son utilisation dans une méthode de traitement d'une pathologie lie un effet excessif du TNF-alpha et pour son utilisation dans une méthode de traitement du corps humain ou animal comme inhibiteur direct du TNF alpha.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/811,144 US8975399B2 (en) | 2010-07-19 | 2011-07-19 | Benzenesulfon amide-compound treatment of a pathological condition linked to an excessive effect of TNF |
| EP11754705.9A EP2595620A2 (fr) | 2010-07-19 | 2011-07-19 | Traitement d'une pathologie liee a un effet excessif du tnf par un compose de benzene sulfonamide |
| CA2805206A CA2805206A1 (fr) | 2010-07-19 | 2011-07-19 | Traitement d'une pathologie liee a un effet excessif du tnf par un compose de benzene sulfonamide |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1055867 | 2010-07-19 | ||
| FR1055867A FR2962649B1 (fr) | 2010-07-19 | 2010-07-19 | Traitement d'une pathologie liee a un effet excessif du tnf par un compose de benzene sulfonamide |
| US201161443132P | 2011-02-15 | 2011-02-15 | |
| US61/443,132 | 2011-02-15 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2012017166A2 WO2012017166A2 (fr) | 2012-02-09 |
| WO2012017166A3 true WO2012017166A3 (fr) | 2012-07-19 |
Family
ID=43566620
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/FR2011/051742 Ceased WO2012017166A2 (fr) | 2010-07-19 | 2011-07-19 | Traitement d'une pathologie liee a un effet excessif du tnf par un compose de benzene sulfonamide |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8975399B2 (fr) |
| EP (1) | EP2595620A2 (fr) |
| CA (1) | CA2805206A1 (fr) |
| FR (1) | FR2962649B1 (fr) |
| WO (1) | WO2012017166A2 (fr) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2011302295B2 (en) * | 2010-09-13 | 2015-08-20 | Microbiotix, Inc. | Inhibitors of viral entry into mammalian cells |
| PT3021839T (pt) * | 2013-07-18 | 2021-07-30 | Baylor College Medicine | Composições para o tratamento da fibrose |
| WO2015010107A1 (fr) * | 2013-07-18 | 2015-01-22 | Baylor College Of Medicine | Méthodes et compositions de traitement de l'atrophie musculaire, de la faiblesse musculaire, et/ou de la cachexie |
| DK3021840T3 (da) * | 2013-07-18 | 2020-06-15 | Baylor College Medicine | Sammensætninger til forebyggelse af allergenreaktion |
| US10301258B2 (en) | 2014-02-26 | 2019-05-28 | Howard University | Benzende sulfonamide derivatives as HIV integrase inhibitors |
| JP2017534627A (ja) | 2014-11-06 | 2017-11-24 | ノースウエスタン ユニバーシティNorthwestern University | 癌細胞運動性の阻害 |
| US10975051B2 (en) | 2015-08-12 | 2021-04-13 | Memorial Sloan Kettering Cancer Center | Phenylsulfonamido-benzofuran derivatives and uses thereof in the treatment of proliferative diseases |
| CN105085450A (zh) * | 2015-09-14 | 2015-11-25 | 中国药科大学 | 苯并呋喃类衍生物、其制备方法及其治疗作用 |
| CN109803951B (zh) * | 2016-11-08 | 2020-12-04 | 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 |
| US10494334B2 (en) * | 2018-03-28 | 2019-12-03 | Academia Sinica | Compounds to inhibit calcium/calmodulin dependent protein kinase II and applications thereof |
| CN112367984B (zh) | 2018-04-19 | 2024-05-10 | 特维迪疗法公司 | Stat3抑制剂 |
| US11026905B2 (en) | 2018-04-19 | 2021-06-08 | Tvardi Therapeutics, Inc. | STAT3 inhibitors |
| CN111067889B (zh) * | 2019-11-15 | 2022-11-18 | 徐州医科大学 | 2-甲基萘并[1,2-b]呋喃类化合物在制备与糖尿病肾病有关药物方面的应用 |
| CN113004222B (zh) | 2019-12-19 | 2022-11-18 | 复旦大学 | 一种氨基二硫代过酸硫酯类化合物及其制备方法和应用 |
| MX2022008914A (es) | 2020-01-24 | 2022-08-16 | Tvardi Therapeutics Inc | Compuestos terapeuticos, formulaciones y usos de los mismos. |
| WO2021150912A1 (fr) * | 2020-01-24 | 2021-07-29 | Tvardi Therapeutics, Inc. | Composés thérapeutiques, formulations et leurs utilisations |
| WO2022243574A1 (fr) | 2021-05-21 | 2022-11-24 | Cemm - Forschungszentrum Für Molekulare Medizin Gmbh | Inhibiteurs de slc16a3 à base de 3-(phtalazin-1-yl) benzènesulfonamide et leur utilisation thérapeutique |
| JP2025520456A (ja) | 2022-06-15 | 2025-07-03 | トゥヴァルディ セラピューティクス,インク. | Stat3阻害剤のプロドラッグ |
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Also Published As
| Publication number | Publication date |
|---|---|
| CA2805206A1 (fr) | 2012-02-09 |
| FR2962649A1 (fr) | 2012-01-20 |
| US20130123266A1 (en) | 2013-05-16 |
| US8975399B2 (en) | 2015-03-10 |
| FR2962649B1 (fr) | 2025-10-24 |
| WO2012017166A2 (fr) | 2012-02-09 |
| EP2595620A2 (fr) | 2013-05-29 |
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