ECSP066695A - Derivados de n-(1,5-difenil-1h-pirazol-3-il) sulfonamida con afinidad por los receptores cb1 - Google Patents
Derivados de n-(1,5-difenil-1h-pirazol-3-il) sulfonamida con afinidad por los receptores cb1Info
- Publication number
- ECSP066695A ECSP066695A EC2006006695A ECSP066695A ECSP066695A EC SP066695 A ECSP066695 A EC SP066695A EC 2006006695 A EC2006006695 A EC 2006006695A EC SP066695 A ECSP066695 A EC SP066695A EC SP066695 A ECSP066695 A EC SP066695A
- Authority
- EC
- Ecuador
- Prior art keywords
- alkyl
- unsubstituted
- halogen atom
- group
- alkoxy
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- 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
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- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole 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
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- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Addiction (AREA)
- Rheumatology (AREA)
- Obesity (AREA)
- Urology & Nephrology (AREA)
- Pulmonology (AREA)
- Ophthalmology & Optometry (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Transplantation (AREA)
- Virology (AREA)
Abstract
Compuesto que responde a la fórmula (I):en la que - R1 representa" alquilo(C1-C6);" cicloalquilo(C3-C7) no sustituido o sustituido una o varias veces con un grupo alquilo (C1-C3);" cicloalquilmetilo(C3-C7) no sustituido o sustituido una o varias veces en el carbociclo con alquilo(C1-C3);" fenilo no sustituido o mono, di o trisustituido con un sustituyente elegido de manera independiente entre un átomo de halógeno, alquilo(C1-C4), alcoxi(C1-C3), ciano, radical trifluorometilo, radical trifluorometoxi, grupo S(O)nAlk, grupo alquilcarbonilo(C1-C3) o fenilo;" bencilo no sustituido o mono o disustituido con un sustituyente elegido de manera independiente entre un átomo de halógeno, alquilo(C1-C3), alcoxi(C1-C3) o radical trifluorometilo;" tienilo no sustituido o sustituido con un átomo de halógeno o con un isoxazolilo;- R2 representa un átomo de hidrógeno o alquilo(C1-C3);- R3 representa un átomo de hidrógeno o alquilo(C1-C5);- R4, R5, R6, R7, R8 y R9 representan cada uno de manera independiente un átomo de hidrógeno, átomo de halógeno, alquilo(C1-C7), alcoxi(C1-C5), radical trifluorometilo o grupo S(O)nAlk;- n representa 0, 1 ó 2;- Alk representa alquilo(C1-C4).en forma de base o de sal de adición de ácido, así como en forma de hidrato o solvato.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0400257A FR2864958B1 (fr) | 2004-01-12 | 2004-01-12 | Derive de n-[(1,5-diphenyl-1h-pyrazol-3-yl)methyl] sulfonamide, leur preparation et leur application en therapeutique. |
Publications (1)
Publication Number | Publication Date |
---|---|
ECSP066695A true ECSP066695A (es) | 2006-10-31 |
Family
ID=34684951
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EC2006006695A ECSP066695A (es) | 2004-01-12 | 2006-07-11 | Derivados de n-(1,5-difenil-1h-pirazol-3-il) sulfonamida con afinidad por los receptores cb1 |
Country Status (31)
Country | Link |
---|---|
US (1) | US7294645B2 (es) |
EP (1) | EP1720837B1 (es) |
JP (1) | JP4723514B2 (es) |
KR (1) | KR20060105050A (es) |
CN (1) | CN1910157A (es) |
AR (1) | AR047096A1 (es) |
AT (1) | ATE465995T1 (es) |
AU (1) | AU2005209441B2 (es) |
CA (1) | CA2551141C (es) |
CR (1) | CR8468A (es) |
CY (1) | CY1110651T1 (es) |
DE (1) | DE602005020907D1 (es) |
DK (1) | DK1720837T3 (es) |
EC (1) | ECSP066695A (es) |
ES (1) | ES2344850T3 (es) |
FR (1) | FR2864958B1 (es) |
HR (1) | HRP20100283T8 (es) |
IL (1) | IL176710A0 (es) |
MA (1) | MA28422B1 (es) |
NO (1) | NO20063621L (es) |
NZ (1) | NZ548442A (es) |
PL (1) | PL1720837T3 (es) |
PT (1) | PT1720837E (es) |
RS (1) | RS51365B (es) |
RU (1) | RU2366657C2 (es) |
SI (1) | SI1720837T1 (es) |
TN (1) | TNSN06203A1 (es) |
TW (1) | TWI323255B (es) |
UA (1) | UA85079C2 (es) |
WO (1) | WO2005073197A1 (es) |
ZA (1) | ZA200605657B (es) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7030141B2 (en) * | 2001-11-29 | 2006-04-18 | Christopher Franklin Bigge | Inhibitors of factor Xa and other serine proteases involved in the coagulation cascade |
FR2880023B1 (fr) * | 2004-12-23 | 2007-02-23 | Sanofi Aventis Sa | Derives de n-[(4,5-diphenyl-3-alkyl-2-thienyl) methyl] amine leur preparation et leur application en therapeutique |
FR2880890B1 (fr) * | 2005-01-19 | 2007-03-30 | Sanofi Aventis Sa | Derives de n-[(4,5-diphenyl-2-thienyl)methyl]sulfonamide, leur preparation et leur application en therapeutique |
FR2881744B1 (fr) | 2005-02-09 | 2007-04-27 | Sanofi Aventis Sa | Derives de n-[(4,5-diphenyl-2-thienyl)methyl]amine, leur preparation et leur application en therapeutique |
FR2894579B1 (fr) * | 2005-12-12 | 2008-01-18 | Sanofi Aventis Sa | Derives diaryltriazolmethylamine, leur preparation et leur application en therapeutique. |
FR2894578B1 (fr) | 2005-12-12 | 2008-02-01 | Sanofi Aventis Sa | Derives heterocycliques, leur preparation et leur application en therapeutique. |
EP1829867A1 (en) | 2006-03-03 | 2007-09-05 | Laboratorios Del Dr. Esteve, S.A. | Imidazole compounds having pharmaceutical activity towards the sigma receptor |
FR2899899A1 (fr) * | 2006-04-14 | 2007-10-19 | Sanofi Aventis Sa | Derives d'aminomethyl pyridine, leur preparation et leur application en therapeutique |
EP1878723B1 (fr) * | 2006-07-11 | 2010-05-26 | Sanofi-Aventis | Dérivés de N-[(1,5-diphényl-1H-pyrazol-3-yl)méthyl]sulfonamide antagonistes des récepteurs CB1 des cannabinoïdes |
US7297710B1 (en) * | 2006-07-12 | 2007-11-20 | Sanofi-Aventis | Derivatives of N-[(1,5-diphenyl-1H-pyrazol-3-yl)methyl]sulfonamide, their preparation and their application in therapeutics |
JP2008019205A (ja) * | 2006-07-12 | 2008-01-31 | Sanofi-Aventis | N−[(1,5−ジフェニル−1h−ピラゾール−3−イル)メチル]スルホンアミド誘導体、その調製法および治療におけるその応用 |
WO2008062424A2 (en) * | 2006-07-31 | 2008-05-29 | Cadila Healthcare Limited | Substituted 4,5-dihydro-1h-pyrazole derivatives as cannabinoid modulators |
US7875647B2 (en) | 2006-09-29 | 2011-01-25 | Green Cross Corporation | Heteroaryl-pyrazole derivatives as cannabinoid CB1 receptor antagonists |
EP1911747A1 (en) * | 2006-10-11 | 2008-04-16 | Laboratorios del Dr. Esteve S.A. | Sulfonamide substituted pyrazoline compounds, their preparation and use as CB1 modulators |
FR2911136B1 (fr) | 2007-01-05 | 2009-02-20 | Sanofi Aventis Sa | Derives de n-(4-cyano-1h-pyrazol-3-yl)methylamine substitues leur preparation et leur application en therapeutique. |
FR2919184A1 (fr) * | 2007-07-26 | 2009-01-30 | Sanofi Aventis Sa | L'acide 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4- methylpyrazole-3-carboxylique, ses esters, ses sels pharmaceutiquement acceptables et leurs solvates pour leur utilisation comme medicament. |
SG11201501133WA (en) * | 2012-08-16 | 2015-04-29 | Janssen Pharmaceutica Nv | Pyrrolopyrazoles as n-type calcium channel blockers |
SG11201501130PA (en) | 2012-08-16 | 2015-04-29 | Janssen Pharmaceutica Nv | Substituted pyrazoles as n-type calcium channel blockers |
WO2014111356A1 (en) * | 2013-01-17 | 2014-07-24 | F. Hoffmann-La Roche Ag | Oxytocin receptor agonists for the treatment of cns diseases |
US9453002B2 (en) | 2013-08-16 | 2016-09-27 | Janssen Pharmaceutica Nv | Substituted imidazoles as N-type calcium channel blockers |
KR101685993B1 (ko) * | 2014-05-15 | 2016-12-13 | 한국과학기술연구원 | 전압개폐 칼슘이온채널 억제 활성화능을 갖는 n-(피라졸릴메틸)아릴설폰아마이드 화합물 및 이를 포함하는 약학적 조성물 |
CN109689045A (zh) | 2016-05-04 | 2019-04-26 | 因美制药公司 | 大麻素的局部制剂在治疗大疱性表皮松解症和相关结缔组织病症中的用途 |
US20240000806A1 (en) * | 2020-11-20 | 2024-01-04 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Methods and materials for inhibiting cb1 activity |
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FR2713225B1 (fr) * | 1993-12-02 | 1996-03-01 | Sanofi Sa | N-pipéridino-3-pyrazolecarboxamide substitué. |
FR2692575B1 (fr) * | 1992-06-23 | 1995-06-30 | Sanofi Elf | Nouveaux derives du pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant. |
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