AR079849A1 - DERIVATIVES OF THIOCHROMAN, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM, PROCEDURE FOR PREPARATION AND USE OF THE SAME IN THE TREATMENT OF DISEASES OF THE NERVOUS CENTRAL SYSTEM, SUCH AS ALZHEIMER AND PARKINSON, AMONG OTHERS. - Google Patents
DERIVATIVES OF THIOCHROMAN, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM, PROCEDURE FOR PREPARATION AND USE OF THE SAME IN THE TREATMENT OF DISEASES OF THE NERVOUS CENTRAL SYSTEM, SUCH AS ALZHEIMER AND PARKINSON, AMONG OTHERS.Info
- Publication number
- AR079849A1 AR079849A1 ARP110100041A ARP110100041A AR079849A1 AR 079849 A1 AR079849 A1 AR 079849A1 AR P110100041 A ARP110100041 A AR P110100041A AR P110100041 A ARP110100041 A AR P110100041A AR 079849 A1 AR079849 A1 AR 079849A1
- Authority
- AR
- Argentina
- Prior art keywords
- branched
- linear
- substituted
- unsubstituted
- nitrogen atom
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D335/00—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom
- C07D335/04—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D335/06—Benzothiopyrans; Hydrogenated benzothiopyrans
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Reivindicacion 1: Compuestos de formula (1): en la que R1, R2, R3 y R4 idénticos o diferentes, representan cada uno un átomo de hidrogeno, un átomo de halogeno, o un grupo ciano ; hidroxi ; tio ; nitro; alquilo C1-6 lineal o ramificado sustituido opcionalmente ; arilo ; alcoxi C1-6 lineal o ramificado no sustituido o sustituido con uno o varios átomos de halogeno ; ariloxi ; alquiltio C1-6 lineal o ramificado ; ariltio; carboxi; alcoxicarbonilo C1-6 lineal o ramificado ariloxicarbonilo ; aciloxi C1-6 lineal o ramificado ; arilcarboniloxi; acilo C1-6 lineal o ramificado ; arilcarbonilo; amino no sustituido o sustituido con uno o dos grupos alquilo C1-6 lineal o ramificado, idénticos o diferentes ; arilamino no sustituido o sustituido en el átomo de nitrogeno con un grupo alquilo C1-6 lineal o ramificado ; acilamino C1-6 lineal o ramificado no sustituido o sustituido en el átomo de nitrogeno con un grupo alquilo C1-6 lineal o ramificado; arilcarbonilamino no sustituido o sustituido en el átomo de nitrogeno con un grupo alquilo C1-6 lineal o ramificado; aminocarbonilo no sustituido o sustituido con uno o dos grupos alquilo C1-6 lineal o ramificado, idénticos o diferentes arilaminocarbonilo no sustituido o sustituido en el átomo de nitrogeno con un grupo alquilo C1-6 lineal o ramificado ; alquilsulfonilamino C1-6 lineal o ramificado no sustituido o sustituido en el átomo de nitrogeno con un grupo alquilo C1-6 lineal o ramificado ; o arilsulfonilamino no sustituido o sustituido en el átomo de nitrogeno con un grupo alquilo C1-6 lineal o ramificado; sus enantiomeros y sus diastereoisomeros, así como sus sales de adicion con un ácido o una base farmacéuticamente aceptable, entendiéndose que: el término ½arilo y el término ½aril contenido en los grupos ariloxi, ariltio, ariloxicarbonilo, arilcarboniloxi, arilcarbonilo, arilamino, arilcarbonilamino, arilaminocarbonilo, y arilsulfonilamino, representan el grupo fenilo no sustituido o sustituido con uno o varios grupos, idénticos o diferentes, elegidos entre un átomo de halogeno, o un grupo ciano ; hidroxi; tio; nitro; alquilo C1-6 lineal o ramificado sustituido opcionalmente ; alcoxi C1-6 lineal o ramificado no sustituido o sustituido con uno o varios átomos de halogeno ; alquiltio C1-6 lineal o ramificado ; carboxi; alcoxicarbonilo C1-6 lineal o ramificado ; amino no sustituido o sustituido con uno o dos grupos alquilo C1-6 lineal o ramificado, idénticos o diferentes ; aciloxi C1-6 lineal o ramificado ; acilamino C1-6 lineal o ramificado no sustituido o sustituido en el átomo de nitrogeno con un grupo alquilo C1-6 lineal o ramificado ; aminocarbonilo no sustituido o sustituido con uno o dos grupos alquilo C1-6 lineal o ramificado, idénticos o diferentes aminosulfonilo no sustituido o sustituido con uno o dos grupos alquilo C1-6 lineal o ramificado, idénticos o diferentes ; alquilsulfonilamino C1-6 lineal o ramificado no sustituido o sustituido en el átomo de nitrogeno con un grupo alquilo C1-6 lineal o ramificado ; o N-hidroxicarboximidamida; la expresion ½sustituido opcionalmente destinada al término alquilo significa que este grupo puede estar sustituido con uno o varios átomos de halogeno, o con un grupo ciano; hidroxi; tio; nitro; arilo ; alcoxi C1-6 lineal o ramificado no sustituido o sustituido con uno o varios átomos de halogeno ; alquiltio C1-6 lineal o ramificado ; carboxi; alcoxicarbonilo C1-6 lineal o ramificado ; aciloxi C1-6 lineal o ramificado ; amino no sustituido o sustituido con uno o dos grupos alquilo C1-6 lineal o ramificado, idénticos o diferentes ; acilamino C1-6 lineal o ramificado no sustituido o sustituido en el átomo de nitrogeno con un grupo alquilo C1-6 lineal o ramificado ; aminocarbonilo no sustituido o sustituido con uno o dos grupos alquilo C1-6 lineal o ramificado, idénticos o diferentes aminosulfonilo no sustituido o sustituido con uno o dos grupos alquilo C1-6 lineal o ramificado, idénticos o diferentes ; alquilsulfonilamino C1-6 lineal o ramificado no sustituido o sustituido en el átomo de nitrogeno con un grupo alquilo C1-6 lineal o ramificado ; o N-hidroxicarboximidamida.Claim 1: Compounds of formula (1): wherein R1, R2, R3 and R4 identical or different, each represent a hydrogen atom, a halogen atom, or a cyano group; hydroxy; uncle ; nitro; linear or branched C1-6 alkyl optionally substituted; aryl; linear or branched C1-6 alkoxy not substituted or substituted with one or more halogen atoms; aryloxy; linear or branched C1-6 alkylthio; arylthio; carboxy; linear or branched C 1-6 alkoxycarbonyl aryloxycarbonyl; linear or branched C1-6 acyloxy; arylcarbonyloxy; linear or branched C1-6 acyl; arylcarbonyl; amino unsubstituted or substituted with one or two linear or branched C1-6 alkyl groups, identical or different; unsubstituted or substituted arylamino in the nitrogen atom with a linear or branched C1-6 alkyl group; linear or branched C1-6 acylamino unsubstituted or substituted on the nitrogen atom with a linear or branched C1-6 alkyl group; unsubstituted or substituted arylcarbonylamino in the nitrogen atom with a linear or branched C1-6 alkyl group; aminocarbonyl unsubstituted or substituted with one or two linear or branched C1-6 alkyl groups, identical or different arylaminocarbonyl unsubstituted or substituted on the nitrogen atom with a linear or branched C1-6 alkyl group; linear or branched C1-6 alkylsulfonylamino unsubstituted or substituted on the nitrogen atom with a linear or branched C1-6 alkyl group; or unsubstituted or substituted arylsulfonylamino in the nitrogen atom with a linear or branched C1-6 alkyl group; their enantiomers and their diastereoisomers, as well as their addition salts with a pharmaceutically acceptable acid or base, it being understood that: the term ½aryl and the term ½aryl contained in the aryloxy, arylthio, aryloxycarbonyl, arylcarbonyloxy, arylcarbonyl, arylamino, arylcarbonylamino, arylaminocarbonylamino groups , and arylsulfonylamino, represent the phenyl group unsubstituted or substituted with one or more groups, identical or different, chosen from a halogen atom, or a cyano group; hydroxy; uncle; nitro; linear or branched C1-6 alkyl optionally substituted; linear or branched C1-6 alkoxy not substituted or substituted with one or more halogen atoms; linear or branched C1-6 alkylthio; carboxy; linear or branched C1-6 alkoxycarbonyl; amino unsubstituted or substituted with one or two linear or branched C1-6 alkyl groups, identical or different; linear or branched C1-6 acyloxy; linear or branched C1-6 acylamino unsubstituted or substituted on the nitrogen atom with a linear or branched C1-6 alkyl group; aminocarbonyl unsubstituted or substituted with one or two linear or branched C1-6 alkyl groups, identical or different aminosulfonyl unsubstituted or substituted with one or two linear or branched C1-6 alkyl groups, identical or different; linear or branched C1-6 alkylsulfonylamino unsubstituted or substituted on the nitrogen atom with a linear or branched C1-6 alkyl group; or N-hydroxycarboximidamide; the term "substituted" optionally intended for the term "alkyl" means that this group may be substituted with one or more halogen atoms, or with a cyano group; hydroxy; uncle; nitro; aryl; linear or branched C1-6 alkoxy not substituted or substituted with one or more halogen atoms; linear or branched C1-6 alkylthio; carboxy; linear or branched C1-6 alkoxycarbonyl; linear or branched C1-6 acyloxy; amino unsubstituted or substituted with one or two linear or branched C1-6 alkyl groups, identical or different; linear or branched C1-6 acylamino unsubstituted or substituted on the nitrogen atom with a linear or branched C1-6 alkyl group; aminocarbonyl unsubstituted or substituted with one or two linear or branched C1-6 alkyl groups, identical or different aminosulfonyl unsubstituted or substituted with one or two linear or branched C1-6 alkyl groups, identical or different; linear or branched C1-6 alkylsulfonylamino unsubstituted or substituted on the nitrogen atom with a linear or branched C1-6 alkyl group; or N-hydroxycarboximidamide.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1000070A FR2955107B1 (en) | 2010-01-08 | 2010-01-08 | NOVEL THIOCHROMAN DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
Publications (1)
Publication Number | Publication Date |
---|---|
AR079849A1 true AR079849A1 (en) | 2012-02-22 |
Family
ID=42935687
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP110100041A AR079849A1 (en) | 2010-01-08 | 2011-01-07 | DERIVATIVES OF THIOCHROMAN, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM, PROCEDURE FOR PREPARATION AND USE OF THE SAME IN THE TREATMENT OF DISEASES OF THE NERVOUS CENTRAL SYSTEM, SUCH AS ALZHEIMER AND PARKINSON, AMONG OTHERS. |
Country Status (3)
Country | Link |
---|---|
AR (1) | AR079849A1 (en) |
FR (1) | FR2955107B1 (en) |
WO (1) | WO2011083264A1 (en) |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1088945A (en) | 1976-10-18 | 1980-11-04 | Pfizer Limited | Hydantoin derivatives as therapeutic agents |
FR2722502B1 (en) | 1994-07-12 | 1996-08-23 | Adir | NOVEL BENZOTHIADIAZINE DERIVATIVE, ITS PREPARATION METHOD AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME |
WO1998012185A1 (en) * | 1996-09-17 | 1998-03-26 | The Regents Of The University Of California | Benzothiadiazide derivatives and their use as allosteric up-modulators of the ampa receptor |
EE200000468A (en) * | 1998-02-18 | 2002-04-15 | Neurosearch A/S | The compounds, their use and the pharmaceutical composition |
JP2005508352A (en) * | 2001-10-10 | 2005-03-31 | ニューロサーチ、アクティーゼルスカブ | Novel benzothiazine derivative, method for producing the same and method for using the same |
-
2010
- 2010-01-08 FR FR1000070A patent/FR2955107B1/en not_active Expired - Fee Related
-
2011
- 2011-01-06 WO PCT/FR2011/000008 patent/WO2011083264A1/en active Application Filing
- 2011-01-07 AR ARP110100041A patent/AR079849A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
FR2955107B1 (en) | 2012-03-02 |
FR2955107A1 (en) | 2011-07-15 |
WO2011083264A1 (en) | 2011-07-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CL2018000666A1 (en) | New spiro compounds [3h-indole-3,2'-pyrrolidin] -2 (1h) -one and derivatives as inhibitors of mdm2-p53. | |
UY35242A (en) | 3-QUINASA PHOSFATIDYLINOSITOL INHIBITORS | |
DOP2015000158A (en) | PRMT5 INHIBITORS AND THEIR USES | |
PH12017500252B1 (en) | New spiro[3h-indole-3,2`-pyrrolidin]-2(1h)-one compounds and derivatives as mdm2-p53 inhibitors | |
UY35243A (en) | 3-CINASA PHOSFATIDYLINOSITOL INHIBITORS | |
AR075894A1 (en) | OXIDIZED DERIVATIVES OF USEFUL TRIAZOLILPURINS AS ADENOSINE A2A RECEIVER LINKS AND THEIR USE AS MEDICATIONS. | |
AR085004A1 (en) | SELECTIVE INHIBITORS OF GLYCOSIDASES AND USES OF THE SAME | |
UY35617A (en) | 3-QUINASA PHOSFATIDYLINOSITOL INHIBITORS | |
CO7160015A2 (en) | N-substituted benzamides and their use in the treatment of pain | |
AR093244A1 (en) | SUBSTITUTED BENZENE COMPOUNDS USED IN THE TREATMENT OF EZH2-DISORDERS | |
NI201400107A (en) | HETEROCYCLYL COMPOUNDS AS MEK INHIBITORS | |
AR084553A1 (en) | HIDEROCICLIC INHIBITING IMIDAZOLIC DERIVATIVES OF b-SECRETASE, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND USE OF THE SAME TO TREAT NEURODEGENERATIVE DISEASES, IN PARTICULAR ALZHEIMER | |
UY33501A (en) | Acyl sulfonamide derivatives and their pharmaceutically acceptable salts for use in medicine | |
AR063602A1 (en) | DERIVATIVES OF SPIROINDOLINONE, PHARMACEUTICAL FORMULATIONS THAT CONTAIN THEM AND THEIR USE IN THE OBTAINING OF A MEDICINAL PRODUCT FOR THE TREATMENT OF ONCOLOGICAL DISORDERS. | |
AR087309A1 (en) | HETEROCICLIC COMPOUND OF SUBSTITUTED CONDENSED RINGS, PHARMACEUTICAL COMPOSITION THAT INCLUDES IT AND ITS USE FOR THE MANUFACTURE OF A MEDICINAL PRODUCT FOR THE TREATMENT OF NEUROGENERATIVE DISEASES AND ATEROSCLEROSIS | |
DOP2014000036A (en) | PIRIDAZINONE COMPOUNDS AND ITS USE AS DAAO INHIBITORS | |
AR078278A1 (en) | ANTAGONISTS OF TIAZOL AND OXAZOL HEPCIDINE, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND USE OF THE SAME FOR THE TREATMENT OF ANEMIAS AND ILLNESSES ASSOCIATED WITH IRON DEFICIENCIES. | |
AR072819A1 (en) | DERIVATIVES OF TRIAZOLO [4,3-A] PIRIDINE, PREPARATION PROCEDURE, INTERMEDIARIES OF SUCH PROCESS, PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND AND USE THE SAME, AS INHIBITORS OF MET PROTEINQUINASE, FOR THE TREATMENT OF CANCERESIST, PSCESESIS, PSC CENTRAL NERVOUS AND OTHER | |
CL2017002354A1 (en) | Compounds derived from bicyclic heteroaryls fused with activity as phd inhibitors. | |
CO7280475A2 (en) | Azaindole derivatives that act as pi3k inhibitors | |
AR072518A1 (en) | IMIDAZO DERIVATIVES [1,2-A] PIRIDINE, ITS PREPARATION PROCEDURE, PHARMACEUTICAL COMPOSITIONS AND ITS PARTICULAR USE AS MET INHIBITORS. " | |
UY33191A (en) | PIRAZINE DERIVATIVES | |
GT201400167A (en) | NEW DERIVATIVES OF BENCIL SULFONAMIDE USEFUL AS INHIBITORS OF MOGAT-2 | |
UY33490A (en) | NEW KINOLINE ESTERS USEFUL FOR THE TREATMENT OF SKIN DISORDERS. | |
TR201819805T4 (en) | FLAVAGLIN DERIVATIVES. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FB | Suspension of granting procedure |