WO2001060374A1 - Utilisation de derives de paullones pour la fabrication de medicaments - Google Patents
Utilisation de derives de paullones pour la fabrication de medicaments Download PDFInfo
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- WO2001060374A1 WO2001060374A1 PCT/FR2001/000455 FR0100455W WO0160374A1 WO 2001060374 A1 WO2001060374 A1 WO 2001060374A1 FR 0100455 W FR0100455 W FR 0100455W WO 0160374 A1 WO0160374 A1 WO 0160374A1
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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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- 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
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- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Definitions
- Their act. - e because d- * ru ⁇ ⁇ ⁇ ole ⁇ rreca "- e: because the link to cvclir.es rui varies during cell cycle Binding to CDK m ers causes CDK deactivation
- GSK-3 ⁇ is an essential element of the NT signal pathway. It is involved in multiple physiological processes regulating the cell cycle by controlling Dl cvclme and ⁇ -catenm levels, dorsoventral formation during development, action of 1 insulin on glycogen synthesis, axonal outgrowth, neurotoxicity of KIV-1 mediated by Tat, and others.
- GSK- ⁇ and CDK5 are responsible for a large part of the abnormal hyperphosphorylation of the tau protein binding microtubules as observed in the helically paired filaments in Alzheimer's disease and other "taupathies" neurodegenerative.
- GSK-3 ⁇ inhibitors disclosed to date are constituted by lithium and certain purine derivatives.
- the selectivity of lithium has not been raoD-ortée, but given the atomic nature of the product, it is likely that it must be very low.
- lithium only acts at considerable doses (IC 50 around
- the invention provides a solution to these problems with the use, for the manufacture of drugs which inhibit GSK-3 ⁇ and, where appropriate, CDKs, of pauUones of high efficiency, exhibiting, with respect to GSK-3 ⁇ , IC 50 values lower than 10 ⁇ M, and even for a good number of them lower than 5 ⁇ M, or even 1 ⁇ . Some of these compounds even have IC 50 values of less than 50 rM and reaching values for some less than 10 r_M.
- redundant paullone derivatives are used with the general formula (I):
- - Z represents C or N
- - Y represents, with the adjacent ring, a phenyl or thiazolyl residue; the ring or rings constituting these derivatives being optionally substituted by one or more: halogen atoms, hydroxy groups, alkylenehydroxy, alkynealkylenehydroxy, alkynehydroxycyclohexyl, alkyl, alkoxy, alkyleneealkoxy, alkylenecyano, the alkylene group being saturated or unsaturated, these radicals being straight or branched chain, from C1 to C18, said chain being optionally substituted by one or more hydroxy or amino groups; one or more trifluoromethyl groups, • -COiM -COOM; or -CKCOOM (with M representing a hydrogen atom, a C1 to C1 alkyl group, straight chain or branched, substituted where appropriate by one or more hydroxy groups and / or amir.o); nitroso; r.itro; or cyano, -
- R D represents a hydrogen atom or a C L to C 5 alkyl group
- R " represents a hydrogen atom, or a group -C-C0 2 - (CH 3 ) 3 , and the salts of these physiological derivatives are acceptable.
- This family corresponds to the general formula (II):
- R ⁇ to R 4 , R 7 to R 11 identical or different, represent a hydrogen atom, a halogen atom (F, CI, Br, I), a hydroxy group, alkylenehydroxy, alkynealkylenehydroxy, alkynehydroxycyclohexyl, alkyl, alkoxy , alkylenealkoxy, alkylenecyano, these radicals being with straight or branched chain, from C1 to C18, the alkylene group being saturated or unsaturated, said chain being optionally substituted by one or more hydroxy or amino groups; a tri luoromethyl group; a -COM group; -COOM; or -CH.COCM, (with M representing a hydrogen atom, a C1 to C13 alkyl group, straight or branched chain, optionally substituted by one or more hydroxy groups and / or a ino); a nitrcsc group; a nitro group; or a cyano group; and the physiological radicals
- X represents CS-CH 3 or CS.
- the derivatives of the invention advantageously have an IC 50 with respect to GSK-3 ⁇ of less than 10 ⁇ M and for a good number of them at 1 ⁇ M, IC 50 of less than 100 nM and even at 10 nM can be obtained.
- Particularly preferred pauUones of these groups belong to the families of formula (II) or of formula (III) with R 9 chosen from -N0 2 , -CN, -C1, -Br, -CF 3 , C1 to C5 alkyl, in particular methyl, or a hydrogen atom, R. and / or R chosen from alkoxy (C 1 to C 3 for the alkyl radical) and in particular methoxy, alkylenecyano, vinylalkoxy, or propylene, the other substituents being hydrogen.
- 9-cyano-2,3-dimethoxypaullone is a new product and as such falls within the scope of the invention.
- the invention therefore makes it possible to have medicaments having the selectivity required for a given application.
- these drugs are of great interest for the treatment of neurodegenerative diseases, such as Alzheimer's disease.
- the hyperphosphorylation of the tau protein caused by CDK5 and GSK-3 ⁇ can indeed be inhibited by the derivatives of pauUones.
- These drugs also find an application of great interest for the treatment of manic-depressive illnesses.
- cardiovascular sphere can also be used in the cardiovascular sphere to treat or prevent in particular, atherosclerosis, restenosis or angiogenesis, by modifying the balance between proliferation and apoptosis, and by controlling ⁇ -catenm levels.
- the active ingredients used in therapeutically effective amounts, are mixed with the pharmaceutically acceptable vehicles for the chosen mode of administration.
- the drugs are prepared in the form of capsules, tablets, dragees, capsules, pills, drops and the like. Such drugs may contain from 1 to 100 mg of active ingredient per unit.
- the drugs come in the form of sterile or sterilizable solutions. They can also be suspensions or emulsions.
- the doses per unit of intake can vary from 1 to 50 mg of active ingredient.
- the daily dosage is chosen so as to obtain a final concentration of at most 100 ⁇ M of paullone derivative in the blood of the treated patient.
- the dosage used in humans corresponds to the following doses: thus, for example, the patient is administered in one or more doses 10 to 50 mg / day for the treatment of tumors or parasitoses.
- FIGS. 1 to 6, which respectively represent
- FIG. 1A the inhibitory activity vis-à-vis CDKs, CDK1 / CDK2, and GSK-3 alsterpaullone (fig. 1A) and kenpaullone (fig. 1B) concentration of these pauUones
- FIG. 2 the pauUones formulas according to the invention
- FIGS. 3A to 3C the ICs of pauUones according to the invention with respect to one of the kmase protein GSK3,
- CDK1 / cyclin B CDK5 / p25 according to their IC 5 vis-à-vis the other 2 kmase proteins
- Elemental analyzes were performed using an elemental analysis device from CHN Perkin-
- the buffers used have the following compositions: Homogenization buffer: - 60 mM of ⁇ -glycerophosphate, 15 miM of p-nitrcphenylphosphate, 25 M of Moos (pK 7.2), 15 mM of TAGTA, 15 mM of MgCl 2 , 1 mM DTT, 1 mM sodium vanadate, 1 mM NaF, 1 mM phenylpho ⁇ phate, 10 ⁇ g leupeptin / ml, 10 ⁇ g aprotinin / ml, 10 ⁇ g soybean trypsin inhibitor / ml and 100 ⁇ M of ber.zamidine.
- Buffer A 10 mM MgCl 2 , 1 mM ⁇ GTA, 1 mM DTT, 25 mM Tris-HCl pH, 5, 50 ⁇ g heparin / ml.
- Buffer C homogenization buffer, but containing 5 mM of EGTA, and devoid of NaF and protease inhibitors.
- microcystin 5 ⁇ M of microcystin, 100 ⁇ g / ml of each of the following products: leupeptin, aprotinin, pepstatin. .
- Kinase preparations and activity determinations 5 ⁇ M of microcystin, 100 ⁇ g / ml of each of the following products: leupeptin, aprotinin, pepstatin. .
- the kinase activities were determined in buffer A or C (unless otherwise indicated), at 30 ° C, at a final ATP concentration of 15 ⁇ .
- the values of the blank tests were subtracted and the activities calculated in o oles of phosphate incorporated for a 10 min incubation.
- the values of the activities are generally expressed as% of maximum activity, that is, in the absence of inhibitors.
- the GSK-3 ⁇ used is either the enzyme purified from rabbit muscle or expressed and purified from Sf9 insect cells (Hughes et al, 1992, Eur. J. Biochem., 203: 305,311). The determinations were carried out with a 1/100 dilution in 1 mg of BSA / ml of
- the CDKl / cyclin B used was extracted using a homogenization buffer from oocytes from starfish (Marthasterias glacialis) and purified by
- the kinase activity was determined in buffer C, with 1 mg of histone Kl / ml, in the presence of 15 ⁇ M of [ ⁇ " P] ATP ((3000 Ci / mmol; 1 mCi / ml) in a final volume 30 ⁇ l After 10 minutes of incubation at 30 ° C., 25 ⁇ l aliquots of supernatant were deposited on phosohocellulose P81 papers and treated as described above.
- CDK5 / p35 was reconstituted by mixing equal amounts of CDKS and recombinant mammalian p35, expressed in ⁇ . coli in the form of GST fusion protein (Glutathione-S-transferase) and purified by affinity chromatography on glutathione-agarose. The enzymatic activity of the complex was determined in buffer C as described for CDK1 / cyclin 3.
- Phosphorylation of tau in vi tro was performed using purified GSK-3 ⁇ and the recombinant human tau-32 protein as a substrate. After 30 minutes of incubation in the presence of different concentrations of alsterpaullone, under the study conditions for GSK-3 ⁇ described above, the kinase reaction was stopped by adding Laemmli buffer. The tau protein was resolved in SDS-PAG ⁇ at 10% and its phosphorylation rate visualized by autoradiography.
- Tau transfection we excised, from a bacterial expression vector pNG2 (3iernat et al., 1993, Neuron 11: 153-163) and the gene coding for htau23,
- the shortest human tau isoform with Xbal and BamHI.
- the gene was inserted into the baculovirus transfer vector pVL1392 cut with the same endonucleases.
- BaculoGold system was used for the construction of the vector containing the baculovirus tau.
- BaculoGold DNA is a modified type of baculovirus containing a lethal deletion.
- Co-transfection of the BaculoGold DN with a complement baculovirus transfer vector makes it possible to recover the lethal deletion of this viral DNA and to reconstitute viable virus particles carrying the sequence coding for htau23.
- the plasmid DNA used for the transfections was purified using CIAGEN cartridges (Hilden, Germany).
- Sf9 cells cultured in monolayers (2x10 cells in a 60 mm cell culture vessel) were co-transfected with baculovirus DNA (0.5 ⁇ g of BaculoGold DNA) and with derivatives of pVL1392 (2 ⁇ g) using the calcium phosphate co-precipitation method.
- the presence of recombinant protein was examined in the infected cells 5 days after infection with SDS-PAG ⁇ and Western blot.
- Treatment of Sf9 cells with kinase inhibitors Treatment of Sf9 cells with kinase inhibitors
- Sf9 cells infected with baculovirus expressing htau23 were treated 36 hours after infection, (when the cells have already expressed levels of tau sufficient for the development of cellular processes) with 20 ⁇ M of inhibitors for 3 hours before being collected.
- Sf9 cells were infected with a recombinant virus at an MOI of 1 to 5.
- HLB hypotonic lysis buffer
- Equal amounts of protein (80 ⁇ g) are subjected to an SDS-PAG ⁇ using a 15% acrylamide gel, transferred by electrophoresis to a nitrocellulose membrane and subjected to an immunoblot with a specific phosphorylation antibody which selectively detects DARPP -32 phosphorylated on Thr75.
- Example 1 2 - Iodo-7, 12 -dihydro- indolo [3,2-] [1] be ⁇ z zépine- 6 (5ff) -one (2 -iodopaullone)
- Example 6 7, 8-d methoxy-5- (4-n ⁇ trophenylhydrazono) -, 5- dihydro-1H- [1] benzazepm-2 (3H) -one Stirring is carried out in glacial acetic acid (10 ml), during lh at 70 ° C, 7,8 -di etnoxy-1H- [1] benzazepine-2, 5 (3h, 4H) dione (235 mg, 1 mole), (Schultz C. et al, (1999) J. Med.Chem., 42, 2909-2919), hydrochloride 4-nitrophenylhydrazine (569 mg, 3 mmol), and sodium acetate (246 mg, 3 mmol).
- Example 7 Study of the inhibition of GSK-3 ⁇ , CDK5 / p35 and CDKl / cyclin B by pauUones. . alsterpaullone
- alsterpaullone has been studied on several highly purified kinases.
- GSK-3 ⁇ GS1 peptide
- CDKs histone H1
- Activity is expressed as a percentage of maximum activity. The results obtained are given in FIG. 1 and in Table 1. The values of IC 5 ⁇ were calculated from the dose / response curves and are expressed in ⁇ M.
- FIGS. 3A to 3C To compare the effects of the active compounds on GSK-3 ⁇ and the CDKs, we report in FIGS. 3A to 3C the values of IC S0 with respect to each enzyme (CDKl / cyclin B, CDK5 / p25 and GSK-3 ⁇ ) as a function of the IC 50 values vis-à-vis the other 2 kinases.
- Example 8 Study of the inhibition by GSK-3 ⁇ paullones by competition with ATP.
- FIG. 4A The kinetic data for, determination of the activity of GSK-3 ⁇ at different concentrations of alsterpaullone are reported in FIG. 4. The enzymatic activities are described as determined above.
- Figure 4A primary curve l / V poured l / ATP. The ATP concentrations in this reaction mixture vary from 0.5 to 4 ⁇ M. The GS-1 concentration is kept constant at 4 ⁇ . The box shows the slopes as a function of concentration from the primary curves. The apparent inhibition constant (Ki) is indicated by an arrow.
- the inhibitory effect of alsterpaullone on the activity of GSK-3 ⁇ was determined on a tau protein binding microtubules.
- the reco binante human tau protein expressed in bacteria can be phosphorylated in vitro by GSK-3 ⁇ and this phospnorylation is inhibited in a dose-dependent manner by alsterpaullone with an ICM close to 33nM.
- the phophorylation rate of DARPP-32 on Thr75 was monitored by Western blot with a phosphospecific antibody and evaluated by quantification of the fingerprints. The results obtained are respectively represented in FIGS. 5A and 5B. It is found that 1 alsterpaullone is capable of inhibiting the phospnorylation of D7ARPP-32 m if you.
- Example 11 preparation of a capsule using 9-n tropaullone as active ingredient.
Abstract
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001559470A JP2003522793A (ja) | 2000-02-15 | 2001-02-15 | 製薬におけるパウロン誘導体の使用 |
EP01907815A EP1255551A1 (fr) | 2000-02-15 | 2001-02-15 | Utilisation de derives de paullones pour la fabrication de medicaments |
AU2001235691A AU2001235691A1 (en) | 2000-02-15 | 2001-02-15 | Use of paullone derivatives for making medicines |
CA002397560A CA2397560A1 (fr) | 2000-02-15 | 2001-02-15 | Utilisation de derives de paullones pour la fabrication de medicaments |
US10/203,977 US7232814B2 (en) | 2000-02-15 | 2001-02-15 | Use of paullone derivatives for making medicines |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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FR0001862A FR2804959B1 (fr) | 2000-02-15 | 2000-02-15 | Utilisation de derives de paullones pour la fabrication de medicaments |
FR00/01862 | 2000-02-15 |
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WO2001060374A1 true WO2001060374A1 (fr) | 2001-08-23 |
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PCT/FR2001/000455 WO2001060374A1 (fr) | 2000-02-15 | 2001-02-15 | Utilisation de derives de paullones pour la fabrication de medicaments |
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US (1) | US7232814B2 (fr) |
EP (1) | EP1255551A1 (fr) |
JP (1) | JP2003522793A (fr) |
AU (1) | AU2001235691A1 (fr) |
CA (1) | CA2397560A1 (fr) |
FR (1) | FR2804959B1 (fr) |
WO (1) | WO2001060374A1 (fr) |
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WO2004100977A1 (fr) * | 2003-03-25 | 2004-11-25 | The Board Of Trustees Of The University Of Illinois | Procede d'inhibition de proliferation de cellules tumorales |
JP2005528380A (ja) * | 2002-04-04 | 2005-09-22 | エンゾン,インコーポレーテッド | インドールのポリマー性アシル誘導体 |
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JP6902025B2 (ja) | 2015-06-18 | 2021-07-14 | ティン セラピューティックス エルエルシー | 聴覚損失の予防および治療のための方法および組成物 |
WO2016201581A1 (fr) | 2015-06-18 | 2016-12-22 | The Hospital For Sick Children | Procédé de traitement de médulloblastome |
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- 2001-02-15 CA CA002397560A patent/CA2397560A1/fr not_active Abandoned
- 2001-02-15 AU AU2001235691A patent/AU2001235691A1/en not_active Abandoned
- 2001-02-15 JP JP2001559470A patent/JP2003522793A/ja active Pending
- 2001-02-15 WO PCT/FR2001/000455 patent/WO2001060374A1/fr active Application Filing
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WO1999021859A1 (fr) * | 1997-10-10 | 1999-05-06 | Glaxo Group Limited | Azaoxindole, derives et applications |
WO1999065910A1 (fr) * | 1998-06-16 | 1999-12-23 | The Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services | Inhibiteurs de kinases dependantes de la cycline sous forme d'azepinone fusionnee |
Cited By (36)
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WO2001070231A3 (fr) * | 2000-03-22 | 2002-06-20 | Centre Nat Rech Scient | Utilisation de substances modulatrices de l'expression ou de la fonction d'une proteine impliquee dans le cycle cellulaire pour le traitement ou la prevention des lesions neurales aiguës |
WO2001070231A2 (fr) * | 2000-03-22 | 2001-09-27 | Centre National De La Recherche Scientifique -Cnrs- | Utilisation de substances modulatrices de l'expression ou de la fonction d'une proteine impliquee dans le cycle cellulaire pour le traitement ou la prevention des lesions neurales aiguës |
CN100391959C (zh) * | 2001-09-21 | 2008-06-04 | 赛诺菲-安万特 | 嘧啶-5-(1h)-酮衍生物 |
JP2005528380A (ja) * | 2002-04-04 | 2005-09-22 | エンゾン,インコーポレーテッド | インドールのポリマー性アシル誘導体 |
US7351407B2 (en) | 2002-04-30 | 2008-04-01 | Alcon, Inc. | Agents which regulate, inhibit, or modulate the activity and/or expression of connective tissue growth factor (CTGF) as a unique means to both lower intraocular pressure and treat glaucomatous retinopathies/optic neuropathies |
EP1616568A3 (fr) * | 2002-04-30 | 2006-06-21 | Alcon, Inc | Inhibiteurs de GSK-3 et de CDK comme agents antiglaucome |
EP1616568A2 (fr) * | 2002-04-30 | 2006-01-18 | Alcon, Inc | Inhibiteurs de GSK-3 et de CDK comme agents antiglaucome |
WO2004058766A2 (fr) * | 2002-12-23 | 2004-07-15 | Faustus Forschungs Cie. Translational Cancer Research Gmbh | Derives d'azepinones condensees inhibiteurs de tumeurs |
DE10260618B4 (de) * | 2002-12-23 | 2005-06-09 | Faustus Forschungs Cie. Translational Cancer Research Gmbh | Tumorhemmende annellierte Azepinonderivate |
WO2004058766A3 (fr) * | 2002-12-23 | 2004-08-26 | Faustus Forschungs Cie | Derives d'azepinones condensees inhibiteurs de tumeurs |
DE10260618A1 (de) * | 2002-12-23 | 2004-07-08 | Faustus Forschungs Cie. Translational Cancer Research Gmbh | Tumorhemmende annellierte Azepinonderivate |
US8431522B2 (en) | 2003-03-25 | 2013-04-30 | The Board Of Trustees Of The University Of Illinois | Methods of inhibiting tumor cell proliferation |
WO2004100977A1 (fr) * | 2003-03-25 | 2004-11-25 | The Board Of Trustees Of The University Of Illinois | Procede d'inhibition de proliferation de cellules tumorales |
US7799896B2 (en) | 2003-03-25 | 2010-09-21 | The Board Of Trustees Of The University Of Illinois | Methods of inhibiting tumor cell proliferation |
US7635673B2 (en) | 2003-03-25 | 2009-12-22 | The Board Of Trustees Of The University Of Illinois | Methods of inhibiting tumor cell proliferation |
AU2005239811B2 (en) * | 2004-05-12 | 2010-06-17 | Bayer Cropscience Ag | Plant growth regulation |
EA013072B1 (ru) * | 2004-05-12 | 2010-02-26 | Байер Кропсайенс Аг | Применение конденсированных производных азепинона для регулирования роста растений, композиция для регулирования роста растений и ее применение и способ регулирования роста растений |
US7767664B2 (en) | 2004-05-12 | 2010-08-03 | Bayer Cropscience Ag | Plant growth regulation |
WO2005107471A1 (fr) * | 2004-05-12 | 2005-11-17 | Bayer Cropscience Gmbh | Regulation de croissance de plantes |
US7605153B2 (en) * | 2004-10-15 | 2009-10-20 | Centre National De La Recherche Scientifique - Cnrs | Use of paullone derivatives for the production of medicaments for the treatment of mucoviscidosis and diseases related to protein addressing errors in cells |
WO2006117212A2 (fr) | 2005-05-04 | 2006-11-09 | Develogen Aktiengesellschaft | Utilisation des inhibiteurs gsk-3 dans la prevention et le traitement des maladies auto-immunes pancreatiques |
WO2007006566A1 (fr) * | 2005-07-12 | 2007-01-18 | Abbott Gmbh & Co. Kg | Composes pyridazine utilises comme inhibiteurs de la glycogene synthase kinase 3 |
US7994160B2 (en) | 2005-07-12 | 2011-08-09 | Abbott Gmbh & Co. Kg | Pyridazine compounds as glycogen synthase kinase 3 inhibitors |
EP2275096A2 (fr) | 2005-08-26 | 2011-01-19 | Braincells, Inc. | Neurogenese par modulation des recepteurs muscariniques |
EP2258359A2 (fr) | 2005-08-26 | 2010-12-08 | Braincells, Inc. | Neurogenèse par modulation des récepteurs muscariniques avec sabcomeline |
EP2275095A2 (fr) | 2005-08-26 | 2011-01-19 | Braincells, Inc. | Neurogenese par modulation des recepteurs muscariniques |
EP2258357A2 (fr) | 2005-08-26 | 2010-12-08 | Braincells, Inc. | Neurogenèse avec inhibiteur de l'acetylcholinestérase |
EP2258358A2 (fr) | 2005-08-26 | 2010-12-08 | Braincells, Inc. | Neurogenèse avec un inhibiteur de l'acetylcholinestérase |
EP2377530A2 (fr) | 2005-10-21 | 2011-10-19 | Braincells, Inc. | Modulation de neurogénèse par inhibition PDE |
EP2314289A1 (fr) | 2005-10-31 | 2011-04-27 | Braincells, Inc. | Modulation de la neurogenese dont la médiation est assurée par récepteur gaba |
EP2377531A2 (fr) | 2006-05-09 | 2011-10-19 | Braincells, Inc. | Neurogénèse par modulation de l'angiotensine |
EP2382975A2 (fr) | 2006-05-09 | 2011-11-02 | Braincells, Inc. | Neurogénèse par modulation d'angiotensine |
US8029980B2 (en) | 2006-09-29 | 2011-10-04 | The Board Of Trustees Of The University Of Illinois | Identification and use of agents that modulate oncogenic transcription agent activity |
WO2010099217A1 (fr) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation de neurogenèse à l'aide de combinaisons de d-cyclosérine |
WO2011063115A1 (fr) | 2009-11-19 | 2011-05-26 | Braincells Inc. | Combinaison d'un agent nootropique avec un ou plusieurs agents neurogènes ou à effet neurogène par synergie pour stimuler ou intensifier la neurogenèse |
WO2011091033A1 (fr) | 2010-01-20 | 2011-07-28 | Braincells, Inc. | Modulation de la neurogenèse par des agents ppar |
Also Published As
Publication number | Publication date |
---|---|
JP2003522793A (ja) | 2003-07-29 |
US7232814B2 (en) | 2007-06-19 |
CA2397560A1 (fr) | 2001-08-23 |
AU2001235691A1 (en) | 2001-08-27 |
FR2804959A1 (fr) | 2001-08-17 |
EP1255551A1 (fr) | 2002-11-13 |
US20030181439A1 (en) | 2003-09-25 |
FR2804959B1 (fr) | 2006-04-28 |
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