WO2007074176A1 - Nuevos derivados pirrólicos con actividad inhibidora de desacetilasas de histonas - Google Patents
Nuevos derivados pirrólicos con actividad inhibidora de desacetilasas de histonas Download PDFInfo
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- WO2007074176A1 WO2007074176A1 PCT/ES2005/000708 ES2005000708W WO2007074176A1 WO 2007074176 A1 WO2007074176 A1 WO 2007074176A1 ES 2005000708 W ES2005000708 W ES 2005000708W WO 2007074176 A1 WO2007074176 A1 WO 2007074176A1
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- 0 CC(C)(CC(C)(C)*C(c1c(*)c(*)c(*)[n]1*)=O)*C(*)=* Chemical compound CC(C)(CC(C)(C)*C(c1c(*)c(*)c(*)[n]1*)=O)*C(*)=* 0.000 description 3
- YLQWEJYYVHBAEW-UHFFFAOYSA-N COc1cc(-c2c(C(NCCCCNC(NO)=O)=O)[nH]c(-c3cc(OC)cc(OC)c3)c2)cc(OC)c1 Chemical compound COc1cc(-c2c(C(NCCCCNC(NO)=O)=O)[nH]c(-c3cc(OC)cc(OC)c3)c2)cc(OC)c1 YLQWEJYYVHBAEW-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
- C07D207/42—Nitro radicals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
Definitions
- the invention relates to new compounds derived from pyrrols, with methods for their preparation and with the use thereof as drugs for the treatment of cancer in pharmaceutical compositions thanks to their inhibitory activity on certain histone deacetylases .
- HDACs histone deacetylase inhibitors
- HDAC inhibitors can be increased by combining synergistically with other treatments by improving the transcriptional profile of genes that hinder the development of resistance (Keen et al. Cancer Res. Treat. 2003, 81, 177. Egger et al. Nature 2004, 429, 457).
- HDAC inhibitors Several families of HDAC inhibitors are known, whose general characteristics can be found in various reviews (Villar-Garea and Esteller Int. J. Cancer 2004, 112, 171 and Curr. Drug Metab. 2003, 4, 11. Grozinger et al. Chem. Biol. 2002, 9, 3. McLaughlin et al., Drug Discov. Today 2003, 8, 793. Monneret Eur. J. Med. Chem. 2005, 40, 1, Biel et al. Angew. Chem. Int. Ed. 2005, 44, 3186).
- the structures of the most active inhibitors are characterized by a cyclic or polycyclic part of a predominantly hydrophobic nature linked by a spacer carbon chain to a unit capable of coordinating the metal ion of the active center of the HDAC.
- HDAC inhibitors 3- (4-aroyl-1-methyl-1H-2-pyrrolyl) - ⁇ / -hydroxy-2-propenamides
- the spacer chain is unsaturated and positions 3 and 5 of the pyrrole ring are not substituted, resulting in a linear molecular geometry.
- the therapeutic utility thereof is not without problems, among which the selectivity of inhibition of different HDACs, some of which are not useful therapeutic targets in oncology, toxicity, and The chemical instability.
- the present invention describes a general method of synthesis of new HDAC inhibitors that incorporates the possibility of generating a wide variety of functional groups, resulting in molecules chemically stable and with various polycyclic systems, spacer sizes and coordinating units to the metal atom of the enzymes to be inhibited.
- the problem thus posed by the present invention is to provide compounds and compositions with a high selectivity in the inhibition of different HDACs related to the appearance and development of neoplastic processes, with high chemical stability and low toxicity.
- the proposed solution comprises the use of pyrrolic derivatives of general formula I.
- These compounds have aryl or heteroaryl substituents in positions 3 and 5, as well as electron-attractant groups such as the nitro group in position 4 and heterogeneous groups in position 2 comprising spacers of different nature and the use of groups ⁇ / -hydroxyurea, ⁇ / -alkylamino (aryl) urea, / V-hydroxythiourea and N-alkylamino (aryl) thiourea as coordinators to the metal atom of the HDACs.
- These pyrrole derivatives demonstrate a great capacity to inhibit cell proliferation and tumor growth.
- the present invention solves the need that existed to have histone deacetylase inhibitors that had advantages such as good pharmacological properties, chemical stability in solid phase and in solution, the ease and efficiency of chemical synthesis thereof and the accessibility and variability of the starting chemical compounds.
- Figure 1 shows the effect determined in vito of some of the compounds object of the present invention on the histone deacetylase activity of the HCT116 cell line (human colon carcinoma), compared with the compounds TSA (acronym for tr ⁇ costatin A) and SAHA (acronym for suberoylanilide hydroxamic acid) used as a positive control.
- TSA acronym for tr ⁇ costatin A
- SAHA acronym for suberoylanilide hydroxamic acid
- Figure 2 shows the in vitro effect of representative examples of the compounds object of the present invention on the histone deacetylase activity of the MOLT4 cell line (human fibroblastic leukemia), compared with the TSA and SAHA compounds used as positive control.
- MOLT4 cell line human fibroblastic leukemia
- Figure 3 shows the quantification of the level of acetylation by HPCE (high efficiency capillary electrophoresis) of histones H3 and H4 of the line Jurkat cell of human promyelocytic leukemia treated with some of the compounds object of the invention in a concentration of 10 ⁇ M.
- HPCE high efficiency capillary electrophoresis
- Figure 4 shows the measurement of the percentage of apoptotic and necrotic cells in the presence of various concentrations of SAHA and two of the inhibitors object of the present invention.
- the data obtained in the control sample and in a sample treated with DMSO are also included.
- the exposed data correspond to the human colon carcinoma model HCT116.
- Figure 5 shows the measurement of the percentage of apoptotic and necrotic cells in the presence of various concentrations of SAHA and two of the inhibitors object of the present invention.
- the data obtained in the control sample and in a sample treated with DMSO are also included.
- the data presented correspond to the human acute myeloid leukemia model HL60.
- Figure 6 shows the inhibition of tumor growth of human colon carcinoma HCT116 in nude nude mice, caused by intraperitoneal administration of some of the compounds object of the invention.
- the xenoimplants were performed intra-splenicly and the inhibitors were injected intraperoneally, according to the procedure detailed in Example No. 18.
- Figure 7 shows the antitumor activity in vivo in nude nude mice of some of the compounds object of the invention in the MOLT4 human fibroblastic leukemia model.
- the xenoimplants were performed intra-spleen according to the procedure detailed in example No. 17.
- the present invention relates to the pyrrole derivatives of general formula I:
- Another object of the present invention are the processes for preparing said compounds of general formula I.
- Another additional object of the invention is the use of these derivatives for the treatment of various forms of cancer by restricting tumor growth through the inhibition of the action of certain deacetylases of (lathones.
- this invention has as its object the elaboration of a pharmaceutical composition comprising some pyrrole derivative of general formula I and at least one pharmaceutically acceptable excipient.
- the present invention provides pyrrole-derived compounds that have the following formula I:
- R 1 and R 3 independently represent each other a phenyl radical; mono or polysubstituted phenyl in the different ring positions; or a heteroaryl group
- R 2 represents a hydrogen atom or an electron-attractant group such as the nitro group; or an amino or amido group;
- R 4 represents a hydrogen atom or a C1-C6 linear, branched or cyclic alkyl group
- (n) represents a number of methylene groups between 1 and 8, both inclusive;
- (X) indistinctly represents a secondary amino group, an oxygen atom or a sulfur atom;
- (Y) represents a group selected from methylene, substituted methylene and secondary amino;
- (Z) indistinctly represents an oxygen or sulfur atom; and (W) represents a group selected from hydroxyl, hydroxyamino, hydrazino and alkyl, aryl or heteroaryl hydrazino.
- said compounds of general formula I are: Hexanoic 6- (3,5-diphenyl-1W-pyrrol-2-carboxamide) acid, with the following structural formula:
- Another aspect of the invention refers to different processes for obtaining the compounds of general formula I.
- the following methods A to E describe the procedures for obtaining compounds of general formula (Ia), (Ib), (Ic) and (Id) as We'll see later.
- Said compounds (Ia) to (Id) are compounds whose general formula falls within the general formula I.
- Method A represents a process for the preparation of compounds of general formula (Ia):
- the reaction mixture formed by the four compounds of phases a) to d) can be carried out by adding one of the components to the previous mixture of the other three in the organic solvent and at the temperature of -85 0 C at +25 0 C, preferably at temperatures close to 0 0 C. Then a time is left to complete the reaction, being able to reach room temperature. Once the coupling reaction is completed, the ester obtained after following the general procedure is reacted with the mixture of lithium or sodium hydroxide, dimethoxyethane and water thus yielding, after the corresponding treatment, the compounds of general formula (Ia).
- Method B represents a process for the preparation of compounds of general formula (Ib):
- reaction mixture formed by the four compounds of phases a) to d) can be carried out by adding one of the components to the previous mixture of the other three in the organic solvent and at the temperature of -85 0 C at +25 0 C, preferably at temperatures close to 0 0 C.
- R 5 is tert-butoxycarbamoyl (NHBoc) or benzyloxycarbamoyl
- the reaction mixture formed by the four compounds of phases a) to d) can be carried out by adding one of the components to the previous mixture of the other three in the organic solvent and at the temperature of -85 0 C at +25 0 C, preferably at temperatures close to 0 0 C. Then a time is left to complete the reaction, being able to reach room temperature.
- R 5 in compound III that is, depending on whether R 5 represents tert-butoxycarbamoyl (NHBoc) or benzyloxycarbamoyl (NHCBz)
- subsequent treatments will be different.
- R 5 is NHBoc
- the resulting product must be subjected to an acid treatment which preferably consists of the reaction at room temperature with trifluoroacetic acid in a halogenated solvent.
- R 5 represents NHCBz
- the resulting product is subjected to hydrogenolysis, preferably by reaction with hydrogen gas or ammonium formate in a short chain alcohol as solvent and in the presence of a heterogeneous palladium catalyst.
- phosgene or some of its derivatives such as diphosgene or triphosgene or also thiophosgene.
- the final compound (Ic) When the reaction is with phosgene, diphosgene or triphosgene, the final compound (Ic) will have the meaning of Z an oxygen atom. If on the contrary the treatment is with thiophosgene Z it will be a sulfur atom.
- Method D represents a process for the preparation of compounds of general formula (Id):
- R 1 , R 2 , R 3 , R 4 , X, Z and n have the significance given above and R 6 is a 5, 6-membered H, C1-C6 alkyl, aryl or heteroaryl with 1 or more heteroatoms selected from O, N or S, which comprises reacting a mixture consisting of: a) A 1 H-pyrrole-2-carboxylic acid of formula II,
- R 5 is tert-butoxycarbamoyl (NHBoc) or bezyloxycarbamoyl (NHCBz), c) An activation reagent of the carboxyl group; and d) A tertiary amine, selected from cyclic or acyclic aliphatics with C3-C10 carbons and alkanoaromatics with C9-C15 carbons, deprotect the product obtained by acid or hydrogenolysis treatment and react with phosgene or its analogues such as diphosgene, triphosgene or thiophosgene, obtaining a socianato or thioisocyanate which is treated with hydrazine or alkyl, aryl or heteroaryl hydrazines.
- phosgene or its analogues such as diphosgene, triphosgene or thiophosgene
- the reaction mixture formed by the four compounds of phases a) to d) can be carried out by adding one of the components to the previous mixture of the other three in the organic solvent and at the temperature of -85 0 C at +25 0 C, preferably at temperatures close to 0 0 C. Then a time is left to complete the reaction, being able to reach room temperature.
- R 5 in compound III that is, depending on whether R 5 represents tert-butoxycarbamoyl (NHBoc) or benzyloxycarbamoyl (NHCBz)
- subsequent treatments will be different.
- R 5 is NHBoc
- the resulting product must be subjected to an acid treatment which preferably consists of the reaction at room temperature with trifluoroacetic acid in a halogenated solvent.
- R 5 represents NHCBz
- the resulting product is subjected to hydrogenolysis preferably by reaction with hydrogen gas or ammonium formate in a short chain alcohol as solvent and in the presence of a heterogeneous palladium catalyst.
- phosgene or some of its derivatives such as diphosgene or triphosgene or also thiophosgene.
- the final compound (Ic) When the reaction is with phosgene, diphosgene or triphosgene, the final compound (Ic) will have the meaning of Z an oxygen atom. If on the contrary the treatment is with thiophosgene Z it will be a sulfur atom.
- Method E represents an additional procedure for the preparation of compounds of general formula (Id):
- R 1 , R 2 , R 3, R 4 , X, Z and n have the significance given above and R 6 is a 5, 6-membered alkyl, aryl or heteroaryl H, C1-C6 with 1 or more heteroatoms selected from O, N or S, which comprises reacting a mixture consisting of: a) A 1 H-pyrrol-2-carboxylic acid of formula II,
- the activation reagent of the carboxyl group is preferably phenyl dichlorophosphate, diethyl phosphorothiamidate (DEPC) or the system formed by 1-hydroxybenzotriazole and N- (3- dimethylaminopropyl) -N'-ethylcarbodiimide .
- a tertiary amine is a common reagent to methods A and B, selected from cyclic or acyclic aliphatic with C3-C10 carbons and alkanoaromatic with C9-C15 carbons.
- this tertiary amine is selected from N-methyl pyrrolidine or N-methylmorpholine. It is also preferable to carry out the reaction between elements a) to d) of each of the methods A to E by microwave irradiation.
- R 3 has the significance given above; b) A configuration mine (E) or (Z) with the following formula V,
- R 1 has the significance given above, and R 6 represents a C1-C6 alkyl or aryl group; c) A metal salt, preferably selected from lithium perchlorate, silver perchlorate or silver acetate, and d) A tertiary organic base, selected from aliphatic with C3-C10 carbons or alkanoaromatic with C9-C15 carbons.
- the reaction mixture formed by the four components indicated above can be performed by microwave irradiation or by adding one of the components over the other three, in an organic solvent and the temperature of -25 0 C to +25 0 C, preferably at temperatures close to +25 0 C.
- a mixture of 2-alkoxycarbonyl pyrrolidines corresponding to the substituents selected for each particular reaction is obtained.
- Said mixture is dissolved in a cyclic ether such as high-boiling tetrahydrofuran or acyclic ether such as bis (2-methoxyethyl) ether, also known as "diglyme” and an oxidizing agent such as manganese dioxide, hydrogen peroxide is added. or 2,3-dichloro-5,6-dicyano-1,4-benzoquinone.
- Acids of general formula Il are obtained by hydrolysis alkaline of the above esters, preferably by treating them with lithium or sodium hydroxide in a mixture of water and dimethoxyethane.
- a further aspect of this invention relates to the use of the compounds of general formula I for the treatment of cancer.
- the mechanism of action of said compounds is explained by their antagonistic properties with histone deacetylases involved in blocking the synthesis of proteins responsible for the regulation of processes such as apoptosis or cell growth and proliferation. Said properties prevent or block the binding of deacetylases and enzyme complexes related to their natural substrates, such as N-acetylated Usine residues in the ⁇ position of the terminal lysine residues of histones, so that they remain in the mono- or polyacetylated state.
- a final aspect of the invention refers to a composition comprising at least one of the compounds of general formula I and one or more pharmaceutically acceptable excipients.
- the compounds of formula I of the present invention can be administered both as a pure substance and in the form of pharmaceutical formulations, although it is preferable to administer the compound in combination.
- the combination of the medicament is preferably in the form of a formulation Ia which: i) Contains the compound of general formula I alone;
- excipients and / or transport substances Contains one or more excipients and / or transport substances; and iii) May contain some additional therapeutically active substance.
- the excipients, transport substances and auxiliary substances must be pharmaceutically and pharmacologically tolerable, so that they can be combined with other components of the formulation or preparation and do not exert adverse effects on the treated organism.
- the formulations include those that are suitable for oral or parenteral administration (including subcutaneous, intradermal, intramuscular and intravenous), although the best route of administration will depend on the patient's condition.
- the formulations can be in the form of single doses and are prepared according to methods known in the field of pharmacology.
- the amounts of active substances to be administered may vary depending on the particularities of The therapy although generally vary between 1 and 500 mg per day in one or several doses.
- DMSO-de 162.5, 157.9, 134.4, 131.3, 131.2, 130.3, 128.6, 127.9, 127.0, 125.1, 119.8, 113.0, 112.9, 109.3, 55.0, 54.9;
- Anal. Cale, for C 18 H 15 NO 3 C, 73.71; H, 5.15; N, 4.78. Found: C, 73.56; H, 5.08; N, 4.81%.
- Triethylamine (1.15 ml, 8.25 mol), 1- hydroxybenzotriazole (0.22 g, 1.65 mmol), ⁇ / - (3-dimethylaminopropyl) hydrochloride - ⁇ / '- Ethylcarbodümide (0.32 g, 1.65 mmol) and ⁇ / -methylmorphol (0.165 ml, 1.5 mmol) were added successively, and the mixture was stirred at 0 ° C for 2 h, and for 96 more hours at room temperature.
- the methyl ester obtained was dissolved in ethylene glycol dimethyl ether (6 ml) and the solution was cooled to 0 0 C. Then, an aqueous solution of 1N LiOH (3.6 ml) was added dropwise and the resulting mixture was stirred at 0 0 C. The progress of the reaction was monitored by thin layer chromatography. Once the reaction was completed, 10% citric acid (3.6 ml, aqueous solution) was added (pH ⁇ 6). The solution was extracted with methylene chloride (3 x 5 mL), and the combined organic fractions were dried over MgSO 4 and evaporated under reduced pressure. The reaction crude was triturated in diethyl ether to give 0.42 g of a white solid. Rdto.
- Methyl 6- (3-phenyl-5- (4-methoxyphenyl) -1 H- pyrrol-2-carboxamido) hexanoate (0.53 g, 1.25 mmol), prepared from 3-phenyl-5- (4-methoxyphenyl) ) -1H-pyrrol-2-carboxylic acid and 6-aminohexanoic acid methyl ester hydrochloride according to the procedure described in Example 4, and sodium methoxide in methanol (5.0 mmol, 1.4 ml of a previously prepared solution) were added successively. The mixture was stirred for 26h, observing the formation of a dense precipitate. After this time, water (3 ml) was added to the reaction medium.
- This material was prepared by a procedure substantially similar to that of Example 10, using benzyloxyamlna instead of methylhydrazine. After the previously specified addition-deprotection sequence, the title compound was obtained as the trifluoroacetate of the corresponding ammonium salt. Rdto.
- This material was prepared by a procedure substantially similar to that of Example 11, from 3,5-bis (3,5-dimethoxyphenyl) -1H-carboxylic acid and trifluoroacetate of the ammonium salt of 1- (4- aminomethyl) -3- (benzyloxy) urea. Rdto.
- the samples for the scintillation reader were prepared by mixing 500 ⁇ l of the upper phase and 5 ml of scintillation liquid.
- the cells of the Jurkat human lines were treated for 24 hours with different concentrations of the HDAC inhibitor compounds object of the present invention.
- the nuclei were isolated by adding RSB buffer (10 mM Tris pH 7.5, 10 mM sodium chloride and 3 mM magnesium chloride) with 1% Nonidet-P40 and protease inhibitor.
- RSB buffer 10 mM Tris pH 7.5, 10 mM sodium chloride and 3 mM magnesium chloride
- To extract the histones 0.25M HCI was added to the nuclei, and the mixture was stirred at 4 ° C for 16 h. Then, the histones were precipitated by adding 8 volumes of acetone.
- the histone mixture obtained was separated by reverse phase high performance liquid chromatography (HPLC), using a C18 column with a gradient of acetonitrile (20-60%) in 0.3% trifluoroacetic acid.
- the separation of the non-acetylated, mono-, di-, tri-, and tetra-acetylated species from each fraction of histones H3 and H4 was carried out by high resolution capillary electrophoresis (HPCE), using a silica capillary ( 60.2 cm x 75 ⁇ m, effective length of 50 cm).
- HPCE high resolution capillary electrophoresis
- the elution conditions used were: 25 ° C, 12 kV voltage, 214 nm absorbance detector, and 110 mM phosphate elution buffer (pH 2.0) and cellulose-HPM (0.03% w / v).
- the system was washed for 3 minutes with 0.1 M NaOH, followed by another 2 minute wash with 0.5 M H 2 SO 4 , and equilibrated with the elution buffer for 3 minutes. Buffers and wash solutions were prepared with filtered MiIIi-Q water through a 0.45 ⁇ m pore filter. The samples were injected under pressure of 0.3 psi for 3 seconds. All samples were analyzed in duplicate.
- the quantification of the amount of apoptotic cells was performed by studying the change in permeability of the cytoplasmic membrane by flow cytometric analysis, using the YoPro ⁇ commercial kit as a staining agent. The procedure followed is explained below.
- the cells of the human lines HCT116 and HL60 (10 6 cells per treatment) were treated for 24 hours with different concentrations of the HDAC inhibitor compounds object of the invention. After this period, the cells were washed twice with cold 1X PBS, resuspended in 1 ml of 1X PBS and 1 ⁇ l of YoPro® and 1 ⁇ l of propidium iodide were added. The mixture was incubated protected from light for 30 minutes on ice. The amount of apoptotic cells was measured by flow cytometry.
- Figure 4 shows the data related to the human colon carcinoma model
- FIG. 1 shows the data related to the human acute myeloid leukemia model HL60.
- Example 18 Measurement of biological activity in vivo.
- mice in the control group were administered 200 ⁇ l of PBS to mimic the stress of the inoculation.
- volume d 3 x ⁇ / 6
- mice were sacrificed and the tumors were removed and weighed.
- Figure 7 shows the data related to the human colon carcinoma model HCT116.
- Figure 8 shows the data related to the MOLT4 human fibroblastic leukemia model.
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Abstract
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Priority Applications (18)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2005800524523A CN101351444B (zh) | 2005-12-27 | 2005-12-27 | 具有组蛋白脱乙酰基酶抑制活性的吡咯衍生物 |
ES05850516T ES2369705T3 (es) | 2005-12-27 | 2005-12-27 | Nuevos derivados pirrólicos con actividad inhibidora de desacetilasas de histonas. |
AT05850516T ATE516268T1 (de) | 2005-12-27 | 2005-12-27 | Neue pyrrolderivate mit histondeacetylase- hemmwirkung |
HK09104096.6A HK1125926B (en) | 2005-12-27 | Pyrrole derivatives with histone deacetylase inhibitor activity | |
DK05850516.5T DK1975158T3 (da) | 2005-12-27 | 2005-12-27 | Hidtil ukendte pyrrolderivater med histondeacetylase-inhibitoraktivitet |
AU2005339535A AU2005339535B2 (en) | 2005-12-27 | 2005-12-27 | New pyrrolic derivatives with histone deacetylase inhibitory activity |
PL05850516T PL1975158T3 (pl) | 2005-12-27 | 2005-12-27 | Nowe pochodne pirolu o aktywności inhibitującej deacylazę histonową |
PT05850516T PT1975158E (pt) | 2005-12-27 | 2005-12-27 | Novos derivados de pirrole com actividade inibidora de histona desacetilase |
CA2635392A CA2635392C (en) | 2005-12-27 | 2005-12-27 | New pyrrolic derivatives with histone deacetylase inhibitory activity |
SI200531342T SI1975158T1 (sl) | 2005-12-27 | 2005-12-27 | Novi derivati pirola z učinki inhibitorja histonske deacitilaze |
BRPI0520806-8A BRPI0520806A2 (pt) | 2005-12-27 | 2005-12-27 | derivados pirrólicos, processos para a preparação de compostos, seu uso e composição farmacêutica que os contém |
JP2008547990A JP4975758B2 (ja) | 2005-12-27 | 2005-12-27 | ヒストンデアセチラーゼ阻害活性を有する新規ピロール誘導体 |
RU2008130876/04A RU2416600C2 (ru) | 2005-12-27 | 2005-12-27 | Новые производные пиррола с ингибирующей гистондеацетилазу активностью |
US10/571,497 US7638550B2 (en) | 2005-12-27 | 2005-12-27 | Pyrrolic derivatives with histone deacetylase inhibitory activity |
PCT/ES2005/000708 WO2007074176A1 (es) | 2005-12-27 | 2005-12-27 | Nuevos derivados pirrólicos con actividad inhibidora de desacetilasas de histonas |
EP05850516A EP1975158B9 (en) | 2005-12-27 | 2005-12-27 | Novel pyrrole derivatives with histone deacetylase inhibitor activity |
MX2008008470A MX2008008470A (es) | 2005-12-27 | 2005-12-27 | Nuevos derivados pirrolicos con actividad inhibidora de desacetilasa de histonas. |
CY20111100951T CY1111899T1 (el) | 2005-12-27 | 2011-10-05 | Καινοφανη παραγωγα πυρρολης με δραστηριοτητα αναστολεα της απακετυλασης της ιστονης |
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PCT/ES2005/000708 WO2007074176A1 (es) | 2005-12-27 | 2005-12-27 | Nuevos derivados pirrólicos con actividad inhibidora de desacetilasas de histonas |
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US (1) | US7638550B2 (es) |
EP (1) | EP1975158B9 (es) |
JP (1) | JP4975758B2 (es) |
CN (1) | CN101351444B (es) |
AT (1) | ATE516268T1 (es) |
AU (1) | AU2005339535B2 (es) |
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Cited By (2)
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EP2305643A1 (en) | 2009-10-02 | 2011-04-06 | Ikerchem, S.L. | New histone deacetylase inhibitors based simultaneously on trisubstituted 1h-pyrroles and aromatic and heteroaromatic spacers |
EP2508510A1 (en) | 2011-04-06 | 2012-10-10 | Ikerchem, S.L. | Hydroxyphenyl pyrrole compounds containing an hydroxamic acid as hdac inhibitors and medicinal applications thereof |
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WO2006108864A2 (en) * | 2005-04-15 | 2006-10-19 | Dominion Pharmakine S.L. | New nitrogenated trans-stilbene analogs, method for the obtention and medical applications thereof |
CN103373969B (zh) * | 2012-04-27 | 2015-09-16 | 中国科学院上海有机化学研究所 | 苯基唑环取代酰胺类化合物及其制备方法和用途 |
MY195058A (en) * | 2015-05-22 | 2023-01-05 | Chong Kun Dang Pharmaceutical Corp | Heterocyclicalkyl Derivative Compounds as Selective Histone Deacetylase Inhibitors and Pharmaceutical Compositions Comprising the Same |
CN106565583A (zh) * | 2016-11-15 | 2017-04-19 | 淮阴师范学院 | 多取代吡咯衍生物的制备方法 |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2305643A1 (en) | 2009-10-02 | 2011-04-06 | Ikerchem, S.L. | New histone deacetylase inhibitors based simultaneously on trisubstituted 1h-pyrroles and aromatic and heteroaromatic spacers |
WO2011039353A1 (en) | 2009-10-02 | 2011-04-07 | Ikerchem, S.L. | New histone deacetylase inhibitors based simultaneously on trisubstituted 1h-pyrroles and aromatic and heteroaromatic spacers |
US8685992B2 (en) | 2009-10-02 | 2014-04-01 | Universidad Del País Vasco | Histone deacetylase inhibitors based simultaneously on trisubstituted 1H-pyrroles and aromatic and heteroaromatic spacers |
AU2010302572B2 (en) * | 2009-10-02 | 2016-10-20 | Ikerchem, S.L. | New histone deacetylase inhibitors based simultaneously on trisubstituted 1H-pyrroles and aromatic and heteroaromatic spacers |
KR101754940B1 (ko) | 2009-10-02 | 2017-07-06 | 이케르쳄 에스.엘. | 3-치환된 1h-피롤 및 방향족 및 헤테로 방향족 스페이서에 동시에 기반한 신규한 히스톤 디아세틸라아제 저해제 |
EP2508510A1 (en) | 2011-04-06 | 2012-10-10 | Ikerchem, S.L. | Hydroxyphenyl pyrrole compounds containing an hydroxamic acid as hdac inhibitors and medicinal applications thereof |
WO2012136722A1 (en) | 2011-04-06 | 2012-10-11 | Ikerchem, S.L. | Hydroxyphenyl pyrrole compounds containing an hydroxamic acid as hdac inhibitors and medicinal applications thereof |
Also Published As
Publication number | Publication date |
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CA2635392A1 (en) | 2007-07-05 |
CA2635392C (en) | 2013-07-23 |
EP1975158A4 (en) | 2009-11-11 |
EP1975158B1 (en) | 2011-07-13 |
CN101351444A (zh) | 2009-01-21 |
RU2416600C2 (ru) | 2011-04-20 |
CN101351444B (zh) | 2011-07-13 |
PL1975158T3 (pl) | 2011-12-30 |
ATE516268T1 (de) | 2011-07-15 |
AU2005339535B2 (en) | 2012-02-23 |
EP1975158A1 (en) | 2008-10-01 |
MX2008008470A (es) | 2008-09-26 |
JP4975758B2 (ja) | 2012-07-11 |
SI1975158T1 (sl) | 2011-10-28 |
RU2008130876A (ru) | 2010-02-10 |
JP2009521519A (ja) | 2009-06-04 |
DK1975158T3 (da) | 2011-10-24 |
EP1975158B9 (en) | 2012-02-29 |
BRPI0520806A2 (pt) | 2009-06-09 |
CY1111899T1 (el) | 2015-11-04 |
AU2005339535A1 (en) | 2007-07-05 |
US7638550B2 (en) | 2009-12-29 |
ES2369705T3 (es) | 2011-12-05 |
HK1125926A1 (en) | 2009-08-21 |
PT1975158E (pt) | 2011-09-23 |
US20080262073A1 (en) | 2008-10-23 |
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