WO2001022968A1 - Agents anticancereux - Google Patents
Agents anticancereux Download PDFInfo
- Publication number
- WO2001022968A1 WO2001022968A1 PCT/JP2000/006786 JP0006786W WO0122968A1 WO 2001022968 A1 WO2001022968 A1 WO 2001022968A1 JP 0006786 W JP0006786 W JP 0006786W WO 0122968 A1 WO0122968 A1 WO 0122968A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compound
- general formula
- cancer
- anticancer
- anticancer agents
- Prior art date
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Classifications
-
- 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
- A61K31/495—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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Definitions
- the present invention relates to an anticancer agent that suppresses the growth of cancer, that is, an antineoplastic agent, and in particular, to the growth of human cancer cells containing a diphenylmethylbiperazine derivative.
- the present invention relates to a pile cancer drug that suppresses the occurrence of cancer, that is, an antineoplastic agent.
- the present invention provides a method for suppressing fibrotic diseases caused by proliferation of fibroblasts and proliferative lesions of pulmonary fibrosis diseases caused by proliferation of fibroblasts as a side effect of an anticancer drug.
- the present invention relates to a fibrosis inhibitor containing a diphenylmethylbiperazine derivative for treating proliferative lesions in mammals including humans.
- pile cancer or antineoplastic agents include: (i) melphalan, methylamine and cyclophosphamide, etc., and (2) B CNU, CCNU, methyl—CCNU and A Nitrosopreas such as CNU, 3 Thiotepa, mitomycin AZQ, carbone, azirines and epoxides such as dianhydrogalactitol and dibromodarcitol, and 4 alkylating agents such as procarpazine, dacarbazine and hexamethylene melamine.
- ⁇ Metrexrexant MTX
- 6-Mercaptopurine (6-MP)
- 6-Thoguanine (6-TG)
- 5-Fluorouracil (5-FU)
- Tegafur UFT
- 5'-DFUR 5-Fluorouracil
- Antimetabolites such as 5-fluoropyrimidine and related compounds such as pink listin, pimplastin and Pinto-alliloid compounds such as ndesine, ethoside compounds such as etoposide and teniposide, taxanes such as paclitaxel and docetaxel, and camptothecin compounds such as irinotecan.
- Plant-derived anticancer agents 7 adriamycin, selvidin, actinomycin D, anti-cancer antibiotics such as cosmegen, plenoxan, munomycin, medamicin and novanttron, 3 adenocorticoid, Hormonal agents such as estrogen, progestin, anti-estrogens, anti-alomose inhibitors, androgens, anti-androgens, and LH-RH analogs; enzymes such as luas paraginase; and cisplatin, carboplatin and Platinum complex compounds such as nedaplatin (254-S), 11 non-specific immunostimulants, 12 Ru centers Ferron and 13 TNF such Nadogaa
- cisplatin is used in the treatment of solid tumors.
- cisplatin has been shown to have nephrotoxicity, gastrointestinal toxicity, ototoxicity and peripheral neurotoxicity, and has a low cure rate, which is a problem.
- An object of the present invention is to solve the problems of these anticancer agents.
- the present invention has a large anticancer activity (ie, an anti-neoplastic tumor activity) against various cancers or a property of suppressing the growth of lung fibroblasts.
- An object of the present invention is to provide a less toxic compound, a salt thereof, and a derivative thereof, which have both a cancer activity (ie, an anti-neoplastic tumor activity) and a property of inhibiting the growth of lung fibroblasts. Disclosure of the invention
- a salt thereof, a derivative thereof, or a prodrug thereof is less toxic than cisplatin, and has a large anticancer effect on various cancers as compared with cisplatin.
- the present invention has been found to have an action and to suppress the growth of fibroblasts, and thus has reached the present invention.
- the present invention provides a compound represented by the general formula [I]:
- FIG. 1 is a graph showing the cell growth inhibitory effect of the compound represented by the general formula [I] shown in Example 2 on fibroblasts.
- the compound represented by the general formula [I] a salt thereof, a derivative thereof, or a prodrug thereof (hereinafter, collectively referred to as a compound represented by the general formula [I]).
- I] a compound represented by the general formula [I]
- the compound represented by the general formula [I] further suppresses hyperconstriction and hyperextension of the myocardium without a cardiac depressing action, and protects the myocardium from necrosis. It is disclosed that the compound has an action, has a therapeutic and preventive effect on myocardial infarction, and has a suppressive and preventive effect on myocardial necrosis.
- the present inventors have found that the compound represented by the general formula [I] and the like in vivo (in vivo) and in vitro (in vitro) are more effective than cisplatin and other anticancer agents. It has been found that it has excellent anticancer activity against various cancers and exhibits a broad anticancer spectrum against various cancers, and it has been found that the compound represented by the general formula (I) Found that they inhibited fibroblast proliferation.
- anticancer agent includes a therapeutic agent for cancer and / or a fibrosis inhibitor.
- the "salt" of the compound represented by the general formula [I] Means a pharmaceutically acceptable salt, for example, an inorganic acid addition salt such as hydrochloride, hydrobromide, sulfate, phosphate or nitrate; acetate, propionate, succinate Acid, glycolate, lactate, lignate, oxalate, tartrate, citrate, maleate, fumarate, methanesulfonate, benzenesulfonate, p-toluenesulfonic acid Salts or organic acid addition salts such as ascorbate, or amino acid addition salts such as aspartate or glutamate, and also includes, but is not limited to, hydrates and hydrates Not something.
- an inorganic acid addition salt such as hydrochloride, hydrobromide, sulfate, phosphate or nitrate
- acetate, propionate, succinate Acid glycolate, lactate, lignate, oxalate, tartrate
- the “prodrug” of the compound represented by the general formula [I] has a group that can be chemically or metabolically degraded, and is hydrolyzed or solvolyzed, or under physiological conditions. It exhibits activity as an anticancer agent by being decomposed with, and is a derivative of the compound represented by the general formula [I].
- the compound represented by the general formula [I] or the like according to the present invention has an excellent anticancer effect. That is, the pile cancer drug of the present invention contains the compound represented by the general formula [I] or the like as a main drug.
- the anticancer drug of the present invention when administered in combination with other anticancer drugs, can exert the anticancer effect of pile cancer drugs even on cancers that have become resistant. it can.
- the compound represented by the general formula [I] according to the present invention when used as an anticancer agent, it can be usually administered systemically or locally, orally or parenterally.
- the anticancer agent of the present invention may be administered simultaneously with another pile cancer drug, or may be administered before or after administration of another anticancer agent.
- the dosage varies depending on age, body weight, symptoms, therapeutic effect, administration method and processing time, but is usually for adults (average weight 60 kg). Alternatively, it is orally or parenterally administered once or several times a day in the range of 0.001 mg to lg, preferably in the range of 100 to 50 mg. When administered parenterally, it can be administered continuously for over 12 hours.
- a solid composition for oral administration is prepared by using the compound represented by the general formula [I] of the present invention as a main drug
- dosage forms such as tablets, pills, powders, and granules are possible.
- one or more active ingredients may be combined with one or more active diluents, dispersants or adsorbents, such as lactose, mannitol, glucose, hydroxypropylcellulose, It can be mixed with crystalline cellulose, starch, polyvinyl borolidone, magnesium aluminate metasilicate or powdered silicate. Further, the composition may be mixed with additives other than the diluent according to a conventional method.
- sucrose, gelatin, hydroxypropyl cellulose or hydroxymethylcellulose may be used, if necessary. It may be coated with a film of a gastric or enteric substance such as sulfate, or may be coated with two or more layers. In addition, capsules may be made with substances such as gelatin or ethylcellulose.
- a liquid composition for oral administration is prepared by using the compound represented by the above general formula [I] of the present invention as a main drug, a pharmaceutically acceptable emulsion, dissolving agent, or suspension agent
- a pharmaceutically acceptable emulsion, dissolving agent, or suspension agent Dosage forms such as syrup, elixir and the like are possible.
- the diluent used includes, for example, purified water / ethanol, vegetable oil, and emulsifier.
- these compositions may contain, in addition to diluents, wetting agents, suspending agents, and sweeteners. Auxiliaries such as flavoring agents, flavoring agents, fragrances or preservatives may be mixed.
- a sterile aqueous or non-aqueous solution or solubilizer is used.
- a suspending agent or emulsifier can be used.
- aqueous solutions, solubilizing agents, and suspending agents include water for injection, distilled water for injection, physiological saline, cyclodextrin and its derivatives, triethanolamine, diethanolamine, and monoethanol.
- organic amines such as amine and triethylamine, or inorganic alkaline solutions.
- a water-soluble solution for example, a vegetable oil such as propylene glycol, polyethylene glycol or olive oil, or ethanol.
- a solubilizing agent for example, a surfactant (formation of mixed micelles) such as polyoxyethylene hydrogenated castor oil and sucrose fatty acid ester, or lecithin or hydrogenated lecithin (formation of ribosome) can be used.
- an emulsion preparation comprising a water-insoluble solubilizer such as vegetable oil, lecithin, polyoxyethylene hydrogenated castor oil, polyoxyethylenepolypropylene glycol, or the like can be used.
- compositions for parenteral administration include one or more active compounds, i.e., the compound represented by the above general formula (I), and are formulated by a method known per se.
- the main drug was 1- [1-4-((diphenylmethyl) piperazinyl) 13- [11- (4- (4-chlorophenyl) 14).
- —Hydroxy] piberdinyl] -12-propanol hereinafter referred to as compound 1 is used.
- D-sorbitol and citrate were dissolved in a sufficient amount of water for injection.
- Compound 1 was dissolved in the obtained solution, and the pH was adjusted to 3.2 to 3.3 with sodium hydroxide. Then, with stirring, the remaining water for injection was added. The solution was filtered, packed into 20.0 ml ampules and sealed. The contents of this ampoule were autoclaved and sterilized.
- Human non-small cell lung cancer cell line PC-14, human small cell lung cancer cell line SBC-3, human breast cancer cell line MCF-7, human ovarian cancer cell line SK OV3, human leukemia cell Strain HL60 and human colorectal cancer cell strain W iDR were converted into single cells using trypsin treatment or cell scraper in RPMI 1640 medium, respectively.
- Compound 1 was dissolved in dimethyl sulfoxide as a pile cancer drug, and added so that the concentration of compound 1 was in the range of 0.5 to 1 ⁇ M. I put in one hundred fifty-five centimeters. This plate was heated at 37 ° C with 5% carbon dioxide and saturated water. The cells were cultured for 96 hours under steam conditions.
- MTT [3- (4,5-dimethylthiazol-2-yl) -12,5-diphenyltetrazolamide was dissolved in D-PBS (-) at a concentration of 5 mgZml.
- the amount of formazan was measured with a multiplate reader for the absorbance at a wavelength of 562-63 nm.
- a tumor volume growth curve was drawn with the average growth rate of the negative control being 0% and the average growth rate of the positive control being 100%, and the 50% human cancer cell growth inhibitory concentration of Compound 1 was calculated. . This is shown in Table 1.
- the values in Table 1 are the mean values of the cancer cell growth inhibitory concentration (IC 5 () ) value of 50% of MTT ATSSE in three independent cancer cell culture experiments using Compound 1. Shown by the error range (M). As shown in Table 1, Compound 1 has a concentration of 0.5 to 1.1 M. The results showed a 50 % growth inhibitory effect ( IC5Q ) for various cancers. The IC5 () value for Compound 1 is much lower than the IC5 () value of cisplatin, which is considered to be the most effective for solid tumors, measured by the MTT Atsey method, which is 2 to 3 M. Yes, IC 5 for compound 1. The value of indicates that compound 1 has a large anticancer effect, and is effective as an anticancer agent. In addition, it shows a broad antitumor spectrum against solid tumor cells such as lung cancer, breast cancer, colorectal cancer, and ovarian cancer as well as leukemia cells. is there.
- mice B AL BZc nu / nu (6 weeks old), the 2 X 1 0 7 single human non-small cell lung carcinoma lines PC- 1 4 cells were to saline suspension, implanted subcutaneously in the back The progress of engraftment was observed at. On the 7th day after transplantation, confirm the tumor status and select testable individuals. The animals were randomized so that no bias occurred, and the animals were divided into a control line, a first test line, and a second test line, each of which was addressed to 6 animals.
- the tumor volume of each implanted tumor is measured by measuring the minor axis of the tumor and the major axis of the tumor, and the product of the square of the minor axis of the tumor and the major axis of the tumor, that is, the formula: (minor axis of the tumor) 2 X ( (Major axis).
- Compound 1 administration was started on day 7 after tumor implantation.
- Compound 1 was administered to 6 animals in the subject group with series number 1 for 1 day, 7 days, 8 days, 9 days, 10 days, and 11 days after tumor implantation.
- 3 mg of compound 1 / kg body weight was injected via the tail of a nude mouse, and six of the subjects with the seq. No. 2 received 7 days, 8 days and 9 days after tumor implantation.
- the control group of subject No. 1 was a series to which Compound 1 was not administered, and the administration and treatment of Compound 1 were not performed at all.
- 1,2,3,4-Tetrahydroisoquinoline 25.Og was dissolved in acetonitrile (100 ml), and sodium carbonate (40.0 g) and epipromohydrin were added. (31.0 g) was added and the mixture was heated and refluxed for 4 hours. After the salt was filtered off, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Cogel C-200, 500 g), and eluted with a mixed solvent of 99 parts of chloroform and 1 part of methanol to give 2— [1— ( (2,3_epoxy) propyl] -1,2,3,4-tetratetrasoquinoline (15.6 g) was obtained.
- the compound represented by the general formula [I] and the like according to the present invention have less toxicity than conventional anticancer agents, for example, cisbratin, and are more various than conventional anticancer agents. It has a large anti-cancer effect on cancer and exhibits a broad anti-cancer spectrum. Compared to conventional anticancer drugs, it has a greater effect on cancer (solid cancer) and other malignant tumors. It greatly contributes to cancer treatment.
- the present invention also has an effect of suppressing fibroblast proliferation such as pulmonary fibrosis, and has an excellent effect of suppressing fibrosis as compared with conventional therapeutic agents such as pulmonary fibrosis and keloids. However, pulmonary fibrosis is a major contributor in the treatment of keloids.
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- Medicinal Chemistry (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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DE60032620T DE60032620T2 (de) | 1999-09-30 | 2000-09-29 | Antikrebsmittel |
EP00962991A EP1222924B1 (en) | 1999-09-30 | 2000-09-29 | Anticancer agents |
US10/089,718 US6683083B1 (en) | 1999-09-30 | 2000-09-29 | Anticancer agents |
CA002385996A CA2385996C (en) | 1999-09-30 | 2000-09-29 | Anticancer agents |
AU74498/00A AU776745B2 (en) | 1999-09-30 | 2000-09-29 | Anticancer agents |
Applications Claiming Priority (2)
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JP11/280874 | 1999-09-30 | ||
JP28087499 | 1999-09-30 |
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WO2001022968A1 true WO2001022968A1 (fr) | 2001-04-05 |
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PCT/JP2000/006786 WO2001022968A1 (fr) | 1999-09-30 | 2000-09-29 | Agents anticancereux |
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US (1) | US6683083B1 (ja) |
EP (2) | EP1637140B1 (ja) |
AT (2) | ATE359788T1 (ja) |
AU (1) | AU776745B2 (ja) |
CA (1) | CA2385996C (ja) |
DE (2) | DE60034494T2 (ja) |
TW (1) | TWI289450B (ja) |
WO (1) | WO2001022968A1 (ja) |
Families Citing this family (14)
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US7879840B2 (en) * | 2005-08-25 | 2011-02-01 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
US7393652B2 (en) * | 2000-05-10 | 2008-07-01 | The Trustees Of Columbia University In The City Of New York | Methods for identifying a chemical compound that directly enhances binding of FKBP12.6 to PKA-phosphorylated type 2 ryanodine receptor (RyR2) |
US20040229781A1 (en) * | 2000-05-10 | 2004-11-18 | Marks Andrew Robert | Compounds and methods for treating and preventing exercise-induced cardiac arrhythmias |
US20060293266A1 (en) * | 2000-05-10 | 2006-12-28 | The Trustees Of Columbia | Phosphodiesterase 4D in the ryanodine receptor complex protects against heart failure |
US8022058B2 (en) | 2000-05-10 | 2011-09-20 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
US20040048780A1 (en) * | 2000-05-10 | 2004-03-11 | The Trustees Of Columbia University In The City Of New York | Method for treating and preventing cardiac arrhythmia |
US6489125B1 (en) * | 2000-05-10 | 2002-12-03 | The Trustees Of Columbia University In The City Of New York | Methods for identifying chemical compounds that inhibit dissociation of FKBP12.6 binding protein from type 2 ryanodine receptor |
US7718644B2 (en) * | 2004-01-22 | 2010-05-18 | The Trustees Of Columbia University In The City Of New York | Anti-arrhythmic and heart failure drugs that target the leak in the ryanodine receptor (RyR2) and uses thereof |
US7544678B2 (en) * | 2002-11-05 | 2009-06-09 | The Trustees Of Columbia University In The City Of New York | Anti-arrythmic and heart failure drugs that target the leak in the ryanodine receptor (RyR2) |
EP1603450A4 (en) | 2003-03-07 | 2009-07-29 | Univ Columbia | METHODS USING TYPE 1 RYANODINE RECEPTOR |
US8710045B2 (en) * | 2004-01-22 | 2014-04-29 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the ryanodine receptors |
US7704990B2 (en) * | 2005-08-25 | 2010-04-27 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
US20070052304A1 (en) * | 2005-09-07 | 2007-03-08 | Philippe Masson | Multi-pattern high temperature superconducting motor using flux trapping and concentration |
JP5318938B2 (ja) * | 2011-06-09 | 2013-10-16 | 株式会社アエタスファルマ | ジフェニルメチルピペラジン誘導体、及びそれを用いた医薬組成物 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0363212A2 (en) * | 1988-10-06 | 1990-04-11 | MITSUI TOATSU CHEMICALS, Inc. | Novel heterocyclic compounds and anticancer-drug reinforcing agents containing them as effective components |
JPH04134070A (ja) * | 1990-09-21 | 1992-05-07 | Mitsui Toatsu Chem Inc | 新規ピリジン誘導体及びそれを有効成分として含有する制癌剤効果増強剤 |
US5304558A (en) * | 1990-07-10 | 1994-04-19 | Kirin Brewery Co., Ltd. | Diphenylmethyl piperazine derivatives |
-
2000
- 2000-09-29 EP EP05077245A patent/EP1637140B1/en not_active Expired - Lifetime
- 2000-09-29 DE DE60034494T patent/DE60034494T2/de not_active Expired - Lifetime
- 2000-09-29 AT AT05077245T patent/ATE359788T1/de active
- 2000-09-29 WO PCT/JP2000/006786 patent/WO2001022968A1/ja active IP Right Grant
- 2000-09-29 AT AT00962991T patent/ATE349212T1/de active
- 2000-09-29 CA CA002385996A patent/CA2385996C/en not_active Expired - Fee Related
- 2000-09-29 DE DE60032620T patent/DE60032620T2/de not_active Expired - Lifetime
- 2000-09-29 EP EP00962991A patent/EP1222924B1/en not_active Expired - Lifetime
- 2000-09-29 AU AU74498/00A patent/AU776745B2/en not_active Ceased
- 2000-09-29 US US10/089,718 patent/US6683083B1/en not_active Expired - Fee Related
- 2000-09-30 TW TW089120410A patent/TWI289450B/zh not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0363212A2 (en) * | 1988-10-06 | 1990-04-11 | MITSUI TOATSU CHEMICALS, Inc. | Novel heterocyclic compounds and anticancer-drug reinforcing agents containing them as effective components |
US5304558A (en) * | 1990-07-10 | 1994-04-19 | Kirin Brewery Co., Ltd. | Diphenylmethyl piperazine derivatives |
JPH04134070A (ja) * | 1990-09-21 | 1992-05-07 | Mitsui Toatsu Chem Inc | 新規ピリジン誘導体及びそれを有効成分として含有する制癌剤効果増強剤 |
Also Published As
Publication number | Publication date |
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CA2385996C (en) | 2008-02-12 |
DE60032620D1 (de) | 2007-02-08 |
ATE359788T1 (de) | 2007-05-15 |
DE60032620T2 (de) | 2007-10-04 |
EP1222924A4 (en) | 2004-08-04 |
ATE349212T1 (de) | 2007-01-15 |
AU7449800A (en) | 2001-04-30 |
EP1637140A1 (en) | 2006-03-22 |
EP1222924A1 (en) | 2002-07-17 |
TWI289450B (en) | 2007-11-11 |
US6683083B1 (en) | 2004-01-27 |
EP1222924B1 (en) | 2006-12-27 |
CA2385996A1 (en) | 2001-04-05 |
EP1637140B1 (en) | 2007-04-18 |
DE60034494T2 (de) | 2008-01-03 |
AU776745B2 (en) | 2004-09-23 |
DE60034494D1 (de) | 2007-05-31 |
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