EP0772607A1 - Wasserlösliche methin-derivate und diese enthaltende pharmazeutische zusammensetzung für krebsbehandlung - Google Patents
Wasserlösliche methin-derivate und diese enthaltende pharmazeutische zusammensetzung für krebsbehandlungInfo
- Publication number
- EP0772607A1 EP0772607A1 EP95925127A EP95925127A EP0772607A1 EP 0772607 A1 EP0772607 A1 EP 0772607A1 EP 95925127 A EP95925127 A EP 95925127A EP 95925127 A EP95925127 A EP 95925127A EP 0772607 A1 EP0772607 A1 EP 0772607A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- ring
- group
- ion
- carbon atoms
- methine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/64—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/84—Naphthothiazoles
Definitions
- Water-soluble methine compound and pharmaceutical composition for treatment of cancer comprising the same
- the present invention relates to a methine compound useful as a photograhic material, medicine or the like, and to a pharmaceutical composition for treatment of cancer comprising the methine compound.
- J. P. KOKAI Japanese Patent Unexamined Published Application
- an object of the present invention is to provide a methine compound which falls in rhodacyanine dyes and which has a high solubility.
- Another object of the present invention is to provide a good pharmaceutical composition for treatment of cancer.
- Zi represents a non-metallic atomic group necessitated for forming a five-membered nitrogen-containing heterocyclic ring together with -N(R ⁇ )-C-
- Zi represents a non-metallic atomic group necessitated for forming a f ive-membered nitrogen-containing heterocyclic ring together with -N + (R.
- R t , Ri and Rj each represent an alkyl group and at least one of R ⁇ , R-, and RJ represents an alkyl group substituted with a polyethylene oxide group wherein one end of the polyalkylene oxide having a degree of polymerization of 2 to 6 is terminated with a hydrophobic group or substituted with a heterocyclic ring containing two or more oxygen atoms , Q represents an anion , k represents a numeral neces sitated to control the charge in the mol ecul e at zero , p represents 0 or 1 , and Y represents a methine group or nitrogen atom.
- a pharmaceutical composition for treatment of cancer which comprises a therapeutically effective amount of the methine compound and a pharmaceutically acceptable diluent and/or carrier .
- Z together with -N(R ⁇ )-C- represents a non-metallic atomic group necessitated for forming a thiazolidine ring, benzothiazoline ring , benzoxazoline ring , naphthothiazoline ring or naphthoxazoline ring , i and W 2 each represent a hydrogen atom or they together form a non- metallic atomic group necessitated for forming a naphthalene condensed ring or benzene condensed ring , Q represents a halogen ion or organic acid anion , p represents 0 or 1 , Y represents a methine group or nitrogen atom, Ri , R, and R 5 each represent an alkyl group and at least one of Ri , R» and Ri has a substituent of the following formula Ill-a or Ill-b:
- the heterocyclic rings formed by Zi and -N(R_ )-C- together are preferably thiazolidine ring, benzothiazoline ring, naphthothiazoline ring and nahthoxazoline ring. More preferred are benzothiazoline ring and naphthothiazoline ring. Among them, benzothiazoline ring is the most preferred.
- the heterocyclic ring formed by Zi and -N(R ⁇ )-C- together may have a substituent. The substituent is preferably a halogen atom, alkyl group, alkoxy group, hydroxyl group or the like. The most preferred is methoxy group.
- the condensed ring formed by W x and W 2 may have a substituent, which is preferably a halogen atom, alkyl group, alkoxy group, hydroxyl group or the like.
- the alkyl groups represented by R. , Ri and Rj are preferably those having 1 to 5 carbon atoms, more preferably those having 1 to 3 carbon atoms .
- Particularly preferred are ethylene oxide polymers .
- the degree of polymerization is preferably 3 to 5 , particularly preferably 3 to 4.
- the hydrophobic groups which terminate the polyalkylene oxide are preferably lower alkyl groups such as those having 1 to 3 carbon atoms .
- the mode of the termination is , for example , an ether bond or ester bond .
- Particularly preferred is the ether bond with an alkyl group having 1 to 3 carbon atoms , and most preferred is with methyl group .
- Examples of the heterocyclic rings containing two or more oxygen atoms include dioxolane and dioxane . Particularly preferred are 1 , 3 - dioxolanyl group and 1 , 3-dioxanyl group.
- the alkyl group substituted with a polyalkylene oxide group having a degree of polymerization of 2 to 6 and terminated with a hydrophobic group or substituted with a heterocyclic ring containing two or more oxygen atoms is preferably R, .
- the halogen ion or organic acid anion represented by Q is preferably an iodide ion , chloride ion or sulfonic acid ion . Among them , the chloride ion is more preferred.
- Y is preferably a methine group, and p is preferably 0.
- the methine compound of the present invention is usable as a spectral sensitizing dye or anticancer agent.
- the methine compound of the present invention can be usually synthesized by a synthesis method described in ⁇ . S . Patent No. 2 , 388 , 963 .
- the methine compounds of the present invention are widely usable as spectral sensitizing dyes or medicines such as anticancer agents.
- one of the methine compounds of the present invention is used as a medicine, it is usually administered, for example, by the following preferred method: the methine compound, dissolved in, for example, 5 % glucose solution or together with a suitable carrier or diluent, is injected into a vein, abdominal cavity, muscle or bladder.
- the practical solubility suitable for the injection preparations is 0.1 to 1 % by weight.
- compositions of this invention containing one or more compounds of the general formulas (I) to (II) described above can be effectively used to treat various types of cancer including melanomas, hepatomas, gliomas, neuroblasto as, sarcomas and carcinomas of the lung, colon, breast, bladder, ovary, testis, prostate, cervix, pancreas, stomach, small intestine and other organs .
- compositions of this invention can contain one or more compounds of the general formulas (I) to (II) and a pharmaceutically acceptable diluent and/or carrier, and if desired, can further contain other therapeutic agents including conventional anti- tumor agents known in the art.
- conventional anti-tumor agents which can be used include adriamycin, cisplatin, colchicine, CCNU (Lomastine), BCNU (Carmustine) , Actinomycin D, 5- f luorouracil , thiotepa, cytosinearabinoside , cyclophosphamide, mitomycin C, and the like.
- Suitable examples of the pharmaceutical carriers or diluents include glucose, sucrose, lactose, ethyl alcohol, glycerin, mannitol, sorbitol , pentaerythritol, diethylene glycol, triethylene glycol, ethylene glycol, propylene glycol, dipropylene glycol, polyethylene glycol 400, other polyethylene glycols, mono-, di- and triglycerides of saturated fatty acids such as glyceryl trilaurate, glyceryl monostearate, glyceryl tristearate and glyceryl distearate, pectin, starch, alginic acid, xylose, talc, lycopodium, oils and fats such as olive oil, peanut oil, castor oil, corn oil, wheat germ oil, sesame oil, cottonseed oil, sunflower seed oil and cod-liver oil, gelatin, lecithin, silica, cellulose, cellulose derivatives such as
- compositions may also be appropriate for this invention.
- the pharmaceutically effective amount of the compound of the general formulas (I) to (II) and the mode or manner of administration will be dependent upon the nature of the cancer, the therapy sought, the severity of the disease, the degree of malignancy, the extent of metastatic spread, the tumor load, general health status, body weight, age, sex, and the genetic or racial background of the patient.
- suitable modes of administration include intravenous, hypodermic, intraperitoneal, intramuscular or intravesicular injection or oral use in the form of, for example, a compound of the general formulas (I) to (II) in, e.g., a 5% glucose aqueous solution or with other appropriate carriers or diluents as described above.
- a suitable therapeutically effective amount of a compound of the general formulas (I) to (II) in the composition is about 0.01% by weight to about 10% by weight, more generally 0.1% by weight to about 1%, based on the weight of the composition.
- a suitable therapeutically effective amount of the compound of the general formulas (I) to (II) generally can range from 10 mg to 500 mg, more generally 100 mg to 200 mg, administered per day per 70 kg of body weight, in single or multiple doses, as determined appropriate for the therapy involved.
- methine compounds of the present invention as photosensitive materials for photography or as medicines such as anticancer agent is expected, since they have a solubility in water or the like far higher than that of an analogous rhodacyanine dye.
- Example 1 The following Examples will further illustrate the present invention.
- Example 1 The following Examples will further illustrate the present invention.
- the reaction liquid was cooled to room temperature.
- the crystals thus formed were suction-filtered and washed with 50 ml of ethyl acetate.
- the crude crystals thus formed were dissolved in 50 ml of chloroform/methanol (1:1). 400 ml of ethyl acetate was added to the solution, and the crystals thus formed were suction-filtered.
- the resultant mixture was heated to 60 ⁇ C . 2 ml of triethylamine was added dropwise to the mixture. After stirring the mixture at that temperature for 5 minutes followed by addition of 150 ml of ethyl acetate, the reaction liquid was cooled to room temperature. The resultant crystals were suction-filtered and then washed with 50 ml of ethyl acetate.
- Test 1 5 mg of a methine compound is fed into a test tube, to which 5 ml of ion-exchanged water is added, the resultant mixture is shaken at room temperature for 5 minutes, and the solubility thereof is macroscopically confirmed (1 mg/ l solution).
- Test 2 5 mg of a methine compound is fed into a test tube, to which 0.5 ml of ion-exchanged water is added, the resultant mixture is shaken at room temperature for 5 minutes, and the solubility thereof is macroscopically confirmed (10 mg/ml solution) .
- the results of the solubility test 1 are given in Table 3, and those of the test 2 are given in Table 4.
- the human colonic epithelial carcinoma cell lines LS174T there was used the established line by trypsinizing piece of LS174T obtained from the operating theatre of the original adenocarcinoma of colon in such that the piece becomes suitable for cultivation .
- this cultured cells LS174T are hypodermically injected to a nude mouse , the cells can be easily grown in the body of the nude mouse as a moderately to sufficiently differentiated human colonic epithelial carcinoma .
- the cel l s LS174T produce CEA in high level and can proliferate in hamster cheek pouches or immunodeprived mice , so that it has been proven that the cells LS174T have neoplastic properties .
- mice Male, five weeks age ) available from Charles River Japan Inc . were placed in an atmosphere having no pathogen .
- Tumors formed by the hypodermic injection of human colonic epithelial carcinoma cell lines LS174T into the mice were cut off under the aseptic condition, and the surrounding skin and connective tissue of the tumor tissues as well as the necrotic tissue located in the center of the tumor tissues were removed .
- the tumor tissues were cut in the form of 3-5 mm square, and the resulting one tissue was charged into a needle for transplantation to hypodermically transplant it into the mouse .
- the resulting mice were randomly divided into control group ( six mice ) and treating group ( six mice ) .
- the intravenous administration of the pharmaceutical composition into the treating group started next day .
- the amount and schedule of the administration were determined based on the experience, mainly the knowledge from the pretoxic-test data of LD 50 and LD 10. 5 % glucose solution or physiologic saline for injection was injected to the control group in the same amount as that to be intravenously injected to the treating group.
- the pharmaceutical composition was dissolved in 5 % glucose solution or physiologic saline for injection in such that the amount of the pharmaceutical composition contained in the glucose solution or physiologic saline is 5 ml per one kg of weight of the mouse to be injected so as to prepare an injection liquid.
- the proliferation of tumor in the control group reached exponential growth phase and the size of the tumor became detectable by touch with hand, i.e., generally three weeks after the transplantation, the experiment was stopped. Then the tumor of each mouse was cut off and the weight of the resulting tumor was measured by use of chemical balance. Regarding each group, tumor inhibition percentage between the treating group and control group was calculated. The results obtained are shown in Table 5.
- LOX a human melanoma cell line, grown subcutaneously in nude mice was excised, trypsinized to yield a single cell suspension using a metal grid with a 4 mm mesh. Red blood cells were lysed by incubation with 0.17 molar ammonium chloride at 4 "C for 20 minutes. Five million viable trypan blue negative cells made up in 0.1 ml of Dulbecco modified Eagles' medium (DME) were injected into the peritoneal cavity of a male athymic Swiss nu/nu mouse. The control group and each treatment group consisted of 5 to 10 mice. Treatment was commenced the following day by intraperitoneal injection.
- DME Dulbecco modified Eagles' medium
- T/C is the ratio, expressed as a percentage of the mean survival age of the treated group to the mean survival age of the untreated control group.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP169582/94 | 1994-07-21 | ||
JP16958294 | 1994-07-21 | ||
US420481 | 1995-04-12 | ||
US08/420,481 US5599825A (en) | 1994-07-21 | 1995-04-12 | Water-soluble methine compound and pharmaceutical composition for treatment of cancer comprising the same |
PCT/JP1995/001408 WO1996003393A1 (en) | 1994-07-21 | 1995-07-14 | Water-soluble methine compound and pharmaceutical composition for treatment of cancer comprising the same |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0772607A1 true EP0772607A1 (de) | 1997-05-14 |
Family
ID=26492853
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP95925127A Ceased EP0772607A1 (de) | 1994-07-21 | 1995-07-14 | Wasserlösliche methin-derivate und diese enthaltende pharmazeutische zusammensetzung für krebsbehandlung |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0772607A1 (de) |
JP (1) | JPH10506878A (de) |
AU (1) | AU678116B2 (de) |
CA (1) | CA2187445A1 (de) |
WO (1) | WO1996003393A1 (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004331545A (ja) * | 2003-05-06 | 2004-11-25 | Japan Science & Technology Agency | 抗リーシュマニア剤 |
JP4553355B2 (ja) * | 2004-10-04 | 2010-09-29 | 富士フイルム株式会社 | トリパノソーマ原虫寄生感染症の予防又は治療用医薬組成物 |
EP1894920A1 (de) * | 2005-06-24 | 2008-03-05 | Japan Science and Technology Agency | Pharmazeutische zusammensetzung, enthaltend eine azarhodacyaninverbindung als wirkstoff |
US10221171B2 (en) | 2015-01-09 | 2019-03-05 | The Regents Of The University Of California | Oxathiazole thiazolium Hsp 70 inhibitors |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2919447A1 (de) * | 1978-05-17 | 1979-11-22 | Takeda Chemical Industries Ltd | Tumorhemmendes mittel |
JPS6267068A (ja) * | 1985-09-18 | 1987-03-26 | Mitsubishi Chem Ind Ltd | シアニン化合物および光学記録体 |
AU1144688A (en) * | 1987-03-17 | 1988-09-15 | Dana-Farber Cancer Institute, Inc. | A pharmaceutical composition comprising cyanine dye |
JP2824917B2 (ja) * | 1989-08-30 | 1998-11-18 | 株式会社林原生物化学研究所 | 抗腫瘍剤 |
HUT64224A (en) * | 1991-08-13 | 1993-12-28 | Dana Farber Cancer Inst Inc | Process for the production of the medical preparatives containing rodacimin applicable for treatment of cancer |
JP2864188B2 (ja) * | 1992-09-01 | 1999-03-03 | 富士写真フイルム株式会社 | 水溶性メチン化合物 |
-
1995
- 1995-07-14 CA CA002187445A patent/CA2187445A1/en not_active Abandoned
- 1995-07-14 WO PCT/JP1995/001408 patent/WO1996003393A1/en not_active Application Discontinuation
- 1995-07-14 AU AU29366/95A patent/AU678116B2/en not_active Ceased
- 1995-07-14 EP EP95925127A patent/EP0772607A1/de not_active Ceased
- 1995-07-14 JP JP8505639A patent/JPH10506878A/ja not_active Ceased
Non-Patent Citations (1)
Title |
---|
See references of WO9603393A1 * |
Also Published As
Publication number | Publication date |
---|---|
CA2187445A1 (en) | 1996-02-08 |
WO1996003393A1 (en) | 1996-02-08 |
AU2936695A (en) | 1996-02-22 |
JPH10506878A (ja) | 1998-07-07 |
AU678116B2 (en) | 1997-05-15 |
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