Patent Application
20090042962
The present invention relates to a therapeutic agent for a keratoconjunctival disorder such as dry eyes, corneal ulcer, keratitis, conjunctivitis, superficial punctate keratopathy, corneal epithelial defects, conjunctival epithelial defects, keratoconjunctivitis sicca, superior limbic keratoconjunctivitis or filamentary keratitis, comprising as an active ingredient, a biphenylmethyl derivative or a salt thereof.
Cornea is a transparent avascular tissue having a diameter of about 1 cm and a thickness of about 1 mm, while conjunctiva is a mucosal membrane covering the eyeball surface posterior to the corneal margin, and the back face of the eyelid. It is known that when the cornea or the conjunctiva is damaged, the visual function is significantly affected. Keratoconjunctival disorders caused due to a variety of diseases such as corneal ulcer, keratitis, conjunctivitis, dry eyes and the like may adversely affect normal architecture of corneal epithelium or conjunctival epithelium, and as a result, they may impair structures and functions of the corneal stroma and corneal endothelium. In these years, with the development of cell biology, factors participating in cell proliferation, migration, adhesion, extension, differentiation and the like have been elucidated, and it has been reported that these factors play important roles in repair of keratoconjunctival disorders (Japanese Review of Clinical Opthalmology, 46, 738-743 (1992), Ophthalmic Surgery, 5, 719-727 (1992)).
On the other hand, it is disclosed that a biphenylmethyl derivative, which is an active ingredient of the present invention, inhibits the action of angiotensin II and is useful as a therapeutic agent for cardiovascular diseases such as hypertension and heart failure (Japanese patent No. 2709225, Japanese patent No. 2868313, JP-B-5-29351, etc.).
However, there is no report of study on a pharmacological action of such a biphenylmethyl derivative on an eye disease, particularly a keratoconjunctival disorder, and also there is no suggestion as to what type of biphenylmethyl derivative with what basic chemical structure is useful for a keratoconjunctival disorder.
Accordingly, it is a very interesting subject to research a compound useful as a therapeutic agent for a keratoconjunctival disorder among these numerous known biphenylmethyl derivatives.
The present inventors have made intensive studies on effects of biphenylmethyl derivatives in treatment of a corneal disorder, and as a result, they found that a biphenylmethyl derivative having a specific basic chemical structure exhibits an excellent improving effect on a corneal disorder in a test for therapeutic effect using corneal disorder models, and thus the present invention has been accomplished.
That is, the present invention is directed to:
(1) a therapeutic agent for a keratoconjunctival disorder comprising as an active ingredient a compound represented by the following general formula (I) or a salt thereof:
(wherein X represents
the ring Y represents a substituted or unsubstituted nitrogen-containing heterocyclic ring,
R1 represents a carboxy group or a substituted or unsubstituted nitrogen-containing 5-membered heterocyclic ring, and
R2 and R3 may be the same or different and represent a hydrogen atom, a substituted or unsubstituted alkyl group or a substituted or, unsubstituted alkylcarbonyl group);
(2) the therapeutic agent for a keratoconjunctival disorder according to the above (1), wherein in the general formula (I),
X represents
the ring Y represents
R1 represents a carboxy group,
R4 represents a hydrogen atom, a hydroxy group, an alkoxy group or an alkyl group,
R5 and R6 may be the same or different and represent a halogen atom, a hydroxyalkyl group or an alkoxyalkyl group, and
R7, R6, R9 and R10 may be the same or different and represent a hydrogen atom, a hydroxy group, an alkoxy group or a carboxy group or an ester thereof;
(3) the therapeutic agent for a keratoconjunctival disorder according to the above (1) or (2), wherein in the general formula (I),
X represents
the ring Y represents
R1 represents a carboxy group or
R4 represents an alkoxy group or an alkyl group,
R5 represents a halogen atom or a hydroxyalkyl group, and
R6 represents a halogen atom, a hydroxyalkyl group or a carboxy group or an ester thereof;
(4) the therapeutic agent for a keratoconjunctival disorder according to the above (1) or (2), wherein in the general formula (I),
X represents
the ring Y represents
R1 represents
R4 represents an alkyl group;
(5) the therapeutic agent for a keratoconjunctival disorder according to the above (1) or (2), wherein in the general formula (I),
X represents
the ring Y represents
R1 represents a carboxy group or
R4 represents an alkoxy group or an alkyl group,
R7 represents a hydrogen atom or an alkyl group,
R8 represents a hydrogen atom,
R9 represents a hydrogen atom or
R10 represents a hydrogen atom or a carboxy group or an ester thereof;
(6) the therapeutic agent for a keratoconjunctival disorder according to the above (3) or (5), wherein the ester of a carboxy group is
(7) the therapeutic agent for a keratoconjunctival disorder according to the above (1), wherein in the general formula (I),
X represents
R1 represents
R2 and R3 may be the same or different and represent a hydrogen atom, a carboxyalkyl group or an alkylcarbonyl group;
(8) the therapeutic agent for a keratoconjunctival disorder according to the above (1) or (7), wherein in the general formula (I),
X represents
R1 represents
R2 represents a carboxyalkyl group, and represents an alkylcarbonyl group;
(9) the therapeutic agent for a keratoconjunctival disorder according to the above (1), wherein 4′-[[4-methyl-6-(1-methylbenzimidazol-2-yl)-2-n-propylbenzimidazol-1-yl]methyl]-1,1′-biphenyl-2-carboxylic acid, 2-n-butyl-4-spirocyclopentane-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-2-imidazolin-5-one, 2-butyl-4-chloro-5-hydroxymethyl-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]imidazole, 2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-1H-benzimidazol-7-carboxylic acid, 1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-1H-benzimidazol-7-carboxylate, N-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-N-valeryl-L-valine, 4-(1-hydroxy-1-methylethyl)-2-n-propyl-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]imidazol-5-carboxylic acid or (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-(1-hydroxy-1-methylethyl)-2-n-propyl-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]imidazol-5-carboxylate, or a salt thereof is contained as an active ingredient;
(10) the therapeutic agent according to any one of the above (1) to (9), wherein the keratoconjunctival disorder is dry eyes, corneal ulcer, keratitis, conjunctivitis, superficial punctate keratopathy, corneal epithelial defects, conjunctival epithelial defects, keratoconjunctivitis sicca, superior limbic keratoconjunctivitis or filamentary keratitis; and
(11) the therapeutic agent for a keratoconjunctival disorder according to any one of the above (1) to (10), wherein the dosage form is an eye drop or an ophthalmic ointment.
The groups defined in the biphenylmethyl derivative having a basic chemical structure represented by the above general formula (I) of the present invention (hereinafter referred to as the “present compound”) will be described in further detail. The halogen refers to fluorine, chlorine, bromine or iodine. The alkyl refers to straight-chain or branched alkyl having 1 to 6 carbon atoms such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl and isohexyl. The alkoxy refers to straight-chain or branched alkoxy having 1 to 6 carbon atoms such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, tert-butoxy, n-pentyloxy and n-hexyloxy.
The substituted or unsubstituted nitrogen-containing heterocyclic ring refers to a nitrogen-containing heterocyclic ring which may have a substituent, and examples of the nitrogen-containing heterocyclic ring include pyridine, pyrimidine, pyrrole, imidazole, pyrazole, triazole, tetrazole, triazine, tetrahydroquinoline, tetrahydroisoquinoline, indole, quinoline, phenanthridine, benzimidazole and the like. The substituted or unsubstituted nitrogen-containing 5-membered heterocyclic ring refers to a nitrogen-containing 5-membered heterocyclic ring which may have a substituent, and examples of the nitrogen-containing 5-membered heterocyclic ring include pyrrole, imidazole, pyrazole, triazole, tetrazole, triazine and the like.
Further, the ester of a carboxy group refers to an ester composed of a carboxy group and a substituted or unsubstituted alkyl alcohol, a substituted or unsubstituted aryl alcohol or the like. Specific examples of the alkyl alcohol include methanol, ethanol, propanol, butanol and the like, and specific examples of the aryl alcohol include phenol, naphthol and the like.
Preferred examples of R1 in the general formula [1] include a carboxy group,
Preferred examples of R2 and R3 include an n-butylcarbonyl group and a 1-carboxy-2-methyl-propyl group.
Preferred examples of R4 include an n-propyl group, an n-butyl group and an ethoxy group.
Preferred examples of R5 include a chlorine atom and a 1-hydroxy-1-methylethyl group.
Preferred examples of R6 include a carboxy group, a hydroxymethyl group, and
Preferred examples of R7 include a hydrogen atom and a methyl group.
Preferred examples of R8 include a hydrogen atom.
Preferred examples of R9 include a hydrogen atom, and
Preferred examples of R10 include a hydrogen atom, a carboxy group, and
Specific preferred examples of the present compound include 4′-[[4-methyl-6-(1-methylbenzimidazol-2-yl)-2-n-propylbenzimidazol-1-yl]methyl]-1,1′-biphenyl-2-carboxylic acid, 2-n-butyl-4-spirocyclopentane-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-2-imidazolin-5-one, 2-butyl-4-chloro-5-hydroxymethyl-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]imidazole, 2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-1H-benzimidazol-7-carboxylic acid, 1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-1H-benzimidazol-7-carboxylate, N-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-N-valeryl-L-valine, 4-(1-hydroxy-1-methylethyl)-2-n-propyl-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]imidazol-5-carboxylic acid, (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-(1-hydroxy-1-methylethyl)-2-n-propyl-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]imidazol-5-carboxylate, 2-ethoxy-1-[[2′-(5-oxo-2H-1,2,4-oxadiazol-3-yl)-1,1′-biphenyl-4-yl]methyl]benzimidazol-7-carboxylic acid, 2-butyl-4-chloro-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]imidazol-5-carboxylic acid and the like.
The salt of the present compound is not particularly limited as long as it is a pharmaceutically acceptable salt, and examples thereof include sodium salts, potassium salts, lithium salts, calcium salts, magnesium salts, salts with an inorganic acid such as hydrochloric acid, nitric acid or sulfuric acid, salts with an organic acid such as acetic acid, fumaric acid, maleic acid, succinic acid or tartaric acid, and the like. Quaternary ammonium salts are also included in the salt according to the present invention. Preferred salts are sodium salts and potassium salts. The present compound may be in a form of a hydrate or a solvate. Further, optical isomers, geometric isomers, tautomers, polymorphisms and the like of the present compound are also included in the scope of the present invention.
The present compound can be produced based on the method described in Japanese patent No. 2709225, Japanese patent No. 2868313, JP-B-5-29351, Japanese patent No. 2853611, Japanese patent No. 2514282, Japanese patent No. 2749458, JP-B-7-25738, Japanese patent No. 2645962 or Japanese patent No. 3465215.
The keratoconjunctival disorder as used herein means the state of damaged cornea and/or conjunctiva due to various factors, and examples thereof include dry eyes, corneal ulcer, keratitis, conjunctivitis, superficial punctate keratopathy, corneal epithelial defects, conjunctival epithelial defects, keratoconjunctivitis sicca, superior limbic keratoconjunctivitis, filamentary keratitis and the like.
The therapeutic agent for a keratoconjunctival disorder of the present invention may be administered either orally or parenterally.
Examples of the dosage form include eye drops, ophthalmic ointments, injections, tablets, capsules, granules, powders and the like. In particular, eye drops are preferred. These can be prepared using any of generally used techniques. For example, the eye drops can be prepared using a tonicity agent such as sodium chloride or concentrated glycerin, a buffer such as sodium phosphate or sodium acetate, a surfactant such as polyoxyethylene sorbitan monooleate, polyoxyl 40 stearate or polyoxyethylene hydrogenated castor oil, a stabilizer such as sodium citrate or sodium edetate, a preservative such as benzalkonium chloride or paraben as needed. The pH of the eye drops is permitted as long as it falls within the range that is acceptable as an ophthalmic preparation, but is preferably in the range of from 4 to 8.
The ophthalmic ointments can be prepared with a generally used base such as white soft paraffin or liquid paraffin. Also, oral preparations such as tablets, capsules, granules and powders can be prepared by adding an extender such as lactose, crystalline cellulose, starch or vegetable oil, a lubricant such as magnesium stearate or talc, a binder such as hydroxypropyl cellulose or polyvinyl pyrrolidone, a disintegrant such as carboxymethyl cellulose calcium or low-substituted hydroxypropylmethyl cellulose, a coating agent such as hydroxypropylmethyl cellulose, macrogol or a silicone resin, a film forming agent such as gelatin film, and the like, as needed.
The present invention also relates to a method for treating a keratoconjunctival disorder comprising administering to a patient a therapeutically effective amount of a compound represented by the general formula (1) or a salt thereof.
The dose of the present compound can be properly selected depending on the symptoms, age, dosage form and the like. In the case of an eye drop, it may be instilled once to several times a day at a concentration of from 0.00001 to 5% (w/v), preferably from 0.001 to 3% (w/v). In the case of an oral preparation, it may be administered once or divided into several times at a dose of generally from 0.1 to 5000 mg per day, preferably from 1 to 1000 mg per day.
As will be described below, when a test for a therapeutic effect on a corneal damage was carried out, any of the present compounds exhibited an excellent improving effect in corneal disorder models. Therefore the present compounds are useful as a therapeutic agent for a keratoconjunctival disorder such as dry eyes, corneal ulcer, keratitis, conjunctivitis, superficial punctate keratopathy, corneal epithelial defects, conjunctival epithelial defects, keratoconjunctivitis sicca, superior limbic keratoconjunctivitis, filamentary keratitis and so on.
Hereinafter, results of a pharmacological test and preparation examples will be shown, however, these examples are for understanding the present invention well, and are not meant to limit the scope of the present invention.
Using male SD rats, corneal disorder models were produced in accordance with the method of Fujihara et al. (Invest. Opthalmol. Vis. Sci. 42 (1): 96-100 (2001)) After the production of the corneal disorder models, the corneal damage score was evaluated in accordance with the method of Murakami et al. (Journal of the eye 21 (1): 87-90 (2004)), and the improvement ratio of a corneal damage after instillation was obtained.
Male SD rats were systemically anesthetized by an administration of Nembutal. Subsequently the exorbital lacrimal gland of each rat was removed and a corneal damage was induced over a period of 2 months.
Then, 4′-[[4-methyl-6-(1-methylbenzimidazol-2-yl)-2-n-propylbenzimidazol-1-yl]methyl]-1,1′-biphenyl-2-carboxylic acid (hereinafter referred to as “Compound A”), 2-n-butyl-4-spirocyclopentane-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-2-imidazolin-5-one (hereinafter referred to as “Compound B”), 2-butyl-4-chloro-5-hydroxymethyl-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]imidazole monopotassium salt (hereinafter referred to as “Compound C”), 2-ethoxy-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-1H-benzimidazol-7-carboxylic acid (hereinafter referred to as “Compound D”) # N-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]-N-valeryl-L-valine (hereinafter referred to as “Compound E”), or 4-(1-hydroxy-1-methylethyl)-2-n-propyl-1-[[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl]imidazol-5-carboxylic acid monohydrate (hereinafter referred to as “Compound F”) was administered to the rats as follows.
A physiological saline solution containing Compound A (0.005%) was instilled into both eyes 6 times a day for 14 days (one group consisting of 4 animals, 8 eyes).
A physiological saline solution containing Compound B (0.04%) was instilled into both eyes 6 times a day for 14 days (one group consisting of 4 animals, 8 eyes).
A physiological saline solution containing Compound C (0.5%) was instilled into both eyes 6 times a day for 14 days (one group consisting of 3 animals, 6 eyes).
A phosphate-buffered saline solution containing Compound D (0.004%) was instilled into both eyes 6 times a day for 14 days (one group consisting of 4 animals, 8 eyes).
A phosphate-buffered saline solution containing Compound E (0.004%) was instilled into both eyes 6 times a day for 14 days (one group consisting of 4 animals, 8 eyes).
A phosphate-buffered saline solution containing Compound F (0.004%) was instilled into both eyes 6 times a day for 14 days (one group consisting of 4 animals, 8 eyes).
In a control group, physiological saline or phosphate-buffered saline was instilled into both eyes 6 times a day for 14 days (one group consisting of 4 animals, 8 eyes).
Fourteen days after the start of instillation, the damaged parts of the cornea were stained with fluorescein. For each of the upper, middle and lower parts of the cornea, the degree of fluorescein staining was evaluated by scoring according to the criteria shown below and the improvement ratio of corneal damage was calculated from the mean value of the total scores for each of the above-mentioned parts. Also for normal eyes, the mean value of the total scores for each of the above-mentioned parts was obtained.
0: No punctate staining
1: Scattered staining (punctate staining being separated)
2: Moderate staining (a part of punctate staining being adjacent)
3: Heavy staining (punctate staining being barely separated)
By taking the mean value of the total scores for the control group (physiological saline or phosphate-buffered saline) as a standard (improvement ratio: 0%) and according to the equation shown below, the improvement ratios for the Compound A, B and C administration groups were calculated, respectively, which are shown in Table 1. The respective improvement ratios for the Compound D and E administration groups calculated in a similar manner are shown in Table 2, and the improvement ratio for the Compound F administration group is shown in Table 3. Incidentally, the mean value of the scores is a mean of those of 8 cases or 6 cases, respectively.
Improvement ratio (%)={(control)−(the present compound)}/damage degree×100 Damage degree=(control)−(normal eye)
As apparent from the results of the above pharmacological test using rats (Tables 1 to 3), Compounds A to F significantly improved a corneal damage.
Hereinafter, representative preparation examples using Compounds A to F will be shown.
By altering the amount of Compound A to be added, an eye drop at a concentration of 0.001% (w/v), 0.03% (w/v), 0.1% (w/v), 0.3% (w/v), 1.0% (w/v), or 3.0% (w/v) can be prepared.
By altering the amount of Compound B to be added, an eye drop at a concentration of 0.002% (w/v), 0.01% (w/v), 0.25% (w/v), 1.25% (w/v), or 3% (w/v) can be prepared.
In 100 ml,
By altering the amount of Compound C to be added, an eye drop at a concentration of 0.003% (w/v), 0.01% (w/v), 0.03% (w/v), 0.05% (w/v), 0.3% (w/v), 1% (w/v) or 3% (w/v) can be prepared.
By altering the amount of Compound D to be added, an eye drop at a concentration of 0.002% (w/v), 0.01% (w/v), 0.25% (w/v), 1.25% (w/v), or 3% (w/v) can be prepared.
By altering the amount of Compound E to be added, an eye drop at a concentration of 0.003% (w/v), 0.01% (w/v), 0.03% (w/v), 0.05% (w/v), 0.3% (w/v), 1% (w/v) or 3% (w/v) can be prepared.
By altering the amount of Compound F to be added, an eye drop at a concentration of 0.001% (w/v), 0.03% (w/v), 0.1% (w/v), 0.3% (w/v), 1.0% (w/v) or 3.0% (w/v) can be prepared.
By altering the amount of Compound C to be added, an ophthalmic ointment at a concentration of 1% (w/w) or 3% (w/w) can be prepared.
By altering the amount of Compound F to be added, an ophthalmic ointment at a concentration of 1% (w/w) or 3% (w/w) can be prepared.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2005-123791 | Apr 2005 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2006/308382 | 4/21/2006 | WO | 00 | 10/18/2007 |
