US20150306084A1

US20150306084A1 - Adenosine a1 agonists for the treatment of glaucoma and ocular hypertension

Info

Publication number: US20150306084A1
Application number: US14/705,967
Authority: US
Inventors: Hans-Georg Lerchen; Barbara Albrecht-Küpper; Andreas Knorr; Peter Sandner; Daniel Meibom; Carsten Schmeck; Hubert Trübel
Original assignee: Bayer Intellectual Property GmbH
Current assignee: Bayer Intellectual Property GmbH
Priority date: 2010-09-02
Filing date: 2015-05-07
Publication date: 2015-10-29
Also published as: CY1117458T1; US9040566B2; CN103249400A; MA34489B1; EA028411B1; BR112013005224A2; CL2016001164A1; CA2809700A1; AU2011298430B2; CN103249400B; PL2611415T3; US20120058983A1; HRP20160532T1; MX2013002396A; DK2611415T3; TWI516266B; ES2570659T3; EP2611415A1; KR20140091457A; CL2013000599A1

Abstract

The present invention relates to the use of selective adenosine A1 agonists, in particular the dicyanopyridines of formula (I), for the treatment and/or prophylaxis of glaucoma and ocular hypertension as well as the their use for the production of a medicament for the treatment and/or prophylaxis of glaucoma and ocular hypertension.

Description

The present invention relates to selective adenosine A1 agonists, in particular the dicyanopyridines of formula (I), for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof as well as the their use for the production of a medicament for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.

BACKGROUND OF THE INTERVENTION

Glaucoma is a degenerative disease comprising a group of debilitating eye diseases that are a leading cause of permanent loss of visual function due to irreversible damage to the optical nerve. Glaucoma refers further to a disease of the eye, characterized and caused by damage of the optic nerve head, degeneration of ocular tissues, and/or elevated intraocular pressure. There are several functionally or morphologically distinct types of glaucoma which in general are accompanied by elevated intraocular pressure (IOP).
The increased IOP is considered to be causally related to the pathological progress of the disease. In patients with ocular hypertension intraocular pressure is elevated but no apparent loss of visual function has occurred. These patients are considered to be at high risk for a potential development of visual loss associated with glaucoma. Some patients which show a glaucomatous vision field loss have a normal to low intraocular pressure. These so called normotension or low tension glaucoma patients can also benefit form agents that decrease intraocular pressure. The loss of visual function and the progressive deterioration associated with glaucoma and ocular hypertension can generally be ameliorated with medications that reduce elevated intraocular hypertension when glaucoma or ocular hypertension is detected early.
Glaucoma—on the basis of its etiology—refers also to primary or secondary glaucoma. Primary glaucoma in adults (congenital glaucoma) may be either open-angle or acute or chronic angle-closure.
Primary glaucoma is characterized by increased intraocular tension which is due to the obstruction of aqueous humor outflow. In chronic open-angle glaucoma (POAG), the anterior chamber and its anatomic structures appear normal, but drainage of the aqueous humor is hampered. In acute or chronic angle-closure, the filtration angle is narrowed, the anterior chamber is shallow and the iris may obstruct the trabecular meshwork at the entrance of the canal of Schlemm. Dilation of the pupil may push the root of the iris forward against the angle, and may produce pupilary block and thus precipitate an acute attack. A predisposion to acute angle-closure glaucoma attacks with various degrees of severity is know in patients eyes with narrow anterior chamber angles
Secondary glaucoma is characterized and caused by any interference which effects the flow of aqueous humor from the posterior chamber into the anterior chamber and subsequently, into the canal of Schlemm. Also inflammatory disease of the anterior segment may inhibit aqueous outflow by causing complete posterior synechia in iris bombe and may plug the drainage channel with exudates. Other common causes are intraocular tumors, enlarged cataracts, central retinal vein occlusion, trauma to the eye, operative procedures and intraocular hemorrhage.
Several therapies for treating glaucoma or ocular hypertension have been proven to be effective in clinical practice via reduction of IOP by lowering aqueous humor production or by increasing outflow facility. Many of the used drugs are administrated topically direct to the eye or orally. However a relevant number of patients do not respond to the current existing glaucoma treatment options. In addition a significant number of patients face side effects like local intolerance and allergic reactions, subconjunctival hyperemia, miosis or uveitis which lead to cessation of the glaucoma therapy. Therefore the need of new and innovative therapeutic agents which control IOP is given. Since glaucoma is caused by progressive damage to the optic nerve head in particular additional neuroprotective effects in the eye would be beneficial.
Thus intense research efforts are currently ongoing for new glaucoma therapies with improved efficacy and reduced side effect profile (Lee A. J., Goldberg I., Exp. Opin. Emer. Drugs 2011, 16(1), 137-161; Traverso C. E. et al., Exp. Opin. Emer. Drugs 2011, 16(2), 293-307; Fogagnolo P., Rossetti L., Exp. Opin. Investig. Drugs 2011, 20(7), 947-959).
Adenosine, a purine nucleoside, is an ubiquitous modulator of numerous physiological activities which is mediated by specific cell surface receptors. Adenosine is formed intracellularly as an intermediate during the degradation of adenosine 5′-monophosphate (AMP) and S-adenosylhomocysteine, but it can be released from the cell, in which case it acts as a hormone-like substance or neurotransmitter by binding to specific receptors.
The first identified biological action of adenosine was the effect on heart rate, atrioventricular conduction and blood pressure (Drugy A. et al., J. Physiol. 1929, 68, 213-237). Since then it has been reported that adenosine is involved in many physiological processes and that these effects are mainly mediated by four known subtypes of adenosine receptors—referred to as A1, A2a, A2b and A3—each of which has a unique pharmacological profile, tissue distribution and effector coupling (Jacobsen K. A. et al., Exp. Opin. Emer. Drugs 2007, 12, 479-492). According to the invention, “adenosine-receptor-selective ligands” are substances which bind selectively to one or more subtypes of the adenosine receptors, thus either mimicking the action of adenosine (adenosine agonists) or blocking its action (adenosine antagonists).
The actions of these adenosine receptors are mediated intracellularly by the messenger cAMP. In the case of the binding of adenosine to the A2a or A2b receptors, the intracellular cAMP is increased via activation of the membrane-bound adenylate cyclase, whereas binding of adenosine to the A1 or A3 receptors results in a decrease of the intracellular cAMP concentration via inhibition of adenylate cyclase.
In the cardiovascular system, the main consequences of the activation of adenosine receptors are: bradycardia, negative inotropism and protection of the heart against ischemia (“preconditioning”) via A1 receptors, dilation of the blood vessels via A2a and A2b receptors and inhibition of the fibroblasts and smooth-muscle-cell proliferation via A2b receptors. In the case of A1 agonists (coupling preferably via G_iproteins), a decrease of the intracellular cAMP concentration is observed (preferably after direct prestimulation of adenylate cyclase by forskolin). Correspondingly, A2a and A2b agonists (coupling preferably via G_sproteins) leads to an increase and A2a and A2b antagonists to a decrease of the cAMP concentration in the cells. In the case of A2 receptors, a direct prestimulation of adenylate cyclase by forskolin is of no benefit.
The development of many subtype specific adenosine receptor agonists or antagonists have been described and tested in clinical trials for many different diseases e.g. cardiac arrhythmias, neuropathic pain, myocardial perfusion imaging, inflammatory diseases and colon cancer (Jacobsen K. A. et al., Nature Rev. Drug Disc. 2006, 5, 247-264; Müller C. E. et al., Exp. Opin. Emer. Drugs 2003, 8, 537-57).
In humans, activation of A1 receptors by specific A1 agonists leads to a frequency-dependent lowering of the heart rate, without any effect on blood pressure. Selective A1 agonists may thus be suitable inter alia for treating angina pectoris and atrial fibrillation.
The cardioprotective action of the A1 receptors in the heart may be utilized inter alia by activating these A1 receptors with specific A1 agonists for treatment and organ protection in cases of acute myocardial infarction, acute coronary syndrome, heart failure, bypass operations, heart catheter examinations and organ transplantations.
For the adenosine A1 receptor several subtype specific agonists have been reported like NNC-21-0126, GR79236, selodenoson and capadenoson which have been reported to be in clinical development (Jacobsen K. A., Handbook Exp. Pharmacol., 2009, 193, 1-24). Also the effect of adenosine A1 receptor agonists on intraocular pressure has been intensively studied and characterized. It was shown that two relatively selective adenosine A1 agonists N6-cyclohexyl-adenosine (CHA) and R(−)-N6-(2-phenylisopropyl)adenosine (R-PIA) lower intraocular pressure in rabbits (Crosson C. E., Curr. Eye Res. 1995, 11, 453-458; Crosson C. E. et al. J. Ocul. Pharmacol. 1994, 10, 379-383; Crosson C. E., J. Pharmacol. Exp. Ther. 1995, 273, 320-326) and cynomolgus monkeys (Kaufman P. L. et al., Exp. Eye Res. 1997, 64, 979-989). However the use of adenosine A1 agonists as therapeutic drugs for glaucoma or ocular hypertension is significantly limited by the effects on hemodynamic parameters as it is known that adenosine A1 agonists are crucially involved in heart rate and blood pressure regulation (Zablocki J. et al., Handbook Exp. Pharmacol., 2009, 193, 25-58).
Prodrugs are derivatives of an active ingredient which undergo in vivo an enzymatic and/or chemical biotransformation in one or more stages before the actual active ingredient is liberated. A prodrug residue is ordinarily used in order to improve the profile of properties of the underlying active ingredient [P. Ettmayer et al., J. Med. Chem. 47, 2393 (2004)]. In order to achieve an optimal profile of effects it is necessary in this connection for the design of the prodrug residue as well as the desired mechanism of liberation to be coordinated very accurately with the individual active ingredient, the indication, the site of action and the administration route. A large number of medicaments is administered as prodrugs which exhibit an improved bioavailability by comparison with the underlying active ingredient, for example achieved by improving the physicochemical profile, specifically the solubility, the active or passive absorption properties or the tissue-specific distribution. An example which may be mentioned from the wide-ranging literature on prodrugs is: H. Bundgaard (Ed.), Design of Prodrugs: Bioreversible derivatives for various functional groups and chemical entities, Elsevier Science Publishers B.V., 1985. A review of prodrug derivatives based on carboxylic acid esters and possible properties of such compounds can be found, for example, in K. Beaumont et al., Curr. Drug Metab. 4, 461-485 (2003). Also known are dipeptide prodrugs of acyclovir for treating ocular herpes infections (B. S. Anand et al., Curr. Eye Res. 26, No. 3-4, 151-163 (2003)) which interact with the oligopeptide transporter on the cornea, thus increasing the bioavailability of acylovir in the eye.
WO 2008/130520 claims alkinyl-substituted purine derivatives as therapeutic agent for glaucoma or ocular hypertension. WO 2010/127210 describes Adenosine derivatives like INO-8875 for reducing intraocular pressure in humans.
Substituted 3,5-dicyano-4-phenylpyridines and their prodrugs as potent and selective adenosine A1 agonists are disclosed in WO 03/53441, WO 2009/015776, WO 2009/015811, WO 2009/015812, WO 2010/072314, WO 2010/072315 and WO 2010/086101.
The object of the present invention is to provide an effective therapeutic agent for the use in the treatment and/or prophylaxis of glaucoma and/or ocular hypertension without showing the above mentioned side effects.
Surprisingly, it has now been found that the dicyanopyridines of formula (I) lower intraocular pressure after topical application to the eye without effecting hemodynamics and are thus suitable for the production of medicaments for the use in the treatment and/or prophylaxis of glaucoma and ocular hypertension.
The present invention relates to compounds of formula (I)

in which
A is oxygen or sulfur,
R¹is hydrogen or a group of the formula

- in which
- # is the attachment to the oxygen-atom,
- L¹is linear (C₂-C₄)-alkanediyl,
- L²is linear (C₁-C₃)-alkanediyl,
- R⁵and R⁸are identical or different and independently selected from the group consisting of hydrogen or a side group of a natural α-amino acid or its homologues or isomers,
- R⁶and R⁹are independently selected from hydrogen or methyl,
- R⁷is hydrogen or (C₁-C₄)-alkyl,
- or
- R⁷and R⁵form together with the atoms which they are attached to a pyrrolidine- or piperidine-ring,
- R¹⁰and R¹¹are identical or different and are independently selected from hydrogen or (C₁-C₄)-alkyl,
  - wherein (C₁-C₄)-alkyl may be substituted with one group selected from hydroxy, (C₁-C₄)-alkoxy, amino, mono-(C₁-C₄)-alkylamino or di-(C₁-C₄)-alkylamino,
- or
- R¹⁰and R⁸form together with the atoms which they are attached to a pyrrolidine- or piperidine-ring,
- and
- R¹²is hydrogen or hydroxycarbonyl,
R²is hydrogen or a group of the formula —CH₂OR¹,
- wherein R¹is defined as above,
R³is hydrogen, methyl or ethyl,
R⁴is hydrogen, methyl or ethyl,
or
R³and R⁴form together with the nitrogen-atom, which they are bound to, a azetidine-, pyrrolidine- or piperidine-ring,
- wherein the azetidine-, pyrrolidine- or piperidine-ring may be substituted with one or 2 substituents independently selected from the group fluoro, trifluoromethyl, methyl, ethyl, methoxy and ethoxy,
  and its salts, solvates and solvates of the salts,
  for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.

In a preferred embodiment the present invention relates to compounds of formula (I), in which

A is sulfur,
R¹is a group of the formula

- in which
- # is the attachment to the oxygen-atom,
- L¹is ethane-1,2-diyl,
- R⁵is hydrogen, methyl, propane-2-yl, 1-methylpropane-1-yl, 2-methylpropane-1-yl, hydroxymethyl or 1-hydroxymethyl,
- R⁶is hydrogen,
- R⁷is hydrogen,
- R⁸is hydrogen, methyl, propan-2-yl, 1-methylpropan-1-yl, 2-methylpropan-1-yl, imidazol-4-ylmethyl, hydroxymethyl, hydroxyethyl, 2-carboxyethyl, 4-aminobutan-1-yl or 2-aminoethyl,
- R⁹is hydrogen,
- R¹⁰is hydrogen,
- R¹¹is hydrogen,
- or
- R¹⁰and R⁸form together with the atoms which they are attached to a pyrrolidine-ring,
R²is hydrogen,
R³is hydrogen,
R⁴is hydrogen,
or
R³and R⁴form together with the nitrogen-atom, which they are bound to, a azetidine-, pyrrolidine- or piperidine-ring,
and its salts, solvates and solvates of the salts,
for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.

In a preferred embodiment the present invention also relates to compounds of formula (I), in which

A is sulfur,
R¹is hydrogen
R²is hydrogen,
R³is hydrogen,
R⁴is hydrogen,
or
R³and R⁴form together with the nitrogen-atom, which they are bound to, a azetidine-, pyrrolidine- or piperidine-ring,
and its salts, solvates and solvates of the salts,
for the use in a method treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.

In a preferred embodiment the present invention also relates to compounds of formula (I), in which
A is oxygen,
R¹is hydrogen
R²is hydrogen or —CH₂OH,
R³is hydrogen,
R⁴is hydrogen,
and its salts, solvates and solvates of the salts,
for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.
In a preferred embodiment the present invention also relates to compounds of formula (I), in which
A is sulfur,
R¹is a group of the formula

- in which
- # is the attachment to the oxygen-atom,
- R⁵is hydrogen, methyl, propan-2-yl, 2-methylpropan-1-yl, benzyl, hydroxymethyl or 1-hydroxyethyl,
- R⁶is hydrogen,
- R⁷is hydrogen,
- R⁸is hydrogen, methyl, propan-2-yl, 1-methylpropan-1-yl, 2-methylpropan-1-yl, imidazol-4-ylmethyl, 4-aminobutan-1-yl, 2-aminoethyl, 3-aminopropan-1-yl, aminomethyl or 3-guanidinopropan-1-yl,
- R⁹is hydrogen,
- R¹⁰is hydrogen,
- R¹¹is hydrogen,
  R²is hydrogen,
  R³is hydrogen,
  R⁴is hydrogen,
  and its salts, solvates and solvates of the salts,
  for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.

In a preferred embodiment the present invention relates to a compound of the formula (1) selected from:

2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-lysyl-D-alaninate-Dihydrochloride,
2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-arginyl-D-alaninate-Dihydrochloride,
2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-lysyl-D-valinate-Dihydrochloride,
2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-arginyl-D-valinate-Trihydrochloride,
2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-lysyl-D-phenylalaninate-Dihydrochloride,
2-{4-[2-(Azetidin-1-yl)-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-beta-alaninate-Trifluoroacetate,
2-{4-[2-(Azetidin-1-yl)-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-ornithinate-Bis(trifluoroacetate),
2-{4-[2-(Azetidin-1-yl)-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-lysyl-L-alaninate-Bis(trifluoroacetate),
2-{4-[2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyano-6-(pyrrolidin-1-yl)pyridin-4-yl]phenoxy}ethyl-L-alanyl-L-alaninate-Hydrochloride,
2-{4-[2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyano-6-(pyrrolidin-1-yl)pyridin-4-yl]phenoxy}ethyl-L-isoleucyl-L-alaninate-Hydrochloride,
2-{4-[2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyano-6-(pyrrolidin-1-yl)pyridin-4-yl]phenoxy}ethyl-glycyl-L-leucinate-Hydrochloride,
(2S)-3-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}propan-1,2-diyl-(2S,2′S)-bis(2-{[(2S)-2-aminopropanoyl]amino}propanoate)-Dihydrochloride
and their salts, solvates and solvates of the salts for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.

In a preferred embodiment the present invention relates to a compound of the formula (I) selected from:

2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-4-[4-(2-hydroxyethoxy)phenyl]pyridine-3,5-dicarbonitrile
2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-4-[4-(2-hydroxyethoxyl)phenyl]-6-(pyrrolidin-1-yl)pyridine-3,5-dicarbonitrile
2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-4-[4-(2-hydroxyethoxyl)phenyl]-6-(azetidin-1-yl)pyridine-3,5-dicarbonitrile
2-Amino-6-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}sulfanyl)-4-(4-{[(2R)-2,3-dihydroxy-propyl]oxy}phenyl)pyridin-3,5-dicarbonitrile
and its salts, solvates and solvates of the salts,
and their salts, solvates and solvates of the salts for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.

2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-lysyl-D-alaninate-Dihydrochloride,
2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-lysyl-D-valinate-Dihydrochloride,
2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-arginyl-D-valinate-Trihydrochloride,
and their salts, solvates and solvates of the salts for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.

In a preferred embodiment the present invention also relates to compounds of formula (I), in which
R³is hydrogen,
R⁴is hydrogen,
and its salts, solvates and solvates of the salts,
for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.
In a preferred embodiment the present invention also relates to compounds of formula (I), in which

R³and R⁴form together with the nitrogen-atom, which they are bound to, a azetidine-pyrrolidine- or piperidine-ring,
and its salts, solvates and solvates of the salts,
for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.

The compounds of formula (I), their production and their action as potent and selective adenosine A1 agonists are disclosed in WO 03/53441, WO 2009/015776, WO 2009/015811, WO 2009/015812, WO 2010/072314, WO 2010/072315 and WO 2010/086101 respectively. The compounds mentioned in WO 03/53441, WO 2009/015776, WO 2009/015811, WO 2009/015812, WO 2010/072314, WO 2010/072315 and WO 2010/086101 in general and especially the compounds specifically are an explicit part of the description of the present invention and are hereby incorporated by reference.
Depending on the substitution pattern, the compounds of the formula (I) can exist in stereoisomeric forms, which behave either as image and mirror image (enantiomers) or which do not behave as image and mirror image (diastereomers). The invention relates both to the use of the enantiomers or diastereomers and to their respective mixtures. Just like the diastereomers, the racemic forms can be separated into the stereoisomerically uniform constituents in a known manner. Equally, the present invention also relates to the use of the other tautomers of the compounds of the formula (I) and their salts.
Salts of the compounds of the formula (I) can be physiologically acceptable salts of the substances according to the invention with mineral acids, carboxylic acids or sulfonic acids. Particularly preferred salts are, for example, those with hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, toluenesulfonic acid, benzenesulfonic acid, naphthalenedisulfonic acid, trifluoroacetic acid, acetic acid, propionic acid, lactic acid, tartaric acid, citric acid, fumaric acid, maleic acid or benzoic acid.
The compounds of the present invention appear preferably as hydrochlorides or trifluoroacetates.
Salts which can be mentioned are also salts with customary bases, such as, for example, alkali metal salts (e.g. sodium or potassium salts), alkaline earth metal salts (e.g. calcium or magnesium salts) or ammonium salts, derived from ammonia or organic amines such as, for example, diethyl-amine, triethylamine, ethyldiisopropylamine, procaine, dibenzylamine, N-methylmorpholine, dihydroabietylamine, 1-ephenamine or methylpiperidine.
Hydrates or solvates are designated according to the invention as those forms of the compounds of the formula (I) which in the solid or liquid state form a molecular compound or a complex by hydration with water or coordination with solvent molecules. Examples of hydrates are sesqui-hydrates, monohydrates, dihydrates or trihydrates. Equally, the hydrates or solvates of salts of the compounds according to the invention are also suitable.
In the context of the present invention, the substituents, unless stated otherwise, have the following meaning:
“Alkyl” is in the context of the invention a straight-chain or branched alkyl radical having 1 to 4 carbon atoms. The following radicals may be mentioned by way of example and by way of preference: methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl and tert-butyl.
“Alkanediyl” is in the context of the invention a straight-chain or branched divalent alkyl radical having 1 to 4 carbon atoms. Examples which may be preferably mentioned are: ethane-1,2-diyl(1,2-ethylene), ethane-1,1-diyl, propane-1,3-diyl(1,3-propylene), propane-1,1-diyl, propane-1,2-diyl, propane-2,2-diyl, butane-1,4-diyl(1,4-butylene), butane-1,2-diyl, butane-1,3-diyl, butane-2,3-diyl.
“Alkoxy” is in the context of the invention a straight-chain or branched alkoxy radical having 1 to 4 carbon atoms. The following radicals may be mentioned by way of example and by way of preference: methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy and tert-butoxy.
“Mono- or di-(C₁-C₄)-alkylamino” is in the context of the invention an amino group having one or having two identical or different straight-chain or branched alkyl substituents, which in each case contain 1 to 4 carbon atoms. For example, the following may be mentioned: methylamino, ethyl-amino, n-propylamino, isopropylamino, t-butylamino, N,N-dimethylamino, N,N-diethylamino, N-ethyl-N-methylamino, N-methyl-N-n-propylamino, N-isopropyl-N-n-propylamino and N-t-butyl-N-methylamino.
The “side group of an α-amino acid” in the meaning of R³encompasses both the side groups of naturally occurring α-amino acids and the side groups of homologs and isomers of these α-amino acids. The α-amino acid may in this connection have both the L and the D configuration or else be a mixture of the L form and D form. Examples of side groups which may be mentioned are: methyl (alanine), propan-2-yl (valine), propan-1-yl (norvaline), 2-methylpropan-1-yl (leucine), 1-methylpropan-1-yl (isoleucine), butan-1-yl (norleucine), tert-butyl (2-tert-butylglycine), phenyl (2-phenylglycine), benzyl (phenylalanine), p-hydroxybenzyl (tyrosine), indol-3-ylmethyl (tryptophan), imidazol-4-ylmethyl (histidine), hydroxymethyl (serine), 2-hydroxyethyl (homoserine), 1-hydroxyethyl (threonine), mercaptomethyl (cysteine), methylthiomethyl (S-methylcysteine), 2-mercaptoethyl (homocysteine), 2-methylthioethyl (methionine), carbamoylmethyl (asparagine), 2-carbamoylethyl (glutamine), carboxymethyl (aspartic acid), 2-carboxyethyl (glutamic acid), 4-aminobutan-1-yl (lysine), 4-amino-3-hydroxybutan-1-yl (hydroxylysine), 3-aminopropan-1-yl (ornithine), 2-aminoethyl (2,4-diaminobutyric acid), aminomethyl (2,3-diaminopropionic acid), 3-guanidinopropan-1-yl (arginine), 3-ureidopropan-1-yl (citrulline). Preferred α-amino acid side groups in the meaning of R³are methyl (alanine), propan-2-yl (valine), 2-methylpropan-1-yl (leucine), benzyl (phenylalanine), imidazol-4-ylmethyl (histidine), hydroxymethyl (serine), 1-hydroxyethyl (threonine), 4-aminobutan-1-yl (lysine), 3-aminopropan-1-yl (ornithine), 2-aminoethyl (2,4-diaminobutyric acid), aminomethyl (2,3-diaminopropionic acid), 3-guanidinopropan-1-yl (arginine). The L configuration is preferred in each case.
The term “effective amount” as used herein refers to an amount of a compound of formula (I) that is effective for treatment and/or prophylaxis glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.
The present invention relates to selective adenosine A1 agonists, in particular the dicyanopyridines of formula (I), for the use in a method for the treatment and/or prophylaxis of glaucoma, normotensive glaucoma, ocular hypertension and/or combinations thereof.
The compounds of formula (I) act as selective adenosine A1 agonists and show a beneficial profile when administered topically to the eye, and are thus useful as an effective therapeutic agent for the treatment and/or prophylaxis of glaucoma and/or ocular hypertension.
The compounds of the present invention lower intraocular pressure when administered topically to the eye without effecting hemodynamic parameters as demonstrated in section B. Experimental methods.
The present invention relates to compounds of formula (I) for the use in a method for the treatment and/or prophylaxis of glaucoma and/or ocular hypertension.
Furthermore the present invention relates to compounds of formula (I) for the use in a method for the treatment and/or prophylaxis of high IOP resulting from traumatic hyphema, orbital edema, postoperative visco-elastic retention, intraocular inflammation, corticosteroid use, pupillary block, or idiopathic causes.
In addition the compounds of formula (I) are useful for the treatment and/or prophylaxis of various ocular hypertensive conditions, such as post-surgical and post-laser trabeculectomy ocular hypertensive episodes and as presurgical adjuncts.
The present invention further relates to a method of treating glaucoma, or other disease or disorder of the eye related to elevated intraocular pressure.
The present invention further relates to the use of compounds of formula (I) for the manufacture of medicaments for the treatment and/or prophylaxis of glaucoma and/or ocular hypertension.
A further subject of the present invention is a pharmaceutical composition comprising a compound of the formula (I).
A further subject of the present invention is a medicament, comprising a compound of the formula (I) as defined in any of claims 1 to 4 in combination with one or more further active ingredients selected from the group consisting of alpha adrenergic agonist, beta blocker and carbonic anhydrase inhibitor.
A further subject of the present invention is the use of a combination of one or more compounds of the formula (I) with one or more other active compounds in a method for the treatment and/or prophylaxis of glaucoma, high IOP resulting from traumatic hyphema, orbital edema, postoperative visco-elastic retention, intraocular inflammation, corticosteroid use, pupillary block, or idiopathic causes. Examples of suitable combination active ingredients may for example and preferably be mentioned:

- alpha adrenergic agonist such as for example alphagan; iopidin, isoglaucon, catapres, aruclonin
- beta blocker such as for example timolol, timoptol, optimal, carteolol, ocupress, betoptic, betagan
- carbonic anhydrase inhibitor such as for example dorzolamide, trusopt, diamox, Acetazolamid, brinzolamid, dorzolamid, dichlorphenamid, methazolamid.

Further disclosed herein is a method for the treatment and/or prophylaxis of high IOP, including glaucoma, ocular hypertension, normotensive glaucoma or a combination thereof comprising administering an effective amount of at least one compound of formula (I) or of a medicament comprising at least one compound of formula (I) in combination with an inert, non-toxic, pharmaceutically suitable excipent to the eye.
Further disclosed herein is a method for the treatment and/or prophylaxis of high IOP, including glaucoma, ocular hypertension, normotensive glaucoma or a combination thereof comprising administering an effective amount of at least one compound of formula (I) or of a medicament comprising at least one compound of formula (I) in combination with an inert, non-toxic, pharmaceutically suitable excipent to the eye and at least one further active compound selected from the group consisting of alpha adrenergic agonists, beta blockers and carbonic anhydrase inhibitors.
Preferred administration route is topical administration to the eye.
Topical preparations of the invention include solutions, sprays, lotions, gels, creams, powders, powder sprays, pastes, emulsions, foams and sticks which comprise the active ingredient of the formula (I), where appropriate also a plurality of active ingredients.
Suitable pharmaceutically-acceptable carriers for topical application include those suited for use in lotions, creams, gels, solutions, ointments, viscous solutions, eye drops, emulsions, gel-forming solutions and the like.
The topically applicable preparations of the invention comprise 0.1 to 99%, preferably 0.5 to 20% by weight of active ingredient of the formula (I).
Ointments comprise hydrocarbon gels, lipogels, absorption bases, W/O ointment bases, mixed emulsions or polyethylene glycols as base.
Gels comprise solvents such as water, ethanol, isopropanol or propylene glycol and are produced using gel formers such as cellulose ethers, alginates, polyacrylates, bentonite, gelatin, tragacanth, polyvinylpyrrolidone or polyvinyl alcohol. Lipophilic gel bases or microemulsions can also be used.
Advantageously, the composition is sterile and can be in dosage unit form, e.g., suitable for topical ocular use. The composition can be packaged in a form suitable for metered application, such as in container equipped with a dropper.
In a preferred embodiment, the composition is a solution prepared using a physiological saline solution as a carrier. The pH of the solution is, preferably, maintained between 4.5 and 8.0 using an appropriate buffer system. A neutral pH is more preferred. Compositions of the invention can also comprise pharmaceutically acceptable preservatives, stabilizers and/or surfactants.
For this purpose, the active compounds can be converted into the customary preparations in a manner known per se. This takes place using inert, nontoxic, pharmaceutically suitable carriers, excipients, solvents, vehicles, emulsifiers and/or dispersants.
Suitable excipients which may be mentioned are, for example: water, nontoxic organic solvents such as, for example, paraffins, vegetable oils (e.g. sesame oil), alcohols (e.g. ethanol, glycerol), glycols (e.g. polyethylene glycol), solid carriers such as natural or synthetic ground minerals (e.g. talc or silicates), sugars (e.g. lactose), emulsifiers, dispersants (e.g. polyvinylpyrrolidone) and glidants (e.g. magnesium sulfate).
Further disclosed herein is an ophthalmic composition comprising a compound of formula (I) and a pharmaceutically acceptable vehicle or excipient.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A: A graph showing IOP as mmHg in unconscious rats after topical administration of 10 mg/ml of the compound of Example 1, 10 mg/ml N⁶-cyclopentyladenosine, and control

FIG. 1B: A graph showing IOP as percent of zero value in unconscious rats after topical administration of 10 mg/ml of the compound of Example 1, 10 mg/ml N⁶-cyclopentyladenosine, and control.

FIG. 2: A graph of IOP as percent of zero value in unconscious rats, after topical administration of 10 mg/ml of the compound of Example 9 and control.

FIG. 3: A graph of blood pressure in conscious rats after topical administration of 10 mg/ml of the compound of Example 1 and N⁶-cyclopentyladenosine.

FIG. 4: A graph of blood pressure in conscious rats after topical administration of 10 mg/ml of the compound of Example 9 and control.

FIG. 5: A graph of IOP in conscious rabbits after topical administration of INO-8875 and control.

FIG. 6: A graph of IOP in conscious rabbits after topical administration of the compound of Example 1 and control.

FIG. 7: A graph showing the effect on mean arterial pressure of conscious rabbits after topical administration of INO-8875.

FIG. 8: A graph of blood pressure in conscious rabbits after topical administration of the compound of Example 1.

EXAMPLES

TABLE 1

Example	R¹	R³	R⁴	HA

1		H	H		2 HCl

2		H	H		2 HCl

3		H	H		2 HCl

4		H	H		3 HCl

5		H	H		2 HCl

The synthesis of examples 1 to 5 and corresponding starting materials is described in WO 2009/015811 in detail.

TABLE 2

Ex-
ample	R¹	—NR³R⁴	HA

6			CF₃CO₂H

7			CF₃CO₂H

8			CF₃CO₂H

9			HCl

10			HCl

11			HCl

* is the attachment to the dicyanopyridine

The synthesis of examples 6 to 11 and corresponding starting materials is described in WO 2010/086101 in detail.

Example 12

2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-4-[4-(2-hydroxyethoxyl)phenyl]pyridine-3,5-dicarbonitrile

The synthesis of example 12 is described in WO 03/53441 (example 6) in detail.

Example 13

2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-4-[4-(2-hydroxyethoxyl)phenyl]-6-(pyrrolidin-1-yl)pyridine-3,5-dicarbonitrile

The synthesis of example 13 is described in WO 2010/086101 (example 1) in detail.

Example 14

2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-4-[4-(2-hydroxyethoxyl)phenyl]-6-(azetidin-1-yl)pyridine-3,5-dicarbonitrile

The synthesis of example 14 is described in WO 2010/086101 (example 49) in detail.

Example 15

2-Amino-6-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}sulfanyl)-4-(4-{[(2R)-2,3-dihydroxy-propyl]oxy}phenyl)pyridin-3,5-dicarbonitrile

The synthesis of example 15 is described in WO 2009/015776 (example 8A) in detail.

Example 16

(2S)-3-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}propan-1,2-diyl-(2S,2′S)-bis(2-{[(2S)-2-aminopropanoyl]amino}propanoate)-Dihydrochloride

The synthesis of example 16 is described in WO 2010/072314 (example 33) in detail.

B. Experimental Methods

Advantageous pharmacological properties of the compounds of the present invention can be determined by the following methods.
The abbreviations are used in the following experiments:
IOP intraocular pressure
SEM (standard error of mean)
PBS (phosphate buffered saline)
In each experiment the control animals received the corresponding solvent.

B-1. IOP Measurements in Rats

Wistar rats with a body weight of about 300 g were anesthetized with isoflurane (2-3% in O₂:N₂O=1:2). The compounds were dissolved/suspended in an aqueous solution of sodium chloride (0.9%) and administered topically to the eye in 10 μl volume at a concentration of 10 mg/ml. IOP was measured with a rebound tonometer (TonoLab) at different time points after application of the compounds. Ocular pressure and effects of hemodynamic parameters can be monitored in this model. N⁶-Cyclopentyl-Adenosine (CPA) is a known adenosine A1 agonist having the structure shown below:
FIG. 1A shows IOP (as mm Hg) over time after topical administration of control, N⁶-Cyclopentyl-Adenosine (CPA) and Example 1 at a dose of 10 mg/ml.
FIG. 1B shows IOP (as percent of zero value) over time after topical administration of control, N⁶-Cyclopentyl-Adenosine (CPA) and Example 9 at a dose of 10 mg/ml.
Table 3 gives IOP (as percent of zero value) after topical administration of N⁶-Cyclopentyl-Adenosine (CPA) and Example 1 at a dose of 10 mg/ml at time points from 0 min to 120 min

TABLE 3

compound	Time [min]	IOP [%]	±SEM

Control

0	100.0	0.0
Control	15	89.6	3.7
Control	30	92.3	4.8
Control	45	88.6	2.9
Control	60	93.4	5.1
Control	90	95.7	4.4
Control	120	96.3	4.3
Example 1	0	100.0	0.0
Example 1	15	93.6	5.7
Example 1	30	80.6	2.6
Example 1	45	77.7	3.0
Example 1	60	70.0	1.7
Example 1	90	75.9	5.9
Example 1	120	76.6	3.5
CPA	0	100.0	0.0
CPA	15	65.0	3.3
CPA	30	58.5	3.5
CPA	45	46.3	4.9
CPA	60	42.5	3.6
CPA	90	44.8	2.3
CPA	120	59.0	2.0
Example 4	0	100.0	0.0
Example 4	30	73.8	6.1
Example 4	60	80.0	7.9
Example 4	90	76.0	7.7
Example 2	0	100.0	0.0
Example 2	30	95.3	9.9
Example 2	60	73.3	3.9
Example 2	90	73.8	6.6

FIG. 2 shows IOP (as percent of zero value) over time after topical administration of control and Example 9 at a dose of 10 mg/ml.
Table 4 gives IOP (as percent of zero value) after topical administration of Example 9 and control at a dose of 10 mg/ml at time points from 0 min to 120 min.

TABLE 4

compound	Time [min]	IOP [%]	±SEM

Control

0	100.0	0.0
Control	15	96.7	3.8
Control	30	106.9	6.4
Control	60	104.4	6.1
Control	90	97.7	5.5
Control	120	101.7	6.5
Example 9	0	100.0	0.0
Example 9	15	81.6	3.1
Example 9	30	84.4	2.4
Example 9	60	83.7	4.0
Example 9	90	85.3	2.4
Example 9	120	83.7	3.9

B-2. Blood Pressure Measurement in Telemetric Rats

Normotensive wistar rats with a body weight of 300 to 350 g were used for this experimental study. Blood pressure was monitored in freely moving conscious animals by radiotelemetry. Briefly, the telemetric system (DSI Data Science International, MN, USA) is composed on 3 basic elements: implantable transmitters (TA11PA-C40), receivers (RA1010) and a computer-based acquisition software (Dataquest A.R.T 2.1 for Windows). Rats were instrumented with pressure implants for chronic use at least 14 days prior the experiments. Rats were anesthetized with isoflurane (2-3% in O₂:N₂O=1:2). During catheter implantation under anesthesia, rats were kept on a heating mat. A fluid-filled sensor catheter was inserted upstream into the exposed descending aorta between the iliac bifurcation and the renal arteries. According to the DSI guidelines the tip of the telemetric catheter was located just caudal to the renal arteries and secured by tissue adhesive. The transmitter body was affixed to the inner peritoneal wall before closure of abdomen. In a hardware configuration equipped for 24 animals, each rat cage was positioned on top of an individual receiver platform. After activation of the implanted transmitters, A.R.T., an on-line data acqusition system, samples data and converts telemetric pressure signals into mm Hg. The compounds were dissolved/suspended in an aqueous solution of sodium chloride (0.9%) and administered topically to the eye in 10 μl volume at a concentration of 10 mg/ml. Given are % deviations from the control run-in period of 2 hours before substance administration.
FIG. 3 shows effects on mean arterial blood pressure after topical administration of control, N⁶-Cyclopentyl-Adenosine and Example 1 at a dose of 10 mg/ml over time.
Table 5 gives mean arterial pressure (MAP) as percent change of zero value after topical administration of control, N⁶-Cyclopentyl-Adenosine and Example 1 at different time points from −0.25 h to 6.25 h.

TABLE 5

Time	control	CPA	Example 1	Example 4	Example 2

[hours]	MAP	±SEM	MAP	±SEM	MAP	±SEM	MAP	±SEM	MAP	±SEM

−0.25	0.0	0.0	0.0	0.0	0.0	0.0	0.0	0.0	0.0	0.0
0.25	4.5	1.8	−25.4	2.8	1.2	1.3	7.3	1.5	10.7	3.3
0.75	0.1	1.1	−71.3	5.0	−6.1	0.8	1.0	2.3	1.6	2.6
1.25	−4.7	2.0	−58.9	7.7	−6.0	0.5	−2.0	1.5	0.3	2.0
1.75	−1.2	3.4	−42.6	7.1	−2.5	1.2	−0.8	2.0	−0.2	1.8
2.25	4.2	3.3	−30.3	5.5	−2.5	1.6	0.7	2.6	−1.1	1.6
2.75	−3.4	0.8	−17.6	6.1	−1.5	2.3	0.6	2.2	1.9	2.7
3.25	−2.3	1.8	−16.4	5.5	−1.4	3.2	0.1	2.5	2.0	2.3
3.75	−4.9	1.1	−9.0	3.1	−1.6	3.5	1.0	2.9	−2.2	1.5
4.25	−3.4	1.1	−8.4	2.9	−1.5	4.1	−1.5	1.6	−0.9	1.2
4.75	−2.0	1.2	−5.3	3.6	−1.7	3.7	−0.3	1.8	−0.8	1.7
5.25	−3.3	0.9	−0.7	4.4	−6.0	4.4	−1.7	2.3	−3.1	1.4
5.75	4.5	1.7	−2.9	2.2	−3.8	4.6	−3.8	2.2	−4.2	1.8
6.25	−4.6	1.1	−2.7	3.2	−6.0	3.7	−3.6	1.6	−4.0	1.6

FIG. 4 shows effects on mean arterial blood pressure after topical administration of control and Example 9 at a dose of 10 mg/ml over time.
Table 6 gives mean arterial pressure (MAP) as percent change of zero value after topical administration of control and Example 9 at different time points from −0.25 h to 6.25 h.

TABLE 6

Time	Control	Example 9

[hours]	MAP	±SEM	MAP	±SEM

−0.25	0.00	0.0	0.00	0.0
0.25	10.26	2.1	7.05	1.3
0.75	0.04	1.1	0.94	1.8
1.25	−1.16	1.6	−3.02	1.9
1.75	0.74	1.0	−2.50	1.0
2.25	−0.27	1.0	0.37	1.3
2.75	0.62	1.8	−0.95	1.6
3.25	3.67	2.3	−1.51	1.0
3.75	1.38	2.6	0.08	1.1
4.25	−1.52	1.0	−1.54	1.5
4.75	0.46	1.0	−1.99	1.9
5.25	−1.68	1.2	−0.43	1.6
5.75	−1.37	1.8	−0.04	1.9
6.25	−1.03	2.2	−2.42	1.9

B-3. Nerve Crush Model

Mice (all at least 7 weeks old) are deeply anesthetized, and optic nerves are intraorbitally crushed. After treating the mice for two weeks with compounds, i.e. the adenosine A1 agonists they are sacrified and eyes are withdrawn. Flatmounts of the retinas are prepared. The degenerated retinal ganglion cells are analyzed and counted in the different treatment groups.

B-4. Retinal Ischemia Model

Male Lewis rats weighing 200 to 250 g and male C57BL/6J mice weighing 25 to 30 g are anesthetized. The anterior chamber of one eye is cannulated with a needle attached to a line infusing normal saline to increase intraocular pressure. IOP is measured by a handheld tonometer (TonoLab) in rat eyes for the next up to 120 minutes. The other eye of the same animal is set up as a control. After ischemia, the needle is withdrawn, IOP is normalized, and reflow of the retinal circulation is documented visually. Animals are killed at different times after I/R injury.

B-5. IOP Measurements in Conscious Rabbits

Female New Zealand rabbits with a body weight of about 4-5 kg were used to measure inner eye pressure (IOP). The compounds were dissolved/suspended in a solution of 10% transcutol, 10% solutol and 80% PBS, and given by topical administration at the eye in 30 μl volume. IOP was measured with a rebound tonometer (TonoVet) at different time points after application of the drugs. INO-8875 is a known adenosine A1 agonist having the structure shown below:
FIG. 5 shows IOP as percent of zero value in rabbits of INO-8875 at dosages of 1.0, 3.0 and 10.0 mg/mL after topical administration.
Table 7 gives IOP as percent of zero value in rabbits of INO-8875 at dosages of 1.0, 3.0 and 10.0 mg/mL after topical administration.

TABLE 7

	INO-8875	INO-8875	INO-8875
time	(1.0 mg/mL)	(3.0 mg/mL)	(10.0 mg/mL)	control

[min]	IOP	±SEM	IOP	±SEM	IOP	±SEM	IOP	±SEM

0	100.0	0.0	100.0	0.0	100.0	0.0	100.0	0.0
30	85.3	5.0	89.3	3.7	74.0	3.6	105.0	4.7
60	86.7	5.5	81.3	1.3	60.0	2.6	99.0	4.0
90	93.3	5.8	79.0	1.5	61.3	3.0	99.3	5.8
120	100	8.9	87.3	7.4	65.0	4.6	99.0	1.0

FIG. 6 shows IOP as percent of zero value in rabbits of Example 1 at dosages of 3.0 and 10.0 mg/mL after topical administration.
Table 8 gives IOP as percent of zero value in rabbits of Example 1 at dosages of 3.0 and 10.0 mg/mL after topical administration.

TABLE 8

	Example 1	Example 1
Time	(3.0 mg/mL)	(10.0 mg/mL)	control

[min]	IOP	±SEM	IOP	±SEM	IOP	±SEM

0	100.0	0.0	100.0	0.0	100.0	0.0
30	82.7	4.3	79.8	7.0	104.6	3.4
60	76.7	3.1	66.2	4.8	90.6	3-9
90	82.1	3.6	71.3	5.1	98.0	5.2
120	81.9	3.0	68.5	4.8	92.2	4.0

B-6. Assessment of Blood Pressure and Heart Rate in Telemetric Rabbits

Implantation of Telemetric Senders in Female New Zealand Rabbits:

New Zealand rabbits were used for implantation of the telemetric senders. Rabbits were pre-anaesthetized with Rompun® and Ketavet® i.m. at a dose of 5 mg/kg (in 0.25 ml/kg)+40 mg/kg (in 0.40 ml/kg) respectively. Anaesthesia was maintained with an i.v. infusion of Rompun® and Ketavet® (5-15 ml/h) with a solution of Rompun 2 ml (20 mg/1 ml)+Ketavet 4 ml (100 mg/ml) and 60 ml 0.9% aqueous solution of sodium chloride. Before surgery the hairs at the inner side of the back leg were completely removed and the skin were treated with local anaesthetic Xylocain® Spray and disinfected with Braunol®. The rabbits were transferred to a sterile surgery unit and covered with sterile swabs and compressions. The skin was opened and the arteria femoralis was carefully dissected free and the pressure catheter of the telemetric implant C50 PXT® (DSI/Data Science International, St. Paul, Minn., U.S.A.) was inserted in the vein and forwarded abdominally under control of the pressure signal. The signal was detected with the RMC1-DSI® receiver plates and visualized with the PONEMAH® physiology platform software DSI/Data Science International, St. Paul, Minn., U.S.A.). After detection of a stable blood pressure signal the catheter was fixed with tissue-glue “Gewebepad” (DSI) and the two ECG electrodes were cut close to the transmitter. The transmitter was fixed under the skin of the rabbit. The wound was closed and finally treated with Nebacetin® Powder Spray. Post-operative analgesia was done with Metamizol i.m. 50 mg/kg in 0.1 ml/kg for 5 days after surgery. In addition a 5 day antibiotic therapy with Terramycin®/LA 20 mg/kg with 0.1 ml/kg was applied i.m.. All rabbits recovered fully within one week of the surgery and were after 2 weeks adjustment to the measurement procedure used for the blood pressure detection.

Registration of MAP and HR in Conscious Female New Zealand Rabbits:

The rabbits with telemetric implants were housed for 5 hours in a transportation box which was placed on the RMC1-DSI® receiver plates. The signals were visualized, compiled and analyzed with the PONEMAH® physiology platform software. The systolic (SAP), diastolic (DAP) and mean arterial blood pressure (MAP) levels were registered in mmHg and the heart rate (HR) in beat/minutes was calculated from the interval between the systoles. Baseline levels for SAP, DAP and MAP as for HR were registered over a 2 hour equilibration period. The compounds were dissolved/suspended in a solution of 10% transcutol, 10% solutol and 80% PBS, and given by topical administration at the eye in 30 μl volume. Controls received the corresponding solvents. Baseline levels for SAP, DAP and MAP as for HR were registered over a 3 hour period after application.
FIG. 7 shows effects of INO-8875 at dosages of 1.0, 3.0 and 10.0 mg/mL on mean arterial blood pressure after topical administration.
Table 9 gives mean arterial pressure (MAP) as mm Hg of INO-8875 at dosages of 1.0, 3.0 and 10.0 mg/mL after topical administration.

TABLE 9

INO-8875	INO-8875	INO-8875
(1.0 mg/mL)	(3.0 mg/mL)	(10.0 mg/mL)	control

Time	MAP		MAP		MAP		MAP
[min]	[mmHg]	±SEM	[mmHg]	±SEM	[mmHg]	±SEM	[mmHg]	±SEM

0	123.9	12.1	118.5	13.2	114.5	7.3	113.6	9.4
30	111.3	13.3	101.8	17.7	89.5	11.4	114.2	13.2
60	110.9	13.6	104.9	17.8	86.9	10.5	113.8	13.4
90	112.6	13.3	105.7	17.1	90.3	8.9	114.8	10.3
120	106.0	14.5	109.0	20.4	90.0	40.0	108.3	18.2

FIG. 8 shows effects of Example 1 at dosages of 3.0 and 10.0 mg/ml on mean arterial blood pressure after topical administration.
Table 10 gives mean arterial pressure (MAP) as mm Hg of Example 1 at dosages of 3.0 and 10.0 mg/mL after topical administration.

TABLE 10

	Example 1	Example 1
Time	(3.0 mg/mL)	(10.0 mg/mL)	control

[min]	MAP	±SEM	MAP	±SEM	MAP	±SEM

0	117.1	28.6	115.9	10.7	113.6	9.4
30	114.5	29.4	118.8	15.0	114.2	13.2
60	110.4	28.7	112.0	14.2	113.8	13.4
90	117.8	34.0	112.8	14.1	114.8	10.3
120	106-7	31.6	105.4	17.9	108.3	18.2

Claims

1-9. (canceled)

10. An ophthalmic composition, comprising a compound of the formula (I) and at least one active ingredients selected from the group consisting of alpha adrenergic agonist, beta blocker and carbonic anhydrase inhibitor, wherein the compound of formula (I) is:

in which

A is oxygen or sulfur,

R¹is hydrogen or a group of the formula

in which

# is the attachment to the oxygen-atom,

L¹is linear (C₂-C₄)-alkanediyl,

L²is linear (C₁-C₃)-alkanediyl,

R⁵and R⁸are identical or different and independently selected from the group consisting of hydrogen or a side group of a natural α-amino acid or its homologues or isomers,

R⁶and R⁹are independently selected from hydrogen or methyl,

R⁷is hydrogen or (C₁-C₄)-alkyl,

or

R⁷and R⁵form together with the atoms which they are attached to a pyrrolidine- or piperidine-ring,

R¹⁰and R¹¹are identical or different and are independently selected from hydrogen or (C₁-C₄)-alkyl,

wherein (C₁-C₄)-alkyl may be substituted with one group selected from hydroxy, (C₁-C₄)-alkoxy, amino, mono-(C₁-C₄)-alkylamino or di-(C₁-C₄)-alkylamino,

or

R¹⁰and R⁸form together with the atoms which they are attached to a pyrrolidine- or piperidine-ring,

and

R¹²is hydrogen or hydroxycarbonyl,

R²is hydrogen or a group of the formula —CH₂OR¹,

wherein R¹is defined as above,

R³is hydrogen, methyl or ethyl,

R⁴is hydrogen, methyl or ethyl,

or

R³and R⁴form together with the nitrogen-atom, which they are bound to, a azetidine-, pyrrolidine- or piperidine-ring,

wherein the azetidine-, pyrrolidine- or piperidine-ring may be substituted with one or 2 substituents independently selected from the group fluoro, trifluoromethyl, methyl, ethyl, methoxy and ethoxy,

or a salt thereof.

11. The ophthalmic composition of claim 10, wherein in the compound of formula (I),

A is sulfur,

R¹is a group of the formula

in which

# is the attachment to the oxygen-atom,

L¹is ethane-1,2-diyl,

R⁵is hydrogen, methyl, propane-2-yl, 1-methylpropane-1-yl, 2-methyl-propane-1-yl, hydroxymethyl or 1-hydroxymethyl,

R⁶is hydrogen,

R⁷is hydrogen,

R⁸is hydrogen, methyl, propan-2-yl, 1-methylpropan-1-yl, 2-methylpropan-1-yl, imidazol-4-ylmethyl, hydroxymethyl, hydroxyethyl, 2-carboxyethyl, 4-aminobutan-1-yl or 2-aminoethyl,

R⁹is hydrogen,

R¹⁰is hydrogen,

R¹¹is hydrogen,

or

R¹⁰and R⁸form together with the atoms which they are attached to a pyrrolidine-ring,

R²is hydrogen

R³is hydrogen,

R⁴is hydrogen,

or

R³and R⁴form together with the nitrogen-atom, which they are bound to, a azetidine-pyrrolidine- or piperidine-ring.

12. The ophthalmic composition of claim 10, wherein in the compound of formula (I)

A is sulfur,

R¹is a group of the formula

in which

# is the attachment to the oxygen-atom,

R⁵is hydrogen, methyl, propan-2-yl, 2-methylpropan-1-yl, benzyl, hydroxy-methyl or 1-hydroxyethyl,

R⁶is hydrogen,

R⁷is hydrogen,

R⁸is hydrogen, methyl, propan-2-yl, 1-methylpropan-1-yl, 2-methylpropan-1-yl, imidazol-4-ylmethyl, 4-aminobutan-1-yl, 2-aminoethyl, 3-aminopropan-1-yl, aminomethyl or 3-guanidinopropan-1-yl,

R⁹is hydrogen,

R¹⁰is hydrogen,

R¹¹is hydrogen,

R²is hydrogen,

R³is hydrogen, and

R⁴is hydrogen.

13. The ophthalmic composition of claim 10, wherein the compound of formula (I) is selected from:

2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-lysyl-D-alaninate-Dihydrochloride,

2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-arginyl-D-alaninate-Dihydrochloride,

2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-lysyl-D-valinate-Dihydrochloride,

2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-arginyl-D-valinate-Trihydrochloride,

2-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-lysyl-D-phenylalaninate-Dihydrochloride,

2-{4-[2-(Azetidin-1-yl)-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-beta-alaninate-Trifluoroacetate,

2-{4-[2-(Azetidin-1-yl)-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-ornithinate-Bis(trifluoroacetate),

2-{4-[2-(Azetidin-1-yl)-6-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}ethyl-L-lysyl-L-alaninate-Bis(trifluoroacetate),

2-{4-[2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyano-6-(pyrrolidin-1-yl)pyridin-4-yl]phenoxy}ethyl-L-alanyl-L-alaninate-Hydrochloride,

2-{4-[2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyano-6-(pyrrolidin-1-yl)pyridin-4-yl]phenoxy}ethyl-L-isoleucyl-L-alaninate-Hydrochloride,

2-{4-[2-({[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]methyl}sulfanyl)-3,5-dicyano-6-(pyrrolidin-1-yl)pyridin-4-yl]phenoxy}ethyl-glycyl-L-leucinate-Hydrochloride,

(2S)-3-{4-[2-Amino-6-({[2-(4-chlorophenyl)-1,3-oxazol-4-yl]methyl}sulfanyl)-3,5-dicyanopyridin-4-yl]phenoxy}propan-1,2-diyl-(2S,2′S)-bis(2-{[(2S)-2-aminopropanoyl]amino}propanoate)-Dihydrochloride.

14. The ophthalmic composition of claim 10, wherein the compound of formula (I) is

in which

R¹is

R³is hydrogen,

R⁴is hydrogen and

HA is 2 HCl.