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Definitions

• the present invention relates to novel 2-aminobenzoyl derivatives, pharmaceutical formulations containing them, and use of the compounds in the manufacture of medicaments for treating or preventing various diseases.
• the present invention relates generally to novel compounds, their use in therapy, and pharmaceutical formulations containing them.
• L-kynurenine is metabolized by three different enzymes in mammalian tissues: kynurenine 3-hydroxylase which form 3-hydroxy- kynurenine (3-HK); kynureninase which forms anthranilic acid and kynurenine aminotransferase (KAT) which causes the formation of kynurenic acid.
• 3-HK is metabolized by the same KAT to yield xanthurenic acid, a metabolically inert side product of the pathway, or by kynureninase to give rise to 3-hydroxyanthranilic acid, which is eventually converted to quinolinic acid.
• quinolinic acid is metabolized by quinolinic acid phosphoribosyltransferase, yielding nicotinic acid mononucleotide and subsequent degradation products including the end product NAD + .
• Kynurenic acid, 3-hydroxykynurenine and quinolinic acid are all neuroactive intermediates of this catabolic cascade.
• 3-hydroxykynurenine is a free radical generator, which has been shown to cause induction of apoptosis, potentiation of excitotoxicity, cataract formation, neurodegenerative diseases, stroke, traumatic injury, neurovirological diseases and neuroinflammation.
• Quinolinic acid is an ⁇ /-methyl-D- aspartate (NMDA) receptor agonist and free radical generator, and as such it can cause excitotoxicity, neurodegenerative diseases, stroke, traumatic brain injury, epilepsy, cerebral malaria, perinatal hypoxia, neurovirological diseases and neuroinflammation.
• NMDA ⁇ /-methyl-D- aspartate
• KYNA kynurenic acid
• KYNA acts as a competitive blocker of the glycine coagonist site of the NMDA receptor and as a noncompetitive inhibitor of the ⁇ 7 nicotinic acetylcholine receptor.
• affinity of KYNA to these two Ca 2+ -permeable receptors is in the range of KYNA levels in the human brain and reasonably close to the (lower) KYNA content of the rodent brain suggests a physiological function in glutamatergic and cholinergic neurotransmission.
• kynurenines have been suggested to participate not only in the pathophysiology of neurodegenerative and seizure disorders, but also to play a role in a large number of etiologically diverse CNS diseases, it is important to modulate their formation.
• 2-aminobenzoyl derivatives (kynurenine-Iike compounds) described here will be useful for such therapeutic intervention. Suggested mechanism of action could be, but is not limited to, by inhibiting enzymes in the kynurenine pathway, and/or inhibiting intermediate compounds, and/or inhibiting free radical formation.
• the invention relates to compounds having the formula (I):
• A is C- ⁇ -6 alkylene
• R, Ri and R 2 are independently hydrogen, halo, haloalkyl, aryl, a heterocyclic group, a heteroaryl group, alkyl, alkenyl, alkynyl, arylalkyl, arylalkenyl, arylalkynyl, hydroxyalkyl, nitro, amino, cyano, cyanamido, guanidine, amidino, acylamido, hydroxy, thiol, acyloxy, azido, alkoxy, carboxy, carbonylamido, S- alkyl or alkyiyhiol;
• Y is hydrogen, halo, haloalkyl, aryl, a heterocyclic group, a heteroaryl group, alkyl, alkenyl, alkynyl, aryl
• R is hydrogen, methyl or methoxy
• Ri is hydrogen or formyl
• R 2 is hydrogen or carboxyl
• R 3 is hydrogen, halo, haloalkyl, aryl, a heterocyclic group, a heteroaryl group, alkyl, alkenyl, alkynyl, arylalkyl, arylalkenyl, arylalkynyl, hydroxyalkyl, nitro, amino, cyano, cyanamido, guanidine, amidino, acylamido, hydroxy, thiol, acyloxy, azido, alkoxy, carboxy, carbonylamido, S-alkyl or alkyiyhiol, and stereoisomers and pharmaceutically acceptable salts thereof.
• X is 2-furyl, 2-dihydrofuryl, 2-tetrahydrofuryl or (2-R°-COO-)phenyl, any of which may be substituted by 1-2 substituents selected from C ⁇ -4 alkyl, C ⁇ -4 alkoxy, OH, nitro, and Y is hydrogen or styryl which is ring-substituted by up to two substituents independently selected from among halogen, C ⁇ -4 alkyl, C ⁇ - alkoxy, OH, nitro, aryl, aryl-C- ⁇ - 4 alkyl, or aryl-C ⁇ -4 alkoxy, and stereoisomers and pharmaceutically acceptable salts thereof.
• the present invention includes within its scope also the pharmaceutical formulations containing as an active substance a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof as well as any possible isomer, or mixture of isomers, covered by the formula (I) in association with one or more pharmaceutically acceptable diluents, preservatives, solubilizers, emulsifiers, adjuvants, excipients and carriers, particularly those conventionally used in pharmaceutical and veterinary formulations.
• the present pharmaceutical formulations may be adapted for administration to humans and/or animals.
• the compounds of formula (I) are useful for treating and/or preventing, and/or minimizing neuronal loss associated with stroke, ischemia, CNS trauma, hypoglycemia and surgery, CNS disorders including neurodegenerative diseases such as Alzheimer's disease, amyotrophic lateral sclerosis, Huntington's disease, Parkinson's disease and Down's syndrome, treating or preventing the adverse consequences of the over stimulation of the excitatory amino acids, psychiatric disorders, e.g., sleep disorders, epilepsy and other convulsive disorders, anxiety, psychiatric diseases, psychosis, senile dementia, multi-infarct dementia, chronic pain (analgesia), glaucoma, CMV retinitis, urinary incontinence, and inducing anesthesia, as well as enhancing cognition, and preventing opiate tolerance and withdrawal symptoms.
• CNS disorders including neurodegenerative diseases such as Alzheimer's disease, amyotrophic lateral sclerosis, Huntington's disease, Parkinson's
• conditions include impotence; cardiovascular disorders including hypertension, preventing blood coagulation, anti-inflammation, neuropathy, chronobiological-based disorders, e.g., jet lag, circadian sleep disorders such as delayed sleep syndrome, shift-work problems, and seasonal-related disorders, e.g. seasonal affective disorder (SAD); endocrine indications, e.g., contraception and infertility, precocious puberty, premenstrual syndrome, hyperprolactinemia, and growth hormone deficiency; neoplastic diseases including e.g.
• cancer and other proliferative diseases include AIDS, conditions associated with senescence, ophthalmological diseases, cluster headache, migraine, skin-protection, diabetes stabilization and weight gain disorders (leptin, obesity), and as an aid to animal breeding, e.g., regulation of fertility, puberty, pelage color.
• R 2 is hydrogen and at least one of the following conditions applies, namely: R is 5-methoxy; and/or A is CH 2 CH 2 or CH 2 CHCOOH, and within these sub-groups, R-i is preferably also hydrogen.
• R ⁇ is hydrogen and at least one of the following conditions applies, namely: R is 5-methoxy; and/or A is CH 2 CH 2 or CH 2 CHCOOH, and within these sub-groups, R-i is preferably also hydrogen.
• X is -CO- and Y is 2-furyl
• X is -CO- and Y is 2-tetrahydrofuryl
• X is -CH 2 -and Y is 2-tetrahydrofuryl
• X is -CO- and Y is 2-acetoxyphenyl
• X is -CO- and Y is 3,4-dihydroxystyryl or 3,4-dihydroxycinnamoyloxy.
• the present invention also includes within its scope pharmaceutical formulations containing as an active substance a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof as well as any possible isomer, or mixture of isomers, covered by the formula (I) in association with one or more pharmaceutically acceptable diluents, preservatives, solubilizers, emulsifiers, adjuvants, excipients and carriers, particularly those conventionally used in pharmaceutical and veterinary formulations.
• the present pharmaceutical formulations may be adapted for administration to humans and/or animals.
• each unit dosage comprising an amount of said at least one member which lies within the range of 0.0025-1000 mg;
• the pharmaceutical formulations may be utilized as e.g. tablets, capsules, emulsions, solutions, syrups or suspensions.
• the formulations may be utilized as ampoules, or otherwise as suspensions, solutions or emulsions in aqueous or oily vehicles.
• the need for suspending, stabilizing and/or dispersing agents will of course take account of the fact of the solubility or otherwise of the active compounds, in the vehicles that are used in particular embodiments.
• the formulations may additionally contain e.g. physiologically compatible preservatives and antioxidants.
• the active ingredient may be mixed with conventional oleaginous or emulsifying excipients.
• the pharmaceutical formulations may also be utilized as suppositories with conventional suppository bases such as cocoa butter or other glycerides.
• the formulations may be made available in a depot form which will release the active formulation slowly in the body, over a pre-selected time period.
• the compounds of the invention may be administered by using transbuccal, intrapulmonary or transdermal delivery systems.
• the compounds of the present invention are useful for treating and/or preventing, and/or minimizing neuronal loss associated with stroke, ischemia, CNS trauma, hypoglycemia and surgery, CNS disorders including neurodegenerative diseases such as Alzheimer's disease, amyotrophic lateral sclerosis, Huntington's disease, Parkinson's disease and Down's syndrome, treating or preventing the adverse consequences of the overstimulation of the excitatory amino acids, psychiatric disorders, e.g., sleep disorders, epilepsy and other convulsive disorders, anxiety, psychiatric diseases, psychosis, senile dementia, multi-infarct dementia, chronic pain (analgesia), glaucoma, CMV retinitis, urinary incontinence, and inducing anesthesia, as well as enhancing cognition, and preventing opiate tolerance and withdrawal symptoms.
• CNS disorders including neurodegenerative diseases such as Alzheimer's disease, amyotrophic lateral sclerosis, Huntington's disease, Parkinson'
• cardiovascular disorders including hypertension, preventing blood coagulation, anti-inflammatory, neuropathy, chronobiological-based disorders, e.g. jet lag, circadian sleep disorders such as delayed sleep syndrome, shift-work problems, and seasonal-related disorders, e.g. seasonal affective disorder (SAD); endocrine indications, e.g., contraception and infertility, precocious puberty, premenstrual syndrome, hyperprolactinemia, and growth hormone deficiency; neoplastic diseases including e.g.
• cancer and other proliferative diseases include AIDS; conditions associated with senescence; ophthalmological diseases; cluster headache, migraine; skin-protection, diabetes stabilization and weight gain disorders (leptin, obesity), and as an aid to animal breeding, e.g., regulation of fertility, puberty, pelage color.
• Example 1 2-(2-aminobenzoyl)-N-(2,4-dinitrophenyl)ethylamine.
• Kynuramine .2HBr (125 mg) is dissolved in 5 cc of absolute ethanol in a 50 cc flask. A solution of 2,4-dinitrofluorobenzene, 71 mg in EtOH 5 cc is then added (a clear yellow solution is formed). After five minutes, 2 cc of a 10% NaHCO 3 solution are introduced drop-wise in the flask. The reaction is left at room temperature overnight. The following morning the formed light yellow precipitate is filtered, washed with water and ethanol and dried in UHV obtaining 80 mg of product (approx. yield 63%).
• Example 2 3-(2-aminobenzoyl)-2-(2,4-dinitroanilino)propanoic acid.
• mice six month old male C57 BL/6 mice, weighing 22-25 g were used. Following arrival at the laboratory, the mice were allowed to acclimatise for two weeks in a room with controlled temperature (21+1 C), and a constant light-dark schedule (12 hr on/12 hr off, lights on between 06.00 and 18.00 hrs). Free access to food and water was maintained throughout. They were housed in groups of 12 animals and tested only during the hours of light (08.00-15.00 hrs). All testing was performed in a normally lighted room. Each test chamber (i.e. activity test cage) was placed in a soundproofed wooden box with 12 cm thick walls and front panels and had dimmed lighting.
• Behavioral measurements and apparatus An automated device, consisting of macrolon rodent test cages (40 x 25 x 15 cm) each placed within two series of infrared beams (at two different heights, one low and one high, 2 and 8 cm, respectively, above the surface of the sawdust, 1 cm deep), was used to measure spontaneous and/or drug-induced motor activity of MPTP and control mice. The following parameters were measured: LOCOMOTION was measured by the low grid of infrared beams. Counts were registered only when the mouse in the horizontal plane, ambulating around the test-cage. REARING was registered throughout the time when at least one high level beam was interrupted, i.e. the number of counts registered was proportional to the amount of time spent rearing.
• TOTAL ACTIVITY was measured by a sensor (a pick-up similar to a gramophone needle, mounted on a lever with a counterweight) with which the test cage was constantly in contact.
• the sensor registered all types of vibration received from the test cage, such as those produced both by locomotion and rearing as well as shaking, tremors, scratching and grooming.
• Table 1 presents the mean ( ⁇ standard deviations) locomotion, rearing and total activity counts of MPTP-treated and control mice administered either 2-(2- aminobenzoyl)-N-(2,4-dinitrophenyl)ethylamine or vehicle administered with a subthreshold dose of L-Dopa. 1% level of significance is represented by an asterisk (Tukey HSD test).
• 2-(2-aminobenzoyl)-N-(2,4-dinitrophenyl)ethylamine had no effect at any dose the first 60-min period before L-Dopa, as compared to the MPTP-treated vehicle mice.
• 2-(2-aminobenzoyl)-N-(2,4-dinitrophenyl)ethylamine improved significantly all three behavioural parameters when administered together with a subthreshlod dose of L-Dopa.
• 2-(2-aminobenzoyl)-N-(2,4-dinitrophenyl) ethylamine (1 , 3 or 10 mg/kg) improved significantly the locomotion, rearing and total activity of MPTP- treated mice, as compared to the MPTP vehicle group.
• Isolation of hippocampal neurons Wistar rats (12-14 days) were decapitated without anaesthesia and the hippocampus was removed. It was manually cut into slices (0.2-0.4mm), in a solution containing (mM): 150 NaCI; 5 KCl; 1.25 NaH 2 PO 4 ; 2 CaCI 2 ; 2 MgCI 2 ; 26 NaHCO 3 ; 20 glucose. Slices were preincubated in this solution for 30 min at room temperature. The enzymatic treatment proceeded in the same solution with lower Ca2+ concentration (0.5mm) containing 0.4 mg/ml protease from aspergillus oryzae. The incubation in the enzyme solution proceeded at 32°C within 10 min.
• Slices were kept subsequently in enzyme-free solution containing normal Ca2+ concentration and used within 6-8h for obtaining isolated neurons. Throughout the entire procedure the solutions were continuously saturated with a 95% O 2 and 5% CO 2 gas mixture to maintain pH 7.4. For cell dissociation the slice was transferred into the extracellular solution containing (mM): 150 NaCI; 5 KCl; 2 CaCI 2 ; 10 N-2- hydroxyethylpiperazine-N'-2-ethanesulphonic acid (Hepes); pH adjusted with NaOH to 7.4.
• Single cells were isolated from CA and CA3 zones of hippocampal slices by vibrodissociation method. They had diameter 10-15 ⁇ m and preserved a small part of dendritic tree. After isolation they were usually suitable for recording for 1-2h.
• NMDA-activated currents The currents were filtered at 3kHz (three-pole active Bessel filter) digitally sampled at the rate 6000 ⁇ s per point for NMDA activated currents. NMDA-induced transmembrane currents were measured in the presence of 10 ⁇ M glycine and 300 ⁇ M L-aspartate in the control and test solutions. The currents were recorded at holding potential -70 mV.

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• 2003
  • 2003-06-26 IL IL15666903A patent/IL156669A0/xx not_active IP Right Cessation
• 2004
  • 2004-06-16 AR ARP040102095A patent/AR044786A1/es not_active Application Discontinuation
  • 2004-06-18 PE PE2004000604A patent/PE20050230A1/es not_active Application Discontinuation
  • 2004-06-22 PA PA20048605401A patent/PA8605401A1/es unknown
  • 2004-06-23 UY UY28382A patent/UY28382A1/es not_active Application Discontinuation
  • 2004-06-24 CA CA2527112A patent/CA2527112C/en not_active Expired - Fee Related
  • 2004-06-24 US US10/562,197 patent/US8309767B2/en not_active Expired - Fee Related
  • 2004-06-24 MX MXPA06000022A patent/MXPA06000022A/es active IP Right Grant
  • 2004-06-24 NZ NZ544908A patent/NZ544908A/en unknown
  • 2004-06-24 AU AU2004249012A patent/AU2004249012B2/en not_active Ceased
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  • 2004-06-24 AT AT04744907T patent/ATE460391T1/de not_active IP Right Cessation
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  • 2004-06-24 TW TW093118235A patent/TWI342210B/zh not_active IP Right Cessation
  • 2004-06-24 DE DE602004025937T patent/DE602004025937D1/de not_active Expired - Lifetime
  • 2004-06-24 DK DK04744907.9T patent/DK1644316T3/da active
  • 2004-06-24 CN CN200480017943XA patent/CN1835910B/zh not_active Expired - Fee Related
  • 2004-06-24 UA UAA200600303A patent/UA85187C2/ru unknown
  • 2004-06-24 EA EA200600115A patent/EA011255B1/ru not_active IP Right Cessation
  • 2004-06-24 HN HN2004000224A patent/HN2004000224A/es unknown
  • 2004-06-24 WO PCT/IL2004/000567 patent/WO2004112690A2/en not_active Ceased
  • 2004-06-24 EP EP04744907A patent/EP1644316B1/en not_active Expired - Lifetime
  • 2004-06-24 ES ES04744907T patent/ES2341958T3/es not_active Expired - Lifetime
  • 2004-06-24 PL PL04744907T patent/PL1644316T3/pl unknown
  • 2004-06-24 KR KR1020057025006A patent/KR101115196B1/ko not_active Expired - Fee Related
  • 2004-06-24 SI SI200431416T patent/SI1644316T1/sl unknown
  • 2004-06-24 BR BRPI0411382-9A patent/BRPI0411382A/pt not_active IP Right Cessation
• 2006
  • 2006-01-16 IS IS8235A patent/IS8235A/is unknown
  • 2006-01-25 NO NO20060420A patent/NO20060420L/no not_active Application Discontinuation
• 2010
  • 2010-05-25 CY CY20101100463T patent/CY1110043T1/el unknown

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