Aralkyl bridged diazabicycloalkane derivatives for CNS disorders

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

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514183, 514211, 540456, 540460, 540461, 540468, 540472, 540477, 540500, 540502, 540503, 540552, 540556, A61K 3155, C07D47108, C07D48708

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056796730

ABSTRACT:
Certain aralkyl diazabicycloalkyl compounds are described for treatment of CNS disorders such as cerebral ischemia, psychoses and convulsions. Compounds of particular interest are of the formula: ##STR1## wherein each of R, R.sup.1, R.sup.4, R.sup.5, R.sup.6 and R.sup.7 is independently selected from hydrido, lower-alkyl, benzyl, and haloloweralkyl; wherein each of R.sup.2, R.sup.3 and R.sup.10 through R.sup.13 is independently selected from hydrido, hydroxy, loweralkyl, benzyl, phenoxy, benzyloxy and haloloweralkyl; wherein each of R.sup.8 and R.sup.9 is selected from hydrido, loweralkyl, benzyl and haloloweralkyl; wherein m is an integer of from two to four; wherein A is selected from phenyl, naphthyl, benzothiophenyl, benzofuranyl and thienyl; wherein any of the foregoing A groups can be further substituted with one or more substituents independently selected from hydrido, hydroxy, loweralkyl, loweralkoxy, halo, haloloweralkyl, amino, monoloweralkylamino and diloweralkylamino; or a pharmaceutically acceptable salt thereof.

REFERENCES:
patent: 4204003 (1980-05-01), Szmuszkovicz
patent: 4463013 (1984-07-01), Collins et al.
patent: 4801604 (1989-01-01), Von Voightlander
patent: 4826839 (1989-05-01), King et al.
H!-(+)-pentazocine, a highly potent and selective radioligand for .sigma. receptors", FEBS Letters 251(1,2): 53-58 (Jul. 1989).
Rodd's Chemistry of Carbon Compounds, 2nd ed., Coffey, ED., vol. IV, Part H, Chapter 37, pp. 259, 278-284-Elsevier Scientific Publishing Company (1978).
Rothman, et al., Annals of Neurology, 19(2): 105-11 (1986).
Carter, et al., J. Pharm. Exp. Ther., 247(3): 1222-1232 (1988).
Gilman, et al., The Pharmacological Basis of Therapeutics, 7.sup.th ed., p. 404 Macmillan (1985).
Parsons, et al., Neuropharm, 25(2): 217-220 (1986).
Lason, et al., Brain Res., 482: 333-339 (1989).
DeCosta, et al., J. Med. Chem., 32(8): 1996-2002 (1989).
Long, et al., Soc. Neurosci. Abst., 16: 1122, Abst. 461.4 (1990).
Contreras, et al., Brain Res., 546: 79-82 (1991).
Scopes, et al., J. Med. Chem., 35:490-501 (1992).
DeCosta, et al., J. Med. Chem., 35(1): 38-47 (1992).
Radesca, et al., J. Med. Chem., 34(10): 3058-65 (1991).
Cheesman, et al., Derwent Abstract WO/92128 (1992).
Giardina, Biosistemi Come Targets Farmacologici, Recettori Peptidergici, Analgesisi Oppiodi Kappa: Sintesi E Relazioni Struttura-Attivita 'Di Piperidine Sostituite, pp. 21-63 (1992).
Rees, Biosistemi Come Targets Farmacologici, Recettori Peptidergici, Synthesis & Biological Activity of Kappa-Opioid Agonists Leading to the Selection of CI-9777 (Enadoline) for Clinical Investigation, pp. 65-101 (1992).
Ronsisvalle, Biosistemi Come Targets Farmacologici, Recettori Peptidergici, Requisiti Strutturali Per I Liganti Oppioidi: E'Possible Modulare La Selecttivita, pp. 102-133 (1992).
Aram et al., J. Pharmacol. Exp. Ther., 248, 320-328 (1989) Abstract only.
Bailey et al., Eur. J. Pharmacol., 240, 243-250 (1993).
Canoll et al., J. Neurosci. Res., 24, 311-328 (1989) Abstract only.
Clissold et al., J. Pharmacol. Exp. Ther., 265, 876-886 (1993).
Cook et al., J. Pharmacol. Exp. Ther., 263, 1159-1166 (1992) Abstract only.
DeCoster et al., Brain Res., 671, 45-53, (1995) Abstract only.
DeHaven-Hudkins et al., Life Sci., 56, 1571-1576 (1995) Abstract only.
Gewirtz et al., Neuropsychopharmacology, 10, 37-40 (1994).
Itzhak et al., FASEB J., 3, 1868-1872 (1989).
Kirk et al., J. Pharmacol. Exp. Ther., 271, 1080-1085 (1994) Abstract only.
Klein et al., J. Pharmacol. Exp. Ther., 260, 990-999 (1992) Abstract only.
Klein et al., Eur. J. Pharmacol., 254, 239-248 (1994).
Lasage et al., Synapse, 20, 156-64 (1995) Abstract only.
Loscher et al., Eur. J. Pharmacol., 238, 191-200 (1993).
Lysko et al., Stroke, 23, 414-419 (1992) Abstract only.
Lysko et al., Stroke, 23, 1319-1323 (1992) Abstract only.
Pontecorvo et al., Brain Res. Bull., 26, 461-465 (1991) Abstract only.
Reddy et al., J. Med. Chem., 37, 260-267, (1994) Abstract only.
Roth et al., Eur. J. Pharmacol., 236, 327-331 (1993).
Takahashi et al., Stroke, 26, 1676-1682 (1995) Abstract only.
Tam in Sigma Receptors, Y. Itzhak ed., Academic Press, Harcourt Brace & Co. Publishers, London (1994) ISBN 0-12-376350-9.
Tortella et al., Trends Pharmacol. Sci., 10:501-507 (1990).
Tortella et al., Trends Pharmacol. Sci.,11:146-147 (1990).
Weissman et al., Biol. Psych., 29, 41-54 (1991).
Witkin et al., J. Pharmacol. Exp. Ther., 266, 473-482 (1993).
Rennie, "The Mice That Missed", Scientific American, Jul. 1992, pp. 20, 26.
Schnabel, Science vol. 260, Jun. 18, 1993, pp. 1719-1720.

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