Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Ether doai
Reexamination Certificate
2006-09-19
2006-09-19
Keys, Rosalynd (Department: 1621)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Ether doai
C514S719000, C514S720000, C514S721000, C568S644000, C568S645000, C568S646000
Reexamination Certificate
active
07109245
ABSTRACT:
Methods and compounds for reversing pathological vasodilation of blood vessels, for example vasodilation caused by activation of CB1-like receptors, by administering to a subject a therapeutically effective amount of a compound sufficient to induce vasoconstriction, the compound comprising:wherein dashed lines independently represent either a single or a double bond, R1is a lower alkyl, R2is a lower alkyl, R3is a lower alkyl or halogen, R4is a lower alkyl or hydrogen, R5is a lower alkyl or hydrogen, R6is a hydrogen, lower alkyl or halogen, and R7is a hydrogen, lower alkyl or halogen. The vasoconstrictor can be used for a variety of purposes, including hemostasis or the treatment of shock, for example vasodilatory shock syndromes such as septic shock.
REFERENCES:
patent: 2304669 (1942-12-01), Adams
patent: 3919322 (1975-11-01), Brossi et al.
patent: 4025516 (1977-05-01), Razdan et al.
patent: 4978332 (1990-12-01), Luck et al.
patent: 5227537 (1993-07-01), Stoss et al.
patent: 5296466 (1994-03-01), Kilbourn et al.
patent: 5342971 (1994-08-01), Herlt et al.
patent: 5747524 (1998-05-01), Cullinan et al.
patent: 5939429 (1999-08-01), Kunos et al.
patent: 6274635 (2001-08-01), Travis
patent: 6563009 (2003-05-01), Kunos et al.
patent: WO 99/53917 (1999-10-01), None
patent: WO 01/03690 (2001-01-01), None
Bukoski et al., “CD1Receptor Antagonist SR141716A Inhibits Ca2+-Induced Relaxation in CB1Receptor-Deficient Mice,”Hypertension 39:251-257 (2002).
Childers et al., “A Novel Approach to the Synthesis of the Cannabinoids,”J. Org. Chem. 49:5276-5277 (1984).
Consroe et al., “Antiepileptic Potential of Cannabidiol Analogs,”J. Clin. Pharmacol. 21:428S-436S (1981).
Ferraro et al., “The Cannabinoid Receptor Agonist WIN 55,212-2 Regulates Glutamate Transmission in Rat Cerebral Cortex: an In Vivo and In Vitro Study,”Cereb. Cortex 11:728-733 (2001).
Járai et al., “Cannabinoid-Induced Mesenteric Vasodilation Through an Endothelial Site Distinct from CB1 OR CB2 Receptors,”PNAS 96:14136-14141 (1999).
Korte et al., “Chemical Classification of Plants, XXIX. Hashish, 8, Synthesis of DL-Cannabidiol and its Methyl Homologs,”Justus Liebigs Annalen der Chemie 693:165-170 (1966).
Martin et al., “Structure-Anticonvulsant Activity Relationships of Cannabidiol Analogs,”NIDA Research Monograph 79:48-58 (1987).
Srebnik et al., “Base-Catalysed Double-Bond Isomerizations of Cannabinoids: Structural and Stereochemical Aspects,”J. Chem. Soc. Perkin Trans.—:2881-2886 (1984).
Varga et al., “Platelet- and Macrophage-Derived Endogenous Cannabinoids are Involved in Endotoxin-Induced Hypotension,”FASEB J. 12:1035-1044 (1998).
Chemical Abstracts, 65:7221e.
Burstein et al., “Prostaglandins and Cannabis XV. Comparison of Enantiomeric Cannabinoids in Stimulating Prostaglandin Synthesis in Fibroblasts,” Life Sciences, 39(19):1813-1823 (1986).
Mechoulam et al., “Enantiomeric Cannabinoids: Stereospecificity of Psychotropic Activity,” Experientia, 44:762-764 (1988).
Thakur et al., “Enantiomeric Resolution of a Novel Chiral Cannabinoid Receptor Ligand,” J. Biochem. Biophys. Methods, 54:415-422 (2002).
Kunos George
Razdan Raj K.
Keys Rosalynd
Klarquist & Sparkman, LLP
Organix Inc.
The United States of America as represented by the Secretary of
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