1,3-Propane diol esters and ethers and methods for their use...

Details 1,3-Propane diol esters and ethers and methods for their use... 1,3-Propane diol esters and ethers and methods for their use...

2008-09-02

2008-09-02

Anderson, Rebecca L (Department: 1626)

Drug, bio-affecting and body treating compositions

Designated organic active ingredient containing

Carbohydrate doai

C554S227000, C554S082000, C514S420000, C549S039000, C548S496000, C560S038000, C560S128000

Reissue Patent

active

11405041

ABSTRACT:
The invention relates to compounds of formula:wherein R1is selected from the group consisting of fatty acid acyl groups of 12 to 30 carbon atoms and fatty alcohol groups of 12 to 30 carbon atoms, and wherein R2is selected from the group consisting of H, fatty acid acyl of 12 to 30 carbon atoms and fatty alcohol groups of 12 to 30 carbon atoms, the same as or different from R1, and the residue of a nutrient, drug, or other bioactive compound, and to the use of these compounds to deliver drugs and other bioactive compounds.

REFERENCES:
patent: 2924528 (1960-02-01), Barsky et al.
patent: 2993063 (1961-07-01), Alsop et al.
patent: 3291816 (1966-12-01), Goldblatt et al.
patent: 4268426 (1981-05-01), Williams et al.
patent: 4668664 (1987-05-01), Rougier et al.
patent: 4851426 (1989-07-01), Ladkani et al.
patent: 5286512 (1994-02-01), Klemann et al.
patent: 5321145 (1994-06-01), Schafer
patent: 0 018 342 (1983-02-01), None
patent: 0 087 864 (1983-09-01), None
patent: 0 139 480 (1985-05-01), None
patent: 0 139 780 (1985-05-01), None
patent: 0161114 (1985-11-01), None
patent: 0 173 478 (1986-03-01), None
patent: 0 057 797 (1986-06-01), None
patent: 0 184 058 (1986-06-01), None
patent: 0 056 189 (1986-08-01), None
patent: 0 222 155 (1987-05-01), None
patent: 0 246 540 (1987-11-01), None
patent: 0 161 422 (1989-03-01), None
patent: 0319126 (1989-06-01), None
patent: 0 321 128 (1989-06-01), None
patent: 0 393 920 (1990-10-01), None
patent: 0 405 873 (1991-01-01), None
patent: 0 405 874 (1991-01-01), None
patent: 0 574 312 (1993-12-01), None
patent: 0 611 569 (1994-08-01), None
patent: 0 675 103 (1995-10-01), None
patent: 1 782 (1963-04-01), None
patent: 0 888 162 (1962-01-01), None
patent: 1 135 647 (1968-12-01), None
patent: 1 293 277 (1972-10-01), None
patent: 1 493 098 (1977-11-01), None
patent: 1 529 762 (1978-10-01), None
patent: 1 556 197 (1979-11-01), None
patent: 2 161 477 (1987-09-01), None
patent: 57-067511 (1982-04-01), None
patent: 61-129190 (1986-06-01), None
patent: 2-129119 (1990-05-01), None
patent: 4-99784 (1992-03-01), None
patent: 05-051355 (1993-03-01), None
patent: WO 91/09831 (1991-07-01), None
patent: WO 94/26262 (1994-11-01), None
patent: WO 95/04030 (1995-02-01), None
patent: WO 96/33155 (1996-10-01), None
Breusch et al., Chemische Berichte, vol. 88, pp. 1511-1519, 1955.
Langen et al., Chemical Abstracts, vol. 92, No. 1, #461a, 1980.
Lion Corp., Patent Abstracts of Japan, vol. 6, No. 143(C-117), 1982.
Vajdi et al., Chemical Abstracts, vol. 95, No. 5, #41676e, 1981.
Hounsom et al., Oxidative Stress and Disease (2000), 4(Antioxidants in Diabetes Management), 155-172.
Watanabe et al, Chemical Abstracts, vol. 107, No. 3, #23659p, 1987.
Bertelsen, O. et al., “Structural Elucidation of Alkyl-Branched Chain Aliphatic Alcohols and Fatty Acids by Mass Spectrometry of their Respective Alkyl Nicotinate and Picolinylcarboxylate Derivatives,”Chemical Abstracts, 104:108841 (1986).
Christie, W.W., et al., “Mass Spectra of the Picolinyl Ester Derivatives of Some Isomeric Dimethylene-Interrupted Octadecadiynoic Acids,”Chemical Abstracts, 109:210389(1988).
Christie, W.W., et al., “Mass Spectra of the Picolinyl Esters of Isomeric Mono-and Dienoic Fatty Acids,”Chemical Abstracts107:55235 (1987).
Deterding, L. et al., “Fast-Atom-Bombardment and Tandem Mass Spectrometry for Determining Structures of Fatty Acids and Their Picolyl Ester Derivatives,”Chemical Abstracts, VI. 110:38801 (1989).
Deterding, L., et al., “Tandem Mass Spectrometry for Identifying Fatty Acid Derivatives that Undergo Charge-Remote Fragmentations,”Chemical Abstracts110:56917 (1989).
Harvey, D.J., Picolinyl Derivatives for the structural Determination of Fatty Acids byChemical Abstracts101:166564 (1984).
Harvey, D.J., “Pyridine-Containing Derivatives for the Structural Elucidationof the Alkyl Chains of Lipids by Mass Spectrometry and a Comparison with the Spectra of Related Heterocyclic Derivatives,”Chemical Abstracts, 114:206360 (1991).
Jie, et al., “Mass Spectra of Picolinyl Ester Derivatives of Some Conjugated Diacetylenic Fatty Acids,”Chemical Abstracts, 118:191384 (1993).
Kimura, K. et al., Higher Unsaturated Fatty Alcohol Esters Having Antiucler Activity,Chemical Abstracts, vol. 87, 1997 Abstract No. 53462e.
Koori, S., “Unsaturated Higher Akuogatuc Esters of Nicotinic Acid,”Chemical Abstracts, vol. 77, Abstract No. 164488f (1972).
Kumokawa, Y. et al. γ-Linolenic Acid Derivatives As Platelet Aggregation Inhibitors,Chemical Abstracts, vol. 105, 1986, Abstract No. 78532f.
Spitzer, V. et al., “Curupira Tefeensis II: Occurrence of Acetylenic Fatty Acids,”Fat Sci. Technol., No. 5, (1991) pp. 169-174.
Terumo Corp., “Trienoic Fatty Acid Pyridylmethyl Esters,”Chemical Abstracts, vol. 101, 1984 Abstract No. 171104v.

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