Substituted 5-aryl-benzothiepines having activity as inhibitors

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

514431, 514249, 514314, 544236, 544176, C07D33700, C07D48700, A61K 3138, A61K 31495

Patent

active

061074942

ABSTRACT:
Provided are novel benzothiepines, derivatives, and analogs thereof; pharmaceutical compositions containing them; and methods of using these compounds and compositions in medicine, particularly in the prophylaxis and treatment of hyperlipidemic conditions such as those associated with atherosclerosis or hypercholesterolemia, in mammals.

REFERENCES:
patent: 3287370 (1966-11-01), Mohrbacher et al.
patent: 3389144 (1968-06-01), Mohrbacher et al.
patent: 3444176 (1969-05-01), Mohrbacher et al.
patent: 3520891 (1970-07-01), Mohrbacher
patent: 3694446 (1972-09-01), Houlihan et al.
patent: 3714190 (1973-01-01), Boissier et al.
patent: 3962261 (1976-06-01), Zinnes et al.
patent: 4207239 (1980-06-01), McCall
patent: 4251526 (1981-02-01), McCall
patent: 5158943 (1992-10-01), Sohda et al.
patent: 5430116 (1995-07-01), Kramer et al.
patent: 5491152 (1996-02-01), Wilde et al.
patent: 5512558 (1996-04-01), Enhsen et al.
patent: 5610151 (1997-03-01), Glombik et al.
Stedronsky, "Interaction of bile acids and cholesterol with nonsystemic agents having hypocholesterolemic properties", Biochimica et Biophysica Acta, 1210 (1994) 255-287.
Heubi, J.E. et al., "Primary Bile Acid Malabsorption: Defective In Vitro Ileal Active Bile Acid Transport", Gastroenterology, 1982:83:804-11.
Reihner, E., et al., "Regulation of hepatic cholesterol metabolism in humans: stimulatory effects of cholestyramine on HMG-CoA reductase activity and low density lipoprotein receptor expression in gallstone patients", Journal of Lipid Research, vol. 31, 1990, 2219-2226.
Suckling, et al., "Cholesterol lowering and bile acid excretion in the hamster with cholestyramine treatment", Atherosclerosis, 89(1991) 183-190.
Kramer, et al., "Intenstinal Bile Acid Absorption", The Journal of Biological Chemistry, vol. 268, No. 24, Aug. 25, 1993, 18035-18046.
PCT/US95/10863 "International Search Report"; Jan. 10, 1996.
PCT/US97/04076 "International Preliminary Examination Report" June 16, 1998.
D. Huckle et al. "4-Amino-2,3,4,5,-tetrahydro-1-benzoxepin-5-ols, 4-Amino-2,3,4,5-tetrahydro-1-benzothiepin-5-ols, and Related Compounds"; Journal Chemical Society (C), 1971; pp. 2252-2260.
R. Patra et al., "Conformational And Steric Requirements Of the Side Chain For Sulfur Participation In Benzothiepin Derivatives", Tetrahedron Letters, vol. 30, No. 32, pp. 4279-4282, 1989.
Y. Ishiro et al., "Novel Synthesis Of 4, 5-Bis (arylthio)-2, 3,4,5-tetrahydro-1-benzothiepins: Noteworthy Cyclization By the Reaction Of 2-Butynediol With Arenethiols In the Presence of Zinc Iodide", Synthesis, (9), pp. 827-9, 1987.
F. Kvis et al., "Benzocycloheptenes And Heterocyclic Analogs As Potential Drugs. VII.", Collect. Czech. Chem. Commun., vol. 37, pp. 3808-3816, 1972.
K. Sindelar et al. "Benzocycloheptenes And Heterocyclic Analogues As Potential Drugs. III. Further Synthetic Experiments In The Series of 1-Benzothiepine Derivatives", Collect. Czech. Chem. Commun., vol. 37, pp. 1195-1206, 1972.
D. Huckle et al., "4-Amino-2,3,4,5-tetrahydro-1-benzoxepin-5-ols, 4-Amino-2,3,4,5-tetrahydro-1-benzothiepin-5-ols, And Related Compounds", J. Chem. Soc. (C), pp. 2252-2260, 1971.
K. Sindelar et al. "Neurotropic And Psychotropic Compounds XXIX. Derivatives Of 2,3,4,5-tetrahydro-1-benzothiepin", Collect. Czech. Chem. Commun., vol. 33, pp. 4315-4327, 1968.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Substituted 5-aryl-benzothiepines having activity as inhibitors does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Substituted 5-aryl-benzothiepines having activity as inhibitors , we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Substituted 5-aryl-benzothiepines having activity as inhibitors will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-582800

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.