Phosphorus-containing squalene synthetase inhibitors

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Phosphorus containing other than solely as part of an...

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

558156, 558157, 558158, 558161, 562 9, 562 10, 562 11, 562 13, 562 21, C07F 940, A61K 3166

Patent

active

052121640

ABSTRACT:
Compounds which are inhibitors of cholesterol biosynthesis (by inhibiting de novo squalene biosynthesis), and thus are useful as hypocholesterolemic agents and antiatherosclerotic agents are provided which have the structure ##STR1## wherein m is 0, 1, 2 or 3; n is 0, 1, 2, 3 or 4;

REFERENCES:
patent: 4871721 (1989-10-01), Biller
Schweizer et al. in J. Org. Chemistry, vol. 33, No. 1 pp. 336-339 (1968).
Poulter C. D. et al. J. Org. Chem. 51, 4768 (1986).
Poulter C. D. et al, J.A.C.S 109, 5542 (1987).
Poulter C. D., et al., Biosynthesis of Isoprenoid Compounds, "Conversion of Farnesyl Pyrophosphate to Squalene", vol. 1, Chapter 8, pp. 413-441, J. Wiley and Sons, 1981.
Faust, J. R., et al., Proc. Nat. Acad. Sci., USA, "Squalene synthetase activity in human fibroblasts: Regulation via the low density lipoprotein receptor", 1979, 76, 5018-5022.
de Montellano, P. Ortiz, et al., J. Med. Chem., "Inhibition of Squalene Synthetase by Farnesyl Pyrophosphate Analogues", 1977 20, 243-249.
Corey and Volante, J. Am. Chem. Soc. "Application of Unreactive Analogs of Terpenoid Pyrophosphates to Studies of Multistep Biosynthesis, Demonstration that `Presqualene Pyrophosphate` is an Essential Intermediate on the Path to Squalene", 1976, 98, 1291-3.
Sandifer, R. M. et al., J, Am. Chem. Soc., 1982, 104, 7376-8, "Squalene Synthetase, Inhibition by an Ammonium Analogue of a Carbocationic Intermediate in the Conversion of Presqualene Pyrophosphate to Squalene".
Bertolino, A., et al., Biochim. Biophys. Acta., 1978, 530, 17-23, "Polyisoprenoid Amphiphilic Compounds as Inhibitors of Squalene Synthesis and Other Microsomal Enzymes".
Davisson, V. J. et al., J. Org. Chem., 1986, 51, 4768-4779, "Phosphorylation of Isoprenoid Alcohols".
Stremler, K. E. et al., J.A.C.S., 1987 109, 5542, "Methane and Difluoromethanediphosphonate Analogues of Geranyl Diphosphate: Hydrolysis-Inert Alternate Substrates".
McClard, R. W., et al., J. Am. Chem. Soc., 1987, 109, 5544-5545, "Novel Phosphonylphosphinyl (P-C-P-C) Analogues of Biochemically Interesting Diphosphates, Syntheses and Properties of P-C-P-C Analogues of Isopentenyl Diphosphate and Dimethylallyl Diphosphate".
Capson, T. L., PhD dissertation, Jun. 1987, Dept. of Medicinal Chemistry, the University of Utah, Abstract, Table of Contents, pp. 16, 17, 40-43, 48-51, Summary.
Stowell, M. H. B., et al, "The Phosphonylphosphinyl Dianion: A Convenient Synthon for the Preparation of Biologically Interesting Phoshonylphosphinyl (P-C-P-C) Compounds," Tetrahedron Letters, vol. 30, No. 4, pp. 411-414, 1989.
Biller, S. A. et al, "Isoprenoid (Phosphinylmethyl)phosphonates as Inhibitors of Squalene Synthetase," J. Med. Chem., Oct. 1988, 31, 1869.

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

Phosphorus-containing squalene synthetase 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 Phosphorus-containing squalene synthetase inhibitors, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Phosphorus-containing squalene synthetase inhibitors will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-804579

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