Immunosuppressive cyclolignan derivatives

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Lignin or derivative doai

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

514468, 549299, A61K 3134, C07D30777, C07D30792

Patent

active

057391149

ABSTRACT:
Immunosuppressive cyclolignan derivatives are provided of formula (I) or (II): ##STR1## in which R.sup.1 is hydrogen, hydroxy, alkoxy; R.sup.2 and R.sup.3 are hydrogen, alkyl, acyl, or together R.sup.2 and R.sup.3 form a group --CHR.sup.4 --; R.sup.4 is hydrogen, alkyl, alkenyl, hydroxyalkyl, (poly)haloalkyl, aryl, acyloxyalkyl, alkoxy, carboxyalkyl, alkoxycarbonyl, carbamoyl; R.sup.5 when present is hydrogen, alkyl, alkenyl, aryl, (poly)haloalkyl, acyl, carbamoyl, or thiocarbamoyl; R.sup.6 is alkyl, hydroxyalkyl, haloalkyl, acyl, acyloxyalkyl, carboxy or alkoxycarbonyl; Ar is 3,4,5-trialkoxyphenyl or 4-hydroxy-3,5-dialkoxyphenyl; and X is nitrogen or oxygen.

REFERENCES:
patent: 4567253 (1986-01-01), Durst et al.
patent: 4644072 (1987-02-01), Vyas et al.
Hartwell and Schrecker, "The Chemistry of Podophyllum", Progress in the Chemistry of Organic Natural Products, pp. 84-166, 1957.
Terada et al., "Antitumor Agents. I. DNA Topoisomerase II Inhibitory Activity and the Structural Relationship of Podophyllotoxin Derivatives as Antitumor Agents", Chem. Pharm. Bull., 40(10) 2720-2727, 1992.
Thurston et al., "Antitumor Agents. 78. Inhibition of Human DNA Topoisomerase II by Podophyllotoxin and .alpha.-Peltatin Analogues", J. Med. Chem., 29:1547-1550, 1986.
Hansen et al., "New Compounds Related to Podophyllotoxin and Congeners: Synthesis, Structure Elucidation and Biological Testing". Acta Chemica Scandinavica, vol. 47 (1993), pp. 1190-1200.
Jones et al., "Synthesis of (.+-.)-4-Deoxypodophyllotoxin, (.+-.)-Podophyllotoxin and (.+-.)-Epipodophyllotoxin", Journal of the Chemical Society, Perkin Transactions 1, Nov., 1993, pp. 2541-2548.
Buchardt et al., "Thermal Chemistry of Podophyllotoxin in Ethanol and a Comparison of the Cytostatic Activity of the Thermolysis Products", Journal of Pharmaceutical Sciences, vol. 75, No. 11, Nov. 1986, pp. 1076-1080.
Forsey et al., "Comprehensive Synthetic Route to Eight Diastereomeric Podophyllum Lignans", The Journal of Organic Chemistry, vol. 54, No. 18, 1 Sep. 1989, pp. 4280-4290.
Gordaliza et al., "Antineoplastic and antiviral activities of podophyllotoxin related lignans", Chemical Abstracts, vol. 120, No. 19, Abstract No. 120: 235425c. (May 9, 1994).
Gordaliza et al., "Antineoplastic and Antiviral Activities of Podophyllotoxin Related Lignans,", Arch Pharm., vol. 327, No. 3, 1994, pp. 175-179.
Terada et al., "Antitumor Agents. I. DNA Topoisomerase II Inhibitory Activity and the Structure Relationship of Podophyllotoxin Derivatives as Antitumor Agents", Chemical & Pharmaceutical Bulletin, vol. 40, No. 10, Oct. 1992, pp. 2720-2727.
Thurston et al., "Antitumor Agents. 100. Inhibition of Human DNA Topoisomerase II by Cytotoxic Ether and Ester Derivatives of Podophyllotoxin and .alpha.-Peltatin", Journal of Medical Chemistry, vol. 32, No. 3, Mar. 1986, pp. 604-608.

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

Immunosuppressive cyclolignan derivatives does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Immunosuppressive cyclolignan derivatives, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Immunosuppressive cyclolignan derivatives will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-634635

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