Use of substituted chromans, some of which are known, as medicam

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

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Details

514320, 546196, 546199, A61K 31445, C07D40514

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active

054929180

ABSTRACT:
The present invention relates to the use of substituted chromans of the general formula (I) ##STR1## in which the substituents have the meaning indicated in the description, for the production of medicaments, in particular as HIV protease-inhibiting agents, new active compounds and processes for their preparation.

REFERENCES:
patent: 4957928 (1990-09-01), Frostl
patent: 4977166 (1990-12-01), Hardy
patent: 4997836 (1991-03-01), Sugihara
patent: 5030639 (1991-07-01), Davis
patent: 5240943 (1993-08-01), Desai
patent: 5371094 (1994-12-01), Heine
Journal of Medicinal Chemistry, vol. 34, No. 8, Aug. 1991; Perspective, "HIV Protease: A Novel Chemotherapeutic Target for AIDS", J. R. Huff, pp. 2306-2314.
Bioorganic & Medicinal Chemistry Letters, vol. 2, No. 6, pp. 541-546, 1992; "The Use of HIV-1 Protease Structure in Inhibitor Design", R. E. Babine et al.
J. Med. Chem., 1992, vol. 35, pp. 2525-2533; "A Series of Potent HIV-1 Protease Inhibitors Containing a Hydroxyethyl Secondary . . . ", T. J. Tucker et al.
The EMBO Journal, vol. 7, No. 6, pp. 1785-1791, 1988; "Partial purification and substrate analysis of bacterially-express HIV . . . ", J. Hansen et al.
Journal of Virological Methods, vol. 22, 1988, pates 309-317; "Antibodies to Human Cytomegalovirus Structural Polypeptides . . . ", M. P. Landini et al.

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