The grant is designed to cover new secondary metabolites from higher plants which have novel chemical structures and which have potential for clinical use as antibiotics in the treatment of infections caused by microorganisms against which current fermentation-derived antibiotics are unsatisfactory in some significant way. Central to this effort is the use of rational modern testing methods and the proven presence amongst higher plant extracts of structurally and therapeutically novel agents. Once confirmed to be active, the most potent plant extracts are fractionated guided by bioassay techniques in order to isolate the active constituents in pure form. These products are then evaluated for their antimicrobial spectrum and comparative potency in vitro in comparison with established antibiotics. In vivo evaluation in infected mice is carried out on the most potent agents. The new agents uncovered are often present in small amount so synthesis often has to be explored in order to confirm the structures, prepare enough for significant evaluation and to prepare analogues to explore the relationship between structure and activity. The latter is necessary because there are usually no precedent structures in the antibiotic literature to guide us and because of our desire to improve the medicinal potential of substances whose intrinsic activity is too weak for clinical use by themselves. The diseases under attack by these methods include tuberculosis, infections due to Gram-negative bacteria, venereal diseases, infections by organisms resistant to known antibiotics and fungal diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI013155-11
Application #
3125404
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Project Start
1976-09-01
Project End
1986-08-31
Budget Start
1985-09-01
Budget End
1986-08-31
Support Year
11
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Kansas Lawrence
Department
Type
Schools of Pharmacy
DUNS #
072933393
City
Lawrence
State
KS
Country
United States
Zip Code
66045
Mitscher, L A; Baker, W (1998) Tuberculosis: a search for novel therapy starting with natural products. Med Res Rev 18:363-74
Mitscher, L A; Jung, M; Shankel, D et al. (1997) Chemoprotection: a review of the potential therapeutic antioxidant properties of green tea (Camellia sinensis) and certain of its constituents. Med Res Rev 17:327-65
Gollapudi, S R; Telikepalli, H; Jampani, H B et al. (1994) Alectosarmentin, a new antimicrobial dibenzofuranoid lactol from the lichen, Alectoria sarmentosa. J Nat Prod 57:934-8
Devasthale, P V; Mitscher, L A; Telikepalli, H et al. (1992) Dactylocyclines, novel tetracycline derivatives produced by a Dactylosporangium sp. III. Absolute stereochemistry of the dactylocyclines. J Antibiot (Tokyo) 45:1907-13
Mitscher, L A; Drake, S; Gollapudi, S R et al. (1987) A modern look at folkloric use of anti-infective agents. J Nat Prod 50:1025-40
Mitscher, L A (1987) Chemistry of newer antibiotics directed toward overcoming bacterial resistance. Bull N Y Acad Med 63:269-94
Boger, D L; Yasuda, M; Mitscher, L A et al. (1987) Streptonigrin and lavendamycin partial structures. Probes for the minimum, potent pharmacophore of streptonigrin, lavendamycin, and synthetic quinoline-5,8-diones. J Med Chem 30:1918-28
Mitscher, L A; Drake, S; Gollapudi, S R et al. (1986) Isolation and identification of higher plant agents active in antimutagenic assay systems: Glycyrrhiza glabra. Basic Life Sci 39:153-65
Boger, D L; Mitscher, L A; Mullican, M D et al. (1985) Antimicrobial and cytotoxic properties of 9,10-dihydrophenanthrenes: structure-activity studies on juncusol. J Med Chem 28:1543-7