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Anticandidal activity

Hufford, C. D., Liu, S., Clark, A. M. and Oguntimein, B. O. 1987. Anticandidal activity of eupolauridine and onychine, alkaloids from Cleistopholispatens. Journal of Natural Products, 50 961-964. [Pg.263]

Fig. 1. Anticandidal activity of IV-benzyl aminocyclic urea PS-SCL. Each graph represents the activity of a sublibrary, and each bar within a graph represents the percent inhibition of the growth of C. albicans ATCC 10231 by a separate mixture. The line represents the average activity for all of the mixtures making up the corresponding sublibrary. Fig. 1. Anticandidal activity of IV-benzyl aminocyclic urea PS-SCL. Each graph represents the activity of a sublibrary, and each bar within a graph represents the percent inhibition of the growth of C. albicans ATCC 10231 by a separate mixture. The line represents the average activity for all of the mixtures making up the corresponding sublibrary.
Anticandidal Activity of Most Active A-benzyl Aminocyclic Urea Mixtures... [Pg.330]

Cassone A, De Bemardis F, Torosantucci A, Tacconelli E, Tumbarello M, Cauda R In vitro and in vivo anticandidal activity of human immunodeficiency vims protease inhibitors. J. Infect Dis 1999 180 448 53. [Pg.127]

Kingsbury, W. D., Boehm, J. C., Mehta, R. J., Grappel, S. R Transport of antimicrobial agents using peptide carrier systems anticandidal activity of m-fluorophenylalanine peptide conjugates. J. Med. Chem. 1983,26,1725-1729. [Pg.744]

Cyathocaline exhibited moderate but selective activity in our yeast bioassay and also in a cytotoxicity assay against the A-549 human lung carcinoma cell line (Table 11). Three azafluorenone alkaloids have previously been tested for ( otoxic activity and were found to be inactive [53] but one has been reported to have anticandidal activity [54]. [Pg.485]

Substitution at position 4 will reduce the anticandidal activity, while some 4-substituted analogs retain activity against C. neoformans. [Pg.8]

Hufford CD, Liu S, Clark AM, Oguntimein BO. Anticandidal activity of eupolaur-idine and onychine, alkaloids from Cleistopholis patens. J Nat Prod 1987 50 961-4. [Pg.246]

In an effort to develop highly potent antifungal agents, Chauhan et al. [29] have reported potent antifungal rhodanine analogs. Some derivatives XXI, XXII, and XXIII were found to be very effective (MIC=0.78 pg/mL) against C. albicans MTCC183. The potent compoimds were further tested for in vitro anticandidal activity and amphotericin B-resistant strain of C. albicans. [Pg.54]

S. Sheikh, R.A. Sheikh, R. Bhatia, A.A. Hashmi, N. Manzoor, L.A. Khan, Anticandidal activity of ciimamaldehyde, its ligand and Ni (II) complex Effect of increase in ring and side chain, Microb. Pathogenesis 49 75-82, 2010. [Pg.350]


See other pages where Anticandidal activity is mentioned: [Pg.202]    [Pg.466]    [Pg.49]    [Pg.327]    [Pg.231]    [Pg.758]    [Pg.137]    [Pg.215]    [Pg.346]   
See also in sourсe #XX -- [ Pg.20 , Pg.485 ]

See also in sourсe #XX -- [ Pg.20 , Pg.485 ]




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Onychine anticandidal activity

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