ANTIBACTERIAL ACTIVITY;
ANTIFUNGAL ACTIVITY;
ARTICLE;
CANDIDA ALBICANS;
CHEMICAL MODIFICATION;
CONTROLLED STUDY;
DISK DIFFUSION;
DRUG POTENCY;
DRUG PROTEIN BINDING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME ACTIVE SITE;
ENZYME CONFORMATION;
ESCHERICHIA COLI;
IN VITRO STUDY;
LIPOPHILICITY;
MICROMYCETE;
MOLECULAR DOCKING;
MOLECULAR MODEL;
MOLECULAR RECOGNITION;
NONHUMAN;
STAPHYLOCOCCUS AUREUS;
Synthesis and antibiotic activity of a small molecules library of 1,2,3-triazole derivatives
Aufort, M., Herscovici, J., Bouhours, P., Moreau, N. and Girard, C. (2008). Synthesis and antibiotic activity of a small molecules library of 1,2,3-triazole derivatives. Bioorg. Med. Chem. Lett. 18: 1195-1198.
Antibacterial and antifugal mono- and di-substituted symmetrical and unsymmetrical triazine-derived Schiff-bases and their transition metal complexes
Chohan, Z.H., Pervez, H., Rauf, A., Khan, K.M., Maharvi, G.M. and Supuran, C.T. (2004). Antibacterial and antifugal mono- and di-substituted symmetrical and unsymmetrical triazine-derived Schiff-bases and their transition metal complexes. J. Enzyme Inhib. Med. Chem. 19: 161-168.
Safety of a weekly high dose of liposomal amphotericin B for prophylaxis of invasive fungal infection in immunocompromised patients: Prophysome Study
Cordonnier, C., Mohty, M., Faucher, C., Pautas, C., Robin, M. Vey, N., Monchecourt, F., Mahi, L. and Ribaud, P. (2008). Safety of a weekly high dose of liposomal amphotericin B for prophylaxis of invasive fungal infection in immunocompromised patients: Prophysome Study. Int. J. Antimicrob. Agents 31: 135-141.
Synthesis and SAR studies of biaryloxy-substituted triazoles as antifungal agents
Liu, P., Zhu, S., Li, P., Xie, W., Jin, Y., Sun, Q., Wu, Q., Sun, P., Zhang, Y., Yang, X., Jiang, Y. and Zhang, D. (2008). Synthesis and SAR studies of biaryloxy-substituted triazoles as antifungal agents. Bioorg. Med. Chem. Lett. 18: 3261-3265.
Discovery of uracil-based histone deacetylase inhibitors able to reduce acquired antifungal resistance and trailing growth in Candida albicans
Liu, Z., Yang, G. and Qing, X. (2001). Discovery of uracil-based histone deacetylase inhibitors able to reduce acquired antifungal resistance and trailing growth in Candida albicans. J. Chem. Technol. Biotechnol. 76: 1154-1158.
Discovery of uracil-based histone deacetylase inhibitors able to reduce acquired antifungal resistance and trailing growth in Candida albicans
Mai, A., Rotili, D., Massa, S., Brosch, G., Simonetti, G., Passariello, C. and Palamarai, A.T. (2007). Discovery of uracil-based histone deacetylase inhibitors able to reduce acquired antifungal resistance and trailing growth in Candida albicans. Bioorg. Med. Chem. Lett. 17: 1221-1225.
Improved outcomes associated with advances in therapy for invasive fungal infections in immunocompromised hosts
Metcalf, S.C. and Dockrell, D.H. (2007). Improved outcomes associated with advances in therapy for invasive fungal infections in immunocompromised hosts. J. Infect. 55: 287-299.
Crystal structure of cytochrome P450 14 -sterol demethylase (CYP51) from Mycobacterium tuberculosis in complex with azole inhibitors
Podust, L., Poulos, T.L. and Waterman, M.R. (2001). Crystal structure of cytochrome P450 14 -sterol demethylase (CYP51) from Mycobacterium tuberculosis in complex with azole inhibitors. Proc. Natl. Acad. Sci. USA. 98: 3068-3073.
Multiple patterns of resistance to fluconazole in Candida glabrata isolates from a patient with oropharyngeal candidiasis receiving head and neck radiation
Redding, S.W., Kirkpatrick, W.R., Saville, S., Coco, B.J., White, W., Fothergill, A., Rinaldi, M., Eng, T., Patterson, T.F. and Lopez- Ribot, J. (2003). Multiple patterns of resistance to fluconazole in Candida glabrata isolates from a patient with oropharyngeal candidiasis receiving head and neck radiation. J. Clin. Microbiol. 41: 619-622.
Use of prophylactic antifungals in the immunocompromised host
Ship, J.A., Vissink, A. and Challacombe, S.J. (2007). Use of prophylactic antifungals in the immunocompromised host. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 103: 1-14.
Synthesis, determination of the lipophilicity, anticancer and antimicrobial properties of some fused 1,2,4-triazole derivatives
Sztanke, K., Tuzimski, T., Rzymowska, J., Pasternak, K. and Kandefer-Szersze ZM. (2008). Synthesis, determination of the lipophilicity, anticancer and antimicrobial properties of some fused 1,2,4-triazole derivatives. Eur. J. Med. Chem. 43: 404-419.
In vitro antifungal activity of KP-103, a novel triazole derivative, and its therapeutic efficacy against experimental plantar tinea pedis and cutaneous candidiasis in guinea pigs
Tatsumi, Y., Yokoo, M., Arika, T. and Yamaguchi, H. (2001). In vitro antifungal activity of KP-103, a novel triazole derivative, and its therapeutic efficacy against experimental plantar tinea pedis and cutaneous candidiasis in guinea pigs. Antimicrob. Agents Chemother. 45: 1493-1499.
Novel effect of voriconazole on conidiation of Aspergillus species
Varanasi, N.L., Baskaran, I., Alangaden, G.J., Chandrasekar, P.H. and Manavathu, E.K. (2004). Novel effect of voriconazole on conidiation of Aspergillus species. Int. J. Antimicrob. Agents 23: 72-79.
Selective sensitivity to carboxyamidotriazole by human tumor cell lines with DNA mismatch repair deficiency
Yang, J.L., Qu, X.J., Yu, Y., Kohn, E.C. and Friedlander, M.L. (2008). Selective sensitivity to carboxyamidotriazole by human tumor cell lines with DNA mismatch repair deficiency. Int. J. Cancer 123: 258-63