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Inhibition of wild type Candida albicans MY1055 1,3-beta-D-glucan synthase using UDP[6,3H]-glucose as substrate after 60 mins by liquid scintillation counting analysis
Assay data:2 Active, 1 Activity ≤ 1 nM, 2 Activity ≤ 1 µM, 2 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition Assay from Article 10.1016/S1074-5521(02)00240-5: "Crystal structures of Candida albicans N-myristoyltransferase with two distinct inhibitors."
Assay data:6 Active, 1 Activity ≤ 1 nM, 5 Activity ≤ 1 µM, 6 Tested
Inhibition of Candida albicans chitin synthase 1 expressed in Saccharomyces cerevisiae RRA400-1U cells using [3H]UDP-GlcNAc as substrate by scintillation counting method
Antimicrobial activity against Candida albicans ATCC 90028 assessed as inhibition of microbial growth by CLSI based method
Assay data:2 Active, 2 Activity ≤ 1 nM, 8 Activity ≤ 1 µM, 8 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed Citation
Inhibition of Candida albicans ATCC 90028 NMT using GLTISKLFRR-NH2 as substrate assessed as reduction in [3H]-myristoylated peptide reaction product formation preincubated with substrate for 10 mins followed by enzyme addition measured after 10 mins by HPLC analysis
Antifungal activity against Candida albicans HLY4123 after 16 hrs in presence of 0.25 ug/ml of fluconazole by ten fold serial dilution method
Assay data:11 Active, 2 Activity ≤ 1 nM, 11 Activity ≤ 1 µM, 14 Tested
Competitive inhibition of Candida albicans DHFR preincubated for 2 mins followed by substrate addition in presence of dihydrofolate
Assay data:1 Active, 1 Activity ≤ 1 nM, 1 Activity ≤ 1 µM, 1 Tested
Inhibition of candida albicans beta-(1,3)-glucan synthase assessed as decrease in transfer of radiolabelled glucose from UDP-[3H]-glucose onto acceptor
Assay data:4 Active, 1 Activity ≤ 1 nM, 3 Activity ≤ 1 µM, 4 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µM
Time dependent inhibition of Candida albicans ATCC 38247 membrane inositol phosphorylceramide synthase using ceramide as substrate
Inhibition of candida N-myristoyltransferase
Assay data:25 Active, 1 Activity ≤ 1 nM, 15 Activity ≤ 1 µM, 28 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMRelated BioAssays by Target
Inhibition of Candida albicans inositol phosphorylceramide synthase
Assay data:2 Active, 2 Activity ≤ 1 nM, 2 Activity ≤ 1 µM, 2 Tested
Inhibition of Candida albicans ATCC 38247 inositol phosphorylceramide synthase preincubated for 30 mins
Assay data:4 Active, 2 Activity ≤ 1 nM, 3 Activity ≤ 1 µM, 6 Tested
Inhibition of Candida albicans OSC
Inhibition of Candida albicans N-myristoyltransferse
Assay data:33 Active, 2 Activity ≤ 1 nM, 32 Activity ≤ 1 µM, 47 Tested
Compound was tested for inhibition of purified Oxidosqualene-lanosterol cyclase from Candida albicans
In vitro inhibitory activity against candida albicans Nmt (CaNmt) using substrate peptide GLTISKLFR-R-NH2 (0.5 uM) and myristoyl-CoA (0.5 uM)
In vitro inhibitory activity against Candida albicans Nmt (CaNmt) using substrate peptide GLTISKLFR-R-NH2 (0.5 uM) and myristoyl-CoA (0.5 uM)
Assay data:9 Active, 3 Activity ≤ 1 nM, 8 Activity ≤ 1 µM, 9 Tested
Inhibitory activity against cell free dihydrofolate reductase (DHFR) from Mycobacterium lufu
Assay data:35 Active, 1 Activity ≤ 1 nM, 15 Activity ≤ 1 µM, 43 Tested
Inhibitory activity against cell free dihydrofolate reductase (DHFR) from Escherichia coli
Assay data:40 Active, 1 Activity ≤ 1 nM, 24 Activity ≤ 1 µM, 43 Tested
Inhibition of Dihydrofolate reductase enzyme from Candida albicans
Assay data:23 Active, 17 Activity ≤ 1 nM, 23 Activity ≤ 1 µM, 23 Tested
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