Page last updated: 2024-08-05 14:53:00

fungal xenobiotic metabolite

Any fungal metabolite produced by metabolism of a xenobiotic compound in fungi.

ChEBI ID: 76968

Members (9)

MemberDefinitionClass
1-hydroxy-2-naphthoic acidA naphthoic acid with the carboxy group at position 2 and carrying a hydroxy substituent at the 1-position. It is a xenobiotic metabolite produced by the biodegradation of phenanthrene by microorganisms.1-hydroxy-2-naphthoic acid
1-naphthoic acidA naphthoic acid carrying a carboxy group at position 1.1-naphthoic acid
2-amino-4,6-dinitrotolueneAn amino-nitrotoluene that is 4,6-dinitrotoluene substituted at position 2 by an amino group.2-amino-4,6-dinitrotoluene
4-amino-2,6-dinitrotolueneAn amino-nitrotoluene that is 2,6-dinitrotoluene substituted at position 4 by an amino group.4-amino-2,6-dinitrotoluene
4-ethylphenolA member of the class of phenols carrying an ethyl substituent at position 4.4-ethylphenol
4',7-dihydroxyflavanoneA dihydroxyflavanone in which the two hydroxy substituents are located at positions 4' and 7.4',7-dihydroxyflavanone
6-hydroxyflavanoneA monohydroxyflavanone that is flavanone substituted by a hydroxy group at position 6.6-hydroxyflavanone
9-fluorenoneThe simplest member of the class fluoren-9-ones that is 9H-fluorene bearing an oxo substituent at position 9.fluoren-9-one
melilotic acidA monocarboxylic acid that is propionic acid in which one of the hydrogens at position 3 is substituted by a 2-hydroxyphenyl group.3-(2-hydroxyphenyl)propanoic acid

Research

Studies (379)

TimeframeStudies, Drugs with This Role(%)All Drugs %
pre-199035 (9.23)18.7374
1990's31 (8.18)18.2507
2000's128 (33.77)29.6817
2010's161 (42.48)24.3611
2020's24 (6.33)2.80

Study Types

Publication TypeStudies, Drugs with this Role (%)All Drugs (%)
Trials2 (0.47%)5.53%
Reviews7 (1.65%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other414 (97.87%)84.16%

Protein Targets (19)

Potency Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
67.9K proteinVaccinia virusPotency0.501211
activating transcription factor 6Homo sapiens (human)Potency55.607111
AR proteinHomo sapiens (human)Potency55.926422
LuciferasePhotinus pyralis (common eastern firefly)Potency72.953111
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency28.029622
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency55.821733

Inhibition Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
Androgen receptorHomo sapiens (human)IC503.300011
Androgen receptorRattus norvegicus (Norway rat)IC5018.620911
Heat shock protein HSP 90-alphaHomo sapiens (human)IC501.000011
Indoleamine 2,3-dioxygenase 1Homo sapiens (human)IC50200.000011
L-lactate dehydrogenase A chainHomo sapiens (human)IC50500.000022
L-lactate dehydrogenase A chainRattus norvegicus (Norway rat)IC50500.000011
L-lactate dehydrogenase B chainHomo sapiens (human)IC50500.000011
NeuraminidaseInfluenza A virus (A/Wilson-Smith/1933(H1N1))IC50100.000011
Neuraminidase Influenza A virus (A/Wilson-Smith/1933(H1N1))IC501,000.000011
Tyrosine-protein phosphatase non-receptor type 1Homo sapiens (human)IC50850.000011

Activation Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
Chain A, TrichosurinTrichosurus vulpecula (common brushtail)Kd30.000011
glycogen synthase kinase-3 beta isoform 1Homo sapiens (human)EC50300.000011
L-lactate dehydrogenase A chainHomo sapiens (human)Kd640.000022
L-lactate dehydrogenase A chainRattus norvegicus (Norway rat)Kd640.000011

Other Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
Sulfotransferase 1A1 Rattus norvegicus (Norway rat)Km10.000011