fungal metabolite |
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CHEBI:76946 |
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Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds. |
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![](images/goldenstar.gif) ![](images/goldenstar.gif)
This entity has been manually annotated by the ChEBI Team.
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CHEBI:75765, CHEBI:76947
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Members of
fungal metabolite Class |
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F-9775A
Mass :394.37410
Formula :
C22H18O7
F-9775B
Mass :394.37410
Formula :
C22H18O7
ilicicolin
Definition :
Any member of the class of antibiotic polyketides originally isolated from the fungus Cylindrocladium ilicicola, isolated from the dead leaf of beach (Fagus sp.).
YW3548
Mass :574.78840
Formula :
C34H54O7
psilocin
Mass :204.26820
Formula :
C12H16N2O
cladoniamide
Definition :
A family of tryptophan-derived alkaloids produced in culture by Streptomyces uncialis, a lichen-associated actinomycete strain.
hispidin
Mass :246.218
Formula :
C13H10O5
D-iditol
Mass :182.17176
Formula :
C6H14O6
eburicol
Mass :440.745
Formula :
C31H52O
(1S,2R,3R,6S,7R,8S,11S,14S,15S,18R)-18-hydroxy-5,6,15-trimethyl-8-(2-methylpropyl)-19-oxa-9-azapentacyclo[13.3.1.02,14.03,11.07,11]nonadec-4-ene-10,12-dione
Mass :401.547
epichlicin
Mass :1043.17320
Formula :
C48H74N12O14
1,8-dihydroxynaphthalene-melanin
Definition :
A melanin pigment produced by certain fungi. It plays important roles in UV protection, oxidative stress and pathogenesis. In Aspergillus fumigatus, it is used as a virulence factor and plays an important role in the survival of the fungus during unfavorable conditions both in vivo and in vitro, and protects it from the host immune system. The pigment is generally synthesised from the pentaketide pathway in which 1,8-dihydroxynaphthalene is the immediate precursor which is polymerized to 1,8-dihydroxynaphthalene-melanin by a laccase enzyme.
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CHEBI:182065 (1S,2R,3R,6S,7R,8S,11S,14S,15S,18R)-18-hydroxy-5,6,15-trimethyl-8-(2-methylpropyl)-19-oxa-9-azapentacyclo[13.3.1.02,14.03,11.07,11]nonadec-4-ene-10,12-dione
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![](/chebi/images/ontology/checked/is_a.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3)
is a
![](/chebi/images/ontology/checked/has_part.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3)
has part
![](/chebi/images/ontology/checked/is_conjugate_base_of.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3)
is conjugate base of
![](/chebi/images/ontology/checked/is_conjugate_acid_of.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3)
is conjugate acid of
![](/chebi/images/ontology/checked/is_tautomer_of.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3)
is tautomer of
![](/chebi/images/ontology/checked/is_enantiomer_of.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3)
is enantiomer of
![](/chebi/images/ontology/checked/has_functional_parent.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3)
has functional parent
![](/chebi/images/ontology/checked/has_parent_hydride.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3)
has parent hydride
![](/chebi/images/ontology/checked/is_substituent_group_from.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3)
is substituent group from
![](/chebi/images/ontology/checked/has_role.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3)
has role
![](/chebi/images/checked_status.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3) Checked
![](/chebi/images/unchecked_status.gif;jsessionid=37C548E5912C8107EBC234022CDA56A3) Unchecked
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